MCT8 - AHDS Foundation

Welcome to MCT8 - AHDS Foundation

Ultra-Rare Syndrome | Striving For A Cure | Empowering Families

The symptoms of rare disease, MCT8 deficiency, otherwise known as Allan Herndon Dudley Syndrome, are different in severity in each individual. Click here to learn more.

Hear directly from other parents about their journey. Hear first hand how other families cope.

Your contribution is more than a donation; it is how we will work towards research for a cure, raise awareness and empower families.

Our Partners

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