We are honoured to welcome The Sanders’ Mito Mission, based in Dagenham which is run by daughter and niece Amber.
The Sanders’ story shows how mitochondrial disease can affect multiple members of the same family but in different ways and also the implications of a maternally inherited variant across generations.
If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.
Last week we were honoured to welcome The Sanders’ Mito Mission, based in Dagenham which is run by daughter and niece Amber.
The Sanders’ story shows how mitochondrial disease can affect multiple members of the same family but in different ways and also the implications of a maternally inherited variant across generations.
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 Daisy’s Mito Mission, based in Armagh, Northern Ireland who has joined our Mito Mission family today.
You can read Daisy’s story on her webpage.
Daisy’s story shows how difficult diagnosing mitochondrial disease can be and how long this process can take. After 6 years and seeing lots of different medical professionals, Daisy was eventually diagnosed with mito through genetic testing via the 100,000 Genome Project.
Any support for Daisy’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 Daisy’s Mito Mission, based in Armagh, Northern Ireland who has joined our Mito Mission family today.
Daisy’s story shows how difficult diagnosing mitochondrial disease can be and how long this process can take. After 6 years and seeing lots of different medical professionals, Daisy was eventually diagnosed with mito through genetic testing via the 100,000 Genome Project.
Any support for Daisy’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 Jade’s Mito Mission, based in York, North Yorkshire, to our growing team.
Jade’s story story shows how important it is for all the many different variants of mitochondrial disease to be identified. Without the gene that impacts being discovered Jade, she would still be waiting for diagnosis.
Jade is keen to raise awareness of mitochondrial disease, as well as possibly some fundraising, along with her friends and family.
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 Jade’s Mito Mission, based in York, North Yorkshire, to our growing team.
Jade’s story shows how important it is for all the many different variants of mitochondrial disease to be identified. Without the gene that impacts being discovered Jade, she would still be waiting for diagnosis.
Jade is keen to raise awareness of mitochondrial disease, as well as possibly some fundraising, along with her friends and 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 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 Reiff’s Mito Mission, based in Nottingham, to our Mito Mission family.
Reiff very sadly passed away just at two years old in April 2025. His 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, which is run by his 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 Ezra’s Mito Mission, based in Hull, Yorkshire who has joined our Mito Mission family today.
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.
You can read Ezra’s story on his webpage.
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 Lauren’s Mito Mission to our growing team. Lauren and her family are based in Nuneaton, Warwickshire.
Lauren’s story shows how hearing and sight issues eventually led to a mitochondrial disease diagnosis, and how further symptoms evolved over time.
Lauren’s mission is to raise awareness of mitochondrial disease by having her story out there for everyone to read.
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 Lauren’s Mito Mission to our growing team. Lauren and her family are based in Nuneaton, Warwickshire.
Lauren’s story shows how hearing and sight issues eventually led to a mitochondrial disease diagnosis, and how further symptoms evolved over time.
Lauren’s mission is to raise awareness of mitochondrial disease by having her story out there for everyone to read.
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 the Merryweathers’ Mito Mission, based in Birmingham.
You can read the Merryweathers family’s story here. It 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 Charlotte’s Mito Mission, based in Crewe, Cheshire, who has joined our Mito Mission family today.
You can read Charlotte’s story on her 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 Jason’s Mito Mission, based in Chatham, Kent, who has joined our Mito Mission family today.
You can read Jason’s story here. 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.
A massive congratulations and thank you to all of our incredible Three Peak and One Peak participants on Saturday!
These fabulous fundraisers took the blustery, wet weather in their stride and took on a remarkable challenge to raise vital funds & awareness for mitochondrial disease.
We were thrilled to see both Lillia’s and Emma’s missions represented. I think we can safely say on behalf of all the people and families we support that we are incredibly grateful for any support we receive
You can support us too by signing up for a regular donation on our website, or by checking out and signing up for our upcoming events!
THANK YOU
A massive congratulations and thank you to all of our incredible Three Peak and One Peak participants on Saturday 7th June!
These fabulous fundraisers took the blustery, wet weather in their stride and took on a remarkable challenge to raise vital funds & awareness for mitochondrial disease.
We were thrilled to see both Lillia’s and Emma’s missions represented. I think we can safely say on behalf of all the people and families we support that we are incredibly grateful for any support we receive.
You can support us too by signing up for a regular donation on our website, or by checking out and signing up for our upcoming events!
THANK YOU!
