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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
25 February 2021

Lily and partners fund £80k study into mito and neuropsychiatric diseases

The Lily Foundation is proud to announce its latest investment into scientific research to improve the lives of people with mitochondrial diseases. The charity is co-funding an £80,000 study to explore the links between mito and neuropsychiatric diseases – a blanket term that covers a broad range of medical conditions involving neurology and psychiatry.

Research
8 December 2020

Research Focus: Vestibular dysfunction

Amanda Male and Sarah Holmes are physiotherapists specialising in neuromuscular and vestibular rehabilitation. Here they talk about a new diagnostic framework they’ve developed to identify vestibular (inner ear) causes of balance problems in patients with a mitochondrial disease diagnosis.