Anyone experiance muscle twitching

Discussion in 'Fibromyalgia Main Forum' started by Granolamom, Nov 4, 2002.

  1. Granolamom

    Granolamom New Member

    new here and wondering if anyone has experaince muscle twitching .

    lee
  2. Granolamom

    Granolamom New Member

    new here and wondering if anyone has experaince muscle twitching .

    lee
  3. joyof3

    joyof3 New Member

    All the time and in different parts of my body. your not the only one. stephanie
  4. Phoenix

    Phoenix New Member

    Oh ya! Big time. I don't know of a day, not one, that I have not had twitching...sometimes as many as eight or nine a minute for hours.

    Mine are so bad that I have to take 20 mg of baclofin four times a day...even then the bad ones get through.
  5. Shirl

    Shirl New Member

    Hi Lee, welcome to the board. I had the 'twitching' for years off and on. I started taking Pro Energy (Malic Acid and Magnesium), and ZMA (Zinc, Magnesium and B-6), and to be honest, I had forgotten about the Twitching untill I read your post!(Both products are sold here at Pro Health).

    It was probably a deficiency in one of the above, as I have not had them in months now.

    HOpe this is helpful, twitching is miserable.


    Again, welcome to the board.

    Shalom, Shirl
    [This Message was Edited on 11/04/2002]
  6. JaciBart

    JaciBart Member

    It was a recent one on this.

    Jaci
  7. kristine

    kristine New Member

    ...it stopped after i started taking the magnesium...kristine
  8. karen2002

    karen2002 New Member

    Have Twitching, almost everyday. Its most prevalent at nite. I am taking magnesium...and still muscle twitches.
    Karen
  9. Granolamom

    Granolamom New Member

    Thanks to everyone. It is great to have found this board!!!!
    I am very new at this( just diagnosied last week)

    Granolamom
  10. marcus1243

    marcus1243 New Member

    for the twitching. I think you'll find that it will reduce it, if not completely eliminate it. Both my girlfriend and I (she has CFS, I have FMS) twitch when we're sleeping -- sometimes it's like playing nocturnal football!
    Take care,
    Marcus
  11. pam_d

    pam_d New Member

    ...at least my life since FM...

    Hugs (but my arms will twitch),
    Pam
  12. Granolamom

    Granolamom New Member

    Thanks for all your responses. I love knowing I am not the only one!!!