What does it take to live with mitochondrial disease?
Hope. Courage. Belief. Community.
At The Lily Foundation, we know the challenges that families affected by rare mitochondrial disease face every day. That’s why we’re here – to provide support, fund research and raise awareness.
This video shares what it really takes to live with mitochondrial disease, and how together we can make a difference.
Join us to fight mito and find hope for everyone affected.
The Lily Foundation is the UK’s leading charity dedicated to supporting people affected by mitochondrial disease (mito) – a life-limiting genetic condition that affects energy production in every cell of the body.
Driven by a commitment to fight mito and find hope for everyone affected, we work tirelessly to raise awareness of this little-known but incurable condition, fund pioneering research and provide vital support to patients and families.
We align with the following UN Sustainable Development Goals:
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