10 years ago, The Lily Foundation stood at the heart of the campaign to legalise #mitochondrialdonation. Today, research confirms it’s working, giving families the chance to have healthy, genetically related children 💗 Read more and please share! https://t.co/2fp9DK5IuE

👁️Today is World Sight Day – and we’re proud to reshare some incredible news for the mito community. Idebenone is now available for patients with LHON – a breakthrough that could help preserve vision and improve lives. 📖 Read Mary’s story to learn more: https://t.co/M0hN3PAIas

🔬 Supporting medical research into mitochondrial disease is at the heart of our mission. 👉 Explore our current research projects: https://t.co/jSUbHQbYW8 👉 Discover our past research projects: https://t.co/jSUbHQbYW8 Together, we’re driving hope through science. 💚

Happy International Coffee Day! ✨☕ “The Lily Coffee mornings are the highlight of my week…” - Amy, 28 If you’d like to be part of these wonderful mornings, just drop an email to Janet@thelilyfoundation.org.uk to get involved! ❤️

Throwback Thursday!👀 Today we're throwing it back to our unforgettable Adult Support Weekend — and what a weekend it was! Swipe through these fabulous photos to relive some of the highlights — we hope they bring a smile to your face just like they do for us. 😊

It’s not too late to do your bit for World Mitochondrial Disease Awareness Week! 💚 Did you know... Symptoms of mito include loss of muscle coordination, seizures, loss of vision and/or hearing, and organ failure Please share to show you care: 🔗 https://t.co/QRYTGdM7TK

💡 Tonight, landmarks across the UK will glow green for Light Up for Mito Thank you to everyone who made this happen – you’re all doing your bit to help put mito on the map this World Mitochondrial Disease Week! 💚 It's not too late to play your part: https://t.co/U2l9KsdOQF

It’s not too late to get involved in World Mitochondrial Disease Awareness Week! 💚 All week, we’re shouting loud about mitochondrial disease – raising awareness, sharing stories and putting mito on the map all over the UK. 👉 Find out more: 🔗 https://t.co/QRYTGdM7TK

World Mitochondrial Disease Week is reaching its peak Did you know there is still no cure for mito? We're fighting to change this and have invested over £3 million in pioneering research since 2007. 👉 Here's how you can continue to support us💚 🔗 https://t.co/QRYTGdM7TK

💚Share to show you care this World Mitochondrial Disease Awareness Week! 💚 All week we’re shouting loud about mitochondrial disease – raising awareness, sharing stories and putting mito on the map. 👉 See how you can help: 🔗 https://t.co/QRYTGdM7TK #worldmitoweek2025

💚 It’s World Mitochondrial Disease Week! 💚 This week, we’re shouting loud about #mitochondrialdisease – raising awareness, sharing stories and putting mito on the map. 👉 See how you can get involved: https://t.co/U2l9KsdOQF #worldmitoweek2025 #mitoonthemap #mitoaware

It’s here – World Mitochondrial Disease Awareness Week! 💚 Every share helps raise awareness and brings us closer to better treatments, more support and a cure. Let’s make some noise for the mito community! 💪 👉 Get involved: 🔗 https://t.co/QRYTGdM7TK #worldmitoweek2025

It’s here – World Mitochondrial Disease Awareness Week! Let’s make some noise for the mito community! 👉 See how you can get involved: 🔗 https://t.co/QRYTGdM7TK

💚✨ It’s nearly here… World Mitochondrial Disease Week starts TOMORROW! ✨💚 This is our moment to come together and put mito on the map – but we need your help! 🌍 Are you in? 🙌 https://t.co/tvXNUwWEzW

Today is #TK2dTuesday Learn more about thymidine kinase 2 deficiency (TK2d) and support those affected. https://t.co/SRkY1utz0k #mitochondrialdisease #TK2dAwareness

#LilyFoundation are joining together with the global #mito community to raise awareness of Thymidine kinase 2 deficiency (TK2d), an ultra rare #mitochondrialdisease Find out more: https://t.co/SRkY1utz0k #TK2dTuesday #muscleweakness #mito #TK2dAwareness

Thymidine kinase 2 deficiency (TK2d) is an ultra rare #mitochondrialdisease Find out more: https://t.co/SRkY1utz0k #TK2dTuesday #muscleweakness #mito #TK2dAwareness

Today is TK2d Awareness Day TK2d is a rare form of mitochondrial disease By advocating for patients, we're helping to drive vital progress towards a potential treatment Read more https://t.co/MCR6MgZZTG #TK2dawarenessday #thelilyfoundation #mitochondrialdisease #mitoonthemap

This month is Dystonia Awareness Month.💜 Throughout the month, we’ll be sharing facts and information to help raise awareness, spread understanding. Knowledge is power — and together, we can shine a light on this often misunderstood condition 💡

This is NOT a drill! 🚨 World Mitochondrial Disease Week is just ONE WEEK AWAY!! Have you made your plans to get involved? Let’s stand together and shine a light on mitochondrial disease. 👉 Find out how to get involved here: https://t.co/U2l9KsdOQF

💚 Be a part of something amazing 💚 Light Up for Mito – Saturday 20th September Want to light up a local landmark? We’ve got a ready-to-go email template to help! https://t.co/U2l9KsdOQF