S4K International Kevin Hunter Day The Price of Football Podcast We're so grateful for your support S4K International Raising awareness is key to our work to find effective treatments and one day, a cure for #mitochondrialdisease

Thanks Emily Coady-Stemp & Joshua Askew for sharing news of Kevin Hunter Day 's #marchoftheday raising awareness of #mitochondrialdisease! Putting #mitoonthemap around London & the South East! bbc.com/news/articles/… You can still sponsor Kevin by texting KEVIN to 70560 to donate £10!

Not long to this fabulous fundraiser at Christ Church Bath thanks to the Bath Community Band Bath Comm Big Band Thanks SLJO for joining our fight against #mitochondrialdisease ! #music #fundraiser #Bath

#WorldMitoWeek ended yesterday, but the journey to raise awareness, generate support, and advance innovation continues. Resources for those living with #MitochondrialDisease and their families are available from MitoAction, United Mitochondrial Disease Foundation, Mito Foundation and International Mito Patients (IMP).

From the results of surveyed registrants in mitoSHARE, we have more numbers to share on hearing-related symptoms in our patients with #mitochondrialdisease. Elevating #deafawareness and #mitoawareness on #DeafAwarenessMonth Join mitoshare at umdf.org/mitoshare/regi…

Online first at JCN: A questionnaire for parents in a pediatric #mitochondrialdisease clinic: questions that they would like addressed, primary concerns about their child, and goals for their child journals.sagepub.com/doi/10.1177/08… #humanisminmedicine

Mitochondrial disease can cause fatigue, weakness, seizures, heart problems, liver failure, and more. Contact us to volunteer or join our research. hubs.la/Q02QKpK50 #phdlife #scientists #molecularbiology #lifesciences #inspriational #volunteer #mitochondrialdisease

#WorldMitoWeek 2024 might be over today, but for patients and families with #mitochondrialdisease -- it's every day. Let's continue to #IlluminateTomorrow and share #mito voices today and every day. #MoreEnergyTogether umdf.org

Thank you to everyone who took part in World Mitochondrial Disease Week. Together we've made a huge impact! 💚 Thank you to all the mito community members who have shared your stories and experiences to raise awareness of mito 🙏 #WorldMitoWeek #MitochondrialDisease #mito

Another message from Sara Nowinski, PhD from the Van Andel Institute (VAI) on her hopes for #mitochondrialresearch -- addressing #mitochondrialdisease on a molecular level. #Cures and not just symptom management -- it's our hope, too. Researchers help us #IlluminateTomorrow

CELEBRATING over 2,000 registrants! Thank you!! Join mitoSHARE and add your data to a registry that drives #mitochondrialdisease research and #clinicaltrials forward. It's the simplest way to make transformative impact for the #mito community. Register at umdf.org/mitoshare-regi…

Megan lives with a #mitochondrialdisease called #MERRF syndrome which, for her, started with a seizure when she was 16 years old. Megan gives voice to the same HOPE of so many in the #mito community -- a cure. #IlluminateTomorrow Learn more about MERRF at umdf.org/MERRF

MRIs often reveal symmetrical lesions in the basal ganglia/brainstem in Leigh syndrome, but genetic testing is needed for a definitive diagnosis. That’s a wrap for our #LeighSyndrome fact series this week! 💙 #CureMito #LeighSyndromeAwareness #MitoWeek2024 #MitochondrialDisease"

Thanks so much to mito warrior Riaan's family for arranging for so many landmarks to light up green for World #MitochondrialDisease Week in Cardiff last night. Thanks ITV News for sharing Riaan's story and helping put #mitoonthemap itv.com/news/wales/202…

Concluding the #mitoweek2024 with 2 awesome selections of publications related to #mitochondrialdisease 📚Congrats to all authors! biomed.news/bims-mitdis/20… biomed.news/bims-mitdis/20… Bims: Biomed News Gavin McStay Keshav K Singh, PhD MitoScientists MitoSense Mitochondria & Aging Mitochondria News

There's no cure for #mito...but we're fighting hard to change that!📷Thanks to everyone for sharing & engaging with our posts throughout World #MitochondrialDisease Week, putting #mitoonthemap Keep up to date with our work by signing up to our newsletter: thelilyfoundation.org.uk/contact/

Cure EB Queen Elizabeth Olympic Park Thanks so much for the mention Cure EB We are delighted to have a team of Lily supporters getting involved in this fantastic event Queen Elizabeth Olympic Park next weekend. Raising awareness and funds to help fight #mitochondrialdisease supporting our #raredisease community.

Listen in to Friday's BBC Beds, Herts & Bucks to hear Angela talk about her amazing son, James who bravely battles #mitochondrialdisease Hear James' #mito story from around 1 hr 15 into the show: bbc.co.uk/sounds/play/p0… Share & help The #LilyFoundation put #mitoonthemap

The Crites family is lighting up their home in green for Mitochondrial Disease Awareness Week! 💚 Check it out and share your own picture with us in the comments! #leighsyndrome #mitochondrialdisease #mitoawareness #WorldMitoWeek2024

Are you #mitoaware? 👪Mitochondrial disease can affect anyone at any age!👪 Please share to help raise awareness during World #MitochondrialDisease Week. Learn more by visiting our website: ⬇️⬇️⬇️ ow.ly/C6KC50TshNf