MPS Society
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 Diseases including Fabry Disease, their families, carers and professionals.

Registered Charity No. 1143472

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A selection of charities you may wish to consider: 
Teenage Cancer Trust Heart UK Rethink Mental Illness Bliss Hope for Tomorrow The Scottish Wildlife Trust British Lung Foundation Ovarian Cancer Action

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