Throughout May we are collected money for the The Society for Mucopolysaccharide Diseases(The MPS Society). The MPS Societyis 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. MPS awareness day is the 15th May.
In total we raised £76.95 for this great charity. If you would like to find out more about the MPS Society please visit www.mpssociety.co.uk