Our Foundation is made up of a group of passionate parents and 100% volunteer-based. We are striving to find a cure; improve the quality of life and potential of our children; support hundreds of families around the world; share hope for a brighter future; learn from our collective experiences and; raise awareness of this ultra-rare condition with doctors, researchers and the general public. Our boys with MCT8-AHDS have many challenges to overcome, but we are stronger facing these together.