MCT8 - AHDS Foundation

Welcome to MCT8 - AHDS Foundation

Ultra-Rare Syndrome | Raising Awareness | Supporting & 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 will help us raise awareness of this ultra-rare condition and support and empower families.

Our Partners

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