News. categories: Support,Research,Events,Personal stories,Awareness,Fundraising,Fitness - The Lily Foundation Page 4
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Stay connected with the mitochondrial disease community

Discover the latest updates from The Lily Foundation and the wider mitochondrial disease community. You’ll find news, personal stories, research updates and insights into the vital support we provide for those affected by mitochondrial disease.

From inspiring stories of families living with mitochondrial disease to breakthroughs in mito research and much more, there’s plenty going on. Sign up to our newsletters and follow us on social media to stay informed and connected – don’t miss a thing!

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Research
13 March 2023

Research focus: TRANSFORM study update

The Lily Foundation has been funding a study into a potentially life-changing new treatment for mitochondrial disease patients affected by epileptic seizures. Here to update us on progress is Katrin Bangel, part of the research team at the Wellcome Centre for Mitochondrial Research in Newcastle.

Support Research
3 February 2023

"The one place we can be ourselves"

At the recent 49th British Paediatric Neurology Association conference in Edinburgh, we found ourselves one of just eight exhibitors invited to host a stand and display our work. What’s more, we were excited to discover that The Lily Foundation were the only charity selected to deliver an oral presentation at the event.

Research Awareness
25 January 2023

On the road with the research team

It was a busy end to 2022 for Alison Maguire (Head of Research & Finance) and Katie Waller (Science & Patient Engagement Officer), who have been proudly representing The Lily Foundation at a range of recent mitochondrial disease events aimed at medical professionals, scientists and researchers.