anyone have dysautonomia?

Discussion in 'Fibromyalgia Main Forum' started by Sheila1366, Jan 15, 2011.

  1. Sheila1366

    Sheila1366 New Member

    i was told I had this a few years ago. Thought it had gotten better but right now things aren't looking so good. Just wonder if there are others out there.
  2. AuntTammie

    AuntTammie New Member

  3. rgl

    rgl New Member

    I have NCS neurocardiogenic syncope and POTS Postural Orthastic Tachardia which fall under dysautonomia.

    The symptoms are very similiar to what we experience with FM/CFS is a source of information

    Good luck with dealing with dysautonomia; you can't ignore it! lol
  4. DeborahLynn

    DeborahLynn Member

    I haven't been diagnosed with it per se, but I do have most of the symptoms described on the websites. I have CFS/FMS.


  5. IanH

    IanH Active Member

    Dysautonomia, once though of as a distinct illness has become a loose descriptive term for autonomic dysfunction. Any symptom of any illness which affects the autonomic nervous system is dysautonomia. Probably about 90% of people with ME/CFS or FMS will have dysautonomia.
    gastrointestinal, cardiac, pulmonary, orthopedic, renal and ophthalmologic symptoms