Donate to the MPS Society

Thank you for donating to the MPS Society.  

Your support means we are able to be there for everyone affected, whether that’s a family with a young child recently diagnosed or a young adult transitioning into adulthood.  

 

As a small charity that receives no government funding, we are truly grateful for supporters like you. 

How your money helps

 

£5 could pay for a newly diagnosed family to receive a disease specific information booklet

£16 could pay for specialist equipment to help our researchers better understand treatments and potential therapies for MPS

£25 could support one bereaved family, enabling them to plant a tree in memory of a child or adult who has lost their life to MPS at the MPS Childhood Wood

£60 could enable one family to attend a regional family event such as a trip to Cadbury World, to have fun with other affected families

£100 could pay a Support Officer to visit an affected family providing essential practical and emotional support

£200 could enable a child who lives with a brother or sister with MPS, to attend a Sibling Activity Weekend for an opportunity to share stories and have fun

£1000 could fund 6 specialist MPS clinics in a year so that families can come together to share their experiences, break down isolation and make lasting friendships

Contact us

 

Call the fundraising team on:

0345 389 9901 or 

We are the only registered charity providing professional support to individuals and families affected by MPS, Fabry or a related disease in the UK.

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MPS Society, MPS House,

Repton Place, White Lion Road,

Amersham, Buckinghamshire,

HP7 9LP, United Kingdom

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0345 389 9901

Registered Charity No.1143472 & SCO41012. Registered Company No. 7726882.

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© 2020 Society for Mucopolysaccharide Diseases