Society for Mucopolysaccharide Diseases
MPS House, Repton Place, White Lion Road, Amersham, Buckinghamshire, HP7 9LP, UK
Tel: 0845 389 9901 Fax: 0845 389 9902
National Registered Charity No. 287034
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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:
- To act as a support network for those affected by MPS & Related Diseases
- To bring about more public awareness of MPS & Related Diseases
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To promote and support research into MPS & Related Diseases
To Donate online click here
The European Commission approves first and only enzyme Replacement Therapy for MPSII, Hunter Disease - Press Statement
MPS House
Find out more about MPS House and our Conference and Meeting Venue available for hire.
The Society is a registered umbrella body with the Criminal Records Bureau. Click here for more information on the service we provide.
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