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Re: My big day....

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Good for you cyn, its wonderful when you finally have someone who believes you

because you're starting to doubt yourself ....

My big day....

Yesterday was the big day, I saw my rheumatologist for the first time. He

spent quite a bit of time with me, I guess all of you who've been to a

rheumy know the first-time drill, lol! We talked a long time before the

physical, and a long time afterwards. After the physical, he came in and

told me he had several things to say to me. I thought " right, I don't have

FMS, so I'm going to have to suffer thru this alone " . He took both my hands

and said, in a very kind voice, " I hate to have to tell you, you DO have

Fibromyalgia " . I guess he expected me to be upset, but after years of

doctors ragging on me about making up pain and me being a drug addict just

looking for more drugs, I felt so very RELIEVED.

I am allergic to hormones (when I was pregnant I lost so much weight from

the nausea & vomiting that I weighed 2 lbs less the day the baby was born

than I did before I got pregnant. Birth control pills and different hormone

treatments had the same effect on me). I also have a " retro " effect from

many different drugs, including painkillers, they have the exact opposite

effect on me than they're intended to. He told me to keep on doing yoga,

even when it hurts, as the stretching is good for my muscles and has

probably done me a lot of good in the realm of pain management. He said

then that he needed to find a painkiller I could tolerate, and ended up

prescribing Fiorinal #3 for me, which is what I've been taking, in smaller

doses, over the last 18 years, for migraines. He said I should be taking 4

or 5 pills a day, which is about double the dose I'd been taking. He said

if that doesn't do enough for the pain, he'll consider either increasing

the amount, or give me something else that will work better.

I think he was very surprised by the fact I wasn't upset by the diagnosis

(I guess most people don't want to have FMS...but I have been to so many

doctors who just told me there was nothing wrong or I was having rebound or

not getting enough exercise....) but now I have a dr. and diagnosis that I

can live with. He is also a gynecologist, though he said that he had become

interested in FMS in particular because he'd seen so many women suffering

from it. But he DID get onto me about the fact that I haven't been having

the regular tests and gyno exams I should have at my age, lol!

He also said that they're testing me for lupus and rheumatoid arthritis,

something I never considered. I guess he wants to rule them out....I don't

know if the treatment for them is any different. I am just so happy and

relieved that I have a doctor who believes me when I say I'm in pain, and

he doesn't just tell me to take aspirin or an NSAID and get more exercise.

Other doctors throw the FDA (Federal. Drug Administration) in my face, and

tell me they have to be careful or they'll lose their licenses. There have

been 2 doctors in Nashville busted in the last 2 weeks for being addicted

to Oxycontin, getting it through deals with their secretaries and patients.

One of those doctors was one I'd actually been seeing for about 3 years,

and he was always getting on to me about the FDA....now I know why he was

so paranoid about it. It makes me wonder how many doctors out there are

depriving their patients of quality care because they're secret drug

addicts who don't want to get caught out.

So now I'm feeling relieved and happy, mainly because I now know that my

pain is real and I was well justified in requesting pain medication from my

PCP, who refused to help me. (it makes me wonder if he's one of those

addicts). I think it should send up warning flags to anyone who is seeing a

doctor who refuses to give pain medication because he has to report to the

FDA and doesn't want to lose his license.

My doctor also said that 3 of the meds my other doctors are giving me are

actually recommended for FMS patients....Neurontin, which my neurologist is

giving me to help prevent migraines, Lexapro, an anti-depressant, and

Seroquel, an anti-psychotic I take at bedtime (I'm Bi-Polar, with severe

depression).

I saw my psychiatrist later that afternoon, and he said I looked so much

more relaxed and happy, and he felt I no longer needed ECT treatments,

which is a real relief, because I really didn't want to have to go through

that.

I'm sorry, I know I'm really running off at the mouth right now, but I'm

just so relieved and happy that I finally have a doctor who believes me and

is trying to help me!

Thank you if you've managed (and been willing) to read this far!

>

cyn

clmerritt@...

Time.....time ....time is what turns kittens into cats

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I know that feeling, for years I knew something was terribly wrong with me and

everytime I went to the doctor they treated me like a drug adict. Untill one

day my mother and I got onto the internet where there was a sight where you can

put your symptoms in and it gives you possible diagnoses. At that point I was

extremely suicidal because of the pain. Thank God we found the answer,

fibromyalgia came up as the diagnoses, and then I went looking on the internet

for an fms doctor, found one and he is great...only problem though is that he

won't prescribe oxycontin, which I think would benefit me alot. I have been

going to doctor after doctor requesting this medication for only when the pain

level is at a 10, but I have been turned down every time. The highest pain

medication I've been on is methodone and Duragesic, not to mention xanax,

adavan, and valium. But I hear, and if you guys can help me find a doctor that

can help, that oxycontin really does the trick for fms patients. To I

wish you all the luck in the world, and I know what it is like when you finally

find out what is wrong with you. I went through that, I knew something was

wrong with me but everyone was telling me that it was in my head and they were

wrong. Just goes to show you that even doctors are not perfect.

Jana

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Cyn, Id love a massage just about any moment of any day !!!

Really Im so happy for you that you have a sense of relief. I remember

well once I was diagnosed just being relieved it was not in my head!

Have a wonderful weekend!

Bless you

Deb

--- Merritt wrote:

---------------------------------

Thank you Deb! It took me several years, and several doctors, but I can

tell Dr. Harmuth is a great doctor, with a great deal of empathy.

While I was waiting for my appointment, I saw a man leaving with a TENS

unit. (he didn't have it when he came in) I don't know if the Center

has

them for rent, or if he ordered one, and I didn't think to ask the Dr.

about it. There was also a section devoted to physical therapy, with a

pool, exercise machines, and a massage room (I'd love a good massage!)

Bless YOU too,

cyn

=====

My personal photos, free to view or use

http://photos.yahoo.com/lilacskyz

:) Deb

______________________________________________________________________

Post your free ad now! http://personals.yahoo.ca

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I'd love a massage too! Or some ultra sound with Arnica gel.

Dillion

> Cyn, Id love a massage just about any moment of any day !!!

> Really Im so happy for you that you have a sense of relief. I

remember

> well once I was diagnosed just being relieved it was not in my head!

> Have a wonderful weekend!

> Bless you

> Deb

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I read with interest your repr? drugs.... I get the opposite effect intended

from many drugs so am afriad to take any. dash

My big day....

Yesterday was the big day, I saw my rheumatologist for the first time. He

spent quite a bit of time with me, I guess all of you who've been to a

rheumy know the first-time drill, lol! We talked a long time before the

physical, and a long time afterwards. After the physical, he came in and

told me he had several things to say to me. I thought " right, I don't have

FMS, so I'm going to have to suffer thru this alone " . He took both my hands

and said, in a very kind voice, " I hate to have to tell you, you DO have

Fibromyalgia " . I guess he expected me to be upset, but after years of

doctors ragging on me about making up pain and me being a drug addict just

looking for more drugs, I felt so very RELIEVED.

I am allergic to hormones (when I was pregnant I lost so much weight from

the nausea & vomiting that I weighed 2 lbs less the day the baby was born

than I did before I got pregnant. Birth control pills and different hormone

treatments had the same effect on me). I also have a " retro " effect from

many different drugs, including painkillers, they have the exact opposite

effect on me than they're intended to. He told me to keep on doing yoga,

even when it hurts, as the stretching is good for my muscles and has

probably done me a lot of good in the realm of pain management. He said

then that he needed to find a painkiller I could tolerate, and ended up

prescribing Fiorinal #3 for me, which is what I've been taking, in smaller

doses, over the last 18 years, for migraines. He said I should be taking 4

or 5 pills a day, which is about double the dose I'd been taking. He said

if that doesn't do enough for the pain, he'll consider either increasing

the amount, or give me something else that will work better.

I think he was very surprised by the fact I wasn't upset by the diagnosis

(I guess most people don't want to have FMS...but I have been to so many

doctors who just told me there was nothing wrong or I was having rebound or

not getting enough exercise....) but now I have a dr. and diagnosis that I

can live with. He is also a gynecologist, though he said that he had become

interested in FMS in particular because he'd seen so many women suffering

from it. But he DID get onto me about the fact that I haven't been having

the regular tests and gyno exams I should have at my age, lol!

He also said that they're testing me for lupus and rheumatoid arthritis,

something I never considered. I guess he wants to rule them out....I don't

know if the treatment for them is any different. I am just so happy and

relieved that I have a doctor who believes me when I say I'm in pain, and

he doesn't just tell me to take aspirin or an NSAID and get more exercise.

Other doctors throw the FDA (Federal. Drug Administration) in my face, and

tell me they have to be careful or they'll lose their licenses. There have

been 2 doctors in Nashville busted in the last 2 weeks for being addicted

to Oxycontin, getting it through deals with their secretaries and patients.

One of those doctors was one I'd actually been seeing for about 3 years,

and he was always getting on to me about the FDA....now I know why he was

so paranoid about it. It makes me wonder how many doctors out there are

depriving their patients of quality care because they're secret drug

addicts who don't want to get caught out.

So now I'm feeling relieved and happy, mainly because I now know that my

pain is real and I was well justified in requesting pain medication from my

PCP, who refused to help me. (it makes me wonder if he's one of those

addicts). I think it should send up warning flags to anyone who is seeing a

doctor who refuses to give pain medication because he has to report to the

FDA and doesn't want to lose his license.

My doctor also said that 3 of the meds my other doctors are giving me are

actually recommended for FMS patients....Neurontin, which my neurologist is

giving me to help prevent migraines, Lexapro, an anti-depressant, and

Seroquel, an anti-psychotic I take at bedtime (I'm Bi-Polar, with severe

depression).

I saw my psychiatrist later that afternoon, and he said I looked so much

more relaxed and happy, and he felt I no longer needed ECT treatments,

which is a real relief, because I really didn't want to have to go through

that.

I'm sorry, I know I'm really running off at the mouth right now, but I'm

just so relieved and happy that I finally have a doctor who believes me and

is trying to help me!

Thank you if you've managed (and been willing) to read this far!

>

cyn

clmerritt@...

Time.....time ....time is what turns kittens into cats

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