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.
Read stories from other families about their journey.
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.
We are currently not sending out a newsletter. This is the plan for the future. By providing your email you agree to receive periodic emails from the Foundation.