Our vision is for a world in which every mitochondrial disease patient has a voice and access to treatment, support to improve their life and, ultimately, a cure.
https://www.thelilyfoundation.org.uk/
#mitochondrialdisease
To help put mito on the map during World Mitochondrial Disease Week, our Research Manager @abioblog.bsky.social is here to explain the disease in a really simple way
Watch, learn and share! 💚
#mitoaware
To help put mito on the map during World Mitochondrial Disease Week, our Research Manager @abioblog.bsky.social is here to explain the disease in a really simple way
Watch, learn and share! 💚
#mitoaware
In 2018/19, Lily funded research using zebrafish to test treatments
Find out what happened in our latest Research Zone post with Research Manager Maria and Dr Ben Munro
www.thelilyfoundation.org.uk/affected-by-...
In 2018/19, Lily funded research using zebrafish to test treatments
Find out what happened in our latest Research Zone post with Research Manager Maria and Dr Ben Munro
www.thelilyfoundation.org.uk/affected-by-...
It’s a groundbreaking fertility technique that helps women with faulty mitochondrial DNA have healthy babies
Want to understand more? Watch our explainer video 👇
www.thelilyfoundation.org.uk/affected-by-...
It’s a groundbreaking fertility technique that helps women with faulty mitochondrial DNA have healthy babies
Want to understand more? Watch our explainer video 👇
www.thelilyfoundation.org.uk/affected-by-...
www.thelilyfoundation.org.uk/affected-by-...
www.thelilyfoundation.org.uk/affected-by-...
Here’s our CEO and founder, Liz, to explain why every voice matters
Please share:
mpscom.eu.qualtrics.com/jfe/form/SV_...
Here’s our CEO and founder, Liz, to explain why every voice matters
Please share:
mpscom.eu.qualtrics.com/jfe/form/SV_...