Who are we ?
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, and is managed by the
members themselves. The organisation is entirely supported by voluntary
donations and fundraising activities.
The Irish MPS Society is part of an international network
of MPS Societies worldwide, and through these is involved in promoting
funding ongoing research into the area of MPS-related diseases.