Hello. I'm Laura and my story tells of how I received not only one difficult diagnosis - mitochondrial disease - but also a second challenging diagnosis just a few years later. You can read my story here

Dundee woman Danielle reveals how a DNA test breakthrough brought her relief after a 33-year struggle over an ultra rare condition The Courier MitoMission My Mito Mission thecourier.co.uk/fp/lifestyle/h…

This is Laura, who incredibly sadly died on 27th June 2021. It's her family's wish for her mission to continue - as a tribute and legacy for a beautiful young lady. You can read her story by clicking the link below Laura’s Mito Mission | My Mito Mission

Hello. I’m Lillia, I’m 8 and live in Sheffield with my mummy, daddy and my big brother Harrison. Lillia and her family live with the impact of mitochondrial disease every day. Please take a little time to read their story. Lillia's Mito Mission | My Mito Mission

Hello. I’m Louise and I live in Sheffield. Please take a few minutes to read about my journey with mitochondrial disease. Louise’s Mito Mission | My Mito Mission

New paper on mitochondrial distribution across the human body If you have more mitochondria than the average person in your heart, does that mean you also have more than average in your brain, muscles, kidneys, etc? We investigated inter-organ correlations in mitochondria 🧵

Mitochondrial disease can affect almost any part of the body, especially the major organs which require the most energy. This is one of the reasons why it can be challenging too diagnose.

Hi, I’m Lucas and live in Middleton, Leeds. Lucas has mitochondrial disease and following being admitted to hospital in 2022, he is still feeling the effects. You can read his story by clicking the link below Lucas’s Mito Mission | My Mito Mission

Enter our brand new prize draw for the chance to win a two-night glamping pod break! ✨ crowdfunder.co.uk/p/win-two-nigh…

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

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