I am a 52 year old female, recently diagnosed with Fibromyalgia. I have been in pain for most of my life and for most of my life the doctors tagged me as a hypochondriac! I understand, however it doesn't lessen my pain or anguish. I just saw the Fibro Hope commercial for the first time two weeks ago and it made me cry to know that I am not alone anymore and there are people out there that really do understand just how I feel.
My first debilitating episode was in 1982 and has increased in frequency ever since. My pain is now constantly with me and I take Flexoril and Vicodin. My symptoms include MONSTER migraines, the medication Verapamil does mask the pain but not the aura, dizziness or nausea. The symptoms of migraine occur several times daily so driving is out completely and other things have to be postponed on a regular basis, until my vision clears enough to see.
My mother died from complications of Familial ALS in 2001, she had two uncles who died within ten years of each other and one brother who died several years before her.
Since Fibromyalgia and ALS are both neurological disorders, are they related? What type of tests are done to rule out ALS? Should I be seeing a neurologist? Neither of my family physicians seem to be concerned about ALS, so should I be seeking another?