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

Vincent Gomez

For my son Vincent Scott Gomez. You are never forgotten and always thought of. If love was enough, you would of lived forever.
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Vincent's Story

Vincent was born June 6, 2013. He was diagnosed October 31, 2013 with MPS 1, Hurlers Syndrome. We traveled to Minneapolis, MN to pursue a bone marrow transplant. We started that transplant process as soon as possible. Vincent fought hard all the way to the end, where he grew his wings and left us on May 18, 2014 at the age of eleven months in my arms. Just short of his first birthday. Vincent would be six years old on June 6, 2019. He is missed by his two younger brothers, older brother, older sister, and mommy. You will always be remembered sweet boy. Mommy misses you.

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  • Nana holley nicholson

    NaNa loves and misses you As I look to the heavens above, knowing you are flying in peace

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

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