MCT8-AHDS |

MCT8-AHDS Foundation

Short history of events that lead to the creation of the MCT8-AHDS Foundation

Thyroid Hormone Analog Therapy of Patients With Severe Psychomotor Retardation Caused by Mutations in the MCT8 Thyroid Hormone Transporter: The Triac Trial.

For Families | Patient Stories

Read stories from other families about their journey.

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

About Diagnosing

The symptoms of AHDS depend vastly on how severe each case is and the severity of each case depends essentially on two connecting elements. Click here to learn more.

Patient Stories

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

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

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Please email us at [email protected] with any questions you might have.

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Welcome to MCT8-AHDS Foundation

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

Our Partners

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