Hello Supporter

Without you, our supporters, we wouldn’t be able to help those affected by mitochondrial disease or keep funding research into treatments. But we also rely on you to keep spreading the word about the condition.


This month, read about the lengths one of our supporters has gone to in order to raise awareness, and funds, to help fight mito.

A young mito warrior sitting in front of a group of people wearing Lily Foundation tops

How people power is spreading the word

When his son Jude was diagnosed with mitochondrial disease, like so many other parents Dale had never heard of the condition. But since that day he’s made it his mission to spread the word about our work, doing more than his fair share in the fight against mito.

Sponsor a hole at the Lily Golf Day 2024

Save the date…


We’re delighted to announce that the Lily Comedy Night will be returning to London’s Comedy Store on 3rd February 2025. Tickets will be on sale soon so watch this space…

If you’ve received a mitochondrial disease diagnosis, The Lily Foundation can offer emotional support and practical advice as you navigate your illness.