als

  1. G

    fibro maybe myofascial pain syndrome

    I tested 10 out of 18 on that test, he says no treatment needed and I agree. He thinks instead of fibro maybe myofascial pain syndrome. C-diff is the recurrent colon infection that I had. It when bad bacteria take over good ones. it is caught from the hospital or from taking antibiotics. I got...
  2. G

    Reason for Concern? Long Sorry- New

    Hi, My name is Heather and I've been reading this forum for several months and want to say what a terrific, helpful site this is! I've had "MS" like symptoms on and off for over 25years, and along with those I've had "widespread" fasiculations. I've wasted a lot of time worrying myself sick...
  3. G

    suspected fibromyalgia

    we tried to relieve your fears the last time you was posting but nothing convinced you that you really don't sound like you have als. it sounds like mentally you are still in a bit of a state as you were before. you said you was not going to come back,what has happened to bring you back to the...
  4. G

    is ALS starting? or fibromyalgia?

    :oops:Hello all I'm 27 male, I'm still not diagnose but I have some very frightened symptoms and I want to hear your oppinions. In March of 2007 after very stressful situation I started a lot of symptoms: -Fasciculations all over my body(very strong I can see my body parts twitching)...
  5. G

    my story

    well, I am not sure where to begin. I have had some minor things on and off for along time. Quickly-epstien barr virus at 20. That lasted for a year or so, there was no twitching, just tired and achey. Then 8 yrs ago mis-diagnoised with MS. I was having tingling and numbness, had MRI, came back...
  6. G

    Facial twitching and right-sided perceived weakness

    Corny...I know, but I have lurking around and reading for a couple of months now, and figured I should introduce myself. My journey started about 7 months ago with facial twitching and right-sided perceived weakness. I have had a diagnosis of fibromyalgia for about 20 years, so am thus an...
  7. G

    Fibrofog, symptoms and diagnosis or ALS?

    jattd, I am not a doctor, and don't know of one on this forum that specializes in Neurological symptoms. But, what you describe does not sound like ALS. Your doctor mentioned Fibromyalgia. Have you pursued that avenue of thinking? Have you gone to a pain clinic for evaluation? There are...
  8. G

    Should I be Tested for ALS?

    Ive been pondering if I should be tested for ALS or not. The problem is I dont trust doctors and have avoided going to one for the last 6 years. Here's my story. 9 years ago after more then a year of going to the doctors with complaints of muscle soreness and fatigue I was finally diagnosed...
  9. G

    Needing information

    I joined this group in October and have been reading your posts, almost daily, since then. This is my first post. Due to the fact that the medical community seems to have so few answers I find the antecdotal information on this site very helpful. This is my story: In the middle of August, 2006...
  10. G

    Fatigue

    Good morning! The farther we get into this ALS battle, the more I realise everyone's journey is different, but I'm looking for some feedback on fatigue. My sister's energy levels have dropped significantly in the last month or so. This last week she described going to work and being so...
Back
Top