We are the leading UK charity focusing on all muscle disease. We are dedicated to improving the lives of all babies, children and adults affected by muscle disease.
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A diagnosis of muscular dystrophy or a related condition is likely to be a shock. Here is information to help you come to terms with the news.
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We are here to support anyone affected by muscle disease - children and adults who have a condition, and clinical, education, health and social care professionals.
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Join forces with us to campaign on key issues and to raise vital funds to help us continue our work. Together we’re stronger.
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How to donate. The Muscular Dystrophy Campaign is funded almost entirely by voluntary donations. Your generosity makes our vital work possible.
Contact us Our phone and email Information Service is here weekdays 8.30am- 6pm to address any of your concerns about muscle disease.
Gillian Paton is the regional care advisor in Edinburgh.
Gillian supports both children and adults with muscle disease at:
Clinical Genetics Centre
Western General Hospital
Crewe Road
Edinburgh
EH4 2XU
She also supports clinics in Inverness, Aberdeen, Dundee and Fife.
Contact details:
0131 537 1063
Please note that Gillian works part-time, Mondays-Thursdays.
Tags: Scotland
