Posts belonging to Category 'Asthma And Bronchitis'

Advice Please: Sinus/Lung Infections

Question:

- Hide quoted text — Show quoted text -Search…@mail.con2.com wrote:

Don Brady wrote: On Fri, 14 Jan 2005 03:32:40 GMT, "Steven L." <sdlit…@earthlinkNOSPAM.net wrote: People say that mainly if the problem is so undefined that it is difficult to know what the cause is, or if a lot of risk would arise with a wrong choice. If it’s asthma, then a LOT of risk can result with a wrong choice. Asthma can be fatal if left untreated. Sorry, Don, but undiagnosed shortness of breath is not something I would ever suggest self-treatment for. That’s what I was telling him Steven….. I seem to be failing to get the point across that I don’t have much in the way of options. Thanks to an unfortunate event, things have gotten worse for me. I slipped while walking down wet stairs outside my apartment. My hand was on the rail and I was only a couple of steps from the bottom, but I went down and in the process pulled something deep in my left side, toward the rear. As a result sleeping last night was intermittant, because I now cannot cough without excruciating pain, and almost blacked out when I tried to clear my throat this morning. Basically I’m walking the line in between choking and dealing with pain that feels like I’m being stabbed with a knife in the side. So I’m going through hell fighting the urge to cough, but it’s only a matter of time before I do. I can’t even blow my nose, because it creates internal pressure, like coughing. Like going to the doctor, I can’t afford to take off time from work, so now I desperately need to find a solution.

Reconsider your priorities.  You’re getting sicker and that’s making it harder and harder for you to work.  What happens if your condition deteriorates to the point that you cannot work no matter how hard you try? Good health is an investment. — Steven D. Litvintchouk Email:  sdlit…@earthlinkNOSPAM.net Remove the NOSPAM before replying to me.

Response:

On 14 Jan 2005 03:55:54 -0800, Search…@mail.con2.com wrote: – Hide quoted text — Show quoted text -

I seem to be failing to get the point across that I don’t have much in the way of options. Thanks to an unfortunate event, things have gotten worse for me. I slipped while walking down wet stairs outside my apartment. My hand was on the rail and I was only a couple of steps from the bottom, but I went down and in the process pulled something deep in my left side, toward the rear. As a result sleeping last night was intermittant, because I now cannot cough without excruciating pain, and almost blacked out when I tried to clear my throat this morning. Basically I’m walking the line in between choking and dealing with pain that feels like I’m being stabbed with a knife in the side. So I’m going through hell fighting the urge to cough, but it’s only a matter of time before I do. I can’t even blow my nose, because it creates internal pressure, like coughing. Like going to the doctor, I can’t afford to take off time from work, so now I desperately need to find a solution.

How about the emergency room option?

Response:

ENTconsult wrote:

A radioactive particle or a tagged bacteria from the sinus will apear

in the

trachea in 16 hours. Murray Grossan, M.D. http://www.ent-consult.com

I just received your book in the mail.(I won it on Ebay). I definitely have some form of sinusitis, though not as bad as other people here. Nevertheless, the reason I’m sure it has affected my lungs is because I don’t believe that anyone can get asthma, bronchitis wihthin a 24 hour period. And the shortness of breath(which is never triggered by anything other than physical exersion), Outside of that, since this problem occur, I have a tnedancy to mis-swallow, which I belive is caused by restricted passages. This condition has not gotten any better or worse since it first occured 1-1/2 years ago. Anyway, I’ll be reading your book, for some ideas.(I also recently received your irrigator tips). Thanks. Darren Harris Staten Island, New York.

Response:

Darren’s right. I can’t afford to go to a doctor either. I might try the county health dept. (they suck, but they’re better than nothing). Darren there are free clinics in NYC somewhere. Try looking for one of these. They’ll help you out, probably on a sliding scale (which means you pay what you can afford). — Remove nospam to email <Search…@mail.con2.com

wrote in message

news:1105658218.477376.262980@z14g2000cwz.googlegroups.com… – Hide quoted text — Show quoted text -

Again. I’m saying that if I could afford to get tests done, then I would. I’ve come to no conclusions as to the reason for my problems. The most difficult thing about trying to get ideas from this newsgroup is getting around the "go to your doctor" statements. This is not always an plausible or immediate option.(If so, this newsgroup would have no purpose). Thanks. Darren Harris Staten Island, New York.

Response:

Darren, go to an emergency room or call them and tell them that you’re basically indigent, this will make a diff w/the bill. — Remove nospam to email <Search…@mail.con2.com

wrote in message

news:1105703754.577944.148880@z14g2000cwz.googlegroups.com… – Hide quoted text — Show quoted text -

Don Brady wrote: On Fri, 14 Jan 2005 03:32:40 GMT, "Steven L." <sdlit…@earthlinkNOSPAM.net wrote: People say that mainly if the problem is so undefined that it is difficult to know what the cause is, or if a lot of risk would arise with a wrong choice. If it’s asthma, then a LOT of risk can result with a wrong choice. Asthma can be fatal if left untreated. Sorry, Don, but undiagnosed shortness of breath is not something I would ever suggest self-treatment for. That’s what I was telling him Steven….. I seem to be failing to get the point across that I don’t have much in the way of options. Thanks to an unfortunate event, things have gotten worse for me. I slipped while walking down wet stairs outside my apartment. My hand was on the rail and I was only a couple of steps from the bottom, but I went down and in the process pulled something deep in my left side, toward the rear. As a result sleeping last night was intermittant, because I now cannot cough without excruciating pain, and almost blacked out when I tried to clear my throat this morning. Basically I’m walking the line in between choking and dealing with pain that feels like I’m being stabbed with a knife in the side. So I’m going through hell fighting the urge to cough, but it’s only a matter of time before I do. I can’t even blow my nose, because it creates internal pressure, like coughing. Like going to the doctor, I can’t afford to take off time from work, so now I desperately need to find a solution. Darren Harris Staten Island, New York.

Response:

The original poster does deserve credit for his frankness.  Things could go a little badly for any of us and we could be out of cash. Does anyone know of any free or low-cost otolaryngology clinics in New York CIty?

Response:

A radioactive particle or a tagged bacteria from the sinus will apear in the trachea in 16 hours. Murray Grossan, M.D. http://www.ent-consult.com

Response:

On Fri, 14 Jan 2005 03:32:40 GMT, "Steven L." <sdlit…@earthlinkNOSPAM.net

wrote:

People say that mainly if the problem is so undefined that it is difficult to know what the cause is, or if a lot of risk would arise with a wrong choice. If it’s asthma, then a LOT of risk can result with a wrong choice. Asthma can be fatal if left untreated. Sorry, Don, but undiagnosed shortness of breath is not something I would ever suggest self-treatment for.

That’s what I was telling him Steven…..

Response:

Don Brady wrote:

On Fri, 14 Jan 2005 03:32:40 GMT, "Steven L."

<sdlit…@earthlinkNOSPAM.net

– Hide quoted text — Show quoted text -

wrote: People say that mainly if the problem is so undefined that it is

difficult to

know what the cause is, or if a lot of risk would arise with a

wrong choice.

If it’s asthma, then a LOT of risk can result with a wrong choice. Asthma can be fatal if left untreated. Sorry, Don, but undiagnosed shortness of breath is not something I would ever suggest self-treatment for. That’s what I was telling him Steven…..

I seem to be failing to get the point across that I don’t have much in the way of options. Thanks to an unfortunate event, things have gotten worse for me. I slipped while walking down wet stairs outside my apartment. My hand was on the rail and I was only a couple of steps from the bottom, but I went down and in the process pulled something deep in my left side, toward the rear. As a result sleeping last night was intermittant, because I now cannot cough without excruciating pain, and almost blacked out when I tried to clear my throat this morning. Basically I’m walking the line in between choking and dealing with pain that feels like I’m being stabbed with a knife in the side. So I’m going through hell fighting the urge to cough, but it’s only a matter of time before I do. I can’t even blow my nose, because it creates internal pressure, like coughing. Like going to the doctor, I can’t afford to take off time from work, so now I desperately need to find a solution. Darren Harris Staten Island, New York.

Response:

Don Brady wrote:

On 13 Jan 2005 15:16:58 -0800, Search…@mail.con2.com wrote: Again. I’m saying that if I could afford to get tests done, then I would. I’ve come to no conclusions as to the reason for my problems. The most difficult thing about trying to get ideas from this newsgroup is getting around the "go to your doctor" statements. People say that mainly if the problem is so undefined that it is difficult to know what the cause is, or if a lot of risk would arise with a wrong choice.

If it’s asthma, then a LOT of risk can result with a wrong choice. Asthma can be fatal if left untreated. Sorry, Don, but undiagnosed shortness of breath is not something I would ever suggest self-treatment for. There are certain symptoms that I immediately say "Get thee to a doctor."  Undiagnosed shortness of breath, undiagnosed chest pains, chronic bleeding, etc.

This is not always an plausible or immediate option.(If so, this newsgroup would have no purpose). Actually many of us here have full access to formal medical advise on an insured basis but still learn a lot from the group.    

— Steven D. Litvintchouk Email:  sdlit…@earthlinkNOSPAM.net Remove the NOSPAM before replying to me.

Response:

- Hide quoted text — Show quoted text -Search…@mail.con2.com wrote:

Don Brady wrote: On 13 Jan 2005 14:45:04 -0800, Search…@mail.con2.com wrote: Well, I never stated any origins or causes. You said in part: "In September of 2002, I fell asleep with the window open on a night the temperature dropped sharply. It resulted in me catching a cold which I quickly got over, except for a cough that just would not go away. When it finally began to subside somewhat, I noticed that if I tried to jog for 5 minutes, 20 minutes afterwards I’d experience a bout of coughing that would last for about 5 minutes. But that began to get better also.(Though not completely). The big problem began during on my daily walk to work. I have to walk up a hill, and on this particular day I was winded by the time I reached the top, when I wasn’t winded the previous day I walked up that same hill. In other words, this shortness of breath did not happen progressively, but over the course of a 24 hour period, and I’ve had this problem ever since. Now I get winded whenever I do anything that requires even a little physical exertion." It seemed to me that   ou were saying it strted right there. I was saying that while that might have triggered the first shortness of breath,  the shortness of breath could be due to a completely different cause, such as heart disease.  You do not know until you get the tests done. I’m just trying to get ideas from anyone else who may have had simular symptoms, and possibly treatment options. You should not treat symtoms until you get a firm diagnosis. Again. I’m saying that if I could afford to get tests done, then I would. I’ve come to no conclusions as to the reason for my problems. The most difficult thing about trying to get ideas from this newsgroup is getting around the "go to your doctor" statements. This is not always an plausible or immediate option.(If so, this newsgroup would have no purpose).

Let me put my $0.02 in again here. When I had really bad sinus infections, the infected post nasal drip would get down into my bronchial tubes, causing repeated bouts of bronchitis.  And occasionally these would lead to wheezing and shortness of breath. You can try the wheezing test yourself.  Inhale as deeply as you can–then blow out all the air from your lungs thru your mouth as fully as you can.  If you hear a "whistle" sound that means you’re wheezing. Asthma and bronchitis are the obvious possibilities–either can be exacerbated by a stubborn sinus infection.  Sure it could be a heart problem but it would be quite a coincidence to have started up like that just after a bad cold. If it’s asthma, a bronchodilator inhaler may make you feel much better.   Sometimes they work for bronchitis too, particularly Atrovent.  These meds are available by prescription. If it’s a stubborn infection, either upper or lower respiratory or both, you need to be on antibiotics.  Sinus infections can be very stubborn; you need to be on antibiotics a minimum of a couple of weeks, and possibly much longer than that, in order to completely clear the infection. But at this point, we’re stuck.  We can’t diagnose you by remote control, and we can’t prescribe the types of medications that might help you. No matter what it is, you always need to find a doctor to write the prescriptions! — Steven D. Litvintchouk Email:  sdlit…@earthlinkNOSPAM.net Remove the NOSPAM before replying to me.

Response:

On 13 Jan 2005 15:16:58 -0800, Search…@mail.con2.com wrote:

Again. I’m saying that if I could afford to get tests done, then I would. I’ve come to no conclusions as to the reason for my problems. The most difficult thing about trying to get ideas from this newsgroup is getting around the "go to your doctor" statements.

People say that mainly if the problem is so undefined that it is difficult to know what the cause is, or if a lot of risk would arise with a wrong choice. But certainly you can try irrigation etc. to see if that helps.  It should. It is described at http://www.sinusitisfaq.org/   Getting enough rest is very important too in fighting any infection.   And making sure you are not eating an unusual diet that would be deficient in B viramins or protein etc.

This is not always an plausible or immediate option.(If so, this newsgroup would have no purpose).

Actually many of us here have full access to formal medical advise on an insured basis but still learn a lot from the group.    

Response:

- Hide quoted text — Show quoted text -Don Brady wrote:

On 13 Jan 2005 14:45:04 -0800, Search…@mail.con2.com wrote: Well, I never stated any origins or causes. You said in part: "In September of 2002, I fell asleep with the window open on a night

the

temperature dropped sharply. It resulted in me catching a cold which

I

quickly got over, except for a cough that just would not go away.

When

it finally began to subside somewhat, I noticed that if I tried to

jog

for 5 minutes, 20 minutes afterwards I’d experience a bout of

coughing

that would last for about 5 minutes. But that began to get better also.(Though not completely). The big problem began during on my daily walk to work. I have to walk up a hill, and on this particular day I was winded by the time I reached the top, when I wasn’t winded the previous day I walked up

that

same hill. In other words, this shortness of breath did not happen progressively, but over the course of a 24 hour period, and I’ve had this problem ever since. Now I get winded whenever I do anything that requires even a little physical exertion." It seemed to me that   ou were saying it strted right there. I was saying that while that might have triggered the first shortness

of

breath,  the shortness of breath could be due to a completely

different cause,

such as heart disease.  You do not know until you get the tests done. I’m just trying to get ideas from anyone else who may have had

simular

symptoms, and possibly treatment options. You should not treat symtoms until you get a firm diagnosis.

Again. I’m saying that if I could afford to get tests done, then I would. I’ve come to no conclusions as to the reason for my problems. The most difficult thing about trying to get ideas from this newsgroup is getting around the "go to your doctor" statements. This is not always an plausible or immediate option.(If so, this newsgroup would have no purpose). Thanks. Darren Harris Staten Island, New York.

Response:

On Thu, 13 Jan 2005 15:57:05 -0500, Don Brady <dbr…@pobox.com

wrote: I don;t think that any of these can be dealt with reasobaly

I meant to say – Hide quoted text — Show quoted text -

I don;t think that any of these can be dealt with reasobaly except with the help of medical specialists

Response:

Well that’s disasterous if your identification of the origin is

correct.   I

only say that because it is easy to fool oneself as to the cause of

things.

I have done it myself several times.   One is too close to one’s own

symptoms. Well, I never stated any origins or causes. I’m just trying to get ideas from anyone else who may have had simular symptoms, and possibly treatment options. Thanks. Darren Harris Staten Island, New York.

Response:

On 13 Jan 2005 14:45:04 -0800, Search…@mail.con2.com wrote:

Well, I never stated any origins or causes.

You said in part: "In September of 2002, I fell asleep with the window open on a night the temperature dropped sharply. It resulted in me catching a cold which I quickly got over, except for a cough that just would not go away. When it finally began to subside somewhat, I noticed that if I tried to jog for 5 minutes, 20 minutes afterwards I’d experience a bout of coughing that would last for about 5 minutes. But that began to get better also.(Though not completely). The big problem began during on my daily walk to work. I have to walk up a hill, and on this particular day I was winded by the time I reached the top, when I wasn’t winded the previous day I walked up that same hill. In other words, this shortness of breath did not happen progressively, but over the course of a 24 hour period, and I’ve had this problem ever since. Now I get winded whenever I do anything that requires even a little physical exertion." It seemed to me that   ou were saying it strted right there. I was saying that while that might have triggered the first shortness of breath,  the shortness of breath could be due to a completely different cause, such as heart disease.  You do not know until you get the tests done.

I’m just trying to get ideas from anyone else who may have had simular symptoms, and possibly treatment options.

You should not treat symtoms until you get a firm diagnosis.

Response:

On 13 Jan 2005 12:31:26 -0800, Search…@mail.con2.com wrote:

 Shorttness of breath suggests that asthma or other cause needs to be ruled out…… I wish it were that easy.

Actually there is a simple test for athma.  They measure your lung FEV with and without a drug.  If there is a significant difference, you may have astkma. Many ENT’s can give this test.   I have it it done twice (both negative).

When I went to the doctor last year, she spent 20 seconds looking into my lungs with what was basically a flashlight on the end of a tube, only to say she could see nothing wrong.

I do not  think that asthma would necessary be visible to an endoscope.

That by itself resulted in a bill for $315.00, so I can’t really afford to try the traditional route for diagnosis and treatment.

I think you really need to.   You need to get insurance.  Isn’t it guaranteed issue in New York? You probably have either asthma or other lung or heart ailment if you short of breath on exercise.  I don;t think that any of these can be dealt with reasobaly – Hide quoted text — Show quoted text -

Hence the reason I’m posting here. In September of 2002, I fell asleep with the window open on a night the temperature dropped sharply. It resulted in me catching a cold which I quickly got over, except for a cough that just would not go away. When it finally began to subside somewhat, I noticed that if I tried to jog for 5 minutes, 20 minutes afterwards I’d experience a bout of coughing that would last for about 5 minutes. But that began to get better also.(Though not completely). The big problem began during on my daily walk to work. I have to walk up a hill, and on this particular day I was winded by the time I reached the top, when I wasn’t winded the previous day I walked up that same hill. In other words, this shortness of breath did not happen progressively, but over the course of a 24 hour period, and I’ve had this problem ever since. Now I get winded whenever I do anything that requires even a little physical exertion. When I wake up in the morning I tend to have an ache in my windpipe, and phlegm production in my sinuses and lungs is a problem that has screwed up my digestion system, and makes the first half hour difficult after waking up. I can even pick up the scent of the "infection" when I breath. Unfortunately, I caught a cold last week, which exacerbated my problems(which briefly included spitting blood yesterday morning). As a result, I’m again dealing with bouts of dry coughing throughout the day. It sometimes keeps me up for an hour or so in the middle of the night. Outside of that, my symptoms don’t seem to be triggered by environmental factors.(ie: Temperature changes, dust, ect). Nevertheless, I sometimes cough so hard I get light headed. I used to play basketball for several hours just about every day. But ever since this breathing/coughing/sinus problem began, I’m forced to be sedentary and as a result I’ve gained 50 lbs.

Well that’s disasterous if your identification of the origin is correct.   I only say that because it is easy to fool oneself as to the cause of things. I have done it myself several times.   One is too close to one’s own symptoms. – Hide quoted text — Show quoted text -

Anyway, any ideas or recommendations would be greatly appreciated. Thanks a lot. Darren Harris Staten Island, New York.

Response:

Don Brady wrote:

On Wed, 12 Jan 2005 18:49:50 GMT, "Steven L."

<sdlit…@earthlinkNOSPAM.net

– Hide quoted text — Show quoted text -

wrote: causing shortness of breath when doing anything more than normal activities, and bouts of coughing 20 minutes after physical

exertion?

Thanks a lot. Having said that, the symptoms you’re describing are sometimes associated with asthma or bronchitis.  You need to see a physician

for

an appropriate diagnosis. Yes I agree – I have had lots (and lots) of coughing from nasal drip

but not

shortness of breath.   Shorttness of breath suggests that asthma or

other cause

needs to be ruled out……

I wish it were that easy. When I went to the doctor last year, she spent 20 seconds looking into my lungs with what was basically a flashlight on the end of a tube, only to say she could see nothing wrong. That by itself resulted in a bill for $315.00, so I can’t really afford to try the traditional route for diagnosis and treatment. Hence the reason I’m posting here. In September of 2002, I fell asleep with the window open on a night the temperature dropped sharply. It resulted in me catching a cold which I quickly got over, except for a cough that just would not go away. When it finally began to subside somewhat, I noticed that if I tried to jog for 5 minutes, 20 minutes afterwards I’d experience a bout of coughing that would last for about 5 minutes. But that began to get better also.(Though not completely). The big problem began during on my daily walk to work. I have to walk up a hill, and on this particular day I was winded by the time I reached the top, when I wasn’t winded the previous day I walked up that same hill. In other words, this shortness of breath did not happen progressively, but over the course of a 24 hour period, and I’ve had this problem ever since. Now I get winded whenever I do anything that requires even a little physical exertion. When I wake up in the morning I tend to have an ache in my windpipe, and phlegm production in my sinuses and lungs is a problem that has screwed up my digestion system, and makes the first half hour difficult after waking up. I can even pick up the scent of the "infection" when I breath. Unfortunately, I caught a cold last week, which exacerbated my problems(which briefly included spitting blood yesterday morning). As a result, I’m again dealing with bouts of dry coughing throughout the day. It sometimes keeps me up for an hour or so in the middle of the night. Outside of that, my symptoms don’t seem to be triggered by environmental factors.(ie: Temperature changes, dust, ect). Nevertheless, I sometimes cough so hard I get light headed. I used to play basketball for several hours just about every day. But ever since this breathing/coughing/sinus problem began, I’m forced to be sedentary and as a result I’ve gained 50 lbs. Anyway, any ideas or recommendations would be greatly appreciated. Thanks a lot. Darren Harris Staten Island, New York.

Response:

Search…@mail.con2.com wrote:

Can anyone give me an idea of what sinus infections may spread to the lungs,

All of them.  :-) My ENT believes in the "Unified Field Theory of Respiratory Infections" (that’s what he calls it):  Since the epithelium of the nasopharynx is pretty much the same as the tissues of the throat, larynx and trachea, any type of infection (viral, bacterial or fungal) in the upper respiratory tract can spread to the lower respiratory tract.  Carried down there by infected post nasal drip.

causing shortness of breath when doing anything more than normal activities, and bouts of coughing 20 minutes after physical exertion? Thanks a lot.

Having said that, the symptoms you’re describing are sometimes associated with asthma or bronchitis.  You need to see a physician for an appropriate diagnosis. — Steven D. Litvintchouk Email:  sdlit…@earthlinkNOSPAM.net Remove the NOSPAM before replying to me.

Response:

On Wed, 12 Jan 2005 18:49:50 GMT, "Steven L." <sdlit…@earthlinkNOSPAM.net

wrote:

causing shortness of breath when doing anything more than normal activities, and bouts of coughing 20 minutes after physical exertion? Thanks a lot. Having said that, the symptoms you’re describing are sometimes associated with asthma or bronchitis.  You need to see a physician for an appropriate diagnosis.

Yes I agree – I have had lots (and lots) of coughing from nasal drip but not shortness of breath.   Shorttness of breath suggests that asthma or other cause needs to be ruled out……

Response:

Can anyone give me an idea of what sinus infections may spread to the lungs, causing shortness of breath when doing anything more than normal activities, and bouts of coughing 20 minutes after physical exertion? Thanks a lot. Darren Harris Staten Island, New York.

Response:

Tinnitus

Question:

Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

Response:

Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

Some years ago, after a particularly long and loud session, I noticed residual ringing in one of my ears. It never went away…. I use custom-made earplugs to stop the tinnitus level from rising any higher now, though sometimes I wonder whether I should just give up and go classical. Should have been using ‘em all along. My advice: Buy now, before it’s too late… OK, OK, they’re like condoms for the ears (it’s always better without), but better safe than sorry if you’re working with loud music.

Response:

Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

Recovery is possible. Takes time and caution. I’m better now, but had damaged my ears to the point that tinnitus visited occasionally. Among some friends it got to be a chuckle when they’d see me put a finger over my ear to see whether a high pitched noise was inside or outside my head. Be careful, wear plugs, watch out for the snare drum and cymbals and with luck and care you’ll be able to hear the chime and ring of that amp for many more years. Ron

Response:

I’ve got it, too. If you don’t already have it, avoid it… I use earplugs at *every* gig (as player or listener). Avoiding high Sound Pressure Levels is, in my opinion, the only cure. I think that ear-level speaker cabinets were a prime cause in my case (my hearing *range* is significantly narrower in my Right ear  - the one next to the cabinet). My doctor ran through the possible causes and cures. I tried the dietary recommendations (no dairy products) to reduce the level of mucus in the Ear-Nose-Throat system   – no change (no surprise – the problem wasn’t caused by my diet). I tried homeopathic medicine – no change. At first, I couldn’t listen to *any* music without the whine starting up, I thought I’d stopped enjoying music for life! The problem has lessened over the last 15 years – I’ve grown acclimatised to its occasional appearance, it’s no longer a nuisance. Peculiarly, there is a *psychosomatic* element to it (just seeing the *word* "tinnitus" in the subject header set it off!) My doctor had me try to zero-in on the offending frequencies with guitar feedback but: 1. C’mon, d’you think I’ve never heard of the *placebo* effect? 2. I experience Tinnitus as oscillation *far above* my normal range of hearing     (too high for me to discern its musical pitch). I’ll say it yet again… Avoiding high Sound Pressure Levels is, in my opinion, the only cure. Elmo’ 7#9

Response:

Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

Get a jar of those foam plug (available by the box or jar) throw a handful in your gear bag, a handful in your glove compartment, and keep the rest at practice. That way, you’ll always have some handy for you and friends…cheap enough to give away. Tinnitus is a bitch…I’m always glad when I wear them, and usually wish I had when I don’t.

Response:

Mention the tinnitus to your dentist on your next visit.  You could be a night grinder. Hey!  Good name for a band…

Response:

I am 46. When I was 15, the ringing began after being explosed to a particularly loud session in very close range. It has never stopped. For about 10 years (ending about 5 years ago), I rarely played, but still went to loud concerts. After starting to play agin, the ringing got even worse, so I finally bought some custom made plugs to try to reduce the risk of further damage. The ringing annoys me, and worries me that I will someday be able to hear nothing but the ringing. But it is not yet interfering severely with my life.

– Hide quoted text — Show quoted text – Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

Response:

Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

In the 80’s I went to see "The Angels" play down under. The levels were so loud that the whole concert was distortion and it hurt the whole time. Vocals drums, bass, everything was just distortion. The next day I kept thinking that the phone was ringing and tried to answer it. No side effects now, although I guess I may have had some hearing damage. I have a friend who gets tinitus. Not a muso, but a labourer. It really drives this guy nutz!

Response:

Mention the tinnitus to your dentist on your next visit.  You could be a night grinder. Hey!  Good name for a band…

Don’t forget…remove all of your Amalgom and replace with bonded composites. "Amalgom" is not as good as "Night Grinder", but in the context of Dental Conspiracy Band Names…well, it’s a pretty small room. Sunday! Sunday! Sunday! Tinnitus, Night Grinder, and special guest Amalgom. At the Fair Grounds. Be There!

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- Hide quoted text — Show quoted text – Mention the tinnitus to your dentist on your next visit.  You could be a night grinder. Hey!  Good name for a band… Don’t forget…remove all of your Amalgom and replace with bonded composites. "Amalgom" is not as good as "Night Grinder", but in the context of Dental Conspiracy Band Names…well, it’s a pretty small room. Sunday! Sunday! Sunday! Tinnitus, Night Grinder, and special guest Amalgom. At the Fair Grounds. Be There!

Sh1t…’Amalgam’

Response:

Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

I’ve done some work as security manning the rails at concerts. Between having your back to a huge stack of loudspeakers, and safely catching 225 pound crowd surfers and sending them peacefully on their way to do it all over again, earplugs and a back brace are not an option. I’ve never had continuous ringing, just a few hours worth, but it keeps you awake.  When your young it’s a badge of courage. Now that we’re older we know the facts. I hope it works out for all of you, I can’t think of anything worse for a musician.  Imagine poor Beethoven, given the gift to formulate beautiful music, while losing your hearing. cheers… HJA Ears fine, eyes starting to betray me – Hide quoted text — Show quoted text –

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Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

Because of the first day on the rifle range in basic training Aug/Sept 1954, firing one round and coaching two rounds. i was almost completly deaf in both ears for about 3 or 4 days. I have had Tinnitus ever since. The tones will change frequency, and each ear has a differennt frequency. It is very hard to hear an electronic ringer phone, because the sound is almost the same as the tones from the Tinnitus. The apparant volumn will change also. I could not enjoy music for over a year after it happened. As has been said, don’t overload your ears. Dave Foreman

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Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

Every now and then I suffer from a sudden un-explained burst of tinnitus, and then luckily it goes away in about a minute. I hate that ringing in my ears… it reminds me of a blonde girlfriend I had whose head whistled when she walked…  :)

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– Hide quoted text — Show quoted text – Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud! Every now and then I suffer from a sudden un-explained burst of tinnitus,

and then luckily it goes away in about a minute. I hate that ringing in my ears… it reminds me of a blonde

girlfriend I had whose head whistled when she walked…  :)

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i have tinnitus..but i don’t think it’s because of all my playing..i think it’s all because of the machines of all the time at work..i work in a print shop and i’m a technician-prepress operator0-do it all.. the good thing is that i sleep a lot better..i live with 2 snorers..(they’re more like 2 trains..) georgio Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

– spammers suck!!! remover the *no spam* part in my email for reply

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- Hide quoted text — Show quoted text –  who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? I’m 52, got the first case of ringing ears (that lasted all night) the first time I went to a rock club and saw a band live, when I was in my teens.  It comes and it goes, depending on my exposure, the decibels and the duration. A few years back, I had it real bad because I was playing with some idiots who didn’t know what a volume knob was.  There was this harp player who insisted on coming through the monitor on my side, and it was a killer. I’ll NEVER have a harp player in any band again after that.  NEVER. It’s subsided again, but it’s still always there.  And loud bands kill me now. My ears can’t take it anymore, it REALLY hurts. The best thing you can do, other than try to control your exposure to high decibels, is to go to an audiologist and get a pair of the custom fitted "Musicians Earplugs".  I think I paid about $115 for mine.  That’s CHEAP when you try to put a price on your hearing, which is irreplaceable.  CHEAP.  The foam jobs will work, but they’re uncomfortable and nothing sounds good with them.  And forget trying to sing with them in, it’s a lesson in futility. ~kp

I’m not sure that the ringing ears and suppressed hearing that you recover from after exposure to loud noise qualifies as ‘Tinnitus’. My impression was that tinnitus caused a ringing in the ears that may vary in degree from time to time, but *never* goes away. I have that in my right ear. Not extreme, but annoying. Sounds like a 15k carrier signal constantly. Mine comes from exposure to industrial noise so loud that no amount of hearing protection will prevent it. Listening to, and playing in, loud band probably contributed to it as well though. And harp players… Grrr…. I love great harmonica playing, but I’ve had my hearing drilled too many times by a clueless noob that either had an amp too big, or insisted on playing through a cranked vocal mic. It has been truly rare when the band was so loud, or the venue so large, that the harp player needed an amp bigger than 15 watts. Their frequency range carries distances with very little power. I’ve also witnessed a packed house at a jam club instantly vacated *many* times by an annoying, too-loud harmonica. I still love ‘em, but somebody else in the band needs to keep a leash on these guys. ;-) John King "Don’t squat with your spurs on." – (Will Rogers)

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I saw Rick Derringer a few years ago, at an outdoor concert. I was standing right at the stage, about 4 feet from where Rick was standing. Right in front of my line of sight, next to the drums, were 2 – Peavey Classic 50, 4×10’s. Rick was just cranking it out, man, he was just blowing me away, the tones were incredible. That night, when I went to bed, I heard the obligatory after concert ringing. It usually would go away the next day or so. It didn’t. It’s been several years and I still have the ringing, but I don’t really notice it anymore, unless it’s dead quiet and late at night. That was probably one of, if not the greatest concert I have ever been to, and his tones were just indescribable. I don’t know if it will ever go away, probably not, since it’s been several years now. I’d rather not have the ringing, but that concert was so great, that I’ll accept the ringing without regret. Mikey

– Hide quoted text — Show quoted text – Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

Response:

Hello, Most of the time I think it’s knowing where to put your amp and speakers, and, where to stand in relation to where the speaker cabs are, and where the drums are.  Back in the days of full Marshall stacks, I never played mine that way.  I "always" put the cabs side by side, or split `em to each side of the stage. Knowing where that beam or direction/projection of sound is, and how to use it to your good effect, is wonderful.  It allows you to choose to step into (controllable feedback, more sustain, etc.) or out of the beam of sound (protecting your hearing, etc).  I’ve always tried to be mindful of what is pointed or aimed at my head, and to be careful.  It isn’t hard to try an experiment where you aim the cab at your waist and play, and then aim it at your head.  In the latter, your room volume gets higher very quickly. Anytime I use an amp stand or a chair to put a cab or combo on, it never is aimed at my head. About 45 days ago our band played a very small club, and I was about two feet away from the drummer’s crash symbol the whole night.  I got an ear plug and put it in my left ear – the one close to the symbol.  Then I was mindful of my body posture, and I kept my back to that symbol most of the night, keeping my ears away from it. I think I’ve experienced more loud music as a listener in the audience, than on stage.  Our band plays at fairly high stage volume levels, but most of that blows by me and the beam/projection is more like belt-high than head-high.  Rex and I are mindful of where we aim our amps and cabs, so that the audience doesn’t get blasted as well.  I always carry ear plugs with me – they are more for my protection as a potential member of an  audience rather than on stage.  Performing live I rarely use ear plugs, but I’m also very, very careful of what I allow near my head or ears in terms of volume of anything. The offender I find more damaging to me personally that loud amps and drums on stage, is the slightly tipsy guy who insists on having some sort of conversation with me as I’m listening to the band on stage, and leans into me and is yelling in my ear.  That hurts my ears more than most any amps or drum set that I’ve been around.  I "always" find at excuse to move on from that yelling inebriated guy. All the best. Walk in Beauty, Peace.  Scott Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

—–= Posted via Newsfeeds.Com, Uncensored Usenet News =—– http://www.newsfeeds.com – The #1 Newsgroup Service in the World! —–==  Over 100,000 Newsgroups – 19 Different Servers! =—–

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- Hide quoted text — Show quoted text – Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

Yes, tinnitis is an occupational hazard that will pay you back for life. Living in a big city doesn’t help either. I’ve had my share of hearing damage from loud subways, pneumatic drills, as well as the self inflicted damage of standing next to the drummer’s cymbals without understanding (from 16 to maybe 21 years old) how much damage I was doing. I have tinnitis every day.  I live with it.  I accept — if not embrace – it. Mostly it doesn’t bother me anymore.  What is more bothersome is the notch in my hearing at 4K which is widening as I get older. I find myself asking "What?" a lot more than I like and I’m only 49.   I guy I used to work in a band with quit loud music and sold his amp saying that by the time we were 50 we would have to wheel the damn amps behind us with a mic plugged in so we could hear what people were saying.  Not too far off the still works, btw, a Bruce Bass amp. I have been using hearing protection since the late ’70’s but much of the damage was already done, between my own musical ventures and concerts. Getting a hearing test with tinnitis is a riot. They put you in a soundproof booth and a youngish, usually cute, Speech Pathologist asks you to raise your hand when you hear a tone.  Half the time my hand’s going up when she’s not even sending a tone because I’m hearing one in that soundproof booth all the time. Oh well, next life I am going to take up badminton instead of music. Paul Don’t just sit there — DO SOMETHING! PC

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Getting a hearing test with tinnitis is a riot. They put you in a soundproof booth and a youngish, usually cute, Speech Pathologist asks you to raise your hand when you hear a tone.  Half the time my hand’s going up when she’s not even sending a tone because I’m hearing one in that soundproof booth all the time.

They gave me a little button to push, had all these itty bitty transducers of some kind all over my head.  At least they *told* me it was a hearing test. And when you ask for the results, they just tell you your hearing is average for someone of your age, what the hell is that supposed to mean, average for someone who spent his youth in front of bands like the Who and Deep Purple and thus can be expected to hear the dinner bell twenty-four hours a day? Young bastard hearing test technician, glad I let the air out of his tires on the way out.

Response:

Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? As you might have guessed, I have.  Not cool.  I have begun to take steps to minimize my exposure to loud sounds, including not plugging in at all for most part, when I practice.  And I just got a new (old) Vibrolux….man that sweet crisp Fender sound just rings like a bell, but so do my ears after playing too loud!

Well, I’ve gone down the thread, and found everyone’s comments very interesting. So, I thought I’d add a few more. Not common knowledge to most musicians, hearing loss from loud music, is not number one the list of causes. Infection is.  More hearing is lost from infection than loud noises. From a conversation with an ear doctor a number of years ago I also learned that high blood pressure is another cause for ringing in the ears, along with ear wax and inflammation being few others. Ear plugs are a great thing, and so are cigarette filters, tissues, and anything handy when you forget the real things. However, as the saying goes, it’s easier to stay out of trouble, than it is to get out of trouble. Tip 1. For that reason, in the stacks I’ve played through both now and then, I never had any speakers in the top, of the top cabs.  NEVER have any Tip 2. NEVER play in a band with TWO guitar players.  I like to hear the spaces in the music, and the distortion of two guitar players is enough to kill the hearing of a stone.  Plus, when two guitar players are in ego conflict, they try to dominate by their volume. That’s why, power trio’s are my only game.  Well, unless it’s an R&B band with keys and horns, around the vocals. Tip 3. Never get on the stage with a large number of people who can’t get the concept, to DROP OUT, cause the MUSIC is already clogged up with TOO I’ve been on the stage with experienced cat in large numbers, and you will only hear the drums, bass, and a lead instrument through out the musical piece.  Things get passed around, and the musicians have to wait their turn to burn.   Tip 4. Know how to find and/or create SAFE ZONES when you set up the stage. Learn a bit about the acoustic architecture of your environment you are playing in. For example, a 10 watt amp in a closed cement walled garage can sound great, and at the same time kill your ears for life. That same 10 watt amp in the middle of the stage in an old well designed theater can be heard throughout the total seating and hurt no one. But that 10 watt amp in the middle of a football field, will sound like a transistor radio with a weak battery. It is the acoustic environment that controls the amount of sonic energy dissipated on the way to your ears, that is at play here. <Rich comments There are times where you NEED the big watts and times when you DON’T, to be perceived to be at the same volume levels.  This, is really However, that 10 watt amp in the garage can be just as deadly as a Marshall stack in the middle of that football field at full tilt boogie. <thinking I’ve still got my hearing after all these years, because I DON’T LIKE LOUD NOISE!!!!! I used plugs, used safe zones, and stayed out of the line of Even my own!!!!!!! <thinking When MUSIC sounds like NOISE, I’m out of here, and I don’t care who’s making the NOISE. <thinking No two people hear the same sound the same way 100%, by the time the brain cells react, and tell what’s going on.  But, we would like to believe what we hear, is what the other person hears, at the same time BOTH of us are listening to it.  But that ain’t the case.  All we have is related verbal confirmation. With colors, it’s the same thing.  Think of being with a person with color blindness color distortion.  How would that would be relating to them the colors in a painting.  But in this case, instead of it being an EYE thing, it’s an EAR thing with a distorted perception going on. <thinking And, this assumes no tinnitus present, to complicate the matter. Just some thoughts from a tired over worked, I played a gig, got home late, and posted to unwind everything tech. Regards, Rich Koerner, Time Electronics. http://www.timeelect.com Specialists in Live Sound FOH Engineering,        Music & Studio Production, Vintage Instruments, and Tube Amplifiers

Response:

Mention the tinnitus to your dentist on your next visit.  You could be a night grinder. Hey!  Good name for a band… Don’t forget…remove all of your Amalgom and replace with bonded composites.

  Good idea; most people don’t realize that dental amalgam has lead as one of it’s major components. It’s unbelievable that even after all these years of warnings about lead poisoning that dentists still use that shit. — de Jack N2MPU FN20 Modeling the NYC and NYNH&H in HO and CP Rail and D&H in N Proud NRA member

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- Hide quoted text — Show quoted text – Mention the tinnitus to your dentist on your next visit.  You could be a night grinder. Hey!  Good name for a band… Don’t forget…remove all of your Amalgom and replace with bonded composites.   Good idea; most people don’t realize that dental amalgam has lead as one of it’s major components. It’s unbelievable that even after all these years of warnings about lead poisoning that dentists still use that shit.

Um…no they don’t.

Response:

Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty?

I have it so badly 24/7 that I’m disabled.  Any noise at all sets it off worse.  It’s been getting progressively worse for about the last ten years.  I cannot listen to music at any but the very softest levels.  I have to wear industrial earplugs nearly all the time.  I have to speak softly and can no longer sing. If you are experiencing it now after playing, you will eventually have it all the time when you’re not, probably sometime in middle age, maybe as badly as I do – or worse. There is no effective treatment for tinnitus (which is not a disease, but merely a symptom) caused by nerve damage in the ears resulting from high volume environments. Kids, TAKE CARE OF YOUR EARS!  You may live longer than you deserve. E-mail: bongolation<ATmail.md – Change <AT to @ symbol to reply. See COMPLETE headers for more info.  Headers are good – view them. You are not an official member of a.g.a until you are my killfile.

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- Hide quoted text — Show quoted text – Got anyone’s attention?  I want to start by polling the group, who’s experienced residual ringing after playing loud amps to the extent it has caused significant concern/difficulty? I have it so badly 24/7 that I’m disabled.  Any noise at all sets it off worse.  It’s been getting progressively worse for about the last ten years.  I cannot listen to music at any but the very softest levels.  I have to wear industrial earplugs nearly all the time.  I have to speak softly and can no longer sing.

Have you tried the white-noise generating earpieces?

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You seem to be having a lot of problems with your spelling today: irrelevant to the subject ot his grop anyway What does that little snippet mean Mr English? Debs    Moreover, you can’t even read–I never said that I have tinnitus, which is irrelevant to the subject ot his grop anyway. It was the witch Carole who inferred that I have tinnitus and used this inference as an opportunity to ridicule someone she claimed had this illness. You, of course, greeted this abomination with an approving silence. That’s ll we need to know about your value system.

(snipped yet again)

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You’re a mean, twisted person. You have no business on a support group. Why don’t you start a newsgroup dedicated to making fun of the physically or mentally handicapped? Sounds just about your speed.

Piss off. — Fran If you need my email address please ask.

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Piss off.

I notice that you take no umbrage at ridicule of people with physical ailments by Carole, but are moved to vulgar rebuke by those who criticize such cruelty. So much for your integrity. Sounds like you’re already a bit pissed–like your brain is soaked with Ripple or Thunderbird if you can think this way.

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But the point is that I never stated on THIS group that I had tinnitus–so you inferred this from what I wrote on another group. And then you used it as an opportunity to heap ridicule on someone on the grounds of physical debility.     You are beneath contempt.

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I don’t think he ever said he had tinnitus; he only implied that he did.  Never mind the rest… Debs – Hide quoted text — Show quoted text – The people on this ’support’ are dealing with chronic diseases and disabilities yet they still can have a sense of humor to help them get through the rough times.  What IBD do you have William?  You say now you have Tinnitus but when you were busy attacking everyone on that group you also refused to say what was wrong.  UM MOM Susan So you think that ridicule of ailments is funny too? Hardly surprising given your indifference to the people who might find relief through dietary regimens. You’re as twisted as your soulless-mate Carole. Maybe it was diet? ;-) Debs Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

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Your posts ot the tinnitus support group are readable via the google archives, including treatments you mention you have used.  I didn’t "infer" – I reported knowledge that is publicly available to anyone who looks for it.  Of course, if you don’t in fact have it, you posted under false pretenses in the tinnitus group.   – Hide quoted text — Show quoted text –    Moreover, you can’t even read–I never said that I have tinnitus, which is irrelevant to the subject ot his grop anyway. It was the witch Carole who inferred that I have tinnitus and used this inference as an opportunity to ridicule someone she claimed had this illness.

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You have shown support  for people who make public death threats and who ridicule people with illnesses by failing to rebuke them. To that extent you are a blight on this group, and I feel no obligation to have any discourse with you. The group would be better off without you. For the most part you treat this group as a lonely-hearts club where you gossip and exchange personal greetings with people in a way that would be more appropriately done in private.     Moreover, you can’t even read–I never said that I have tinnitus, which is irrelevant to the subject ot his grop anyway. It was the witch Carole who inferred that I have tinnitus and used this inference as an opportunity to ridicule someone she claimed had this illness. You, of course, greeted this abomination with an approving silence. That’s ll we need to know about your value system.

– Hide quoted text — Show quoted text – The people on this ’support’ are dealing with chronic diseases and disabilities yet they still can have a sense of humor to help them get through the rough times.  What IBD do you have William?  You say now you have Tinnitus but when you were busy attacking everyone on that group you also refused to say what was wrong.  UM MOM Susan So you think that ridicule of ailments is funny too? Hardly surprising given your indifference to the people who might find relief through dietary regimens. You’re as twisted as your soulless-mate Carole. Maybe it was diet? ;-) Debs Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

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So you think that ridicule of ailments is funny too? Hardly surprising given your indifference to the people who might find relief through dietary regimens. You’re as twisted as your soulless-mate Carole.

– Hide quoted text — Show quoted text – Maybe it was diet? ;-) Debs Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

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Chortling like a hyena at the crowd that just loves to ridicule people with physical ailments. Why don’t you start a Web site that collects jokes about people with Lou Gehrig’s disease? I’m sure that would provide you with endless hours of mirth.

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You’re a mean, twisted person. You have no business on a support group. Why don’t you start a newsgroup dedicated to making fun of the physically or mentally handicapped? Sounds just about your speed.

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The people on this ’support’ are dealing with chronic diseases and disabilities yet they still can have a sense of humor to help them get through the rough times.  What IBD do you have William?  You say now you have Tinnitus but when you were busy attacking everyone on that group you also refused to say what was wrong.  UM MOM Susan

– Hide quoted text — Show quoted text – So you think that ridicule of ailments is funny too? Hardly surprising given your indifference to the people who might find relief through dietary regimens. You’re as twisted as your soulless-mate Carole. Maybe it was diet? ;-) Debs Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

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Gingko does wonders for tinnitus. Karl

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actually, i suffer from tinnitis terribly.  it was related to the imune mediated inner ear disease (imed) as a result of autoimmunity (sometimes called autoimmune ear disease-aied).  the "extra noise" is not nice. jeff

– Hide quoted text — Show quoted text – Apparently, Mr. K has tinnitus, based on a google search of his posts….perhaps he is just hearing things?

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carole, have bad english and he will get a kick out’a that and give you all kinds of support! jeff

– Hide quoted text — Show quoted text – Probably all that time I spend around tatooed men in handcuffs and fashionable jail clothing has had a negative effect on me. Actually, I previously posted a very nice post, asking what form of IBD you had and how we could help and support you, but you didn’t choose to respond to that one.  I’d be happy to provide support to you in this ng if you provide some indication of your situation and how I (and the rest of the ng) may be of help, or just offer a sympathetic ear. Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

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it doesn’t do $HIT!  (guess this is on topic, hee, hee). jeff

– Hide quoted text — Show quoted text – Gingko does wonders for tinnitus. Karl

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Maybe it was diet? ;-) Debs – Hide quoted text — Show quoted text – Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

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lol Mel :-)

– Hide quoted text — Show quoted text – Maybe it was diet? ;-) Debs Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

Response:

OK, I have a sense of humor…I have IBD..I am full of sh…t – literally.  (How many of the regulars agree that that being full of it is precisely the health issue we deal with daily…  at least disposing of this excess?).. .ok, happy now?  I insulted myself too with my cruel abuse.   Even-Steven.  Let’s everyone lighten up, ok? Let’s get back to support. AND FELLOW POSTERS, WE NEED SOME HUMOR NOW! – Hide quoted text — Show quoted text – Why do you fail to register any offense at Carole’s ridicule of a physical ailment but rather reserve all your bile for a defense against his appalling, cruel abuse? With a twisted ethical perspective like yours, you are no loss to this list. Good riddance. Excuse me for saying this but I am on my way out of this newsgroup…..you Sir are so buried in your own thoughts of being the eternal sole intellect on this newsgroup that it escapes you to be nice.  Do you want a Nobel prize?  Yes? Then do something positive (or maybe getting laid might help you!!).  Maybe they will leave you alone in return. Friendly advice…..outta here…gone……oh, let me say it for "another individual who is warped by her environment thus posting statements that are inept of anything informative to me" No need to reply sir as I did it for you! Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

Response:

"another individual who is warped by her environment thus posting statements that are inept of anything informative to me"

By the way–I take it that English is not your native tongue? Or, in addition to approving of people who ridicule those who ridicule those with tinnitus and other ailments, do you leap onstage on open-mike night at the local comedy club and make fun of Jerry’s Kids?

Response:

Probably all that time I spend around tatooed men in handcuffs and fashionable jail clothing has had a negative effect on me. Actually, I previously posted a very nice post, asking what form of IBD you had and how we could help and support you, but you didn’t choose to respond to that one.  I’d be happy to provide support to you in this ng if you provide some indication of your situation and how I (and the rest of the ng) may be of help, or just offer a sympathetic ear. – Hide quoted text — Show quoted text – Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

Response:

Excuse me for saying this but I am on my way out of this newsgroup…..you Sir are so buried in your own thoughts of being the eternal sole intellect on this newsgroup that it escapes you to be nice.  Do you want a Nobel prize?  Yes? Then do something positive (or maybe getting laid might help you!!).  Maybe they will leave you alone in return. Friendly advice…..outta here…gone……oh, let me say it for "another individual who is warped by her environment thus posting statements that are inept of anything informative to me" No need to reply sir as I did it for you!

– Hide quoted text — Show quoted text – Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

Response:

Why do you fail to register any offense at Carole’s ridicule of a physical ailment but rather reserve all your bile for a defense against his appalling, cruel abuse? With a twisted ethical perspective like yours, you are no loss to this list. Good riddance.

– Hide quoted text — Show quoted text – Excuse me for saying this but I am on my way out of this newsgroup…..you Sir are so buried in your own thoughts of being the eternal sole intellect on this newsgroup that it escapes you to be nice.  Do you want a Nobel prize?  Yes? Then do something positive (or maybe getting laid might help you!!).  Maybe they will leave you alone in return. Friendly advice…..outta here…gone……oh, let me say it for "another individual who is warped by her environment thus posting statements that are inept of anything informative to me" No need to reply sir as I did it for you! Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

Response:

Apparently, Mr. K has tinnitus, based on a google search of his posts….perhaps he is just hearing things?

Response:

Here’s someone who claims to oppose flames and trolling–yet she starts an entire thread devoted to . . . a personal flame. The only consolation here is that her credibility lies in ashes now, especially when she pontificates about trolling.

Response:

Also, notice how here, on a SUPPORT group, compassionate Carole ridicules people with physical ailments. Was she born this vicious, or was she warped by her environment?

Response:

– Hide quoted text — Show quoted text – I had tinnitus and was told I was just going to have to learn to live with it. A friend recommended Ginko Biloba about a year ago. after 6 weeks of taking the ginko 3 times a day there is silence in my ears once again — no more ringing. (I had tests to rule out other causes).  I’m glad you have found some relief.  As time goes on, my tinnitus has been raise another pitch each year for the past four years and it is getting quite annoying.  Any releif would be welcome.  What is Ginko Biloba and where is it available??  

Suggest you subscribe to the newsgroup alt.support.tinnitus. There’s an excellent FAQ covering Gingko etc. David Powner

Response:

I had tinnitus and was told I was just going to have to learn to live with it. A friend recommended Ginko Biloba about a year ago. after 6 weeks of taking the ginko 3 times a day there is silence in my ears once again — no more ringing. (I had tests to rule out other causes).  I’m glad you have found some relief.  As time goes on, my tinnitus has been raise another pitch each year for the past four years and it is getting quite annoying.  Any releif would be welcome.  What is Ginko Biloba and where is it available??   David Booth      Via  ENABEL – Communications & Information Network

David: Gingko Biloba comes from one of the oldest trees in the world, some of these trees live a thousand years. The product is extracted from the roots of the tree. It works by increasing blood circulation, like to the small intricate parts of the ear. Also Valium and Xaanax  work well for tinnitus. More info on Gingko: What drugs, vitamins, and herbs are available for treating tinnitus?    * niacin      Niacin supplements produce a temporary flushing effect that is supposed to      pump more oxygen into the inner ear due to vasodilation. Take niacin on an      empty stomach for best results. You may experience a flush ranging from a      mild sunburn to wondering about spontaneous skin combustion. ;-) You may      also experience a "dry mouth" sensation.      MEGADOSES OF NIACIN CAN DESTROY YOUR LIVER AND KILL YOU. 50mg twice per      day is a common dose for tinnitus. If you experience the flush, then you      are getting the maximum benefit. Caution: niacin can provoke migraine      headache attacks in some people.      Some people report good results from niacin, other people gain nothing.      Your mileage may vary. One contributor advocates taking niacin in      combination with thiamine:           The 1994 text on Myofascial Pain: Trigger Points said that           Niacin without Thiamine will do no good for tinnitus. I don’t           recall the reasoning. Nicotinic Acid (a form of Niacin) if taken           in over 500mg per day should only be done so with Dr. approval.           I take 100mg per day with a B-complex vitamin that already is           balanced properly. You want roughly two parts niacinamide for           each one part thiamine. Most vitamins will come balanced in this           proportion. To my knowledge Nicotinic Acid in large doses like           2-5mg per day over a year or so, could lead to liver damage.           Niacinamide shouldn’t have any negative effects nor should           thiamine. But I suppose if someone swallows a bottle they’d have           a side effect!      There is no clinical proof for the effectiveness of niacin in treating      tinnitus. This is inherently difficult to prove due to a possible "placebo      effect" arising from the niacin flush sensation rather than any      therapeutic value of the underlying vasodilation. Additionally, any      vasodilation that occurs cannot benefit the cochlear hair cells, because      the blood vessel (vas spralie) that feeds these cells cannot expand or      contract.    * lecithin      The following anecdotal report advocates lecithin in combination with      niacin [Ed. note: my nutrition book does not cover lecithin, so I cannot      speculate as to toxicity and side-effects]:           After reading the tinnitus faq I emailed to my father, he           replied that he has helped a number of people cure their own           tinnitus by using Niacin and Lecithin. His theory is that the           lecithin, being an emulsifier, helps disperse the build up of           fats in the capillaries, and the niacin helps dilate the           capillaries to let the lecithin in.           He had meier’s [sic - Meniere's ?] syndrome in the 70’s, and           cured it this way. Our neighbor, a police officer, retired on           disability for the same reason, and Dad practically cured him           that way.           I got tinnitus as a result of childhood ear infections, and it           has done nothing for me, but then, mine is not what I would call           irritating.           It does seem that after chelation, the noise is less.      CAUTION: Smart Drugs & Nutrients, Dean & Morgenthaler, 1991, Heath Freedom      Publications, ISBN 0-9627418-9-2, says that phosphatidyl choline is the      active ingredient of lecithin, and as a precursor of acetylcholine should      be avoided by people who are manic-depressive because it can deepen the      depressive phase.    * gingko biloba      Gingko biloba leaves have been used therapeutically by the Chinese for      centuries for the treatment of asthma and bronchitis. In western countries      a standardized 50:1 concentrate of 24% gingko flavoglycosides is used,      either in liquid or capsule form. Gingko has been shown to increase      circulation throughout the body and the brain.      The article "Ginkgo biloba", The Lancet, Vol 340, Nov 7, 1992, pp.      1136-1139, examines numerous studies on the efficacy of ginkgo on      intermittent claudication (pain while walking), and cerebral      insufficiency, a wide collection of vascular impairment symptoms including      tinnitus. Typical dosages range from 120-160mg per day, divided equally at      meal time.      Most studies showed that between 30-70% of subjects had reduced symptoms      over a 6-12 week period. No serious side effects were observed, and any      minor side effects were not statistically significant compared to subjects      treated only with placebo.      Other references on gingko biloba:      As to tinnitus, Hobbs in reference (1) says:      For example, in 1986 a study statistically proved the effectiveness of      treatment with ginkgo extract for tinnitus: the ringing completely      disappeared in 35% of the patients tested, with a distinct improvement in      as little as 70 days!(2)      Similarly, when 350 patients with hearing defects due to old age were      treated with ginkgo extract, the success rate was 82%. Furthermore, a      follow-up study of 137 of the original group of elderly patients 5 years      later revealed that 67% still had better hearing(3).      References      1.) Ginkgo Elixir of Youth; Christopher Hobbs; Botanica Press, Box 742,      Capitola, CA 95010; 1991; pages 50-51      2.) Tinnitus-multicenter study. A multicentric study of the ear; Meyer,      B.; 1980; Ann. Oto-Laryng. (Paris) 103:185-8      3.) Tebonin-therapy with old hard-of-hearing people. Koeppel, F. W.; 1980;      Therapiewoche 30: 6443-46      Here’s an abstract of a recent paper in Audiology:           Holgers KM; Axelsson A; Pringle I           Ginkgo biloba extract for the treatment of tinnitus.           Department of Audiology, Sahlgren’s Hospital, Goteborg, Sweden.           Language: Eng           Source: Audiology 1994 Mar-Apr;33(2):85-92           Unique Identifier: 94234927           Abstract:           Previous studies have shown contradictory results of Ginkgo           biloba extract (GBE) treatment of tinnitus. The present study           was divided into two parts: first an open part, without placebo           control (n = 80), followed by a double-blind placebo-controlled           study (n = 20). The patients included in the open study were           patients who had been referred to the Department of Audiology,           Sahlgren’s Hospital, Goteborg, Sweden, due to persistent severe           tinnitus. Patients reporting a positive effect on tinnitus in           the open study were included in the double-blind           placebo-controlled study (20 out of 21 patients participated). 7           patients preferred GBE to placebo, 7 placebo to GBE and 6           patients had no preference. Statistical group analysis gives no           support to the hypothesis that GBE has any effect on tinnitus,           although it is possible that GBE has an effect on some patients           due to several reasons, e.g. the diverse etiology of tinnitus.           Since there is no objective method to measure the symptom, the           search for an effective drug can only be made on an individual           basis.      And still another abstract:           I searched the medline for your using PHYSICIANS ON LINE           software, from 1988 to present obtained the following:           Remacle J, Houbion A, Alexandre I, Michiels C           [Behavior of human endothelial cells in hyperoxia and hypoxia:           effect of Ginkor Fort]           Laboratoire de Biochimie Cellulaire, Facultes Universitaires           N.D. de la Paix, Namur, Belgique.           Phlebologie 1990 Apr-Jun;43(2):375-86           Article Number: UI91046351           ABSTRACT:           Recent discoveries have shown that venous diseases have a           multifactorial etiology. One of the factors which is definitely           involved in this pathologic process is the change in the           concentration of oxygen. An increase in the concentration of           oxygen, hyperoxia, or reoxygenation following hypoxia, damages           the tissues by stepping up the production of free radicals. In           addition, a reduction in oxygen concentration, or hypoxia, is           also damaging, probably through a reduction in ATP synthesis.           From a therapeutic standpoint, the veins, and more particularly           the endothelium, must be protected against the impact on the           tissue of these

… read more »

Response:

I had tinnitus and was told I was just going to have to learn to live with it. A friend recommended Ginko Biloba about a year ago. after 6 weeks of taking the ginko 3 times a day there is silence in my ears once again — no more ringing. (I had tests to rule out other causes).

Response:

I had tinnitus and was told I was just going to have to learn to live with it. A friend recommended Ginko Biloba about a year ago. after 6 weeks of taking the ginko 3 times a day there is silence in my ears once again — no more ringing. (I had tests to rule out other causes).   I’m glad you have found some relief.   As time goes on, my tinnitus has been raise another pitch each year for the past four years and it is getting quite annoying.  Any releif would be welcome.   What is Ginko Biloba and where is it available??   David Booth       Via  ENABEL – Communications & Information Network

Response:

I’ve heard that ginkgo can have some positive affects on this; do other remedies exist?  BTW, the cause is from too much loud music/noise over I to suffer from tinnitus. The cause of mine is not know. Have been through a pile of tests. I would also be interested in anything that I used to get it in spells along with backaches and colds. THe answer is Always simple (o.k. not really). When I act like a hypochondriac I take aspirin.  The first signs of aspirin poisoning is Tinitus! so when I’m taking three (15 grains) I’m trading one complaint for another.  If you have Any Tinitus stop using aspirin as it could be setting it off.                                            Elliot Cutler

Sorry, I don’t take aspirin. There are several anti-biotics that have the same effect, but it is usually temporary then. No, mine is not from AB’s, I’m just adding to your "aspirin" list. 8-)  Thomas

Response:

I’ve heard that ginkgo can have some positive affects on this; do other remedies exist?  BTW, the cause is from too much loud music/noise over I to suffer from tinnitus. The cause of mine is not know. Have been through a pile of tests. I would also be interested in anything that

I used to get it in spells along with backaches and colds. THe answer is Always simple (o.k. not really). When I act like a hypochondriac I take aspirin.  The first signs of aspirin poisoning is Tinitus! so when I’m taking three (15 grains) I’m trading one complaint for another.  If you have Any Tinitus stop using aspirin as it could be setting it off.                                                 Elliot Cutler

Response:

Ahhh, but one has to put their head on a pillow at night… and then it becomes super noticable…. Have you tried putting your attention on the sound, taking a break from your thoughts, relaxing into the sound, and riding the waves of sound to sleep?   — Have fun!

Sorry, the "sounds" I hear are far from relaxing. And the last thing I wish to to is concentrate on them, this seems to intensify their effect. There are no "waves" in my ears 8-) Fixating on it makes it seem as though my head is turning inside out or collapsing ;-)  Thomas

Response:

Ahhh, but one has to put their head on a pillow at night… and then it becomes super noticable….

Have you tried putting your attention on the sound, taking a break from your thoughts, relaxing into the sound, and riding the waves of sound to sleep?   — Have fun!

Response:

cause is from too much loud music/noise over too many years…".  This is not the only cause.  Tinnitus can also be caused by damage to the

In an attempt to save bandwidth and boredom, I didn’t include my complete hearing history.  I should have said that *my* tinnitus is from loud noise.  I’ve been to an EN&T and a hearing specialist.  I have custom earplugs.  I’ve played drums for 24 years (rock bands, high school band, drum corps), along with attending lots of concerts and loud clubs.   The experts that I’ve sought out have just been able to recommend abstinence, as it were, to help ensure that things don’t get worse. Now, back to my orginal post: I’ve heard that ginkgo can have a positive affect on tinnitus.  Is this true, and are there other remedies/therapies that anyone has tried? Thanks, Hal

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        I would also be interested in learning about any possible remedies for tinnitus.  I’ve got it in my left ear and have ruled out any tumors via an MRI.

Response:

Intravenous glutamic acid diethyl ester relieves ringing. Deutsche Medizinische Wochenschrift   1992;142

Can you tell us a little bit more? I don’t want to go to the med school to look this up… Paul Edwards

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– Hide quoted text — Show quoted text – I to suffer from tinnitus. The cause of mine is not know. Have been through a pile of tests. I would also be interested in anything that might help out with this. There is more truth to the old saying "Silence is golden" than most realize – I haven’t heard [?] it in about 2+ years. Thomas One remedy I’ve had limited success with is Hydergine. A number of (yes, legitimate double-blind, Steve D) medical studies have documented its effect on tinnitus in about 40-50 percent of patients in doses of appx. 6 mg/day. Since the FDA-approved does is only 3 mg day, you have to do some juggling to get these quantities. What I often did was take 5 mg a day until the prescription ran out, then wait until the next opportunity to fill it. This on-off regimen worked fine. It does give a bit of a buzz, like caffeine, which I eventually found too annoying to contend with any more. My current strategy for tinnitus – the one recommended by Stanford Med School docs – is simply to stop paying attention to it. Like any stimulus which serves no purpose for the organism, if you don’t amplify it by paying attention to it it eventually diminishes  or even ends. — Paul N. Edwards

Ahhh, but one has to put their head on a pillow at night… and then it becomes super noticable. Though you are correct. I have found by keeping busy [taking my mind off it] and keeping a fishtank in my room [to create a little backround noise that helps mask and also soothe the mind] works wonders. But there are times when it is terribly annoying and disconcerting – especially when you want a break from something, enter a "quiet" room and end up having your thoughts drowned out by the "ringing". Thomas

Response:

cause is from too much loud music/noise over too many years…".  This is not the only cause.  Tinnitus can also be caused by damage to the ear from infection, by the effect a tumor has on the hearing nerve, and by a hearing nerve that has been traumatized or severed in the course of removing a tumor.  I know about the last one of these, since I had a tumor removed from my right hearing and balance nerves two years ago. Just added information, to supplement what Hal wrote. — Ted Jardine Voice:  206 867 6280

Response:

Intravenous glutamic acid diethyl ester relieves ringing. Deutsche Medizinische Wochenschrift   1992;142

Response:

I to suffer from tinnitus. The cause of mine is not know. Have been through a pile of tests. I would also be interested in anything that might help out with this. There is more truth to the old saying "Silence is golden" than most realize – I haven’t heard [?] it in about 2+ years. Thomas

One remedy I’ve had limited success with is Hydergine. A number of (yes, legitimate double-blind, Steve D) medical studies have documented its effect on tinnitus in about 40-50 percent of patients in doses of appx. 6 mg/day. Since the FDA-approved does is only 3 mg day, you have to do some juggling to get these quantities. What I often did was take 5 mg a day until the prescription ran out, then wait until the next opportunity to fill it. This on-off regimen worked fine. Hydergine has POWERFUL potentiation effects on caffeine – it’ll give you a killer headache if you drink strong coffee along with it. No major side effects are known, and it is non-toxic. It does give a bit of a buzz, like caffeine, which I eventually found too annoying to contend with any more. My current strategy for tinnitus – the one recommended by Stanford Med School docs – is simply to stop paying attention to it. Like any stimulus which serves no purpose for the organism, if you don’t amplify it by paying attention to it it eventually diminishes  or even ends. — Paul N. Edwards

Response:

I’ve heard that ginkgo can have some positive affects on this; do other remedies exist?  BTW, the cause is from too much loud music/noise over too many years…  

Response:

I’ve heard that ginkgo can have some positive affects on this; do other remedies exist?  BTW, the cause is from too much loud music/noise over too many years…  

I to suffer from tinnitus. The cause of mine is not know. Have been through a pile of tests. I would also be interested in anything that might help out with this. There is more truth to the old saying "Silence is golden" than most realize – I haven’t heard [?] it in about 2+ years. Thomas

Response:

Careful — do a little more reading about tinnitus before you start claiming that you know what its cause is.  Tinnitus can be caused by a variety things, including tumors of the 8th (acoustic) nerve.  It is true that ONE cause is excessive exposure to loud sounds, either over a period of time or after one instant.  Another, much less serious cause is cerumen (wax) build up in the ear canal.  In many cases, the cause of a person’s tinnitus is never determined.  Nonetheless, if one experiences tinnitus over a sustained period of time, one should consult one’s health care provider to at least rule out sinister pathology, especially if the tinnitus occurs in only one ear. -Jane M. Opie, Ph.D., Certified Clinical Audiologist

Response:

Somebody asked for some information on this subject. I too have a problem with this.In th ebook by Dr. Andrew Weiler, MD.called Spontaneous Healing he mentioned that some doctors in Germany do neck adjustments and prescribe yoga exeercises for their patients. Hla N.Tin.

Response:

I have a mild case of Tinnitus in my left ear, aggravated by my taking Zoloft, an SSRI-type antidepressent. Has anyone tried ear-coning for tinnitus, with good result? I have been taking ginkgo for several months to try to remedy the ringing. but it doesn’t seem to help, though I have noticed some cognitive enhancement from it. Are there other substances OTC I can take for tinnitus? Thanks. –Will

Response:

– Hide quoted text — Show quoted text – I had tinnitus and was told I was just going to have to learn to live with it. A friend recommended Ginko Biloba about a year ago. after 6 weeks of taking the ginko 3 times a day there is silence in my ears once again — no more ringing. (I had tests to rule out other causes).  I’m glad you have found some relief.  As time goes on, my tinnitus has been raise another pitch each year for the past four years and it is getting quite annoying.  Any releif would be welcome.  What is Ginko Biloba and where is it available??  

Suggest you subscribe to the newsgroup alt.support.tinnitus. There’s an excellent FAQ covering Gingko etc. David Powner

Response:

I had tinnitus and was told I was just going to have to learn to live with it. A friend recommended Ginko Biloba about a year ago. after 6 weeks of taking the ginko 3 times a day there is silence in my ears once again — no more ringing. (I had tests to rule out other causes).  I’m glad you have found some relief.  As time goes on, my tinnitus has been raise another pitch each year for the past four years and it is getting quite annoying.  Any releif would be welcome.  What is Ginko Biloba and where is it available??   David Booth      Via  ENABEL – Communications & Information Network

David: Gingko Biloba comes from one of the oldest trees in the world, some of these trees live a thousand years. The product is extracted from the roots of the tree. It works by increasing blood circulation, like to the small intricate parts of the ear. Also Valium and Xaanax  work well for tinnitus. More info on Gingko: What drugs, vitamins, and herbs are available for treating tinnitus?    * niacin      Niacin supplements produce a temporary flushing effect that is supposed to      pump more oxygen into the inner ear due to vasodilation. Take niacin on an      empty stomach for best results. You may experience a flush ranging from a      mild sunburn to wondering about spontaneous skin combustion. ;-) You may      also experience a "dry mouth" sensation.      MEGADOSES OF NIACIN CAN DESTROY YOUR LIVER AND KILL YOU. 50mg twice per      day is a common dose for tinnitus. If you experience the flush, then you      are getting the maximum benefit. Caution: niacin can provoke migraine      headache attacks in some people.      Some people report good results from niacin, other people gain nothing.      Your mileage may vary. One contributor advocates taking niacin in      combination with thiamine:           The 1994 text on Myofascial Pain: Trigger Points said that           Niacin without Thiamine will do no good for tinnitus. I don’t           recall the reasoning. Nicotinic Acid (a form of Niacin) if taken           in over 500mg per day should only be done so with Dr. approval.           I take 100mg per day with a B-complex vitamin that already is           balanced properly. You want roughly two parts niacinamide for           each one part thiamine. Most vitamins will come balanced in this           proportion. To my knowledge Nicotinic Acid in large doses like           2-5mg per day over a year or so, could lead to liver damage.           Niacinamide shouldn’t have any negative effects nor should           thiamine. But I suppose if someone swallows a bottle they’d have           a side effect!      There is no clinical proof for the effectiveness of niacin in treating      tinnitus. This is inherently difficult to prove due to a possible "placebo      effect" arising from the niacin flush sensation rather than any      therapeutic value of the underlying vasodilation. Additionally, any      vasodilation that occurs cannot benefit the cochlear hair cells, because      the blood vessel (vas spralie) that feeds these cells cannot expand or      contract.    * lecithin      The following anecdotal report advocates lecithin in combination with      niacin [Ed. note: my nutrition book does not cover lecithin, so I cannot      speculate as to toxicity and side-effects]:           After reading the tinnitus faq I emailed to my father, he           replied that he has helped a number of people cure their own           tinnitus by using Niacin and Lecithin. His theory is that the           lecithin, being an emulsifier, helps disperse the build up of           fats in the capillaries, and the niacin helps dilate the           capillaries to let the lecithin in.           He had meier’s [sic - Meniere's ?] syndrome in the 70’s, and           cured it this way. Our neighbor, a police officer, retired on           disability for the same reason, and Dad practically cured him           that way.           I got tinnitus as a result of childhood ear infections, and it           has done nothing for me, but then, mine is not what I would call           irritating.           It does seem that after chelation, the noise is less.      CAUTION: Smart Drugs & Nutrients, Dean & Morgenthaler, 1991, Heath Freedom      Publications, ISBN 0-9627418-9-2, says that phosphatidyl choline is the      active ingredient of lecithin, and as a precursor of acetylcholine should      be avoided by people who are manic-depressive because it can deepen the      depressive phase.    * gingko biloba      Gingko biloba leaves have been used therapeutically by the Chinese for      centuries for the treatment of asthma and bronchitis. In western countries      a standardized 50:1 concentrate of 24% gingko flavoglycosides is used,      either in liquid or capsule form. Gingko has been shown to increase      circulation throughout the body and the brain.      The article "Ginkgo biloba", The Lancet, Vol 340, Nov 7, 1992, pp.      1136-1139, examines numerous studies on the efficacy of ginkgo on      intermittent claudication (pain while walking), and cerebral      insufficiency, a wide collection of vascular impairment symptoms including      tinnitus. Typical dosages range from 120-160mg per day, divided equally at      meal time.      Most studies showed that between 30-70% of subjects had reduced symptoms      over a 6-12 week period. No serious side effects were observed, and any      minor side effects were not statistically significant compared to subjects      treated only with placebo.      Other references on gingko biloba:      As to tinnitus, Hobbs in reference (1) says:      For example, in 1986 a study statistically proved the effectiveness of      treatment with ginkgo extract for tinnitus: the ringing completely      disappeared in 35% of the patients tested, with a distinct improvement in      as little as 70 days!(2)      Similarly, when 350 patients with hearing defects due to old age were      treated with ginkgo extract, the success rate was 82%. Furthermore, a      follow-up study of 137 of the original group of elderly patients 5 years      later revealed that 67% still had better hearing(3).      References      1.) Ginkgo Elixir of Youth; Christopher Hobbs; Botanica Press, Box 742,      Capitola, CA 95010; 1991; pages 50-51      2.) Tinnitus-multicenter study. A multicentric study of the ear; Meyer,      B.; 1980; Ann. Oto-Laryng. (Paris) 103:185-8      3.) Tebonin-therapy with old hard-of-hearing people. Koeppel, F. W.; 1980;      Therapiewoche 30: 6443-46      Here’s an abstract of a recent paper in Audiology:           Holgers KM; Axelsson A; Pringle I           Ginkgo biloba extract for the treatment of tinnitus.           Department of Audiology, Sahlgren’s Hospital, Goteborg, Sweden.           Language: Eng           Source: Audiology 1994 Mar-Apr;33(2):85-92           Unique Identifier: 94234927           Abstract:           Previous studies have shown contradictory results of Ginkgo           biloba extract (GBE) treatment of tinnitus. The present study           was divided into two parts: first an open part, without placebo           control (n = 80), followed by a double-blind placebo-controlled           study (n = 20). The patients included in the open study were           patients who had been referred to the Department of Audiology,           Sahlgren’s Hospital, Goteborg, Sweden, due to persistent severe           tinnitus. Patients reporting a positive effect on tinnitus in           the open study were included in the double-blind           placebo-controlled study (20 out of 21 patients participated). 7           patients preferred GBE to placebo, 7 placebo to GBE and 6           patients had no preference. Statistical group analysis gives no           support to the hypothesis that GBE has any effect on tinnitus,           although it is possible that GBE has an effect on some patients           due to several reasons, e.g. the diverse etiology of tinnitus.           Since there is no objective method to measure the symptom, the           search for an effective drug can only be made on an individual           basis.      And still another abstract:           I searched the medline for your using PHYSICIANS ON LINE           software, from 1988 to present obtained the following:           Remacle J, Houbion A, Alexandre I, Michiels C           [Behavior of human endothelial cells in hyperoxia and hypoxia:           effect of Ginkor Fort]           Laboratoire de Biochimie Cellulaire, Facultes Universitaires           N.D. de la Paix, Namur, Belgique.           Phlebologie 1990 Apr-Jun;43(2):375-86           Article Number: UI91046351           ABSTRACT:           Recent discoveries have shown that venous diseases have a           multifactorial etiology. One of the factors which is definitely           involved in this pathologic process is the change in the           concentration of oxygen. An increase in the concentration of           oxygen, hyperoxia, or reoxygenation following hypoxia, damages           the tissues by stepping up the production of free radicals. In           addition, a reduction in oxygen concentration, or hypoxia, is           also damaging, probably through a reduction in ATP synthesis.           From a therapeutic standpoint, the veins, and more particularly           the endothelium, must be protected against the impact on the           tissue of these

… read more »

Response:

I had tinnitus and was told I was just going to have to learn to live with it. A friend recommended Ginko Biloba about a year ago. after 6 weeks of taking the ginko 3 times a day there is silence in my ears once again — no more ringing. (I had tests to rule out other causes).

Response:

I had tinnitus and was told I was just going to have to learn to live with it. A friend recommended Ginko Biloba about a year ago. after 6 weeks of taking the ginko 3 times a day there is silence in my ears once again — no more ringing. (I had tests to rule out other causes).   I’m glad you have found some relief.   As time goes on, my tinnitus has been raise another pitch each year for the past four years and it is getting quite annoying.  Any releif would be welcome.   What is Ginko Biloba and where is it available??   David Booth       Via  ENABEL – Communications & Information Network

Response:

I’ve heard that ginkgo can have some positive affects on this; do other remedies exist?  BTW, the cause is from too much loud music/noise over I to suffer from tinnitus. The cause of mine is not know. Have been through a pile of tests. I would also be interested in anything that I used to get it in spells along with backaches and colds. THe answer is Always simple (o.k. not really). When I act like a hypochondriac I take aspirin.  The first signs of aspirin poisoning is Tinitus! so when I’m taking three (15 grains) I’m trading one complaint for another.  If you have Any Tinitus stop using aspirin as it could be setting it off.                                            Elliot Cutler

Sorry, I don’t take aspirin. There are several anti-biotics that have the same effect, but it is usually temporary then. No, mine is not from AB’s, I’m just adding to your "aspirin" list. 8-)  Thomas

Response:

I’ve heard that ginkgo can have some positive affects on this; do other remedies exist?  BTW, the cause is from too much loud music/noise over I to suffer from tinnitus. The cause of mine is not know. Have been through a pile of tests. I would also be interested in anything that

I used to get it in spells along with backaches and colds. THe answer is Always simple (o.k. not really). When I act like a hypochondriac I take aspirin.  The first signs of aspirin poisoning is Tinitus! so when I’m taking three (15 grains) I’m trading one complaint for another.  If you have Any Tinitus stop using aspirin as it could be setting it off.                                                 Elliot Cutler

Response:

Ahhh, but one has to put their head on a pillow at night… and then it becomes super noticable…. Have you tried putting your attention on the sound, taking a break from your thoughts, relaxing into the sound, and riding the waves of sound to sleep?   — Have fun!

Sorry, the "sounds" I hear are far from relaxing. And the last thing I wish to to is concentrate on them, this seems to intensify their effect. There are no "waves" in my ears 8-) Fixating on it makes it seem as though my head is turning inside out or collapsing ;-)  Thomas

Response:

Ahhh, but one has to put their head on a pillow at night… and then it becomes super noticable….

Have you tried putting your attention on the sound, taking a break from your thoughts, relaxing into the sound, and riding the waves of sound to sleep?   — Have fun!

Response:

cause is from too much loud music/noise over too many years…".  This is not the only cause.  Tinnitus can also be caused by damage to the

In an attempt to save bandwidth and boredom, I didn’t include my complete hearing history.  I should have said that *my* tinnitus is from loud noise.  I’ve been to an EN&T and a hearing specialist.  I have custom earplugs.  I’ve played drums for 24 years (rock bands, high school band, drum corps), along with attending lots of concerts and loud clubs.   The experts that I’ve sought out have just been able to recommend abstinence, as it were, to help ensure that things don’t get worse. Now, back to my orginal post: I’ve heard that ginkgo can have a positive affect on tinnitus.  Is this true, and are there other remedies/therapies that anyone has tried? Thanks, Hal

Response:

        I would also be interested in learning about any possible remedies for tinnitus.  I’ve got it in my left ear and have ruled out any tumors via an MRI.

Response:

Intravenous glutamic acid diethyl ester relieves ringing. Deutsche Medizinische Wochenschrift   1992;142

Can you tell us a little bit more? I don’t want to go to the med school to look this up… Paul Edwards

Response:

– Hide quoted text — Show quoted text – I to suffer from tinnitus. The cause of mine is not know. Have been through a pile of tests. I would also be interested in anything that might help out with this. There is more truth to the old saying "Silence is golden" than most realize – I haven’t heard [?] it in about 2+ years. Thomas One remedy I’ve had limited success with is Hydergine. A number of (yes, legitimate double-blind, Steve D) medical studies have documented its effect on tinnitus in about 40-50 percent of patients in doses of appx. 6 mg/day. Since the FDA-approved does is only 3 mg day, you have to do some juggling to get these quantities. What I often did was take 5 mg a day until the prescription ran out, then wait until the next opportunity to fill it. This on-off regimen worked fine. It does give a bit of a buzz, like caffeine, which I eventually found too annoying to contend with any more. My current strategy for tinnitus – the one recommended by Stanford Med School docs – is simply to stop paying attention to it. Like any stimulus which serves no purpose for the organism, if you don’t amplify it by paying attention to it it eventually diminishes  or even ends. — Paul N. Edwards

Ahhh, but one has to put their head on a pillow at night… and then it becomes super noticable. Though you are correct. I have found by keeping busy [taking my mind off it] and keeping a fishtank in my room [to create a little backround noise that helps mask and also soothe the mind] works wonders. But there are times when it is terribly annoying and disconcerting – especially when you want a break from something, enter a "quiet" room and end up having your thoughts drowned out by the "ringing". Thomas

Response:

cause is from too much loud music/noise over too many years…".  This is not the only cause.  Tinnitus can also be caused by damage to the ear from infection, by the effect a tumor has on the hearing nerve, and by a hearing nerve that has been traumatized or severed in the course of removing a tumor.  I know about the last one of these, since I had a tumor removed from my right hearing and balance nerves two years ago. Just added information, to supplement what Hal wrote. — Ted Jardine Voice:  206 867 6280

Response:

Intravenous glutamic acid diethyl ester relieves ringing. Deutsche Medizinische Wochenschrift   1992;142

Response:

I to suffer from tinnitus. The cause of mine is not know. Have been through a pile of tests. I would also be interested in anything that might help out with this. There is more truth to the old saying "Silence is golden" than most realize – I haven’t heard [?] it in about 2+ years. Thomas

One remedy I’ve had limited success with is Hydergine. A number of (yes, legitimate double-blind, Steve D) medical studies have documented its effect on tinnitus in about 40-50 percent of patients in doses of appx. 6 mg/day. Since the FDA-approved does is only 3 mg day, you have to do some juggling to get these quantities. What I often did was take 5 mg a day until the prescription ran out, then wait until the next opportunity to fill it. This on-off regimen worked fine. Hydergine has POWERFUL potentiation effects on caffeine – it’ll give you a killer headache if you drink strong coffee along with it. No major side effects are known, and it is non-toxic. It does give a bit of a buzz, like caffeine, which I eventually found too annoying to contend with any more. My current strategy for tinnitus – the one recommended by Stanford Med School docs – is simply to stop paying attention to it. Like any stimulus which serves no purpose for the organism, if you don’t amplify it by paying attention to it it eventually diminishes  or even ends. — Paul N. Edwards

Response:

I’ve heard that ginkgo can have some positive affects on this; do other remedies exist?  BTW, the cause is from too much loud music/noise over too many years…  

Response:

I’ve heard that ginkgo can have some positive affects on this; do other remedies exist?  BTW, the cause is from too much loud music/noise over too many years…  

I to suffer from tinnitus. The cause of mine is not know. Have been through a pile of tests. I would also be interested in anything that might help out with this. There is more truth to the old saying "Silence is golden" than most realize – I haven’t heard [?] it in about 2+ years. Thomas

Response:

Careful — do a little more reading about tinnitus before you start claiming that you know what its cause is.  Tinnitus can be caused by a variety things, including tumors of the 8th (acoustic) nerve.  It is true that ONE cause is excessive exposure to loud sounds, either over a period of time or after one instant.  Another, much less serious cause is cerumen (wax) build up in the ear canal.  In many cases, the cause of a person’s tinnitus is never determined.  Nonetheless, if one experiences tinnitus over a sustained period of time, one should consult one’s health care provider to at least rule out sinister pathology, especially if the tinnitus occurs in only one ear. -Jane M. Opie, Ph.D., Certified Clinical Audiologist

Response:

Somebody asked for some information on this subject. I too have a problem with this.In th ebook by Dr. Andrew Weiler, MD.called Spontaneous Healing he mentioned that some doctors in Germany do neck adjustments and prescribe yoga exeercises for their patients. Hla N.Tin.

Response:

I have a mild case of Tinnitus in my left ear, aggravated by my taking Zoloft, an SSRI-type antidepressent. Has anyone tried ear-coning for tinnitus, with good result? I have been taking ginkgo for several months to try to remedy the ringing. but it doesn’t seem to help, though I have noticed some cognitive enhancement from it. Are there other substances OTC I can take for tinnitus? Thanks. –Will

Response:

Betadine

Question:

Hi, I am going to try using some betadine with the saline. How much should I use? I had a sinus infection last month and took tequin for it. I actually was almost admitted to the hospital because of asthma and bronchitis that went along with the sinusitis. The tequin seemed to work very well. I still  might have  a little bit of the sinus infection remaining. I am not having any major symptoms ,but I am still getting some colored stuff when I irrigate in the morning and evening. I figured a little betadine might knock it out. Thanks for your input. Jody

Response:

On Wed, 9 May 2001 16:59:19 -0400 (EDT), js…@webtv.net (J Slkw) wrote:

I am going to try using some betadine with the saline. How much should I use?

I use between 1/4 and 1/2  tea-spoon in the waterpic reservoire (with the saline/baking soda [or Breathe-Ease] mix).   I’ve gotten so I just use a short "squirt" from the betadine container, rather than precisely measuring it.  Can’t remember how I arrived at this ratio, but it seems to work a bit better than the saline alone.

Response:

This is the usual amount – so that the solution is colored. Make sure you aren’t allergic to Iodine. Murray Grossan, M.D. http://www.ent-consult.com http://www.TinnitusRelief.net

Response:

"Mike Murray" <mmurr…@uswest.net

wrote in message

news:3afbfa1d.546745146@news.uswest.net…

On Wed, 9 May 2001 16:59:19 -0400 (EDT), js…@webtv.net (J Slkw) wrote: I am going to try using some betadine with the saline. How much should I use? I use between 1/4 and 1/2  tea-spoon in the waterpic reservoire (with the saline/baking soda [or Breathe-Ease] mix).   I’ve gotten so I just use a short "squirt" from the betadine container, rather than precisely measuring it.  Can’t remember how I arrived at this ratio, but it seems to work a bit better than the saline alone.

In what way does it "seem to work a bit better"?

Response:

On Sat, 12 May 2001 10:30:38 -0700, "              MS" <m…@nospam.com

wrote:

In what way does it "seem to work a bit better"?

It’s not like irrigation or nasal steroids, where you feel the results almost instantly.  I’m the first to admit that I haven’t any hard evidence other than a vague sense that it helps, especially with overnight postnasal drainage.  Can’t come close to quantifying it, haven’t kept any usage logs, and there’s a host of other variables involved anyway.   If I go a few weeks or more without using it, it seems like I’m more likely to get a flare-up than if I do.  And, if I *do* get a flare-up, using the betadine seems to clear up the colored drainage sooner. What do I mean when I say "sooner" and to what am I comparing?  Good question.  I had a stubborn episode about 1.5 years ago, where the sinusitus wasn’t clearing up and it went away in about four days when I started using Betadine.  But, maybe it was ready to disappear anyway.

Response:

What exactly is Betadine and where do you get it?

John

Response:

jec wrote:

What exactly is Betadine and where do you get it? John

and how much would you put in one cup of saline solution for irrigation purposes??

Response:

I’ve seen posted here in the past a reference to adding betadine to the nasal irrigation solution. How much should be added to the solution? Thanks, Paul

Response:

"pikaso" <pik…@vivessence.com

wrote in message <news:0LKh9.283068$Rx4.3596452@twister.tampabay.rr.com… I’ve seen posted here in the past a reference to adding betadine to the nasal irrigation solution. How much should be added to the solution? Thanks, Paul

Betadine was always irritating to me, better to use Gentamycin no irritation more effective by my experience.

Response:

"Ray Killeen" <ray_kill…@hotmail.com

wrote in message

news:4338b7f2.0209181000.1ced15db@posting.google.com… > "pikaso" <pik…@vivessence.com

wrote in message

<news:0LKh9.283068$Rx4.3596452@twister.tampabay.rr.com

… Betadine was always irritating to me, better to use Gentamycin no irritation more effective by my experience.

Much more difficult to obtain though! Have to find a doc willing to prescribe it.

Response:

Webby is sick

Question:

I didn’t get any sleep at all last night due to his ragged breathing.  I think he has his seemingly annual bronchitis again.

Purrs and prayers on the way dave

Response:

I don’t remember if I said or not but Prayers and Purrs for you and yours dave – Hide quoted text — Show quoted text – I didn’t get any sleep at all last night due to his ragged breathing.  I think he has his seemingly annual bronchitis again.

Response:

Webby has had this before, it clears up quickly with antibiotics thankfully. The vet thinks he may be allergic to something that starts him off on this time of year.  But thank you for the advice.  I was treating him with his own antibiotics, I have just learned not to let it get too much of a head start on me because he becomes very ill, very quickly when he gets this.

Response:

I am so sorry for poor Webby. He does seem to have his share of troubles. I am praying that the antibiotic helps him soon. Ragged breathing is scary. Poor darlin. Sending headbuts and purrs, CATherine – Hide quoted text — Show quoted text – I didn’t get any sleep at all last night due to his ragged breathing.  I think he has his seemingly annual bronchitis again.  I had some antibiotic that I gave him this morning just in case I can’t get him into see a vet today, ( at least now I have 2 to try to get in to see.)  He kept wheeze coughing during the night, which made me keep thinking cardio myopathy since we just lost Hobbes to it. Hopefully I can get him in and get him a shot in the butt today. Last year when this happened, I gave him the antibiotic, which made him mad and he ran away, got bit on the butt by the groundhog, fell out of the tree and broke his rib and breast bone….  sounds like one of those Rube Goldberg goofy chain of events cartoons doesn’t it?  just wasn’t very funny

Response:

Purrs and a dollop of doggy drool on the way for Webby. Sam – Hide quoted text — Show quoted text – I didn’t get any sleep at all last night due to his ragged breathing.  I think he has his seemingly annual bronchitis again.  I had some antibiotic that I gave him this morning just in case I can’t get him into see a vet today, ( at least now I have 2 to try to get in to see.)  He kept wheeze coughing during the night, which made me keep thinking cardio myopathy since we just lost Hobbes to it. Hopefully I can get him in and get him a shot in the butt today. Last year when this happened, I gave him the antibiotic, which made him mad and he ran away, got bit on the butt by the groundhog, fell out of the tree and broke his rib and breast bone….  sounds like one of those Rube Goldberg goofy chain of events cartoons doesn’t it?  just wasn’t very funny

Response:

Oh, I’m so sorry to hear that. I do hope antibiotics make him all better. Best wishes, healing vibes and purrs, — Polonca & Soncek – Hide quoted text — Show quoted text – I didn’t get any sleep at all last night due to his ragged breathing.  I think he has his seemingly annual bronchitis again.  <snip

Response:

Oo. Please keep us updated and I’ll get the purr machines going. Webby! You get better NOW, you hear me? Karen – Hide quoted text — Show quoted text – I didn’t get any sleep at all last night due to his ragged breathing.  I think he has his seemingly annual bronchitis again.  I had some antibiotic that I gave him this morning just in case I can’t get him into see a vet today, ( at least now I have 2 to try to get in to see.)  He kept wheeze coughing during the night, which made me keep thinking cardio myopathy since we just lost Hobbes to it. Hopefully I can get him in and get him a shot in the butt today. Last year when this happened, I gave him the antibiotic, which made him mad and he ran away, got bit on the butt by the groundhog, fell out of the tree and broke his rib and breast bone….  sounds like one of those Rube Goldberg goofy chain of events cartoons doesn’t it?  just wasn’t very funny

Response:

I didn’t get any sleep at all last night due to his ragged breathing.  

   Here are some purrs from our gang to Webby that he’ll get his shots and be right as rain in no time at all.  Purr-ayers for you as well.   Jeanne Jeanne Hajos spamguard:( u is i, and not is net) === "Anger improves nothing except the arch of a cat’s back."                                           — Coleman Cox My SETI team: http://setiathome.ssl.berkeley.edu/stats/team/team_125874.html

Response:

I didn’t get any sleep at all last night due to his ragged breathing.  I think he has his seemingly annual bronchitis again.  I had some antibiotic that I gave him this morning just in case I can’t get him into see a vet today, ( at least now I have 2 to try to get in to see.)  He kept wheeze coughing during the night, which made me keep thinking cardio myopathy since we just lost Hobbes to it.

Poor you and poor Webby.  Lots of  purrs and good wishes from here that he feels much better soon, and without getting bit on the butt by a gopher. Pam, Tanada, Berfert, QC, Merlin, Penelope and Pine Cone

Response:

Purrs for Webby’s breathing to be easier are on their way from the cats and a hug or two from me for a worried meowmie. — Shirley see my cat pictures at http://communities.msn.co.uk/Friendsfamilyandfelines2

Response:

- Hide quoted text — Show quoted text – I didn’t get any sleep at all last night due to his ragged breathing.  I think he has his seemingly annual bronchitis again.  I had some antibiotic that I gave him this morning just in case I can’t get him into see a vet today, ( at least now I have 2 to try to get in to see.)  He kept wheeze coughing during the night, which made me keep thinking cardio myopathy since we just lost Hobbes to it. Hopefully I can get him in and get him a shot in the butt today. Last year when this happened, I gave him the antibiotic, which made him mad and he ran away, got bit on the butt by the groundhog, fell out of the tree and broke his rib and breast bone….  sounds like one of those Rube Goldberg goofy chain of events cartoons doesn’t it?  just wasn’t very funny Hi,

If Webby has had coughing fits on and off over a period of time, and his breathing is adversely affected during these fits , may I suggest you talk urgently to your vet again about what may be causing his coughing..  It may be that  antibiotics may not be all that Webby now needs. Thalia, my elderly Siamese, started having dry coughing fits last autumn. She would cough several times a day for several days, then would cough no more for a while.  Earlier this year, the coughing led to her producing mucus from her lungs and this developed into a chest infection.  She was put on antibiotics .  Although her chest eventually cleared, she continued to have coughing fits.  At this point, I was advised to have her chest x-rayed to see if her heart was OK and to have taken a bronchial swab to find out whether her coughing had started to cause scar tissue in her bronchii.  The test results showed that her heart was fine but that her bronchii were scarred and had undergone changes consistent with asthma and bronchitis.  In the hope of preventing further damage to her lungs, we have to give her steroids to control the coughing and, when necessary, antibiotics to control any chest infection. I don’t mean to alarm you,  but if Webby does have asthma or bronchitis, he will need different treatment to that which you are giving him.  Unless properly treated, both diseases are life-threatening. If you would like to e:mail me privately, I can tell you in more detail, what happened with Thalia. Sheenah

Response:

I didn’t get any sleep at all last night due to his ragged breathing.  I think he has his seemingly annual bronchitis again.  I had some antibiotic that I gave him this morning just in case I can’t get him into see a vet today, ( at least now I have 2 to try to get in to see.)  He kept wheeze coughing during the night, which made me keep thinking cardio myopathy since we just lost Hobbes to it. Hopefully I can get him in and get him a shot in the butt today. Last year when this happened, I gave him the antibiotic, which made him mad and he ran away, got bit on the butt by the groundhog, fell out of the tree and broke his rib and breast bone….  sounds like one of those Rube Goldberg goofy chain of events cartoons doesn’t it?  just wasn’t very funny

Response:

We will pray for Webby’s quick recovery. We hope it isn’t anything too grave. Jazz & his mama — Irulan from the stars we came, to the stars we return from now until the end of time – Hide quoted text — Show quoted text – I didn’t get any sleep at all last night due to his ragged breathing.  I think he has his seemingly annual bronchitis again.  I had some antibiotic that I gave him this morning just in case I can’t get him into see a vet today, ( at least now I have 2 to try to get in to see.)  He kept wheeze coughing during the night, which made me keep thinking cardio myopathy since we just lost Hobbes to it. Hopefully I can get him in and get him a shot in the butt today. Last year when this happened, I gave him the antibiotic, which made him mad and he ran away, got bit on the butt by the groundhog, fell out of the tree and broke his rib and breast bone….  sounds like one of those Rube Goldberg goofy chain of events cartoons doesn’t it?  just wasn’t very funny

Response:

- Hide quoted text — Show quoted text – I didn’t get any sleep at all last night due to his ragged breathing.  I think he has his seemingly annual bronchitis again.  I had some antibiotic that I gave him this morning just in case I can’t get him into see a vet today, ( at least now I have 2 to try to get in to see.)  He kept wheeze coughing during the night, which made me keep thinking cardio myopathy since we just lost Hobbes to it. Hopefully I can get him in and get him a shot in the butt today. Last year when this happened, I gave him the antibiotic, which made him mad and he ran away, got bit on the butt by the groundhog, fell out of the tree and broke his rib and breast bone….  sounds like one of those Rube Goldberg goofy chain of events cartoons doesn’t it?  just wasn’t very funny

Purrs and get well vibes are going out to Webby!  Hope you can get him into the vet this morning!  Please keep us posted. Christine, Omar, Midnight, Shetra & Oreo

Response:

Health Insurance Options and Costs

Question:

John, It stands for Chronic Obstructive Pulmonary Disease – Emphysema, asthma and bronchitis are COPD’s  (I think.) ~~~~Pat CD Class of 98 "John Riggs"  wrote – Hide quoted text — Show quoted text –     Pardon my ignorance, but what is COPD ( seems the brain is still on vacation )?

Response:

Emphysema, asthma, and CHRONIC bronchitis are COPD.  I have adult onset asthma and chronic bronchitis from work exposure, in addition to CD (class of 97) Ceresse

– Hide quoted text — Show quoted text – John, It stands for Chronic Obstructive Pulmonary Disease – Emphysema, asthma and bronchitis are COPD’s  (I think.) ~~~~Pat CD Class of 98 "John Riggs"  wrote     Pardon my ignorance, but what is COPD ( seems the brain is still on vacation )?

Response:

What were you exposed to at work that caused your COPD?  I have what my doctor calls "an asthmatic condition probably caused from smoking".  I wouldn’t be surprised if I also was in the beginning stages of emphysema.  I use Serevent and Flovent inhalers twice and day and my  breathing is much better with them. ~~~~Pat CD Class of 98 "Ceresse"  wrote – Hide quoted text — Show quoted text – Emphysema, asthma, and CHRONIC bronchitis are COPD.  I have adult onset asthma and chronic bronchitis from work exposure, in addition to CD (class of 97) Ceresse

Response:

very old and mildewed insulation.  The white stuff.  I’m glad the inhalers help you.  Ceresse

– Hide quoted text — Show quoted text – What were you exposed to at work that caused your COPD?  I have what my doctor calls "an asthmatic condition probably caused from smoking".  I wouldn’t be surprised if I also was in the beginning stages of emphysema. I use Serevent and Flovent inhalers twice and day and my  breathing is much better with them. ~~~~Pat CD Class of 98 "Ceresse"  wrote Emphysema, asthma, and CHRONIC bronchitis are COPD.  I have adult onset asthma and chronic bronchitis from work exposure, in addition to CD (class of 97) Ceresse

Response:

    Pardon my ignorance, but what is COPD ( seems the brain is still on vacation )?

– Hide quoted text — Show quoted text – I am in Illinois, am under 65 (43) and am on disability for work exposure related COPD.  If you have some helpful info on this, I would REALLY appreciate it as I truly could find only one Medigap carrier to cover me, at $2000 a year with no prescription coverage!  Thanks, Ceresse Ceresse, I’ve been on Medicare for years, left a Medicare HMO 2 years ago and have had 2 Medigap policies since. If you have Medicare you can get a Medigap Policy. The only difference is if you are under 65. In MD those on Medicare under 65 can only purchase Plan A and C. I pay $90.60 for Plan C which covers all Medicare co-pays and deductibles. What state are you in? one more thing, I have not been able to obtain a Medigap policy due to my health. Ceresse I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

I am in Illinois, am under 65 (43) and am on disability for work exposure related COPD.  If you have some helpful info on this, I would REALLY appreciate it as I truly could find only one Medigap carrier to cover me, at $2000 a year with no prescription coverage!  Thanks, Ceresse

– Hide quoted text — Show quoted text – Ceresse, I’ve been on Medicare for years, left a Medicare HMO 2 years ago and have had 2 Medigap policies since. If you have Medicare you can get a Medigap Policy. The only difference is if you are under 65. In MD those on Medicare under 65 can only purchase Plan A and C. I pay $90.60 for Plan C which covers all Medicare co-pays and deductibles. What state are you in? one more thing, I have not been able to obtain a Medigap policy due to my health. Ceresse I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

Ceresse, I’ve been on Medicare for years, left a Medicare HMO 2 years ago and have had 2 Medigap policies since. If you have Medicare you can get a Medigap Policy. The only difference is if you are under 65. In MD those on Medicare under 65 can only purchase Plan A and C. I pay $90.60 for Plan C which covers all Medicare co-pays and deductibles. What state are you in?

– Hide quoted text — Show quoted text – one more thing, I have not been able to obtain a Medigap policy due to my health. Ceresse I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

Rose Bowl against Nebraska I believe.  Sorry the idea for the RX’s isn’t possible.  As for your family and what you said earlier, coming from a Jewish household with a very strong headed mother, you have to learn to let some of it roll off your back.  My mom is the greatest but she is so strong headed at times that if I didn’t just roll with it I’d probably go nuts at times.  I am very close to her though.  I don’t want to give the wrong idea. UM MOM Susan

– Hide quoted text — Show quoted text – Thanks, Susan.  There are no Eckerd’s or Walgreen’s within 50 miles, and when I’ve discussed these plans with my pharmacies, we’ve discovered that they won’t help my scripts or are unacceptable.  I comparison shop, it’s the best I can do, and my doctor is cooperative with this.  But thanks for the thought!  Ceresse P.S. what bowl game is UM playing in this year? : ) Ceresse there is discounts you can receive on Rx’s at a really reasonable price.  People’s insurance is one that comes to mind, But you can go to your pharmacy and see if they offer this service.  I know Eckerd’s does and I think Walgreens too.  UM MOM Susan one more thing, I have not been able to obtain a Medigap policy due to my health. Ceresse I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

Thanks, Susan.  There are no Eckerd’s or Walgreen’s within 50 miles, and when I’ve discussed these plans with my pharmacies, we’ve discovered that they won’t help my scripts or are unacceptable.  I comparison shop, it’s the best I can do, and my doctor is cooperative with this.  But thanks for the thought!  Ceresse P.S. what bowl game is UM playing in this year? : )

– Hide quoted text — Show quoted text – Ceresse there is discounts you can receive on Rx’s at a really reasonable price.  People’s insurance is one that comes to mind, But you can go to your pharmacy and see if they offer this service.  I know Eckerd’s does and I think Walgreens too.  UM MOM Susan one more thing, I have not been able to obtain a Medigap policy due to my health. Ceresse I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

Ceresse there is discounts you can receive on Rx’s at a really reasonable price.  People’s insurance is one that comes to mind, But you can go to your pharmacy and see if they offer this service.  I know Eckerd’s does and I think Walgreens too.  UM MOM Susan

– Hide quoted text — Show quoted text – one more thing, I have not been able to obtain a Medigap policy due to my health. Ceresse I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

one more thing, I have not been able to obtain a Medigap policy due to my health. Ceresse

– Hide quoted text — Show quoted text – I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

Jonathan, what a predicament you are in!  I am on disability due to my health, and have only Medicare coverage at this time.  The premiums to continue my HMO health insurance from my last job became prohibitive. Medicare’s coverage may be better than what you currently have, as I still pay only 20%, $100 deductible, $750 for hospitalizations, but there is NO prescription coverage.  I cannot get prescription coverage separately.  I could be placed for a reasonably fee under my husband’s policy but 1) it won’t cover pre-existing conditions for a year (as Susan mentioned) and 2) I can’t continue the Medicare for that year while I am signed up and waiting. So, I deal with what I have.  I’m afraid this isn’t very helpful, but it is offered in response to your questions as to how I deal with insurance. An aside–as a former insurance agent, I can tell you that from a strictly insurance stand point, medical insurance is untenable.  Insurance coverage is based upon the principle that not everyone will need it, and that not many (comparatively) will need it at the same time.  But, EVERYONE needs medical insurance.  You see the problem?  For insurance to work the many pay for the needs of the few.  You pay your auto insurance every month, but how many accidents have you ever had?  You’re paying for the protection you MIGHT need if you EVER have an accident.  See?  But just about  everyone needs health coverage just about every year.  So what IS the solution?  I don’t know.  If you speak to people from nations with socialized medicine, there are problems with those systems.  Our system doesn’t work.  The sick go without treatment while many health care providers get rich.  Aren’t plastic surgeons among the richest physicians and isn’t this ironic?  Don’t know what we can do….. I really feel for you in this problem of prohibitive health insurance payments with health problems that require treatment!  Ceresse

– Hide quoted text — Show quoted text – I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

actually, the REAL REASON is the top 1/2 of 1% of the rich get multi-million dollar salaries and bonuses, and typically these individuals are CEO’s and their associates in drug, health insurance companies and hospitals.  if only anyone had any idea where all this $$$ is going…did  you ever wonder?  it is in the lining of the pockets of a only a very few sitting on the very top.  believe me, we pay DEARLY!!!! so just a few can be very, VERY rich!!! (and by the way, they never go without a job or take salary cuts either!) jeff, cd class of o1

– Hide quoted text — Show quoted text – Some more information, just for the record:  -I live in Pennsylvania (Western suburbs of Philadelphia).  -I am not a veteran.  -I didn’t even know that there was an insurance commission. The insurance companies truly make me feel like a 2nd class citizen – like a criminal who has committed some horrendous crime.  I try not to take it personally.  But they are the power brokers in my opinion who impact such a large part of our lives. I feel that one of the key reasons that insurance rates are rising at such an alarming rate, is because their investments aren’t providing the returns that they were a couple of years ago.  Isn’t it interesting that these soaring rate increases started around the time that interest rates had plummeted? Despite these problems, I am counting my blessings, because I currently have a job and am currently not disabled and therefore able to perform my job duties. I will share your information with my wife. Take care and again I really appreciate your respnoses, Jonathan Joseph

Response:

Pearl L: Thanks! This site is very helpful and has already answered some of my questions. Merry Christmas! Jonathan Joseph – Hide quoted text — Show quoted text – Jonathan, Go to your state’s insurance site at: http://www.insurance.state.pa.us/html/health.html

Response:

Jonathan, Your welcome. I love your name. My youngest son is named Jonathan. He is an attorney in Chicago. He has psoriatic arthritis, another expression of the various genes that cause autoimmune diseases. I have been a patient advocate for over 20 years – founded CCFA in MD, National Dir. Pt. Advocacy & Government Relations, CCFA, 3 years in the MD Attorney General’s Office of Health Education and Advocacay and now founder and presidnet of the MD Patient Advocacy Group. If there is anything I can do, let me know.

Pearl L: Thanks! This site is very helpful and has already answered some of my questions. Merry Christmas! Jonathan Joseph

– Hide quoted text — Show quoted text – Jonathan, Go to your state’s insurance site at: http://www.insurance.state.pa.us/html/health.html

Response:

<< and now founder and presidnet of the MD Patient Advocacy Group.

What is the annual budget of the MD Patient Advocacy Group?

Response:

Some more information, just for the record:  -I live in Pennsylvania (Western suburbs of Philadelphia).  -I am not a veteran.  -I didn’t even know that there was an insurance commission. The insurance companies truly make me feel like a 2nd class citizen – like a criminal who has committed some horrendous crime.  I try not to take it personally.  But they are the power brokers in my opinion who impact such a large part of our lives. I feel that one of the key reasons that insurance rates are rising at such an alarming rate, is because their investments aren’t providing the returns that they were a couple of years ago.  Isn’t it interesting that these soaring rate increases started around the time that interest rates had plummeted? Despite these problems, I am counting my blessings, because I currently have a job and am currently not disabled and therefore able to perform my job duties. I will share your information with my wife. Take care and again I really appreciate your respnoses, Jonathan Joseph

Response:

Jonathan, Go to your state’s insurance site at: http://www.insurance.state.pa.us/html/health.html

– Hide quoted text — Show quoted text – Some more information, just for the record:  -I live in Pennsylvania (Western suburbs of Philadelphia).  -I am not a veteran.  -I didn’t even know that there was an insurance commission. The insurance companies truly make me feel like a 2nd class citizen – like a criminal who has committed some horrendous crime.  I try not to take it personally.  But they are the power brokers in my opinion who impact such a large part of our lives. I feel that one of the key reasons that insurance rates are rising at such an alarming rate, is because their investments aren’t providing the returns that they were a couple of years ago.  Isn’t it interesting that these soaring rate increases started around the time that interest rates had plummeted? Despite these problems, I am counting my blessings, because I currently have a job and am currently not disabled and therefore able to perform my job duties. I will share your information with my wife. Take care and again I really appreciate your respnoses, Jonathan Joseph

Response:

Jonathan, if your wife is able to get insurance through her job check that out.  I’m able to get insurance through my husband and I’m not denied for having a pre-existing condition.  And there hasn’t been any waiting period. — Take Care, Sherry  :o)

I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

Pearl You are right in that .. I did some investigating because I was previously covered under my X’s plan and when I changed to the one my company offered they told me that the pre existing clause will be waived as I had continuing medical insurance prior to the change over … the same will apply when I go from my insurance at work, to my husbands insurance company through the Air Force Retirement Program Peace and Love Maryjo

Response:

yeah, i wonder how the CEO’s of some of these health insurance companies enjoyed their million dollar bonuses on us!!! jeff, cd class of o1

– Hide quoted text — Show quoted text – If you change insurance, like to your wife’s all pre-existing health problems will be denied for a year.  They can not deny you coverage but they can make you wait the year.  Are you in the USA?  If so contact the insurance commission about them gouging you.  They are already on insurance companies about this problem.  The only other thing I can suggest is going through the government agencies for care which is lousy I have been told. Are you a Veteran?  They too may be able to help you. Sorry I can’t do more. UM MOM Susan, Who thinks what they are doing is lousy. I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

No – as long as you have been covered previously and do not have a lapse in coverage of more than 63 days, you cannot be denied insurance and there is no pre-exisitng condition waiting period. That is federal law to allow people to change jobs. In Maryland there is also a no pre-exisitng condition clause. Each state has its own laws but federal law of course covers us all. First, check with your insurance commissioner to see what applies in your state. Each state has different plans avaialbe for the self-employed and for small groups. Many of us are on Social Security Disability and after 24 months we are on Medicare with a Medigap Policy. Unfortunately to get around the various federal and state laws mandating coverage of pre-existing conditions companies simply adverse select by raising premiums. Only if you are a member of a group – for instance in Maryland if you are a small group – 2 or more they can only charge you the premium applicable to small groups. Perhaps if you had one employee –  your wife or someone and your state had similar coverage for small groups with premiums set – you could incorporate and go that way – however, I don’t know where you live or what your laws are. I think you should find out!

– Hide quoted text — Show quoted text – If you change insurance, like to your wife’s all pre-existing health problems will be denied for a year.  They can not deny you coverage but they can make you wait the year.  Are you in the USA?  If so contact the insurance commission about them gouging you.  They are already on insurance companies about this problem.  The only other thing I can suggest is going through the government agencies for care which is lousy I have been told. Are you a Veteran?  They too may be able to help you. Sorry I can’t do more. UM MOM Susan, Who thinks what they are doing is lousy. I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

If you change insurance, like to your wife’s all pre-existing health problems will be denied for a year.  They can not deny you coverage but they can make you wait the year.  Are you in the USA?  If so contact the insurance commission about them gouging you.  They are already on insurance companies about this problem.  The only other thing I can suggest is going through the government agencies for care which is lousy I have been told. Are you a Veteran?  They too may be able to help you. Sorry I can’t do more. UM MOM Susan, Who thinks what they are doing is lousy.

– Hide quoted text — Show quoted text – I am self employed, 50 years old, and was diagnosed with Crohns Disease in September 1999 after 6 months of non-stop problems. Fortunately, I had health insurance.  My health insurance plan was and is still an open enrollment PPO plan with Cigna that is available from the IEEE organization and provides coverage for me, my wife and daughter.  Prior to enrolling in this health insuracne plan, I found it impossible to obtain health insurance, because I was previously diagnosed with a mild bipolar disorder. My health insurance premiums have always been high.  However, during the past 12 months, I have seen 3 20% rate increases (one was due to my turning 50 years old).  Financially, I’m reaching the ‘breaking point’ on my ability to pay these premiums and cope with the high deductible, but don’t know what to do about it.  The cost is almost $1100 per month (completely out of my pocket) with a $2000 deductible.  I haven’t explored having my wife apply for health insurance for our family, but since I would need to be covered under her plan, she’d probably be denied family coverage in a non-open enrollment plan. It appears that my options are quite limited. I have the following questions for this newsgroup: -in general, what has been your strategy for insurance coverage? -do you have health insurance? -if so, what type: hmo or ppo? -did you obtain your health before of after being diagnosed? -if you obtained your health insurance after being diagnosed, how did you qualify for health insurance (open enrollment?, through work?) -if you don’t have health insurance, how are you managing to get health care? Thanks for your help and I truly wish everyone a happy holiday free from IBD symptoms. Jonathan Joseph

Response:

Sinus Survival – Is Latest Edition (2000) Worth Getting?

Question:

Mike wrote:

I currently have a copy of the 1995 edition of Robert Ivker’s book, Sinus Survival on loan from my local library. I’d really appreciate it if someone could comment on whether or not there’s enough new content in the 2000 edition to make it worth purchasing.

There’s some updated material, to take into account new meds and new scientific results on sinusitis. But in other ways, there is actually LESS content than the 1995 edition.  Because Dr. Ivker removed the material on asthma and bronchitis–in order to put that material into another book which he is now writing.  So the 2000 edition primarily deals with sinusitis only, not asthma or bronchitis. — Steven D. Litvintchouk                   Email:  sdlit…@earthlink.net     "I guess I could have paid a little closer attention when I was in English class, but it all worked out OK.  I’m gainfully employed."      – President George W. Bush

Response:

I currently have a copy of the 1995 edition of Robert Ivker’s book, Sinus Survival on loan from my local library. I’d really appreciate it if someone could comment on whether or not there’s enough new content in the 2000 edition to make it worth purchasing. Thanks, Mike

Response:

in article 3b13b9e3.13248…@netnews.att.net, Mike at witne…@bigfoot.com wrote on 5/29/01 11:05 AM:

I currently have a copy of the 1995 edition of Robert Ivker’s book, Sinus Survival on loan from my local library. I’d really appreciate it if someone could comment on whether or not there’s enough new content in the 2000 edition to make it worth purchasing. Thanks, Mike

I believe it is worth purchasing.  There is a lot more information in the latest edition.  Check out the table of contents at the website. http://www.sinussurvival.com/book/contents.htm

Response:

Brochospasms?

Question:

Hello, I don’t (think I) have asthma, but this is the only place I can find to ask… I have an intermittent problem where sometimes my throat (or airway) closes up and I can’t breath for about one minute.  It is extremely scary.  Sometimes I think I’m going to die. It is always triggered by something in my throat.  It is very similar, if not the same, as when you take a drink and a little goes "down the wrong tube" and you cough for a little while.  but with me, my throat closes and I can’t cough or breath. Triggers include something really sweet, spicy, or sour touching the back of my throat.  sometimes just saliva will touch something back there and it will happen. This has happened since I was a kid (I’m now 32) and it happens about once a week, on average. One very strange thing about it is that when it’s happening, I actually can breath OUT fairly well.  Then I struggle to breathe in, very slowly, panicking, and again it is fairly easy to breathe out again.  Then of course I have to breathe in again and it is next to impossible.  All of my memories of this traumatic experience are of  not being able to breathe IN, taking sometimes 30 seconds for each inhalation, and then exhaling in just a few seconds. Sometimes I’ve noticed that if I drink some water it helps a little, but it doesn’t help enough, and sometimes not at all. I went to my doctor and he sent me to an ENT specialist.  I was very disapointed because first he doubted that I could have trouble breating in but not out.  His diagnosis was that disease where the valve on your stomach doesn’t close right and the acid comes up your esophagus.  I just really don’t think that’s what it is, since I rarely get heartburn, and this has been happening since I was a kid, and I never had heartburn or other similar symptoms at that age. I searched the internet and found something called Bronchospasms, which seems like this could be it.  According to the articles I read, just about anything can cause Bronchospasms in some people.  Maybe I’m one of those people. But I couldn’t find much more information, like treatment, or whether or not the breathing IN problem is common to this condition. If anyone out there has any suggestions or information about Bronchospasms, please let me know.  I would REALLY appreciate it. Thank you, Gary Beckwith

Response:

- Hide quoted text — Show quoted text – I don’t (think I) have asthma, but this is the only place I can find to ask… I have an intermittent problem where sometimes my throat (or airway) closes up and I can’t breath for about one minute.  It is extremely scary.  Sometimes I think I’m going to die. It is always triggered by something in my throat.  It is very similar, if not the same, as when you take a drink and a little goes "down the wrong tube" and you cough for a little while.  but with me, my throat closes and I can’t cough or breath. Triggers include something really sweet, spicy, or sour touching the back of my throat.  sometimes just saliva will touch something back there and it will happen. This has happened since I was a kid (I’m now 32) and it happens about once a week, on average. One very strange thing about it is that when it’s happening, I actually can breath OUT fairly well.  Then I struggle to breathe in, very slowly, panicking, and again it is fairly easy to breathe out again.  Then of course I have to breathe in again and it is next to impossible.  All of my memories of this traumatic experience are of  not being able to breathe IN, taking sometimes 30 seconds for each inhalation, and then exhaling in just a few seconds.

In asthma it’s just the reverse; asthmatics have trouble in breathing out. So I agree with you this doesn’t sound like asthma. Doesn’t sound like anaphylaxis either since you only have trouble breathing in. Sometimes I’ve noticed that if I drink some water it helps a little, but it doesn’t help enough, and sometimes not at all. I went to my doctor and he sent me to an ENT specialist.  I was very disapointed because first he doubted that I could have trouble breating in but not out.  His diagnosis was that disease where the valve on your stomach doesn’t close right and the acid comes up your esophagus.  I just really don’t think that’s what it is, since I rarely get heartburn, and this has been happening since I was a kid, and I never had heartburn or other similar symptoms at that age.

Gastroespophageal (GE) reflux sounds like a possibility, as your doctor suggested. You could consult a gastroenterologist for another opinion. A faulty spincter valve can allow acid into the esophagus where it can do damage. Lack of heartburn does not rule out GE reflux. Treatment for GE reflux includes elevating head of bed 6" with wood blocks, no meals near bedtime, and drugs like H2 blockers or omaprazole. Sometimes surgery. Link: http://www.vh.org/Providers/ClinRef/FPHandbook/Chapter04/09-4.html University of Iowa Family Practice Handbook, 3rd Edition, Chapter 4 Gastroenterology: Esophageal Diseases http://www.acg.gi.org/patientinfo/frame_gerd.html  GERD I searched the internet and found something called Bronchospasms, which seems like this could be it.  According to the articles I read, just about anything can cause Bronchospasms in some people.  Maybe I’m one of those people. But I couldn’t find much more information, like treatment, or whether or not the breathing IN problem is common to this condition. If anyone out there has any suggestions or information about Bronchospasms, please let me know.  I would REALLY appreciate it. Thank you, Gary Beckwith

Bronchospasm according to Mosby: "an abnormal contraction of the bronchi, resulting in narrowing and blockage of the airway. A cough with wheezing is the usual symptom. Bronchospasm is the main feature of asthma and bronchitis." Your symptoms don’t seem to correspond with bronchospasm. I would vote for GE reflux, but sounds like you need to consult more specialists like a gastro guy. Ellis

Response:

Your laryngospasm should be reported to your otolaryngologist.  If you don’t have one, ask your PCP to refer you to one.  The spasms can result unconsciousness. – Hide quoted text — Show quoted text – I have an intermittent problem where sometimes my throat (or airway) closes up and I can’t breath for about one minute.  It is extremely scary.  Sometimes I think I’m going to die. When this happened to me it was caused by my vocal cords temporarily jamming shut. You can tell it was only temporary by the fact that you are reading this post. Jo.

Response:

I have an intermittent problem where sometimes my throat (or airway) closes up and I can’t breath for about one minute.  It is extremely scary.  Sometimes I think I’m going to die.

When this happened to me it was caused by my vocal cords temporarily jamming shut. You can tell it was only temporary by the fact that you are reading this post. Jo.

Response:

I have an intermittent problem where sometimes my throat (or airway) closes up and I can’t breath for about one minute.  It is extremely scary.  Sometimes I think I’m going to die. When this happened to me it was caused by my vocal cords temporarily jamming shut. You can tell it was only temporary by the fact that you are reading this post. Jo.

Sounds like VCD. See: http://www.njc.org/MFhtml/VCD_MF.html Vocal Cord Dysfunction ‘95, NJC Excerpt: "To understand VCD, it is helpful to know how the vocal cords  function normally. When you breathe in, or inhale, the vocal cords open, allowing air to flow into your windpipe  (trachea) and reach your lungs. However, with Vocal Cord Dysfunction, the vocal cords close together, or  constrict, when you inhale. This leaves only a small opening for air to flow into your windpipe."

why *wouldn't* he try ritalin or something

Question:

Yes Ritalin is meant to be taken before school and once every four hours and most children don’t take it after they leave school.  It is a drug like an amphetamine.  It might help you temporarily (you could use it to attend work) but you would still need an AD for the underlying depression.  My doctor is treating my depression first and once we have that under control and I am ready to go back to work we will look at adding Ritalin or Cylert (I think it is longer acting so a better choice for me).  I think that you should talk to your doctor about all of these issues. If your main goal is to get back to a functional level at work maybe Ritalin is the best choice but you will still have to find an AD that works.  If your main goal is like mine (I am currently unemployed) to treat the depression so I can get to a functional level then you would need to find an AD combo and add Ritalin later. Did any of that make sense – I didn’t get a prescription for Ritalin so I am really having a hard time writing :-( – Hide quoted text — Show quoted text – why would dr phelan be reluctant to try my on ritalin or similar? the drugs work really fast right? like within hours/days rather than weeks/months, so it would just be a very simple and quick trial to do.

Response:

Adderall worked for me within 30 minutes. I took one and felt better.  There’s been a lot of tinkering around with the dosages to find the right stuff, and i’ve heard that generic ritalin doesn’t work very well, but basically, the answer to the question is yes, you would feel something quickly.  it took a few weeks before it really kicked in strong….and i started seeing differences in my behavior.  but my basic mind was effected immediately. he could be hesitant because many doctors feel that if hyperactivity isn’t present, you don’t have it.  that is absolutely not true, but it is still misunderstood.  also because it is a mild amphetamine.  it doesn’t hype you up, it just wakes up the part of the brain that isn’t functioning normally. jaz

– Hide quoted text — Show quoted text – why would dr phelan be reluctant to try my on ritalin or similar? the drugs work really fast right? like within hours/days rather than weeks/months, so it would just be a very simple and quick trial to do.

Response:

sadly ritalin is a contolled drug because it is related to amphetamines the doses used are A LOT less than on the street and the drug has a good safely record (otherwise why would it be used on millions of schoolkids) its all about doctors watching their backs

– Hide quoted text — Show quoted text – why would dr phelan be reluctant to try my on ritalin or similar? the drugs work really fast right? like within hours/days rather than weeks/months, so it would just be a very simple and quick trial to do.

Response:

why would dr phelan be reluctant to try my on ritalin or similar? the drugs work really fast right? like within hours/days rather than weeks/months, so it would just be a very simple and quick trial to do.

Response:

I never thought of it from that perspective.  I guess because my inability to concentrate developed as a side effect from depression, I tend to assume everyone else has the same problem. Narrow minded, sorry.  I guess treatment depends on the diagnosis.  Did you have ADD prior to developing depression? Maggie – Hide quoted text — Show quoted text – not necessarily.  lots of times, adderall has been enough for me.  if it was one or the other, i’d take adderall.  i am NO GOOD on just antidepressants.  i can’t function nearly as well on only anti depressants as i can on only adderall. sometimes depression stems from ADD.  from being overwhelmed by all the projects you can’t finish.  by being unable to find stuff, get organized, get it together, get motivated, take a shower, get out of bed.  it’s not always the other way around. jaz Yes Ritalin is meant to be taken before school and once every four hours and most children don’t take it after they leave school.  It is a drug like an amphetamine.  It might help you temporarily (you could use it to attend work) but you would still need an AD for the underlying depression.  My doctor is treating my depression first and once we have that under control and I am ready to go back to work we will look at adding Ritalin or Cylert (I think it is longer acting so a better choice for me).  I think that you should talk to your doctor about all of these issues. If your main goal is to get back to a functional level at work maybe Ritalin is the best choice but you will still have to find an AD that works.  If your main goal is like mine (I am currently unemployed) to treat the depression so I can get to a functional level then you would need to find an AD combo and add Ritalin later. Did any of that make sense – I didn’t get a prescription for Ritalin so I am really having a hard time writing :-( why would dr phelan be reluctant to try my on ritalin or similar? the drugs work really fast right? like within hours/days rather than weeks/months, so it would just be a very simple and quick trial to do.

Response:

Well, ADD and depression are two completely separate things. You can have one without the other.  If you have ADD, it shouldn’t be because you are depressed.  It’s like some people have asthma and bronchitis.  One doesn’t necessarily cause the other, but can make each other worse.  I think ADD could cause depression, but I don’t see how depression could cause ADD. There are physical differences in the brains of ADDers.  I don’t know which came first for me.  My ADD wasn’t troublesome really until college.  However, I can see strong instances of inattentive behavior and tons of day dreaming from a very young age. I also remember small signs of depression at a young age.  I think that my depression was significantly worsened by the ADD.  I had no idea what the hell was wrong with me, and lost confidence in my brain’s ability.  I was very down on myself.  Learning about the ADD was a tremendous relief.  It had a name, a medication, and it was a common problem.  I wasn’t the only one.  My depression got a lot better as soon as I was on ADD medication.  However, lately I’ve realized that the depression is still an issue, as I’ve had to go back on Anti-depressants.   I do know that depression can give you the inability to concentrate also.  It may be that ADD drugs will help in that circumstance too…but I’m not sure that it could be classified as true ADD.  If you can’t find any ADD symptoms separate from your depression, you probably don’t have ADD.  Does that make sense?  It sounds like your doctor is treating it all as depression.  Of course I’m not a doctor, I’m just going with what my doctor has told me, and all the research that I’ve done.  Once I knew what was wrong with me, I started reading everything I could get my hands on about it.  But I still could be wrong.  Interesting, huh? jaz

– Hide quoted text — Show quoted text – I never thought of it from that perspective.  I guess because my inability to concentrate developed as a side effect from depression, I tend to assume everyone else has the same problem. Narrow minded, sorry.  I guess treatment depends on the diagnosis.  Did you have ADD prior to developing depression? Maggie not necessarily.  lots of times, adderall has been enough for me.  if it was one or the other, i’d take adderall.  i am NO GOOD on just antidepressants.  i can’t function nearly as well on only anti depressants as i can on only adderall. sometimes depression stems from ADD.  from being overwhelmed by all the projects you can’t finish.  by being unable to find stuff, get organized, get it together, get motivated, take a shower, get out of bed.  it’s not always the other way around. jaz Yes Ritalin is meant to be taken before school and once every four hours and most children don’t take it after they leave school.  It is a drug like an amphetamine.  It might help you temporarily (you could use it to attend work) but you would still need an AD for the underlying depression.  My doctor is treating my depression first and once we have that under control and I am ready to go back to work we will look at adding Ritalin or Cylert (I think it is longer acting so a better choice for me). I think that you should talk to your doctor about all of these issues. If your main goal is to get back to a functional level at work maybe Ritalin is the best choice but you will still have to find an AD that works.  If your main goal is like mine (I am currently unemployed) to treat the depression so I can get to a functional level then you would need to find an AD combo and add Ritalin later. Did any of that make sense – I didn’t get a prescription for Ritalin so I am really having a hard time writing :-( why would dr phelan be reluctant to try my on ritalin or similar? the drugs work really fast right? like within hours/days rather than weeks/months, so it would just be a very simple and quick trial to do.

Response:

– Hide quoted text — Show quoted text – Adderall worked for me within 30 minutes. I took one and felt better.  There’s been a lot of tinkering around with the dosages to find the right stuff, and i’ve heard that generic ritalin doesn’t work very well, but basically, the answer to the question is yes, you would feel something quickly.  it took a few weeks before it really kicked in strong….and i started seeing differences in my behavior.  but my basic mind was effected immediately. he could be hesitant because many doctors feel that if hyperactivity isn’t present, you don’t have it.  that is absolutely not true, but it is still misunderstood.  also because it is a mild amphetamine.  it doesn’t hype you up, it just wakes up the part of the brain that isn’t functioning normally. jaz why would dr phelan be reluctant to try my on ritalin or similar? the drugs work really fast right? like within hours/days rather than weeks/months, so it would just be a very simple and quick trial to do.

            bryant tillman Share what you know. Learn what you don’t.

Response:

Well, ADD and depression are two completely separate things. You can have one without the other.   I think ADD could cause depression, but I don’t see how depression could cause ADD. There are physical differences in the brains of ADDers. My ADD wasn’t troublesome really until college.  However, I can see strong instances of inattentive behavior and tons of day dreaming from a very young age. I had no idea what the hell was wrong with me, and lost confidence in my brain’s ability.  I was very down on myself. My depression got a lot better as soon as I was on ADD medication.

Interesting post, jaz.  Someday when I get the backbone, I think I will go to a doctor and ask to try medication for ADD. <shudder  Then again, maybe that day will never come.  I seem to have huge issues around this topic.  Wrinkles in the space time continuum.  :( Then again, does it really matter if it’s just cosmetic? Out of curiosity, what are the physical differences?  I thought ADD just described a set of symptoms and that no organic cause was really known or posited.

Response:

- Hide quoted text — Show quoted text – http://www.amenclinic.com/spect.htm  talks about technology that can show differences in brain functioning. http://www.amenclinic.com/addbrain.htm shows the ADD brain in action. there are other physical traits, such as frequent ear infections as a child, strange sleep patterns/REM functioning and more, things that can actually be measured if one is looking for a physical diagnosis. Usually, if the symptoms are there, most doctors don’t do all of that.  They see if the medication helps.  all diseases are really diagnosed by collecting a set of symptoms….i guess.  They don’t really know what causes it, other than genetic factors. hope that helps a little.

It  does – thanks.

Response:

http://www.amenclinic.com/spect.htm  talks about technology that can show differences in brain functioning. http://www.amenclinic.com/addbrain.htm shows the ADD brain in action. there are other physical traits, such as frequent ear infections as a child, strange sleep patterns/REM functioning and more, things that can actually be measured if one is looking for a physical diagnosis. Usually, if the symptoms are there, most doctors don’t do all of that.  They see if the medication helps.  all diseases are really diagnosed by collecting a set of symptoms….i guess.  They don’t really know what causes it, other than genetic factors. hope that helps a little. jaz

– Hide quoted text — Show quoted text – Well, ADD and depression are two completely separate things. You can have one without the other. I think ADD could cause depression, but I don’t see how depression could cause ADD. There are physical differences in the brains of ADDers. My ADD wasn’t troublesome really until college.  However, I can see strong instances of inattentive behavior and tons of day dreaming from a very young age. I had no idea what the hell was wrong with me, and lost confidence in my brain’s ability.  I was very down on myself. My depression got a lot better as soon as I was on ADD medication. Interesting post, jaz.  Someday when I get the backbone, I think I will go to a doctor and ask to try medication for ADD. <shudder  Then again, maybe that day will never come.  I seem to have huge issues around this topic.  Wrinkles in the space time continuum.  :( Then again, does it really matter if it’s just cosmetic? Out of curiosity, what are the physical differences?  I thought ADD just described a set of symptoms and that no organic cause was really known or posited.

Response:

I’ve kind of been delurking of late ;-) So I’d just like to say hello!

hi – i tried replying to an email you sent me, but it bounced back saying it was an undeliverable address ?? There might be a different way of looking at it. If AD’s aren’t helping and you have ADD then Ritalin treatment could improve function. So if you have ADD and depression an improvement in concentration could help a therapeutic treatment of the depression such as CBT instead of medication.

this is kind of what i’m hoping. i don’t know yet if i’m going to be allowed to try an add med yet – this is all purely self-diagnosis (not that there’s anything wrong with self-diagnosis, mind you) I got diagnosed with ADD just over a week ago and started Ritalin.

you went private? i am going to see a dr rowan at the priory hospital (oh yes, only the best ;) on friday. only because i have a friend of a friend who was diagnosed and treated for add there. but i keep going on like i *know* that that is what my problem is, which i don’t. all i know is that it would be a very quick test to find out. plus, i keep stuff in piles around the house, like jaz, and she has add <this last bit is a joke, btw. The secondary depression is the sense of futility at not being able to organise my life the way I want without considerable stress due to attention deficit.

i get this. i get pissed off at myself for being unable to start anything, unable to finish anything, unable to think of or about anything, unmotivated, unable to concentrate, unable to commit to anythinng. I’ve also come to the conclusion that my resistence to cognitive therapy was because of attention deficit. CBT is a learning therapy and it relies on the person being learning new patterns of positive thoughts.

makes sense.

Response:

not necessarily.  lots of times, adderall has been enough for me.  if it was one or the other, i’d take adderall.  i am NO GOOD on just antidepressants.  i can’t function nearly as well on only anti depressants as i can on only adderall. sometimes depression stems from ADD.  from being overwhelmed by all the projects you can’t finish.  by being unable to find stuff, get organized, get it together, get motivated, take a shower, get out of bed.  it’s not always the other way around. jaz

– Hide quoted text — Show quoted text – Yes Ritalin is meant to be taken before school and once every four hours and most children don’t take it after they leave school.  It is a drug like an amphetamine.  It might help you temporarily (you could use it to attend work) but you would still need an AD for the underlying depression.  My doctor is treating my depression first and once we have that under control and I am ready to go back to work we will look at adding Ritalin or Cylert (I think it is longer acting so a better choice for me).  I think that you should talk to your doctor about all of these issues. If your main goal is to get back to a functional level at work maybe Ritalin is the best choice but you will still have to find an AD that works.  If your main goal is like mine (I am currently unemployed) to treat the depression so I can get to a functional level then you would need to find an AD combo and add Ritalin later. Did any of that make sense – I didn’t get a prescription for Ritalin so I am really having a hard time writing :-( why would dr phelan be reluctant to try my on ritalin or similar? the drugs work really fast right? like within hours/days rather than weeks/months, so it would just be a very simple and quick trial to do.

Response:

Yes Ritalin is meant to be taken before school and once every four hours

they also have extended release which can eliminate the need for additional doses.   most children don’t take it after they leave school.  It is a drug like an amphetamine.

i was abusing it, but i found it wired me if it took it after 2 or 3.   "Come mothers and fathers throughout the land, and dont criticize what you cant understand" ~Bob Dylan

Response:

…you went private? i am going to see a dr rowan at the priory hospital (oh yes, only the best ;) on friday. only because i have a friend of a friend who was diagnosed and treated for add there. but i keep going on like i *know* that that is what my problem is, which i don’t. all i know is that it would be a very quick test to find out. plus, i keep stuff in piles around the house like jaz, and she has add <this last bit is a joke, btw.

If  you’ve suffered from long term depression the appeal of a new diagnosis grows with time ;-) – But seriously it took me several months to convince myself I had it because while my ADD is bad in learning, organising and conversations I also have obsessional traits which means that my house is obsessively tidy. The psychiatrist I saw diagnosed it without any hesitation. I presented my case in note form because I wanted to make the best use of the time.

Response:

you went private? i am going to see a dr rowan at the priory hospital (oh yes, only the best ;) on friday. only because i have a friend of a friend who was diagnosed and treated for add there. but i keep going on like i *know* that that is what my problem is, which i don’t. all i know is that it would be a very quick test to find out. plus, i keep stuff in piles

around the house, like jaz, and she has add <this last bit is a joke, btw.

<jaz looks around at all the piles  joke? :) actually, it’s a lot better than it used to be.  now it’s laundry, mostly, and i get it taken care of faster than i used to. but it still is true!! The secondary depression is the sense of futility at not being able to organise my life the way I want without considerable stress due to attention deficit. i get this. i get pissed off at myself for being unable to start anything, unable to finish anything, unable to think of or about

anything, unmotivated, unable to concentrate, unable to commit to anythinng.

yes, yes yes yes. jaz

Response:

I’ve kind of been delurking of late ;-) So I’d just like to say hello! i read somewhere (on a diagnostic criterion thing??) that add can *cause* depression. tho i don’t know if it can cause *severe* depression. If your main goal is to get back to a functional level at work maybe Ritalin is the best choice but you will still have to find an AD that works.  If your main goal is like mine (I am currently unemployed) to treat the depression so I can get to a functional level then you would need to find an AD combo and add Ritalin later. i agree with all this, and certainly intend to carry on looking for an a/d combo which works for me, but given my track record with responding to drugs, i’m not holding out a great deal of hope. if the best i can do is be functionally depressed, then that’s the best i can do.

There might be a different way of looking at it. If AD’s aren’t helping and you have ADD then Ritalin treatment could improve function. So if you have ADD and depression an improvement in concentration could help a therapeutic treatment of the depression such as CBT instead of medication. I got diagnosed with ADD just over a week ago and started Ritalin. I also came off the AD I was on (Cipramil). I’m in an odd position of feeling depressed and possibly being slighly more depressed (or at least experiencing more sad feelings) yet feeling more functional than I’ve ever been in the 20 years of my diagnosed depression. I seem to suffer from some sort of primary depression and a cronic secondary depression caused by a persistant attention deficit problem. The secondary depression is the sense of futility at not being able to organise my life the way I want without considerable stress due to attention deficit. The ADD seems to have lock the mood at one permenant level. Oddly it may be that the ADD actually reduces the depth of primary depression but worsens the secondary (reactive) depression!!!! I’ve also come to the conclusion that my resistence to cognitive therapy was because of attention deficit. CBT is a learning therapy and it relies on the person being learning new patterns of positive thoughts. This didn’t happen to me because my attention deficit prevents me from getting up the learning curve – both in studying and changing patterns of thought and feeling suffer the same fate. I benefited to a degree though a ‘trickledown effect’

Response:

Yes Ritalin is meant to be taken before school and once every four hours and most children don’t take it after they leave school.  It is a drug like an amphetamine.  It might help you temporarily (you could use it to attend work) but you would still need an AD for the underlying depression.

i read somewhere (on a diagnostic criterion thing??) that add can *cause* depression. tho i don’t know if it can cause *severe* depression. If your main goal is to get back to a functional level at work maybe Ritalin is the best choice but you will still have to find an AD that works.  If your main goal is like mine (I am currently unemployed) to treat the depression so I can get to a functional level then you would need to find an AD combo and add Ritalin later.

i agree with all this, and certainly intend to carry on looking for an a/d combo which works for me, but given my track record with responding to drugs, i’m not holding out a great deal of hope. if the best i can do is be functionally depressed, then that’s the best i can do. Did any of that make sense – I didn’t get a prescription for Ritalin so I am really having a hard time writing :-(

yeh, it makes sense (((maggie))) thank you for being so good to me.

Response:

c.bronchitis vs. asthma

Question:

I’m sorry that you found it rather unbelievable Well that’s a shock isn’t it Norm!!

Not in the least. I had been expecting many more negative responses but, in fact, I have received many personal emails thanking me for providing the Buteyko information. They post to me personally because they don’t wish to provoke further anti-Buteyko postings. – Hide quoted text — Show quoted text -I’m one step ahead of you again – just in case you missed my other message – I’ve set up my own interstellar spamming station – now even extraterrestrials will be prewarned about your spamtastic spuriosity!! You see Norm – once again buteyko fails in the face of scientific rigour and advancement. For those interested SETI – The Search for Extraterrestrial Intelligence – have created a downloadable data-chunk screensaver that will allow you to http://setiathome.ssl.berkeley.edu/ Rich. (Again there are reports of a distinct lack of intelligent life on planet Buteyko!!!!!!!)

I’m amused, I’m sure you can do better than that. I couldn’t find any reference to asthma in you posting at all. ;-) Norman

Response:

Not in the least. I had been expecting many more negative responses but, in fact, I have received many personal emails thanking me for providing the Buteyko information. They post to me personally because they don’t wish to provoke further anti-Buteyko postings.

Then why didn’t you just refer them to the buteyko newsgroup? "The difference between genius and stupidity is that genius has limits." Einstein

Response:

Hi Colin Not in the least. I had been expecting many more negative responses but, in fact, I have received many personal emails thanking me for providing the Buteyko information. They post to me personally because they don’t wish to provoke further anti-Buteyko postings. Then why didn’t you just refer them to the buteyko newsgroup?

I refer them to the most active non-commercial Buteyko group that I am aware of, that is http://www.wt.com.au/~pkolb/buteyko.htm I do not refer them to to alt.support.asthma.buteyko because many Buteyko users avoid this ng, deterred by the many unwanted anti-Buteyko postings that are often posted there. Norman

Response:

I’m amused, I’m sure you can do better than that. I couldn’t find any reference to asthma in you posting at all. ;-) Norman

Of course Norm – despite the fact that ET in the previous thread wanted help by email – as mentioned in said post – this same criticism can be levelled at buteyko – it too has no relevance to asthma.

Response:

: attract more followers. You remind me of adherents to scientology, this is : not really the place for this sort of nonsense. Umm, the Buteyko people are more like the Mormons than scientologists. The scientologists are _bad_news_.  They make this Buteyko lot look like nice guys.  See http://www.cs.cmu.edu/~dst/Secrets/ for more details. Cheers, Kin Hoong

Response:

There are some different Methods to separate Asthma from chron. Bronchitis. Modern methods looks at your blood, asking for inflammations- cells. a) Eosinophile Granulozyten means Asthma, reversibel, well handled with inhaled Cortison, b) Neutrophile Granulozyten means COPD (older form is chronic Bronchitis), not or little reversibel and needs no Cortison in stabile phase (Attention:1. in exerbation yes, 2. treatment must  go 3 month with steroid without change of FEV1), c) Neutrophile and eosinophile Granulos both, small group, with makes problems because Cortison must give high dose but did not good help. bad prognosis so much i knew. Lothar

Response:

I’m sorry that you found it rather unbelievable

Well that’s a shock isn’t it Norm!! I’m one step ahead of you again – just in case you missed my other message – I’ve set up my own interstellar spamming station – now even extraterrestrials will be prewarned about your spamtastic spuriosity!! You see Norm – once again buteyko fails in the face of scientific rigour and advancement. For those interested SETI – The Search for Extraterrestrial Intelligence – have created a downloadable data-chunk screensaver that will allow you to http://setiathome.ssl.berkeley.edu/ Rich. (Again there are reports of a distinct lack of intelligent life on planet Buteyko!!!!!!!)

Response:

Hi jenwolf Thank you for being inquisitive and visiting the site. I’m sorry that you found it rather unbelievable. I felt that way until I’d tried it for a while and experienced the benefits. Norman

Response:

Yes, you can have asthma plus chronic bronchitis plus emphysema, all together. They usually call that COPD, Chronic obstructive pulmonary desease. I have that!

Response:

I agree. But my md listens and listens and can’t hear anything. Through the scope, that is. He listened when I told him about Buteyko. His coment was:" If it works keep doing it."

This does illuminate a problem that arises when regular doctors are told about alt med treatments.  They typically have no idea as to the potential problems of Buteyko.  Since they are unaware of the dangers they cannot caution the patient. A better way of discussing this with a doctor would be to describe buteyko theory and ask if it makes any sense whatsoever. "The difference between genius and stupidity is that genius has limits." Einstein

Response:

but not least…….here’s a thought…..why have asthma deaths and new-onset diagnoses of asthma been rising despite quatum leaps in asthma management…..

Considering that people who use alt med are twice as likely to die from asthma as those who do not, can we not assign some of the blame to the charlatans? "The difference between genius and stupidity is that genius has limits." Einstein

Response:

Yes  you can have asthma and chronic bronchitis at the same time – I have been suffering from Chronic Asthmatic Bronchitis for the past 4 years and experience the same symptoms that you described in your post . Currently , I have no voice , am on 60 milligrams of prednisone  daily , accolate times 2 , Biaxan  1000 milligrams , atrovent 2 times2 , flovent 2 times 4 , a nebulizer and  albuterol as needed . If you are having this problem please see your doctor right away ! teresa m. – Hide quoted text — Show quoted text – so, could it be possible for a person to have both chronic bronchitis and asthma. is c. bronchitis something that always develops/manifests itself later in life? that is, i have had symptoms as far back as i can remember, it’s been very slowly getting worse. and it flares up to an extreme when i’m exposed to smoke, mold or dust. once it starts i cannot tolerate perfumes or chemical odors of any kind. . . or even the smell of the lilacs coming in through the window from a block down the street.

Response:

Hi ScoobyRCP – Hide quoted text — Show quoted text – For all of thsoe who suffer from asthma and it’s rrelated are responsible for your own care ultimately.  If your physician is not listening to you then find another.  If you are not following appropriate medical advice then you will bear the consequences at some point. As for the touted "breathing" technique above I can only say as a practicing respiratory therapist…one with asthma……good luck!  The positions touted by this method have no SOUND and well documented controlled studies to support their claims.  I know that we would all like to see a miracle cure, but at this point there is none on the horizon for asthma. As for breathing techniques is boils down to this…….relaxation will help reduce oxygen use and less muscle fatigue to develop.  This in and of itself is beneficial when trying to breathe through constricted airways.  The more you struggle the more oxygen your body needs….and it starts a vicious cycle.

I agree with everything up to here; except that Buteyko is not a miracle cure, it requires effort by the user to retrain their breathing to reduce their minute volume by use of the Buteyko technique. Hyperventilation IS NOT what asthma is about….it’s about

bronchoconstriction. A Buteyko practitioner  would argue with this, but I’m not one, I’ve simply had success with Buteyko. I’m more interested in results rather than theory. Asthmatics breathe faster at times simply because of a compensatory mechanism that is attempting to maintain adequate control of oxygen and carbon dioxide. This cycle May be broken by early recognition, BUT not always.  Failure to follow established protocols and your physician’s advice may well result in

I agree with this also. My physician is happy with the success I’ve had with Buteyko. My reduction in steroid use has been with his agreement. I always carry my Ventolin with me but I haven’t had to use it since using the Buteyko Breathing technique. I recommend anybody who tries Buteyko should do the same. They are your lungs…….do you want to risk them and your life???  Just a thought….

Are you saying that breathing exercises are dangerous? Rod RCP, EMT-P

Regards Norman

Response:

breathing exercises are not dangerous…….and they are not a substitute for medical management.  adequate pulmonay rehabilitation will reduce the need for some medications in some people, but not all.  And as for the comment about reducing minute volume….that is EXACTLY what you DO NOT want if your disease IS NOT adequately under control.  Your body knows what it needs to provide cellular function…….any efforts to suppress this artificially will be detrimental and will allow CO2 to build up. The best use of this technique is in the confines of a physician managed pulmonary rehab program designed around each individual’s condition.  Nothing "cures" asthma…NOTHING……their are only alleviations and palliatives available.  You can attempt to remove all offending substances from your life but you will very likely find you are allergic to something else. Common sense goes for picking a physician, knowlege of your own disease process, use of your own medications, knowlege of your peak flows and your activity levels.  Last but not least…….here’s a thought…..why have asthma deaths and new-onset diagnoses of asthma been rising despite quatum leaps in asthma management….. Scooby RCP, EMT-P

Response:

[snip] if this is true, then i have both.

Response:

Buteyko is a breathing technique. But unlike many other breathing methods Buteyko’s aim is to breath less.

i don’t even have to be a doctor to know that breathing less will not help me. besides, it’s pretty well known that breathing slows when sleeping — so why hasn’t that cured me? heck, i even wake up feeling worse in the morning than at any other time of the day or night. For a good introducing and more information on Buteyko try http://www.wt.com.au/~pkolb/buteyko.htm.

well, i read a few sentences on the site, and i must say it’s utterly moronic. if anything, i breathe far too shallow-like as it is. i do it trying to avoid feeling the irritation deep in my lungs. over time i believe it has actually reduced my lung capacity and available oxygen. yeah, this method might work in the very short term as nothing better than a method of avoiding pain associated with asthma/bronchitis — but to suggest that it is a medical cure is irrisponsible and downright dangerous (imo). it’s nothing but a bad habit, and anyone who’s got it would do well to break it. my opinion, of course. heck, even if i met an m.d. endorsing this, i wouldn’t heed it.

Response:

For all of thsoe who suffer from asthma and it’s rrelated are responsible for your own care ultimately.  If your physician is not listening to you then find another.  If you are not following appropriate medical advice then you will bear the consequences at some point.

I agree. But my md listens and listens and can’t hear anything. Through the scope, that is. He listened when I told him about Buteyko. His coment was:" If it works keep doing it."

Response:

are responsible for your own care ultimately.  If your physician is not listening to you then find another.  If you are not following appropriate medical advice then you will bear the consequences at some point. As for the touted "breathing" technique above I can only say as a practicing respiratory therapist…one with asthma……good luck!  The positions touted by this method have no SOUND and well documented controlled studies to support their claims.  I know that we would all like to see a miracle cure, but at this point there is none on the horizon for asthma. As for breathing techniques is boils down to this…….relaxation will help reduce oxygen use and less muscle fatigue to develop.  This in and of itself is beneficial when trying to breathe through constricted airways.  The more you struggle the more oxygen your body needs….and it starts a vicious cycle. Hyperventilation IS NOT what asthma is about….it’s about bronchoconstriction.  Asthmatics breathe faster at times simply because of a compensatory mechanism that is attempting to maintain adequate control of oxygen and carbon dioxide. This cycle May be broken by early recognition, BUT not always.  Failure to follow established protocols and your physician’s advice may well result in They are your lungs…….do you want to risk them and your life???  Just a thought…. Rod RCP, EMT-P

Response:

so, could it be possible for a person to have both chronic bronchitis and asthma. is c. bronchitis something that always develops/manifests itself later in life? that is, i have had symptoms as far back as i can remember, it’s been very slowly getting worse. and it flares up to an extreme when i’m exposed to smoke, mold or dust. once it starts i cannot tolerate perfumes or chemical odors of any kind. . . or even the smell of the lilacs coming in through the window from a block down the street.

Response:

so, could it be possible for a person to have both chronic bronchitis and asthma. is c. bronchitis something that always develops/manifests itself later in life? that is, i have had symptoms as far back as i can remember, it’s been very slowly getting worse. and it flares up to an extreme when i’m exposed to smoke, mold or dust. once it starts i cannot tolerate perfumes or chemical odors of any kind. . . or even the smell of the lilacs coming in through the window from a block down the street.

Hi Jenwolf What you describe is very reminiscent of my asthma when is was really bad back in 1991. It started with a bad dose of flu and ended up with both asthma and bronchitis. New triggers seemed to everywhere. It took many months of medication, including antibiotics and oral steroids to drag my health back to my ‘normal’ level. I was eventually stabilised on 800mcg Becotide and 400mcg Ventolin per day. I note from your other posting that medication is not helping your condition much. Since August ‘98 I have been having great success with the Buteyko method. Why not give it a try? Buteyko is a breathing technique. But unlike many other breathing methods Buteyko’s aim is to breath less. Buteyko has improved my asthma, reduced my Ventolin to zero and my steroids by half. I would recommend all asthmatics to try it to see if it works for them. However a word of warning, some have felt so good after using it for a few months they have thrown their medication away. You should continue to carry your medication even though your asthma may be in remission. Buteyko is a great method to help reduce asthma – it is not a miracle cure. For a good introducing and more information on Buteyko try http://www.wt.com.au/~pkolb/buteyko.htm. It is best viewed by using the option to download the whole site and then read at leisure. There is quite a lot of it. See the ‘Get Started Now’ section, to get you started. It is completely free. But for both sides of the camp go to http://home.netscape.com/ and search for Buteyko using SNAP. This will give you other sites of interest including http://home.pacbell.net/colin/ which is Colin Campell’s rejection of the method (which I disagree with). Norman

Response:

bronchitis is the inflamation of the upper airways in response to multiple triggers.  The physiological response to trap the invading triggers is to produce more secretions and therefore wall off the offender and rid them by coughing and clearing the throat.  Asthma as you know is the bronchoconstriction of the lower airways leading to the alveoli.  The wheezing results from the extreme narrowing of the airways there secondary to secretions and reductions of the airway lumen. Yes……you can have both……chronic bronchitis is usually diagnosed if you have a period of time (ususally 3 or more months of the year) where you are constantly bothered by increased secretions.  Smokers and those constantly around inhaled irritants are most prone to having both…. RLB, RCP, EMT-P

Response:

Made it 6 months-baby not gaining-need help!

Question:

Carrie, I am having the same problem with my 1 year old (except he hasn’t grown for about 6 months).  In terms of breastfeeding, you are doing the best for your baby. Nurse him every chance you get (Noah stopped growing when I started putting him on a long schedule — per the pediatrician).  If you do end up having to have blood tests, please check things out very carefully. We went to the peds office last Wednesday to have blood drawn. It was a huge nightmare. We had to retest yesterday, so I looked in to alternative "drawing centers" or outpatient labs. I found out that we could go to the local Children’s Hospital to get the lab work done (where they do this kind of thing all day long). When we got there we found out that they could just prick his finger to get the blood to run the tests (they got more blood this way than when they hit his veins).  The hospital has new equipment that the other labs don’t have, so if we had gone back to the peds office, we would have had to hold him down to draw the blood out of his vein again!  Please check into this before you have any tests done!! Feel free to email me with any other questions or concerns! Myrna and Noah (3-1-98)     Hello All!     I am rejoicing today that my precious Ben has made it 6 months, exclusively bf.  He has never had one bottle of formula, or any supplement.  Ben was born 4 weeks early and was very small, only 5 lb. 13 oz. but was a great nurser from the beginning.  His low birth weight was 5 lb. 6 oz., but regained almost all of his birth weight, except 1 oz. in one week.  He nursed every 2 hours, and after only 2 weeks, he was sleeping through the night (6-8 hours).  Now he only nurses every 3 hours for approximately 30-45 minutes.  The problem we are having now is that in the last six weeks he hasn’t gained any weight.  He had been sick during that period where there was some vomiting. But his sickness never affected his appetite.  When we took him to the emergency room, they weighed him and his weight had dropped.  I’m hoping this is just due to the illness.  Today we took him for his 6 month check-up and his weight was the same as it was 6 weeks ago for his 4 month check-up (I was late getting to his 4 month, that’s why only 6 weeks separated the two appointments.)  My little Ben only weighs 12 lb..  He looks very healthy, just small.  His development is also normal.  We have to go back for a weight check next week and if he hasn’t gained they are going to do a series of blood tests.  I am very worried.  I hope this doesn’t end my bf.  He refuses a bottle.  I have been trying to feed him every 2 hours today and to let him comfort nurse as long as he wants.  So our nursing sessions usually last for about an hour.  As far as solids go, I had tried to get him to eat cereal, and since his illness, he absolutely refuses.  (By the way, his illness was viral induced asthma and bronchitis, with a lot of wheezing, coughing, runny nose, and some vomiting, especially after having a dose of his medicines.)  Is there anything I can do?  I am so worried that this will end my bf.  I really love bf.  Please help me!!!!     Carrie

Response:

Hi Carrie,     About two weeks ago, I had posted a very similar question to this group! Mag reposted her response to my question a little farther up this thread.     My baby was 7mo. old and 15.5 lbs, and had not gained any weight or height for 2.5 months.  He has been exclusively breastfed, with some solids. He also sleeps through the night (10hrs.).  Our doctor did blood tests, urine tests and he wanted me to switch to formula to see exactly how much he was eating a day.  The tests all came back negative, and I decided not to give him formula.  Instead I decided to feed him more often.     He was eating every 3-4 hours, meaning 5 meals a day.  I increased his intake to 8 meals a day (every 2 hours) and put extra breastmilk in his cereal.  Suddenly, like magic, he started growing again.  I don’t know if it was a coincidence, but I feel confident that feeding him more often was the answer.     Many thoughtful people sent me suggestions and reassurance during that two week long torture while we were waiting for the next doctor’s appointment.  Here is what I learned from all these wonderful people, and from the experience:     1. Breastmilk is best, no matter what they say.     2. Babies who sleep longer at night need to nurse more often in the day to make up for the lost meal(s).     3. Breastfed babies have longer and more obvious growth plateaus.     4. Breastfed babies don’t seem to eat as much at one feeding, and want to eat more often because breastmilk digests quicker ( I don’t have any proof of this one, but many people suggested this to me, and from my experience with Cam, it seems true)     5. Babies who have been breastfed for a while don’t like to take a bottle from mommy, no matter what’s inside (learned this the hard way)     6. Doctor’s are not always supportive of non-interventionist perspectives.  Switching to formula sounds like a very attractive idea to a doctor, so they can see the numbers.  It’s not necessarily the best thing to do.  It wasn’t for us.     7. Babies who are not getting enough to eat do not complain!  My baby didn’t.  He never fussed, never asked for food.  It wasn’t until I started feeding him more often that he started showing signs of asking me to nurse him.     8. There are a *lot* of babies out there that are small.  This average size chart should be thrown out the window.  My baby is well below the bottom line of the curve on the chart, yet I meet people all the time with babies that are smaller than him.     9. No matter what you do, there is always something to worry about. Once you’ve tackled this hurdle, something else will come along to take it’s place.  (Right now, Cam’s got a fever of 102, and he’s sleeping all day.  Of course I’m worried!)     10. This newsgroup, the internet and LLL are great places to find support.  I received so many comforting emails and I found many great friends because I came here to find a shoulder to lean on.     Good luck.  Let us all know how things turn out.     P.S. About the blood tests.  Take your baby to a children’s hospital! It is very hard to take blood from a baby. The children’s hospital has special instruments and they work with babies all the time.  It is very traumatizing for the whole family when blood drawing doesn’t go well.  Nip it in the bud and go directly to the children’s hospital, even if it’s a little farther away.     Tammy

Response:

Hi Carrie, It sounds to me like you are doing a great job. I definitely don’t think  your bf relationship has to end at all. It would make a lot of sense that he would not be gaining if he were ill. You are doing the right think offering more nursing, and it sounds like he’s not interested in solids so I wouldn’t push it. Keep up the good work and keep us posted, ok.?  Danette

  bjpind.vcf

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It should end your breastfeeding in fact it sounds like he really needs your milk right know. I had a lady in my office yesterday that her 4 month old hadn’t gained in 6 weeks, but had grown 3 inches. Baby has reoccurrence ear infections and her doctor told her not to worry about it, that that is the reason baby wasn’t gaining well and when she recovers, she will start gaining again. The blood tests will help rule out other causes of the weight loss. Also preemies can’t fit into out mold of normal weight gain. It sounds like you have been doing a great job, keep up with the good work and keep us informed (the test results etc.) Deena (mother of Matthew, 7 and Brandon, 5  and a lactation consultant)   Hello All!   I am rejoicing today that my precious Ben has made it 6 months, exclusively bf.  He has never had one bottle of formula, or any supplement.  Ben was born 4 weeks early and was very small, only 5 lb. 13 oz. but was a great nurser from the beginning.  His low birth weight was 5 lb. 6 oz., but regained almost all of his birth weight, except 1 oz. in one week.  He nursed every 2 hours, and after only 2 weeks, he was sleeping through the night (6-8 hours).  Now he only nurses every 3 hours for approximately 30-45 minutes.  The problem we are having now is that in the last six weeks he hasn’t gained any weight.  He had been sick during that period where there was some vomiting. But his sickness never affected his appetite.  When we took him to the emergency room, they weighed him and his weight had dropped.  I’m hoping this is just due to the illness.  Today we took him for his 6 month check-up and his weight was the same as it was 6 weeks ago for his 4 month check-up (I was late getting to his 4 month, that’s why only 6 weeks separated the two appointments.)  My little Ben only weighs 12 lb..  He looks very healthy, just small.  His development is also normal.  We have to go back for a weight check next week and if he hasn’t gained they are going to do a series of blood tests.  I am very worried.  I hope this doesn’t end my bf.  He refuses a bottle.  I have been trying to feed him every 2 hours today and to let him comfort nurse as long as he wants.  So our nursing sessions usually last for about an hour.  As far as solids go, I had tried to get him to eat cereal, and since his illness, he absolutely refuses.  (By the way, his illness was viral induced asthma and bronchitis, with a lot of wheezing, coughing, runny nose, and some vomiting, especially after having a dose of his medicines.)  Is there anything I can do?  I am so worried that this will end my bf.  I really love bf.  Please help me!!!!   Carrie

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