Welcome to Charlie's Mito Mission!

Charlie news

A family from Glasgow have started a mission for their gorgeous little boy Charlie, who is 4 and was diagnosed with mitochondrial disease this year.

His symptoms were very subtle at first, just a slight tremor noticed by his health visitor, and after 2 years, genetic testing confirmed he has the TARS2 genetic mutation.

By sharing Charlie’s story the family are excited to be raising awareness for a cause that affects them so deeply.

You can read Charlie’s story here.