The MPS Society is a voluntary support group which represents and supports children and adults suffering from Mucopolysaccharide and related diseases, their families, carers and professionals.
It is a registered charity, managed by the members themselves, and entirely supported by voluntary donations and fundraising.
The aims of the Irish MPS Society are as follows:
to act as a support network for those affected by MPS and related diseases
to bring about more public awareness of MPS and related diseases
to promote and support research into MPS and related diseases
Contact
The Irish Society for Mucopolysaccharide Diseases,
