Category: Charity Info

We are honoured to welcome Reiff’s Mito Mission, based in Nottingham, which is run by his loving family.

Reiff’s story shows how a prognosis can be so devastatingly short when mitochondrial disease symptoms appear at an early age. His legacy continues through his mission and is run by Reiff’s loving family.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.

We are honoured to welcome Ezra’s Mito Mission, based in Hull, Yorkshire who has joined our Mito Mission family today.

You can read Ezra’s story on his webpage.

Ezra’s story shows that even with mitochondrial disease in the family, a diagnosis is not always straight forward and how mito can impact differently across generations.

Any support for Ezra’s mission will be hugely appreciated.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.

We are honoured to welcome the Merryweathers’ Mito Mission, based in Birmingham.

You can read the Merryweathers’ story here story shows how a mitochondrial disease diagnosis can impact across different generations, and raise questions about what the future might hold.

Any support for the Merryweather’s mission will be hugely appreciated.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.

We are honoured to welcome Charlotte’s Mito Mission, based in Crewe, Cheshire, who has joined our Mito Mission family today.

You can read Charlotte’s story on his webpage.
With her mission, Charlotte wants to raise as much awareness as possible, even amongst the medical community. She also wants to help all people understand how important mitochondrial research could help everyone, not just those with mito.

Any support for Charlotte’s mission will be hugely appreciated.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.

We are honoured to welcome Jason’s Mito Mission, based in Chatham, Kent, who has joined our Mito Mission family today.

You can read Jason’s story on his webpage. With his mission, Jason wants to raise awareness, help reduce the isolation that can be felt upon diagnosis as well as be an advocate for for timely and correct diagnosis of mitochondrial disease.

Any support for Jason’s mission will be hugely appreciated.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.

We are honoured to welcome Clare’s Mito Mission, based in Cramlington, Northumberland.

You can read Clare’s story on our webpage where her story highlights how as well as dealing with a diagnosis of mitochondrial disease can also bring loneliness, anxiety and depression. It is Clare’s hope that through her mission she can help to power the support that is desperately needed as well as raise awareness and funds for mito research.

Any support for Clare’s mission will be hugely appreciated.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.

We are honoured to welcome Tizzy’s Mito Mission, based in Chepstow, Monmouthshire. This mission is being led by her loving mum Helen, following Tizzy’s passing in 2018.

You can read Tizzy’s story on our webpage where her story shows how the symptoms of mitochondrial disease can suddenly appear at any point, changing lives forever and bringing isolation and loneliness.

Any support for Tizzy’s mission will be hugely appreciated.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.

We’re delighted to be welcoming Aria’s Mito Mission to our growing team. Aria and her family are based in Bradford, West Yorkshire.

Aria’s story story shows how mitochondrial disease can affect many different systems in the body, and how symptoms and a diagnosis can come seemingly out of nowhere.

Aria’s mission is to raise awareness of mitochondrial disease as Aria’s parents hadn’t even heard of mito when the diagnosis came.

We are honoured to welcome Callie’s Mito Mission, based in Ardglass, County Down, who has joined our Mito Mission family today.

You can read Callie’s story on our webpage where her family tell of just how rare her particular mitochondrial disease, PPA2, is. Callie’s family are very keen to raise mitochondrial disease awareness. They
also believe that mitochondrial research should have a much higher profile in the medical community, as it could be the key to treating many illnesses not just mito.

Any support for Callie’s mission will be hugely appreciated.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.