Myofascial syndrome
Feb 2007 I was diagnosed w/ Fibro by my rheumatologist. I am getting all my records for disability insurance and …
Fibromyalgia (FM or FMS or Fibro) is a debilitating chronic syndrome (constellation of signs and symptoms) characterized by diffuse or specific muscle, joint, or bone pain, fatigue...

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Rheumatologist #3
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So today I had an appointment with rheumatologist #3. THe first knew little of fibro, the second just wanted to drug me up and was not friendly at all. The one I went to today was very nice but gave me the whole speil on the medical community still trying to figure out whether fibro is real or not.
She them told me I looked depressed and wanted to treat it with anti depressants. I told her I have slept a total of 5 hours in 2 days and am in pain, why wouldnt I look depressed. I am searching for a medical opinion as to whether or not I should apply for disability or try and work part time. She said she didnt get involved with disability for new patients but didnt ask me to come in for a follow up. UGH!!! So frustrating, I dont know what to do. Why is the medical community still thinking this is made up?? Why in the world would anyone make this up??? Posted on 09/30/08, 04:09 pm |
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I'm sorry you are having such a bad time with Rhuemys. My Dr. ran every test he could think of, then sent me to a rehumy. He did the tender point test, said yes, you haave fibro, and sent me on my way. No help whatssoever!
Thats when I had insurance, now I have none, so cannot afford to see another rhuemy. Maybe you should see a neurologist. I have been reading up on it, and they will sometimes treat fibro. It seems to be a neurological disorder, in my opinion..but we know what opinions are compared to..LOL! I wish they would find something to help ALL of us. NOBODY in their right mind could make up this much pain!
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Ugh!
I was on my search this past summer for a Rheumy, as my doc recommended that I find a good on. As I made the calls, I suddenly found out that Rheumy's will typically only diagnose Fibro, but will not treat it. I waited nearly 6 months to get into a doc down at the university where she too gave me the "we don't know enough about fibro" speach.....told me to start swimming, take a buttload of vitamins (some of which are helping) and to get sleep. I'm still uncertain of her....but I feel this is my last choice. But there is a community class coming up that I want to go to. It's on how to live with Fibro given by a doc. I don't necessarily need to hear the how to live with Fibro.....as I'm alive again today and I think I've figured out the "how to live with it". I need to learn how to manage it part. LOL.......But it's given by a doc, who seems interested in Fibro. And that's what I need. A doc who believes in Fibro! I wish you luck hun...I understand your battles here.
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Thank you, my journey continues I guess.
The Rheumatologist told me that the man who first reported fibro is still alive and is claiming that it is made up!! I felt like saying, "So what??? What about the millions suffering from it now???"
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The rheumatologist I go to does not believe that there is such a thing as fibromyalgia. He thinks it's a hoax. I do have OA and RA and he does belive in that. I have not found any doctors that believe in much of anything except getting the cash out of me. I don't trust doctors and their little pills.
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They think that we make it up so we can get drugs. I can take enough drugs to kill 3 men, and still function fully. It's because I don't get a buzz, or a high, it's because when you are in pain, the meds don't give you a buzz or high, they treat the pain. It's impossible to get a high when you have real pain. Good docs know this.
I had little luck with rheumy's. I still have to see one, to satisfy the ins. co. but the doc that actually helps me live day to day, and have a reason to keep pushing is my Pain Management Doctor. I think you need to consider finding one. My PM doc is my utter salvation (not trying to sound sacrilegious), but true. I decided a long time ago, that I'd rather have quality of life, than quantity. So, since the medical establishment is falling all over themselves trying to decide if FM is real or not, and what new and fascinating drug is the new miracle drug, I've decided that I'd be much happier just treating the pain, thank you very much. IF they ever come out with a drug that helps, then I'll try it (don't get me wrong, I try all the new drugs, I just don't put alot of stock in them). But for me, my narcotic pain meds are the only thing that work for me, all the time, everyday. I'll stick with those, thank you. Otherwise, I'd be in a world of absolute pain, waiting for the new miracle drug to "see" if it's going to work, and see how "well" it's going to work if at all. Nope, not for me. I'll take my narcs thanks. Just see if you can find a PM doc, and hopefully you'll find a good one the first time around. I went to two or three before i found this one. But you know, she was worth the wait. First med she put me on, first day I saw her, once I took that pill, I was 100% pain free! Can't put a price on that. (Well, they can, that particular med would cost me $1437/mo. w/o insurance.) God bless.
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The thing is that I dont take any drugs for my fibro. I changed my diet, walk every day and take vitamin supplements. I'm not asking for drugs, just medical input on treatments i suppose.
I will look into a pain management doctor. Thanks for the replies and the advice :)
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