ATTN HAYLEYCOLE URGENT

Discussion in 'Fibromyalgia Main Forum' started by Lolalee, Sep 18, 2006.

  1. Lolalee

    Lolalee New Member

    Hi Hayley,

    I know this is short notice, but I just read your post where you say that you believe that "within a few years, there will be enough evidence that CFS/FM/ME will be accepted as a neurological disorder."

    I have an appt with my Neurologist today and was wondering if you could direct me to any info on the web that I can print and take to him. He does not believe in FMS. He's had me go through various lab test and other tests and any abnormalities that show up he has ignored. He says its nothing to worry about.

    I'd like to leave him some reading material to educate him.

    Thanks for all you do.

    Lolalee

    [This Message was Edited on 09/18/2006]
  2. Lolalee

    Lolalee New Member

    bump to top
  3. Lolalee

    Lolalee New Member

    Hi Hayley, I just got home 1/2 hour ago...it's almost 9PM. I just wanted to let you know that I didn't get your post before I left for my appt. but I'll be seeing him again soon.

    I am sooooooo exhausted right now. I'll read your responses tomorrow. I appreciate all your time and caring.

    Blessings,

    Lolalee