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Defeat MSA: Joseph G. Fortier Foundation for Multiple System Atrophy's Fundraiser:

Move Today for Those With MSA!

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THE STORY:

Multiple System Atrophy (MSA) is a rare, rapidly progressing neurodegenerative disorder. MSA impairs the systems that regulate blood pressure, heart rate and bladder – many of the basic bodily functions that people take for granted every day. People with MSA suffer from dangerously low blood pressure, speech and swallowing difficulties, sleep disturbances, breathing problems, rigidity and tremors. The life expectancy for those with MSA is typically 3 – 9 years. Patients with advanced MSA often become bed-bound, unable to speak and immobile. At present, there is no cure for MSA, no genetic tests to detect it and very few treatments to manage its debilitating effects.

Help Us Move Forward! Make A Mark in the Fight Against A Little Known But Very Tragic Disease... Help Us Conquer Multiple System Atrophy (MSA)!

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