This website is designed for anyone who is diagnosed with MSA or has a family member or friend with the condition. Most people have never heard of MSA and getting a diagnosis can leave people feeling isolated and alone. Good quality, understandable information about MSA and its treatment can be difficult to find. Exploring this site and finding out more about MSA and the work of the Sarah Matheson Trust is the first step in addressing both these issues.
Visit the photo gallery under our News and Events section to see our brilliant London Marathon runners.
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To improve the accessibility of this site, you can choose to modify the way in which the main text is displayed. You can change the text size, colour and style as well as the background colour by clicking below. Your changes will be automatically saved on your computer so that the site will look the way you want it for the next time you return |
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The regular newsletter of the Sarah Matheson Trust, SMarT news, is packed with information and studies regarding MSA. |
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This website is only one of the Sarah Matheson Trust services. If you are affected by MSA or want further information about your individual situation please write to us or speak to one of our specialist nurses on the phone. |
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If you would like to make a donation, either online, by cheque or regular mandate, please click below. |
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This website provides information for people living with MSA, their families, and their informal and professional carers. The site is not designed as a diagnostic tool and, as with any medical information; the opinion of your doctor should always be sought.
If you intend to reproduce material from this site we politely request that you seek permission before doing so and give full credit to the source of the material.
If you intend to reproduce material from this site we politely request that you seek permission before doing so and give full credit to the source of the material.