MCT8 Children

Hello, I am Alexander. I am one of more than 300 children who live with an MCT8 gene mutation. I trust that scientists and physicians will do their best to find a cure for me and children like me. Until then, I am doing my best and I exercise every day so that maybe I can stand up one day ...

 

Hello, I am Piotr. I am 3 years old and moms little sunshine...

 

Hello, I am Darijan. My mom and dad are very proud of me. I'm 4 years old.

 
 

Hello, I'm Carl. Carl is Mom's and Dad's sunshine and a very bright curious child.

 
 

Hello, I am Fadel. I am 7 years old and my dear mom believes in me very strongly!

 
 

Hello, I'm Szymon. I am 12 years old and I always have the most beautiful smile on my face.

 

Hello, I am Jonas, 7 years old. I love playing with my sister. My parents do everything for me and they fight until the end.

 
 
 

Hi, I'm Max and I'll be soon 2 years old. My mom couldn't decide which photo of me was the cutest one :).

 
 
 
 

The MCT8 Research Foundation is committed to fighting the rare disease - Allan Herndon Dudley Syndrome (AHDS).