The Society For Mucopolysaccharide Diseases

The MPS Society provides professional support to children, adults and families affected by MPS and related Lysosomal Storage Diseases and funds research into treatment and therapies. These diseases are rare, genetic, life-limiting conditions.

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Our top fundraisers

Paul Shields
$81,924.71 raised so far
Katrina Fanneran Burley
$21,217.68 raised so far
JOHN JOHN
$9,800.75 raised so far
Lee Shepherd
$7,041.91 raised so far
Emily Garthwaite
$6,346.67 raised so far
Louis Garthwaite
$5,870.18 raised so far

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Messages from other supporters

On behalf of the Ride4Life cycle challenge in aid of the Genistein trial for Sanfilippo.

Donation by Paul Shields £1,180.00 + £295.00 Gift Aid

Childminders and friends of Anabelle Rose Shepherd donated money on MPS Awareness Wear it Bllue Day - love and miss you baby girl xx

Donation by Sharon Russell £85.00 + £0.00 Gift Aid