Have any of you ever been told you have cervical dystonia?
Hi, I am new to this forum. I was diagnosed about 5 years ago with fibro, after doctors trying o find what caused my severe pain, achiness, headaches, and fatigue. I also suffer from RA, degenerative disc disease, chronic migraines, meniere's disease, diverticulitis, and now the latest diagnosis today was cervical dystonia??? what is wrong with us? I live in beautiful sunny arizona, and could never cope with the cold like I have read many of you do, but find that it is not just cold that triggers me, but even windy days.... and Lord knows we get a lot of wind in southeastern Arizona. I hae also run in to the doctors that think that fibro is nothing but a load of bs...so you are not alone with this. I have recently been blessed with a chronic pain management PA though who is a fibro specialist. How some doctors can say that this is not a real diagnosis is beyond me. Studies in rats with FIBRO have shown how the nerves over react and magnify pain levels. My degenerative disease has caused me to have to have lumbar and cervical fusions, and the pain is so bad that I have to take morphine sulfate to function. But at least on a drug regimine of the ms, muscle relaxers and lyrica, I was starting to actually have good days when I could go fishing, or enjoy the grandkids. I am getting much worse though......had an ongoing headache for 17 days. I thought it was a migraine but nothing helped....now my neurologist says I have this cervical dsytonia where the muscles are in constant spasm causing the migraines. Some days I feel like WHAT ELSE LORD??? wasn't one diagnosis enough, now I have 7 ??? But these spasms seem an awful lot like the ones my son gets with his mild cerebral palsy but his are in his legs.....I take lots of supplements, vitamins, minerals, use chiropractor, massage.....sometimes it seems like it will never end...now have to get botox injections in neck and head?? anyone else gone through this, seems scary.
Hi, I have fibro and cervical dystonia, I was diagnosed with fibro 6 years ago then my head starting having horrible tremors and I couldn't keep my head up with such pain in my neck and headaches. I have yes' and no's and I get botox shots, I just got some today. The shots aren't really that bad but if you have tremors and your head tremors like you're saying no, they can help with that they can't get rid of the yes tremors, it is too dangerous as would probably have trouble with swallowing. It's a horrible disease, both are. I never believed in Fibro but I guess I don't have any choice now. My fibro is just getting worse and I have great problems with meds, I get great depression so I have no relief. Good luck and you are not alone. I also have grandchildren, I am 54 and I can't work, I've been out of work for 2 and half years, the whole thing is devastating. Does any medicines help you besides the morphine uulfate
The Content on this Site is presented in a summary fashion, and is intended to be used for educational and entertainment purposes only. It is not intended to be and should not be interpreted as medical advice or a diagnosis of any health or fitness problem, condition or disease; or a recommendation for a specific test, doctor, care provider, procedure, treatment plan, product, or course of action. Med Help International, Inc. is not a medical or healthcare provider and your use of this Site does not create a doctor / patient relationship. We disclaim all responsibility for the professional qualifications and licensing of, and services provided by, any physician or other health providers posting on or otherwise referred to on this Site and/or any Third Party Site. Never disregard the medical advice of your physician or health professional, or delay in seeking such advice, because of something you read on this Site. We offer this Site AS IS and without any warranties. By using this Site you agree to the following Terms and Conditions. If you think you may have a medical emergency, call your physician or 911 immediately.