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Coping With Multisystem Atrophy

This section is a place to share stories about Coping With Multisystem Atrophy.

Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation.

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May 2008

  • My Mum’s MSA diseas - by Peter - (Mon, May 19 2008)
    Hello, my Mum is 67 of age and a dieseas started 6 years ago. It took german Doctors and Hospitals 5 years to find out what she really has. They first thought it might be a Lupus than Parkinson and finally MSA. [more..]
  • Not finished….yet!! - by Treesee - (Fri, May 09 2008)
    I was on a trip to Ca. with my husband of many years, and we had to come home. I had suddenly lost control of bladder, bowels, blood problems, bleeding, clotting. [more..]
  • FINDING MSA - by s - (Fri, May 09 2008)
    I have had tremors, breathing problems, gait, sitting/posture problems and basically everything to do with this rare disorder except that which is exclusivie to men, for years. [more..]
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