Am I wrong or......
 

right. It is my impression that fibro is in the muscles. Is that right?

The reason I am asking is that I was diagnosed with fibro 10 years ago. When I was diagnosed I had gone in with concerns about my knees and feet. When I got up in the morning, I could barely stand. Things would even out after a couple of hours, but any time I sat down for more than three minutes, my joints screamed. The bottoms of my feet hurt so bad that I could hardly bear to put my feet on the floor.

This is all happening again. I have a friend with RA and she says it sounds exactly like her symptoms. I have TOS and recently had surgery for it. My husband thinks I hurt because I don't excercise enough. I know that is not it. I hurt regardless of my excercise level.

Any suggestions?
Trix

hi trix,
do you have extreme fatigue with the pain and maybe a flu like achiness all over?
I think with fybro you have sensitivity to pressures and touch too - along with tender points.
If there isn't some useful links up above we have some on the TOS forum about Fybro, CMP & RSD.
there here -
http://neurotalk.psychcentral.com/showthread.php?t=304

they can all intermingle/over lap symptom wise a lot.

If the pain is actually feeling like it is in the joints?? more than all over it could be RA or something like that.

Yes, pain does occur in the joints, but there is no swelling or rise in the RA factor in the blood. So it does mimic RA in that way.
The reason it affects the joints is because the tendons and facia (the thin membrane that covers the muscles, like that icky stuff on chicken) that attach the muscles to the bones tighten up or thicken up and make it hard to move. This is why you have pain in the joints and in other places you wouldn't think FM would affect.
I hope all that makes sense.

Fibro since 1984 - in feet also
 

I have had fibro since 1984 whoch started in my face, head, neck, etc. from a dental procedure (trauma) After 5 yers of Trigger P. Inf. it went into semi remission where I no longer needed weekly injections and was actually pain free for weeks a time. Of course- any trauma (car accident) etx. woud trigger it off. then I got an epidual in 2003 and it trigggered off RSD and FM in my entire back. I can just abouty walk.
Now, in sept. I was on my feet all day and they were burning but I just ignored them . Thought it would go away. I was having a party for a friend so I had to be "sociable". I am now suffering for it. I have terrible pain in the soles of my feet, ankles, legs and knees. I spend many days in bed. I take no pain meds as non(35) haave worked so far. I barely make it from day to day. I also have RSD in rt. arm from and IV.
I am now putting lidoderm patches on my feet and that helps the burning a bit and also is a nice cushion. You might want to try that.
This is a cruel disease with little treatment options.(for me- anyway). The only thing tht helps are TPI's sometimes. (only in upper body.--face, head, neck, shoulders, back)
Good luck
Sydney

I've talked to scores of people with FMS, and one thing that seems certain is that the symptoms can vary considerably from person to person. Some complain of severe joint pain. I myself have soreness only in the muscles and occasionally the ligaments. The most important factor in determining FMS are the trigger points. If you have those, chances are very great that you have FMS.

Several times I have run into situations with doctors where they will describe you as having fibro-like symptoms, but deny that you have the illness itself. It seems quite of few of them think of FMS symptoms as just a type of rection that can occur from various illnesses, like fever or nausea does. These docs don't seem to believe that fibro exists as a primary illness.

I hope you manage to get your symptoms under control, Trix! :)