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The Children's Rare Disorder Fund

The Children's Rare Disorders Fund is dedicated to curing rare genetic disorders via funding scientific research & development.

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Founded in September 2022 by parents of a toddler affected by FOXG1, The CRD Fund focuses on underserved communities in the rare disorder space.

The Fund raises funds and distributes it to research projects aimed at curing and/or treating rare disorders, beginning with FOXG1.

Long term, the CRD Fund aims to fund research for as many rare disorders as funding will allow, in order to find treatments and cures for as many children as possible.

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