Top Tweets for #WorldMITOWeek2026
The latest issue of UMDF Connect is here! Check your inbox for a recap of #WorldMitoWeek2026, new #mito support meetings launching, exciting updates coming to mitoSHARE, and more from across the UMDF community. To read the newsletter: https://t.co/zdIRyuvtFk

As World Mitochondrial Disease Awareness Week comes to a close, we want to say thank you to everyone who shared, spoke up, and helped put mito on the map. 💚🌎
Awareness doesn’t stop here—let’s keep the conversation going all year long!
#WorldMitoWeek2026 #PuttingMitoOnTheMap

Mitochondrial disease doesn’t have just one cause. Understanding its genetic complexity is another step toward greater awareness, research, and hope. #PuttingMitoOnTheMap #WorldMitoWeek2026

Want to learn more about #LBSL? Visit UMDF’s Types of Mitochondrial Disease page to learn more about LBSL, including causes, diagnosis, and available resources. Share this information to help raise awareness during #LBSLAwarenessDay and #WorldMitoWeek2026. https://t.co/km4uFSlpGX

Today is the last day of #WorldMitoWeek2026.
Follow us as our Doctors and scientific team work to tackle #mitochondria dysfunction in order to fight chronic disease.

This #LHONAwarenessDay, take a moment to learn more about Leber hereditary optic neuropathy (LHON), a rare inherited mitochondrial disorder. One of the primary signs of #LHON is sudden, painless loss of central vision. Learn more: https://t.co/EIvrGIbqvF #WorldMitoWeek2026

Today, we recognize LHON Awareness Day. 💚
Share this post and help us put LHON—and mitochondrial disease—on the map. 🌎
#LHONAwarenessDay #WorldMitoWeek2026 #PuttingMitoOnTheMap #MitochondrialDisease

https://t.co/qsE59xr5v2
Twelve years ago, our 16-year-old son Stephen said, “Mom, I think I am going blind in my right eye.” He was.
Today I joined @WBRCnews to talk about mitochondrial disease, #LHON & #LHONPlus during #WorldMitoWeek2026.
Watch: https://t.co/ENtKRChJbi
Tomorrow: #LHONAwarenessDay + #LightUpForMito 💚

Our UMDF staff are raising awareness during #WorldMitoWeek2026 and #PuttingMitoOnTheMap in their own communities. Watch the video to see which activities they’re doing during our Virtual National #Mito Movement Challenge happening now and visit https://t.co/INPL1ndt7b to join.
Every action matters this #WorldMitoWeek2026! Whether you join UMDF at an upcoming Energy for Life Walk or participate in our Virtual National Mito Movement Challenge, no action is too small to make a difference. Visit https://t.co/8QAPGupUnu to take action.
#WorldMitoWeek2026 is the perfect time to raise awareness about #mitochondrialdisease. Share the facts with your friends, family, and online community. Every post, share, and conversation helps bring greater visibility to the #mito community. #PuttingMitoOnTheMap.

There is no single picture of mitochondrial disease. 💚 Symptoms, abilities, challenges, and experiences can look completely different from one person to another. Understanding those differences is an important part of understanding mito.
#WorldMitoWeek2026 #PuttingMitoOnTheMap

💚 El 19 de septiembre, el #ICOES se iluminará de verde para sumarse a la campaña de concienciación de la #SemanaMundialEnfermedadesMitocondriales
▶️ LEE: https://t.co/XQNDktxEYU
🫶 @AEPMI
@FEDER_ONG @NoInvisibles @MasVisibles
#lightupformito #WorldMitoWeek2026

Mito is on the map! 🌎📍
From patient stories and organizations to research, events, and landmarks lighting up green, every pin represents another way we’re raising awareness and building connection.
#WorldMitoWeek2026 #PuttingMitoOnTheMap #MitochondrialDisease

World Mitochondrial Disease Awareness Week starts today! 💚🌎
This year, we’re Putting Mito on the Map by raising awareness, sharing stories, and helping more people understand mitochondrial disease and the community it impacts.
#WorldMitoWeek2026 #PuttingMitoOnTheMap

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