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 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.
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.
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.
A warm welcome to Bethany, from Perth, Perthshire who has joined us to raise awareness of mito disease by having her own mission. Bethany lives with the impact of mitochondrial disease 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 Bethany’s mission page.
A warm welcome to Bethany, from Perth, Perthshire who has joined us to raise awareness of mito disease by having her own mission.
Bethany lives with the impact of mitochondrial disease 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 Bethany’s mission page.
A warm welcome to Hazel Allen from Darlington who has joined us to raise awareness of mitochondrial disease by having her own mission. Hazel 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 Hazel’s mission page.
A warm welcome to Hazel Allen, from Darlington, County Durham who has joined us to raise awareness of mitochondrial disease by having her own mission.
Hazel 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 Hazel’s mission page.
It is with incredible sadness that we share the news of the passing of one of our ‘missionees’, Laura.
Our love and thoughts are with Dawn, Laura’s devoted mum, and all Laura’s family and friends at this time.
Laura’s mission and her legacy will live on and continue to raise hopes of treatments and a cure for mitochondrial disease which so tragically impacted her life.
Donations in Laura’s memory are very welcome. Fly high beautiful Laura.
It is with incredible sadness that we share the news of the passing of one of our ‘missionees’, Laura.
Our love and thoughts are with Dawn, Laura’s devoted mum, and all Laura’s family and friends at this time.
Laura’s Mito Mission and her legacy will live on and continue to raise hopes of treatments and a cure for mitochondrial disease which so tragically impacted her life.
Donations in Laura’s memory are very welcome. Fly high beautiful Laura.
Delighted that this month is seeing us welcome a new mission – Ronni & Freddi’s.
Ronni & Freddi are brothers and have been affected in very different ways with mitochondrial disease. Ronni is eight and doing well, but tragically for little Freddi, it was severely
life limiting.
As part of Freddi’s legacy, his family have joined us with their own mission, based in King’s Lynn, Norfolk to help raise awareness, support and funds for research for everyone affected.
Please take a little time to read about the family’s journey with mito on Ronni & Freddi’s webpage
Delighted that this month is seeing us welcome a new mission – Ronni & Freddi’s.
Ronni & Freddi are brothers and have been affected in very different ways with mitochondrial disease. Ronni is eight and doing well, but tragically for little Freddi, it was severely life limiting.
As part of Freddi’s legacy, his family have joined us with their own mission, based in King’s Lynn, Norfolk to help raise awareness, support and funds for research for everyone affected.
Please take a little time to read about the family’s journey with mito on Ronni & Freddi’s webpage
Can you help bring a smile to Regan?
Regan, is one of our ‘missionees’ form
Regan’s Mito Mission and has had some challenging health issues due to having mito recently – that is sadly bringing upset and distress to his usual smiling face.
It would be a fantastic lift if he could receive some ‘happy mail’ – a card, a note, picture, small gift … anything. He loves to get post! Please send them to Regan c/o My Mito Mission, 44d Long Ridge, Brighouse, HD6 3RZ and we’ll swiftly
forward them.
Thank you… and thank you to the family’s lovely friend, Margaret for the idea too.
Can you help bring a smile to Regan?
Regan, is one of our ‘missionees’ form
Regan’s Mito Mission and has had some challenging health issues due to having mito recently – that is sadly bringing upset and distress to his usual smiling face.
It would be a fantastic lift if he could receive some ‘happy mail’ – a card, a note, picture, small gift … anything. He loves to get post! Please send them to Regan c/o My Mito Mission, 44d Long Ridge, Brighouse, HD6 3RZ and we’ll swiftly forward them.
Thank you… and thank you to the family’s lovely friend, Margaret for the idea too.
