Anyone with Fibromyalgia have neurological problems?

I have hyperreflexia, and tremors in my fingers does anyone one else have this also? And also can other symptoms show up later with fibromyalgia?

As FMS has been believed to be a disorder of the central nervous system for about 10 years now--

it is very common to have neuro problems

All people-including healthy people have SOME twitching-but in people with FMS it tends to be significantly more noticable

Fibromyalgia is a complex disease that usually takes years to diagnose. Although it presents itself with many symptoms, that many times mimic other diseases, it takes a lot of medical testing to rule out other conditions.

While fibromyalgia can, and usually does, cause neurological problems, this is only one facet of the disease. A tremor, or a combination of other symptoms that are common to fibromyalgia, does not necessarily mean you are suffering from FMS.

If you are suffering from other symptoms of fibromyalgia, other than just the tremors, see a rheumatologist to determine if it could possibly be FMS.

I HAVE THAT. THEY THOUGHT THAT I HAD PARKINSONS. I TOLD THEM WHAT THEY COULD DO WITH THERE PARKINSON SHAKE. FIBROMYALGIA IS MOSTLY CAUSED BY STREES. THE STREES, OF NOT KNOWING WHERE IT IS GOING TO HIT YOU NEXT. I GET IT THE MOST,AT NIGHT, SLEEPING ON MY SIDE, IN THE HIP SOCKET. THE PAIN WILL WAKE ME UP SOMETIMES SREAMING, IT CAN BE THAT PAINFUL. ...IF YOU ADMIT TO YOURSELF, YOU HAVE IT, THERE IS NOTHING THAT THEY CAN DO FOR IT, SO LIVE WITH IT,...YOU WILL FIND THAT IT IS MUCH MORE EASIER TO LIVE WITH, TALK ABOUT IT,AS A SUBJECT, LIKE YPOU STUBBED YOUR TOE, NO BIG DEAL.....IF YOU MOAN ABOUT IT, AS WHY ME, THIS THING IS GOING TO DISTORY YOU, AND EVERYONE AROUND YOU. FACE IT ,ACCEPT IT,...LIVE IT,.AND YOU WILL SURVIVE IT

I have peripheral neuropathy (sp.) nerve damage to my legs, but I don't know if it is a normal problem with FMS. My doctors have yet to figure out why. I have had FMS, CFS, & IBS for about 9 years and I found most drugs have not helped. I have joined a new support group at:

http://www.webjam.com/woodbridge_fibromy...

and found a lot of information and support on line and at our monthly meetings. I have also found some relief with accupressure, massage, and reflexology (and water exercise).

Good luck

Check out http://www.fibromyalgiasource.com for lots of information about Fibromyalgia including my experience living with it.