The Children’s Rare Disorders Fund is dedicated to finding treatments for FOXG1 Syndrome, with hope to treat as many genetic rare disorders as possible through funding research and replicating successes across disorders. Children with rare disorders are often neurologically and physically disabled. They are often unable to walk, talk, feed themselves, nor do much of what we take for granted every day. Founded by parents of a toddler affected by FOXG1 Syndrome, The CRD Fund is one of the few charities in the world in which 100% of every donation is directed to the cause - in this case, to the development of cures and treatments.
