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MPS Society UK, here for those with rare diseases

Individual and Family Services

Specialities :
Support to those affected by mps and related diseases
Research: promoting and supporting research into mps and related diseases
Awareness: raising the profile of mps and related diseases
Campaigning for improved access to services and equality for all
And patient support
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revenue-icon Revenue
11M - 100M
funding-icon Total Funding
--
size-icon Size
11 - 50
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Frequently Asked Questions About MPS Society UK, here for those with rare diseases

What does Mps society uk, here for those with rare diseases do?+

The Society for Mucopolysaccharide Diseases (MPS Society) is the only UK charity supporting individuals and families affected by MPS and related lysosomal diseases. These are progressive, life-limiting genetic conditions. Since 1982 we have provided support to children, adults and their families affected by MPS and related diseases, funding research into treatments and actively trying to raise awareness about this rare group of diseases. Registered as a Company limited by guarantee in England and Wales No. 7726882. Registered Charity No. 1143472, Charity registered in SCO41012

What are Mps society uk, here for those with rare diseases's specialties? +

Support to those affected by mps and related diseases,research: promoting and supporting research into mps and related diseases,awareness: raising the profile of mps and related diseases,campaigning for improved access to services and equality for all,and patient support

What is Mps society uk, here for those with rare diseases's industry? +

Mps society uk, here for those with rare diseases operates in the Individual and family services industry.

What is Mps society uk, here for those with rare diseases's revenue? +

Mps society uk, here for those with rare diseases's revenue is 11m - 100m

What is Mps society uk, here for those with rare diseases's company size? +

Mps society uk, here for those with rare diseases has 11 - 50 employees.

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