Sure are getting an education tonight on M.E.

Discussion in 'Fibromyalgia Main Forum' started by daylight, Sep 15, 2006.

  1. daylight

    daylight New Member

    As I was reading the symptoms for this DD they match exactly what I've been going through. I've told my doctor for two years that I have more pain and symptoms that the 18 trigger points in FM. I'm curious if anyone knows when FM first got it's name? Also if the insurance companies and SSD had anything to do with the name change. Does it all come down to money? People with a so called syndrome get for less understanding for the medical field than people with a real disease. So if FM and CFS are connected maybe some of us really have M.E. and the insurance and Gov. just don't want to cover the cost to treat it.

    Just a theory .....
  2. justlooking

    justlooking New Member

    found on page 3 bumping for another go around and hopefully someone can assist you


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