Symptoms with movement - Fibromyalgia?
This forum is for questions and support regarding neurology issues such as:
Alzheimer's Disease,
ALS,
Autism, Brain Cancer,
Cerebral Palsy, Chronic Pain,
Epilepsy,
Fibromyalgia, Headaches, MS, Neuralgia, Neuropathy, Parkinson's Disease, RSD, Sleep Disorders,
Stroke, Traumatic Brain Injury

I have gone through some of the same symptons as yourself. I have been diagnosed w/ fibro. and a form of artheritis caused by Crohn's disease (they really haven't given it a specific name). They are currently looking at the possibility of some type of liver damage due to meds. due to the increase of muscle weakness and spasms, they are also considering CFS. However it appears as if you have already undergone blood tests to show anything with the liver. With my symptoms getting worse new ones popping up they still believe I have the Fibro. but in combination with something else (CFS or something). You may have the Fibro. if you have most of the trigger points and symptoms for it along with another problem that could easily be treated. I don't know if I've been of any help to you but maybe it's something you can discuss with your doctor. Good luck to you!
I don't really think I have this. The Drs. answer is unclear. He focused in on twitching - which I do not have. He must have read the word sensation as twitching. By sensation I mean, pain, numbness, tingling, burning, pin pricks, stuff like that. Stuff that you feel.
By the way, I also have a yucky taste in my mouth to go along with the facial numbness. How does your mouth taste?? I sort of have to laugh with that question. I bet you don't have too many total strangers asking you "how does your mouth taste". OH well. Hope I'm not getting too personal.
Sometimes people who don't have it have no clue; sometimes they feel badly about it. Sometimes it is easy to become depressed about having a chronic disease like this, particularly one that not all drs. believe exists. However, more and more of them do believe in it now, so you can feel more justified. It is real. If you have it, just try to go on and do whatever you want to do. Some days I can't do that. However, last August I rode 50 miles in the Hottern' Hell bike ride with the disease. You still can do things. Don't give up. Antidepressants help some, as go good supportive friends and family. I hope you have a good support system as it mcn mmake things much better.
Good luck, and hang in there. --Sherry M--