Fibro conference in LA

Discussion in 'Fibromyalgia Main Forum' started by DebinMN, Sep 8, 2002.

  1. DebinMN

    DebinMN New Member

    I am going. I will grab every bit of info they have and buy a video if they sell them......I will forward the info to the board after I return....I sure hope its worth the $$$ and the pain I will go through......
  2. DebinMN

    DebinMN New Member

    I am going. I will grab every bit of info they have and buy a video if they sell them......I will forward the info to the board after I return....I sure hope its worth the $$$ and the pain I will go through......
  3. selma

    selma New Member

    for going for us. Those of us that can't go really would appreciate the info..

    You are special to do it.

    Love, Selma
  4. Achy-shaky

    Achy-shaky New Member

    Hi DebinMN - Is this the conference on 9/21? I found info in the community board but was not able to go to the website (www.admedcon.com/default.html) noted. Do you know how to register for it & how much it costs? If I can go maybe we could meet there.

    BTW, I'm from Stillwater, MN and have a sister-in-law who lives there & has FMS too - she goes to a great doc - I can ask her who/where and email you.

    Thanks and hope to hear from you soon.

  5. DebinMN

    DebinMN New Member

    I would love to know her doctor.....my primary care doctor doesnt tink its a big deal....REALLY? then why do I wish I could crawl into a hole and stay there? Anyway, my friend in New Mexico and I are going to the conf. We are staying at the hotel where it will be. http://www.admedcon.com is where you register....http://www.fmaware.org site is where all the info is. Would love to meet you. Deb