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Multiple system atrophy (MSA) is a devastating neurodegenerative disease that remains largely unknown by the masses and lacking in treatment options.

Here are some links to videos that can give you a more complete perspective on the impact this disease haas on patients, caregivers and families. Below are a few video links for you to watch.

I know you will.

Austin Crawford, current MSA patient, with his take on the disease: Austin Crawford Fights Multiple System Atrophy

Gettin' the Word Out! Fundraiser March 24, 2018. Music by Smokers Blues Band producer – Tara Denham of Lintz Photography

The Multiple System Atrophy Coalition: A Call to Action (hear patients and caregivers in their own words describe what the disease is to them)

MSA (Multiple System Atrophy NFPO Awareness Video A terminal disease that robs a patient of her ability to do even the most important and entertaining of things-much to the chagrin and sorrow of her good friend Bella

Sophie's Search for a Cure: Sophie, wife and mother, is seen here on a journey few take, no one wants to take and with only one ending; it is a story worth seeing for the awareness and education aspects it presents

To learn more about this rare and terminal neurodegenerative disease, visit the following sites for additional information:

The Multiple Atrophy Coalition webpage

MSA Coalition Link to Website


The MSA Coalition Facebook page:
MSA Coalition Public Discussion Group on Multiple System Atrophy

Vanderbuilt Autonomic Dysfuntion Center:
Vanderbuilt Autonomic Dysfunction Center-Multiple System Atrophy/Shy Drager Syndrome-Vanderbuilt Health


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