YOU are Igniting Hope!
When families learn that their child has been diagnosed with MPS, a rare, progressive and incurable disease that may potentially take their child’s life, it places on them a heavy emotional, physical and financial burden that few can relate to or understand. Most newly diagnosed families have never even heard of the disease and struggle to find adequate information or resources to guide them through the process of seeking treatment. Despite their astounding strength, resilience and optimism, many families struggle to readjust their lives to the overwhelming new reality presented by this disease.
The Canadian MPS Society Works to ensure that children and adults with MPS and related disorders receive the help they need, and receive it now. The support of generous donors like you, enables the Canadian MPS Society to provide family support, raise awareness, advocate, and advance research for treatments and ultimately for a cure.
Thank you for supporting the Canadian MPS Society and the families we serve.