Fighting mito,finding hope.
A donation from you will help fight mitochondrial disease and bring hope to everyone affected by it.
You can support those affected by mito by making a donation in memory of your loved one.
A gift left in your will can help us fight mito and improve the prognosis for those affected by it.
From stamps to raffle prizes, there are lots of ways you can donate to help us keep fighting mito.
Help fight mitochondrial disease every time you shop online – could fundraising be any easier?
Find out why tax-free Payroll Giving is one of the most cost-effective ways to fight mito.
Choose a charity challenge and help us raise vital funds to find a cure for mitochondrial disease.
Discover how to fight mitochondrial disease by fundraising for charity and donating through JustGiving.
Thank you for raising funds to fight mitochondrial disease. Find out how to pay your money in here.
Request a collection tin to leave in a location of your choice and help raise funds to fight mito.
Find out how you can get involved with our charity and support those affected by mitochondrial disease.
Discover ways your company could form a charity corporate partnership with The Lily Foundation.
There are lots of other ways to increase mitochondrial disease awareness and help those affected.
You’ll find plenty of mito-based fun and games to keep the little ones entertained.
Find out all about what mitochondrial disease is and learn more about this rare inherited condition.
Discover how Lily's story turned heartbreak into hope for families facing mitochondrial disease.
We exist to end the suffering caused by mitochondrial diseases through support, research and education.
Read all about our charity’s achievements since we began our fight against mito back in 2007.
Read our Impact Report and see how we’re transforming lives in our fight against mitochondrial disease.
Meet the team behind our mitochondrial disease charity and discover how we're fighting mito.
A selection of useful resources to help you raise funds and awareness about mitochondrial disease.
Aidan died before reaching his 2nd birthday, but his family still raise funds to fight mitochondrial disease in his name.
Alanah Rose was diagnosed with Leigh syndrome in 2023 and sadly lost her battle with mitochondrial disease just 15 months later.
Maisie was a fighter. Help this little girl live on for her parents forever by supporting Team Amazing Maisie and The Lily Foundation.
Siblings Archie and Ava battle mitochondrial disease but don’t let anything stop them! Help their family fundraise on their behalf.
Remembering beautiful Aria, whose laughter, love and light will always shine despite mitochondrial disease.
Born a healthy, happy baby, Aubrey was later diagnosed with mito and lost his battle when he was only 6.
Read the heartbreaking story of Bethaney, who sadly passed away from mitochondrial disease Leigh syndrome aged just 24 years old.
Bills_mito_battle is all about raising money and awareness for a unique little boy called Bill, who was diagnosed with mito in 2020.
Blue-eyed baby Brice lost his fight with mitochondrial disease when he was just 9 months old, and is missed every day.
After losing Connie to mitochondrial disease, her family share their journey of grief, love and finding support through Lily.
Help Daisy’s family raise funds for The Lily Foundation in honour of this cheeky little character who died so young.
Remembering Daisy, a brave little girl taken by mitochondrial disease. Her strength and spirit continue to inspire her family.
Erin lived for just 7 months and 8 days, and only after her death was mitochondrial disease identified. Read her story.
Felix has Leigh syndrome but he’s paving his own way, making his parents grateful for every day they have with him.
Fletcher’s diagnosis of mitochondrial disease turned his family’s world upside down, but they take life day by day together.
Grace died of mitochondrial disease when she was just 3. Help her family raise funds to support The Lily Foundation.
Honouring Harriet and Kimberley, lost to mitochondrial disease. Their legacy inspires awareness, love and hope every day.
Hattie’s parents were besotted by their firstborn but sadly she passed away from mitochondrial disease at just 3 months old.
Hector’s family are supporting The Lily Foundation to raise funds in the fight against mitochondrial disease. Read their story.
Meet Hope – a much-loved daughter, little sister and a true fighter who lives with a rare, life-limiting mitochondrial disease.
Baby Isla Ruby was just 9 months old when she lost her battle with mito. Read about her family’s fundraising efforts in her memory.
Jayden never lets anything get in his way, despite his mitochondrial disease diagnosis that causes him daily pain and fatigue.
Born with early-onset mito, Jude faces daily challenges but inspires everyone with his strength and resilience.
Little Keira, with her huge blue eyes and hair like Rapunzel’s, lost her battle with mitochondrial disease when she was only five.
Sisters Lily and Willow are affected by the same mutation that causes Leigh syndrome, a form of mitochondrial disease.
Read the story of Lillyanna – diagnosed with mito but inspiring her family to raise funds for The Lily Foundation.
Despite her mitochondrial disease, Lily is a resilient, positive child. Help The Lily Foundation by supporting her family today.
Despite prolonged seizures and an induced coma, Matilda fights mitochondrial disease and makes her parents beyond proud.
Olive has mitochondrial disease but faces daily challenges with strength and smiles. Her family fundraise for Lily to support research.
Otto was just 4 months old when he passed away from mitochondrial disease. His family now raise vital funds in his name.
Otto passed away peacefully from mitochondrial disease with his family around him. They’re now raising funds in his name.
Phoebe Grace, born in 2021, faced Leigh syndrome and passed away after a brave fight with mitochondrial disease.
Poppy was diagnosed with mitochondrial disease aged 2, and fights a huge battle against the disease every day. This is her story.
Toby has mitochondrial disease, and suffers epilepsy, is registered blind and can’t walk or talk. Help his family raise funds and hope.
Tirion, diagnosed with mitochondrial disease, faced every challenge with sass. Now her family are fundraising in her memory.
Ruby was diagnosed with Pearson syndrome but thanks to regular blood donations she’s doing better than her parents could hope.
Sebby’s journey with mitochondrial disease touched everyone who met him. His family now fundraise in his memory.
Sophie passed away from mitochondrial disease just a few weeks before her 8th birthday. Help her family honour her memory.
Teddie lost his fight with mitochondrial disease at just 8 years old, but always faced his illness with a cheeky smile.
Teddy is fighting mitochondrial disease with the help of his family who are raising funds in his honour. Support Team Teddy today.
Tommy always had a smile on his face but despite his bright disposition mitochondrial disease took his life when he was only 1.
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