MeanLaureen
<font color=purple>Slam Dancer Extraordinaire<br><
- Joined
- Apr 29, 2001
- Messages
- 6,718
I have a question for someone suffering from Fibromyalgia.
First some background. I was diagnosed with Adult Onset Stills Disease in 2000. (AOSD is a rare autoimmune disease in the same family as Rhuematoid Arthritis - severe joint pains along with fever spikes that can be as high as 104 out of the blue) In 2001 I was told that I had developed Fibromyalgia as a "side effect" to the AOSD.
It was my understanding that the Fibro symptoms were the more muscular pains along with the pain when I was touched or if I laid down. It was keeping me from sleeping at night.
I've had to change doctors a couple of times recently because I am having a hard time finding a specialist that knows enough about AOSD to treat it properly. In the past they had just been filling me up with Methotrexate with no positive results, only bad side effects.
My newest Rheumatologist has told me that a lot of the pain I am in right now (and I am in tremendous pain 24/7) is Fibro related. I tried to tell him that I can tell the difference between Fibro pain and AOSD pain and 80% is AOSD related.
He told me that Fibro causes joint pain. That is completely different than what the other doctors have told me. My question to you guys is...would you consider your pain from Fibro to be mostly in the joints or more muscular that increases greatly to the touch?
I'm afraid he isn't taking me seriously enough when I tell him that the pain in my ankles and knees gets so bad by the end of the day that I can no longer walk without much difficulty or the aid of a cane. Or that the pain in my wrists and fingers is so bad that I can no longer write or even hold a pad of paper. He keeps saying "Oh, that's the Fibro". In the meantime he has suspended my treatment for the AOSD and I'm just getting worse day to day. His treatment for me right now is to dope me up with sleeping pills.
Does this sound like the symptoms and treatment you have gone through?
First some background. I was diagnosed with Adult Onset Stills Disease in 2000. (AOSD is a rare autoimmune disease in the same family as Rhuematoid Arthritis - severe joint pains along with fever spikes that can be as high as 104 out of the blue) In 2001 I was told that I had developed Fibromyalgia as a "side effect" to the AOSD.
It was my understanding that the Fibro symptoms were the more muscular pains along with the pain when I was touched or if I laid down. It was keeping me from sleeping at night.
I've had to change doctors a couple of times recently because I am having a hard time finding a specialist that knows enough about AOSD to treat it properly. In the past they had just been filling me up with Methotrexate with no positive results, only bad side effects.
My newest Rheumatologist has told me that a lot of the pain I am in right now (and I am in tremendous pain 24/7) is Fibro related. I tried to tell him that I can tell the difference between Fibro pain and AOSD pain and 80% is AOSD related.
He told me that Fibro causes joint pain. That is completely different than what the other doctors have told me. My question to you guys is...would you consider your pain from Fibro to be mostly in the joints or more muscular that increases greatly to the touch?
I'm afraid he isn't taking me seriously enough when I tell him that the pain in my ankles and knees gets so bad by the end of the day that I can no longer walk without much difficulty or the aid of a cane. Or that the pain in my wrists and fingers is so bad that I can no longer write or even hold a pad of paper. He keeps saying "Oh, that's the Fibro". In the meantime he has suspended my treatment for the AOSD and I'm just getting worse day to day. His treatment for me right now is to dope me up with sleeping pills.
