MCT8-AHDS Foundation

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Striving for a cure. Empowering families The MCT8-AHDS Foundation aims to raise interest among the research community in the hope of finding a cure for this ultra-rare genetic syndrome, as well as offering support to patients and their families. Last but not least, it aims to raise awareness for MCT8 Deficiency also known as Allan-Herndon-Dudley Syndrome and act as a point of reference for affected families searching for information regarding the syndrome or simply looking to connect with other affected families.

Please help us find a cure for MCT8-ADHS and support children and their families. Join us in...