The Society For Mucopolysaccharide Diseases (The MPS Society)

We support affected individuals & families to raise awareness of rare conditions.

Your support can change lives

£6

could pay for a family to receive a disease-specific booklet

£25

could pay for an advocacy officer to attend a school to offer support

£34

could fund an advocacy officer for 2 hours to support an individual/family

£6

monthly

could pay for a family to receive a disease-specific booklet

£25

monthly

could pay for an advocacy officer to attend a school to offer support

£34

monthly

could fund an advocacy officer for 2 hours to support an individual/family

Give Now

Charity Registration No. 1143472 and Scotland SC041012

www.mpssociety.org.uk

mps@mpssociety.org.uk

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About us

The MPS Society provides specialist support to children, adults and families in the UK who are affected by MPS, Fabry and related lysosomal storage diseases and we fund research into treatment and therapies. These diseases are rare, genetic, life-limiting conditions with no cure.

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