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  Welcome to MPS
The Society for Mucopolysaccharide Diseases (the MPS Society) is a voluntary support group founded in 1982, which represents from throughout the UK over 1200 children and adults suffering from Mucopolysaccharide and Related Lysosomal Storage Diseases including Fabry Disease, their families, carers and professionals. Membership is open to individuals who are resident in the United Kingdom and who meet the agreed criteria. The Society is a registered charity entirely supported by voluntary donations and fundraising and is managed by the members themselves. The Society has the following aims:
Jeans for Genes
 It's fun, it's simple and it's a great cause! Jeans for Genes is a national appeal where everyone across the UK is asked to throw out the usual dress rules, jump into their jeans and donate £1 at schools or £2 at work to help children with genetic disorders. The monies raised go towards pioneering research to develop new treatments and provide advice and support services which bring great hope to many families. Jeans for Genes Day, Friday 3 October 2008.
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Latest News
Expert Meeting on Morquio Disease (MPS IVA)
The opportunity to meet and talk informally with professionals.
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