Severe ME Day of Understanding and Remembrance: Aug. 8, 2017
Determined to paper the Internet with articles about ME, Jody Smith brings some additional focus to Severe Myalgic Encephalomyelitis Day of Understanding and Remembrance on Aug. 8, 2017 ...
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What's worse than CFS/ME

Discussion in 'General ME/CFS News' started by Lee Ann, Apr 15, 2011.

  1. Lee Ann

    Lee Ann

    At this point with atypical CFS?? or secondary CFS, is really not knowing what mystery illness my body possesses. Worse than a disease itself, is not having a definite diagnosis. I don't know what direction to take, what medicines to try, what supplements to buy, what the hell to do. I've carried my lifeless body to so many doctor's offices, (13) I can't stomach the thought of seeing another trained professional (sarcasim) who will give me another round of useless and expensive tests and tell me I am normal...Yippeee.... So, I guess my point to my rambling is, I feel hopeless and like I am stumbling in the dark and I want to scream....Can't somebody please tell me what is happening to my once healthy body....

    Thanks for being here....
    Lee Ann
  2. ixchelkali

    ixchelkali Senior Member

    Long Beach, CA

    Know the feeling. It's not much of an upside, but at least we're all stumbling in the dark together. I'd scream, too, if I had the energy.
  3. *GG*

    *GG* senior member

    Concord, NH
    Could you go see Dr. Klimas? You are closer than mysefl, and I am considering it.


    PS How about the ACAM website for a dr? or Functional Medicine:

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