Ask the Parents

The National MPS Society is able to connect your family with other families who have shared the same experiences.  Please contact Laurie Turner at to connect with other families.

Many National MPS Society member families have consented to offer themselves available to others through email. You may contact them to learn more about the organization and how to cope with day-day issues presented by having a child with an MPS Disease.

We offer these names as an additional resource for affected families and extend our thanks to those listed below for making their email addresses available. Please

Contact Us for additional information on this service.

Locate a contact family from the disease selection lists below: