Coping With Multisystem AtrophyThis 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. You may also Help others by sharing your story. To quickly access health information from your website's browser, download FINDING MSA 
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. I have been to many doctors of various specialties, had numerous tests, but never was given a correct dx. I think with finding this website and one other, I know now what is wrong with me. I will just have to convince one of my doctors. They already know I have lupus fibromyalgia, mgus and tremors, but they diagnosed the tremors as ‘essential’ and said there was no specific cause and act like it isn’t serious. I have had to live with this awful condition and it is getting so much worse. I feel empathy with any others who have had similar situations.
May 2008
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