October 8 is
World MCT8-AHDS Day

MCT8 deficiency is an ultra-rare, genetic disorder that is also known as Allan⁠-⁠Herndon⁠-⁠Dudley Syndrome (AHDS).

There is no cure for this severely debilitating condition that children are born with. It severely impacts both the brain and the rest of the body, and families face many barriers, often waiting years for a diagnosis. It’s time to break down those barriers and shine a light on this rare disorder so we can help guide doctors to diagnose it and families to get the support they deserve.

Want to be a shining light for MCT8 deficiency?
Find out how here: