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

Taheisha Turner

This is for My Daughter Taheisha Turner, My First Born!!!

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Taheisha's Story

Taheisha was diagnosed with MPS 3A and in 2010 I found out about it and at that time I did everything in My Power to Learn about the Disease. Well in 2019 I was able to make it to Taheishas hospital bed side for Her last time in a Hospital. On June 5th Of 2019 Taheisha lost her battle. Or as I Like to say Finished Her Journey and Served Her Purpose. Our Story is Deep because My Child Held Strong Until I Came Home, Yes from Incarceration and from the time My Child Was Diagnosed In 2010, I Became Diagnosed as well because for a Parent to Already be Away and then to be away thru her whole Journey and to come home to Taheisha Final Steps In Her Journey is a Blessing, Because I KNOW SHE WAITED FOR ME, Her Dad!!!

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Our Mission

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

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