I’m doing a talk at Pint of Science Darlington on 13th May! 🥳

I’ll be chatting about all things mitochondria and mitochondrial disease 🙌🏼👇🏼

Clearly my life wasn’t already chaotic enough - meet the newest member of the household and sister to Freya - Mollie (short for Molossus) 😂🙈

New review to read:
DOI: 10.1146/annurev-biochem-052621-092014

Prof Michael Hanna UCLH Robert Pitceathly UCL News Muscular Dystrophy UK London Mitochondrial Centre UCL Brain Sciences We’re delighted to be an integral part of this pioneering project that should bring hope to the whole #mito community. Another great opportunity to work together Prof Michael Hanna Robert Pitceathly UCL Queen Square Institute of Neurology London Mitochondrial Centre UCL Brain Sciences

Only 3 weeks to go until the first ever #Darlingtonpint ! 🍺🧠
Tickets & more info available here: pintofscience.co.uk/events/Darling…
Don't miss out on #pint24

Two of our PhD students, The Lily Foundation funded Jamie Leighton and Lucie Taylor Lucie Taylor had the pleasure of presenting early career work at The 17th UK Neuromuscular Translational Research Conference
ICGNMD UCL_QS_CNMD

If you fancy a fun evening listening to lots of fabulous science, consider coming to a Pint of Science UK talk!

I’ll be speaking on 13th May in Darlington about all things mitochondria 👀🙌🏼

It’s been such a great 2 days being here with The Lily Foundation and hearing from fantastic researchers across the globe.

Excited to be travelling down to UCL_QS_CNMD today for the Neuromuscular Translational Research Conference with Alison, Head of Research The Lily Foundation 🙌🏼

We are very excited to catch up on the latest developments in #NMD and of course #mitochondrialdysfunction 👀

But seriously - how do people not catch every illness at a conference?

This snotty spud was sneezing and coughing at a wedding yesterday and feels like a zombie today.

Reccs for vitamins? 😅☠️

Welcome to our new followers. You can help us spread the word about #mito by sharing this short animation, voiced by actor Bill Nighy which gives a brief overview of the condition. Find out more on The #LilyFoundation website: thelilyfoundation.org.uk

Fantastic to hear from Taylor Lab discussing advances in mitochondrial disease diagnosis at Wellcome Connecting Science Engagement and Society #MitoMed24 conference.

Great to hear about the work of Rob’s lab looking into functional testing to support genomic testing 👏🏼

Calling #Mito #Researchers ! Looking to include the patient voice in your research, look no further! Our Expert Patient Input Committee made up of #mito patients, their families & carers keen to help shape research, clinical care & treatments. Email:[email protected]

This #RareDiseaseDay , our Lily team are proud to represent the voices of mito patients.
Dr Maria O'Hanlon is Teesside University National Horizons Centre for their #RareDiseaseDay event. giving a presentation to the researchers about the work of The #LilyFoundation #LilyRDD24 #mito

So great to be back at Teesside University National Horizons Centre for their Rare Disease Day event!

Proud to be representing The Lily Foundation at the event, and giving a talk later about our work funding mitochondrial research and supporting patients 🙌🏼

#LilyRRD24 #RareDiseaseDay2024

I will never not chuckle to myself when someone stands up and says ‘this is more of a comment than a question’ ☠️😂

There’s a lot going on in the world of #mito #research right now, making it an exciting time in the quest for treatments & a cure. And as the amount of ongoing research has grown, so has our team – welcome to our new Research Manager, Dr Maria O'Hanlon ow.ly/4LT450QuqNG

Really great start to the BPNA 2024 conference with the research team at The Lily Foundation 🙌🏼

So lovely to meet you Thiloka M 💖