A warm welcome to Lillia from Sheffield who has joined us to raise awareness of mitochondrial disease by having her own mission.
Lillia and her family live with the impact of mito every day and any support for her mission will be very welcome.
We are an ‘umbrella’ charity – so whether you support My Mito Mission as a whole or any individual mission – it’s all one great cause!
Please check out Lillia’s mission page.
A warm welcome to Lillia from Sheffield who has joined us to raise awareness of mitochondrial disease by having her own mission.
Lillia and her family live with the impact of mito every day and any support for her mission will be very welcome.
We are an ‘umbrella’ charity – so whether you support My Mito Mission as a whole or any individual mission – it’s all one great cause!
Please check out Lillia’s mission page.
We are thrilled to be able to update you with progress on a research project we were able to part-fund, thanks to our supporters.
Through our friends at The Lily Foundation we have helped to enable gene editing research at The University of Cambridge, which is paving the way for new treatments for incurable mitochondrial disorders
You can read all about the progress that project is making here.
We are thrilled to be able to update you with progress on a research project we were able to part-fund, thanks to our fantastic supporters.
Through our friends at The Lily Foundation we have helped to enable gene editing research at The University of Cambridge, which is paving the way for new treatments for incurable mitochondrial disorders.
You can read all about the progress that project is making here.
We are devastated to share the news of the passing of one of our ‘missionees’, Regan, aged just 13 from mitochondrial disease.
Our love and thoughts are with Mel, Regan’s devoted mum, and all Regan’s family and friends at this time.
Regan’s mission and his legacy will live on and continue to raise hopes of treatments and a cure for mitochondrial disease which so tragically impacted his life.
You will live on in all our hearts, Regan.
We are devastated to share the news of the passing of one of our ‘missionees’, Regan, aged just 13 from mitochondrial disease.
Our love and thoughts are with Mel, Regan’s devoted mum, and all Regan’s family and friends at this time.
Regan’s mission and his legacy will live on and continue to raise hopes of treatments and a cure for mitochondrial disease which so tragically impacted his life.
You will live on in all our hearts, Regan.
Meet Eddie, who we are thrilled has joined us this month – with a brand new Mito Mission based in Leeds.
Eddie is keen to raise awareness, funds for research and hopes of a cure for everyone affected by Mitochondrial Disease.
Read Eddie’s journey with the illness and much more on his mission page here.
Meet Eddie, who we are thrilled has joined us this month – with a brand new Mito Mission based in Leeds.
Eddie is keen to raise awareness, funds for research and hopes of a cure for everyone affected by Mitochondrial Disease. He joins our team of missions around the UK.
Read Eddie’s journey with the condition and much more on his mission page.
Our mito merchandise now proudly includes marvellous My Mito Mugs.
Yes, you now enjoy a cuppa whilst raising one of our mugs – as well as awareness and funds. Your mug or mugs can feature any of our individual mission logos or the main My Mito Mission logo.
Check them out in our shop now.
Our mito merchandise now proudly includes marvellous My Mito Mugs.
Yes, you now enjoy a cuppa whilst raising one of our mugs – as well as awareness and funds. Your mug or mugs can feature any of our individual missions‘ logos or the main My Mito Mission logo.
Check them out in our shop now
Fundraising by our supporters never ceases to warm our hearts as well as boost our funds.
A new fundraiser for Laura’s Mito Mission, based in Cheshire is no exception. Laura’s lovely friend, Andrew has taken on the amazing challenge to ride 1524 miles this year for mito.
Andrew has cerebral palsy and will tackle this awesome challenge in 77 x 20 mile sessions.
Read more, follow his journey and sponsor him here if you can.
Fundraising by our supporters never ceases to warm our hearts as well as boost our funds.
A new fundraiser for Laura’s Mito Mission, based in Cheshire is no exception. Laura’s lovely friend, Andrew has taken on the amazing challenge to ride 1524 miles this year for mito.
Andrew has cerebral palsy and will tackle this awesome challenge in 77 x 20 mile sessions.
Read more, follow his journey and sponsor him here if you can.
Delighted to announce our 11th mission – Bethany’s, based in Norwich, Norfolk.
Bethany and her family joined us to raise awareness of mitochondrial disease.
Please check out Bethany’s mission page.
Delighted to announce our 11th mission – Bethany’s, based in Norwich, Norfolk.
Bethany and her family joined us to raise awareness of mitochondrial disease.
Please check out Bethany’s mission page. If you would like to see where our other 10 missions are based you can find our here
Happy New Year from everyone at My Mito Mission Head Quarters!!
In the aftermath of Christmas and sorting through all your gifts, do you have anything that you don’t want, that could be donated our way?
We can turn your new or used items into ‘Mito Money’ for much needed research into cures and treatments for Mitochondrial Disease.
Last month, Sabrina from Aiman’s Mito Mission, magicked some donated mugs into fab prizes for fundraising – check them out here.
To chat with us about any offers, please use our contact us form here.
Happy New Year from everyone at My Mito Mission Head Quarters!!
In the aftermath of Christmas and sorting through all your gifts, do you have anything that you don’t want, that could be donated our way?
We can turn your new or used items into ‘Mito Money’ for much needed research into cures and treatments for Mitochondrial Disease.
Last month, Sabrina from Aiman’s Mito Mission, magicked some donated mugs into fab prizes for fundraising – check them out here.
To chat with us about any offers of goods, please contact us.
With cases rising and the new Omicron variant becoming more prevalent, face masks are now required in more and more places.
You can stock up on your face masks in our shop to raise awareness of mitochondrial disease as well as raising hopes of a cure.
Stay safe everyone
With cases rising and the new Omicron variant becoming more prevalent, face masks are now required in more and more places.
You can stock up on your face masks in our shop to raise awareness of mitochondrial disease as well as raising hopes of a cure.
Our thoughts are especially with those with mito and other conditions who are more vulnerable at this challenging time.
Stay safe everyone.
We are honoured and moved to have received donations in loving memory of Emily McDowall.
Emily tragically passed away in October at just 5 years old. She was diagnosed with Pearson Syndrome – a form of mitochondrial disease – shortly after birth.
Emily’s family collected £150 at her funeral and her Aunty Sharon has set up a fundraising page for any further kind donations.
This is a sad reminder of just how devastating mitochondrial disease can be. Your donations can and do make a difference. Together we can find treatments and a cure for mito.
We are honoured and moved to have received donations in loving memory of Emily McDowall.
Emily tragically passed away in October at just 5 years old. She was diagnosed with Pearson Syndrome – a form of mitochondrial disease – shortly after birth.
Emily’s family collected £150 at her funeral and her Aunty Sharon has set up a fundraising page for any further kind donations.
This is a tragic reminder of just how devastating mitochondrial disease can be. Your donations can and do make a difference. Together we can find treatments and a cure for mito.
