Pierce Family Fragile X Foundation

Our Story

The Pierce Family Fragile X Foundation was founded by the Pierce family after their sons, Graham and Reid, were diagnosed with Fragile X Syndrome. This journey began with Graham's birth in 2013, where developmental delays and health issues were first noticed. Following extensive medical consultations, Graham was diagnosed in 2015, with Reid's diagnosis following shortly after. The foundation was established to raise funds for research and awareness, driven by the family's commitment to improve the lives of their sons and others affected by this condition.

Impact

The foundation is dedicated to raising funds for research and awareness to find a cure for Fragile X Syndrome, which affects many families. Increased funding is essential for ongoing research and clinical trials that can lead to effective treatments.

Why Donate?

Donations are vital for funding research and treatments for Fragile X Syndrome. All contributions are tax-deductible and will directly support crucial research efforts aimed at finding a cure.

Make a Difference Today

Your support can change lives. Donate cryptocurrency or cash to the Pierce Family Fragile X Foundation and help fund essential research and awareness initiatives. Together, a brighter future for those affected by Fragile X Syndrome is possible!