Our brand new monthly prize draw has gone live today. April’s prize is a fantastic 2 day stay at the stunning Barcaldine Castle. With a bottle of champagne to welcome you and a £25 voucher for Piazza Oban or Ee-Usk … your bound to have a wonderful time.
We’ll have a new prize every month and each draw will run from the 15th to the end of each month. All proceeds will support our work and raise hopes for treatments and a cure for mitochondrial disease.
Our brand new monthly prize draw has gone live today.
April’s prize is a fantastic 2 day stay at the stunning Barcaldine Castle. With a bottle of champagne to welcome you and a £25 voucher for Piazza Oban or Ee-Usk … your bound to have a wonderful time.
We’ll have a new prize every month and each draw will run from the 15th to the end of each month.
All proceeds will support our work and raise hopes for treatments and a cure for mitochondrial disease.
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.
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.
What could be more brilliant than having these gorgeous light up baubles in your home whilst supporting our vital cause?
The beautiful homemade baubles bring a bright green glow and add some mito awareness to your Christmas decorations as well as raising vital funds for research into cures and treatments for mitochondrial disease.
Check them out in our shop now.
What could be more brilliant than having these gorgeous light up baubles in your home whilst supporting our vital cause?
The beautiful homemade baubles bring a bright green glow and add some mito awareness to your Christmas decorations as well as raising vital funds for research into cures and treatments for mitochondrial disease.
Check them out in our shop now.
Brand new to the My Mito Mission shop are our cosy pom-pom beanie hats.
One size fits all with this amazing new way of spreading vital awareness for mitochondrial disease.
If you would like to stay snug with one of these brilliant beanies, click here to go to the shop now.
Brand new to the My Mito Mission Shop are our cosy pom-pom beanie hats.
One size fits all with this amazing new way of spreading vital awareness for mitochondrial disease.
If you would like to stay snug with one of these brilliant beanies, click here to go to the shop now.
It’s not just lighting up that our missions are helping to make happen for World Mito Week (19th-25th September).
Steph from Steph & Jake’s Mito Mission is having her head shaved, with just our logo ‘zap’ left! Jake and Dad Paul will have the ‘zap’ shaved in to the side of their heads.
All donations are gratefully received
It’s not just lighting up that our missions are helping to make happen for World Mito Week (19th-25th September).
Steph from Steph & Jake’s Mito Mission is having her head shaved, with just our logo ‘zap’ left! Jake and Dad Paul will have the ‘zap’ shaved in to the side of their heads. Their local barbers are kindly doing the honours and other local businesses getting involved to help raise awareness.
All donations are gratefully received!
World Mitochondrial Disease Week is with us next month, 19-25th September.
Our brilliant new merchandise help you to ‘Light Up For Mito’…. and raise a little awareness and funds at the same time.
Check it out along with all our other merchandise in our shop now!
World Mitochondrial Disease Week is with us next month, 19-25th September.
Our brilliant new merchandise help you too ‘Light Up For Mito’…. and raise a little awareness and funds at the same time.
Check it out our beautiful candles and baubles – along with all our other merchandise – in our shop now!
