"I believe a cure is possible and we will eliminate the challenges of MPS. Join us to make this a reality for Michael WhitakerRussell and all children living with MPS"

My goal is to raise $1,500
Total: $150

Michael's Story

Michael was diagnosed with MPS II at the age of 18 months. Although there is no cure for MPS II, Michael and I traveled up to Duke University for him to have a unrelated cord blood bone marrow transplant on December 26, 2008.

This has been a trying and difficult path being a single parent, but I would do it all over again if I had to in order to do whatever I could for my child. We would greatly appreciate your contributions with hope it can help find a cure for Michael and others affected by MPS.

Messages in Michael's Guestbook

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  • Shannon Bell

    Sending you prayers and hope for a cure to you and your sweet son.

Our Mission

The National MPS Society exists to cure, support and advocate for MPS and ML.

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