Cri du Chat Research Foundation

EIN: 47-1749667 · Brooklyn, NY

Research into Cri Du Chat Syndrome

Our Story

Founded in July 2014 by Megan and JC Leston, the Cri du Chat Research Foundation emerged from a personal journey filled with hope and determination. After learning that their son would live with Cri du Chat Syndrome, a rare genetic disorder with a challenging prognosis, they were inspired to create a science-focused organization. The foundation aims to change the trajectory for individuals diagnosed with Cri du Chat/5p Minus Syndrome by leveraging advancements in genetic science to identify treatment strategies that can transform lives.

Impact

The mission of the Cri du Chat Research Foundation is to accelerate translational research that utilizes innovative technologies to develop therapeutics aimed at alleviating the major neurological symptoms associated with 5p- syndrome. This mission seeks to enhance the lives and independence of every child and adult affected by this rare disease.

Why Donate?

Your generous donation will directly support critical research into Cri du Chat Syndrome, helping children and families navigate the daily challenges posed by this genetic disorder. Every contribution, no matter the size, brings us closer to breakthroughs that can change lives.

Join the Fight

Help make a difference today! Your support can accelerate research and bring hope to families affected by Cri du Chat Syndrome. Donate cryptocurrency or cash now to empower change!

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