The Multiple System Atrophy Trust is the only charity in the UK dedicated to providing support and information to anyone affected by a rare progressive neurodegenerative disease called multiple system atrophy (MSA).
MSA is a rare progressive neurological disease that currently has no cure. People with MSA will experience difficulty swallowing; falls; vocal chord paralysis; impotence and total incontinence. It's progression is fast and may cause premature death. Due to MSA being a rare condition, and the difficulty in accurately diagnosing it, most people feel lonely and isolated. The MSA Trust is the UK and Eire's only charity supporting people with MSA. We have over 6,000 members including people with MSA, carers, families, friends and health professionals. Our services include MSA nurse support, providing extensive specialist advice to people with MSA and their families in addition to funding research into the cause and ultimately a cure. We also train healthcare professionals so that they are able to correctly diagnose the symptoms of MSA.
We do not receive any government funding and rely entirely on voluntary donations. Without your support we cannot carry out this important work for people with MSA. Thank you in advance for your support.
Charity No: 1137652
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