The Children's Rare Disorders Fund has partnered with FOXG1 Deutschland in order to combine resources, as we work towards curing FOXG1 Syndrome. We are very pleased to announce Tanja Vogel has joined our team as Head of Science.
About The CRD Fund: Founded by parents of a toddler affected by FOXG1 Syndrome, The Children's Rare Disorders Fund is dedicated to finding a cure for FOXG1 Syndrome. The CRD Fund hopes to one day replicate successes across many more rare genetic disorders.
How We Operate: Simply put, we vet potential FOXG1 research projects and make grants to either begin new research or continue current research, for promising projects in need of additional funding in order to continue.



