My Mito Mission
@MyMitoMission
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Missions are run by families affected by #mitochondrialdisease. More research into mitochondrial disease could help so many, not just those with #mito 💚⚡
United Kingdom
Joined August 2017
Introducing PROJECT 1000 STRONG ⚡💪 💚 We're so pleased to be launching our brand new project, aimed at signing up 1000 regular donors and strengthening our future! 🔗 Sign up now to become one of our very first PROJECT 1000 STRONG team members! https://t.co/Un059wisGZ
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Hello, my name is Jake. I am 15 years old and live in Suffolk with my mummy and daddy. And I’m Steph, Jake’s mum. I’m 39 and devoted to my lovely son Jake and husband Paul. You can read our story with mito here Steph & Jake’s Mito Mission | My Mito Mission
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Tragically, Shania died on 10th May 2020, at just 20 years old. Her mission is to raise awareness about mito as well as being a legacy for a special young lady. You can read Shania's story here Shania’s Mito Mission | My Mito Mission
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Sadly, Rory died from mitochondrial disease just days before his 10th birthday, at a time when mito was even less known than it is today. You can read Rory's story here Rory's Mito Mission | My Mito Mission
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Today, we are launching a brand new appeal to help us continue powering support, awareness & research for mitochondrial disease. You can find out more and donate on our JustGiving page: https://t.co/Ya6FUTaaTE Thank you.
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To lose one child to mitochondrial disease is devastating, to lose two beautiful boys is beyond any words. Please read Ronni and Freddi's story and help their family raise awareness . You can read their story here Ronni & Freddi’s Mito Mission | My Mito Mission
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@MyMitoMission Mito is an energy production illness and is one of the most common genetic conditions. It affects all ages, can be debilitating and life-limiting, and there is no treatment or cure. Find out more:
mymitomission.uk
An innovative mitochondrial disease charity - My Mito Mission raises awareness, support and funds for research – could you be a Mito Hero and join us?
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Tonight we're lighting up for Mito! Did you know this week is World Mitochondrial Disease Week? We're thrilled to be joining the global campaign to raise vital awareness for mitochondrial disease. @MyMitoMission
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Individually, mitochondrial disease variants can be very rare. But there are so many variants, that together, they make mito one of the most common genetic illnesses.
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We need your support to continue powering support, awareness and research for mitochondrial disease, like Amanda. Please consider signing up to Project 1000 Strong, our regular donation programme. It's simple, secure, and it makes a huge difference. https://t.co/81GEBsvbfR
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Hello, I’m Rhona from Elderslie in Renfrewshire, Scotland where I live with my husband Graeme, sister Aileen and our adorable pug Jinty. My story illustrates how mito can be misdiagnosed over many years... You can read Rhona's story here Rhona’s Mito Mission | My Mito Mission
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Mitochondrial disease is a genetic condition. It can be inherited or appear spontaneously in a family. Although the gene fault is there from birth, symptoms can onset at any age.
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Incredibly sadly, Regan died on 7th February 2022. His mission goes on as a tribute and legacy for a courageous and inspirational young man. You can read his story here Regan’s Mito Mission | My Mito Mission
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Hello, I’m Paul from Birmingham, West Midlands. My story shows how mitochondrial disease isn't always inherited as I'm an identical twin and my mum and twin aren't impacted. You can read my story here Paul's Mito Mission | My Mito Mission
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Incredibly sadly, Milanna passed away aged just 2 years old on 6th February 2025. Her mission goes on as a tribute and legacy for an amazing, strong little girl. You can read her story here Milanna’s Mito Mission | My Mito Mission
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Enter our brand new prize draw for the chance to win a two-night glamping pod break! ✨ https://t.co/6zOHOMG3Hc
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