The Children’s Rare Disorders Fund

Global Genes Global Advocacy Alliance member focused on rare disease support, education, advocacy, or research. The Children’s Rare Disorders Fund is dedicated to curing rare genetic disorders generally identified in childhood, beginning with FOXG1 Syndrome. Founded by parents of a toddler affected with FOXG1, The CRD Fund focuses research and development projects, aiming to fund research for as many rare disorders as possible, in order to cure as many children as possible. Directory information only; not medical advice, legal advice, or endorsement. Services and eligibility should be confirmed with the organization.