MPS Society

If you or your child is affected by one of the 27 rare diseases we support, you can register to become a member of the MPS Society.

As a member, you will be able to receive specialist advice, support and up to date information about your disease.

If you or one of your family members have been recently diagnosed, then we understand that this can be a difficult time for you. We are here to support you so please complete this form to tell us more about you or your family member so we can get in touch to offer help and support.