Launching our Medical Alert Wristbands!

We’re pleased to announce that our Medical Alert Wristbands are now available to order, free of charge for anybody with a mito diagnosis.
Providing the kind of support those affected by mito want and need is at the very core of what we do.
Time after time, we have heard that people are worried about whether they will get appropriate medical care where mitochondrial disease will be taken into account, either for themselves or a loved one – especially in an emergency situation, or where communication is difficult for any reason.

Launching our Medical Alert Wristbands

Medical Alert wristbands

We’re delighted to announce that our Medical Alert Wristbands are now available to order, free of charge for anybody with a mitochondrial disease diagnosis. 

Read on to find out more about the project, and how to order yours if you’re impacted.

Providing the kind of support those affected by mito want and need is at the very core of what we do. Time after time, we have heard that people are worried about whether they will get appropriate medical care where mitochondrial disease will be taken into account, either for themselves or a loved one – especially in an emergency situation, or where communication is difficult for any reason.

We listened, explored options and liaised further… and these fabulous wristbands are the result. We are thrilled to now be able to provide them free of charge for anyone with mito.

These superb quality wristbands have been developed by The ID Band Company and are adjustable to fit from wrist size 5.25 to 8.25 inches. Known as Medical Ultrabands, they are made from super soft silicone and are totally waterproof and ultra hard wearing, yet smooth, flexible and comfortable to wear.

Callie looking at the wristband Aiman with wristband Mel, Kai and Laci with wristband

(Left to right) Some of our valued missions modelling their wristbands: Callie’s Mito Mission, Ardglass; Aiman’s Mito Mission, Rochdale; Regan’s Mito Mission, Cradley Heath

This unique, bespoke version made especially for My Mito Mission and the mito community is in our vibrant, easily-seen green – the international colour for mito. The clear black text engraved on bright white panels gives direct access via a QR code to specialist mito guidelines and also to the level of additional medical and personal information each wearer would like. The clinical guidelines let medical professionals know if and when they need to alter the standard treatment according to mito patients’ needs, and who they can contact if they need further advice.

Medical wristbands can help communicate your medical needs when you can’t. In an emergency situation, or in a more general medical setting where there is no mito specialism, medical professionals can:

  • be alerted to your condition
  • gain quick access to specialist clinical guidelines
  • be aware of any other medical needs, allergies etc.
  • access personal information such as your name, your emergency contact name and their details

We initially launched the wristbands to our missionees, and have received some incredible feedback so far:

“Having a medical alert wristband gives me reassurance that people will know about my illness should anything happen and I’m unable to tell them.” – Steph, Bury St Edmunds

“Having our medical wristbands makes things easy for hospital stays and appointments; instead of repeating myself about mito each time, they can now scan the QR code and get all information they need.” – Melanie, West Midlands

A huge thank you goes to our valued missionees for their input in developing these bands, to the Newcastle Mitochondrial Disease Clinic, and to The ID Band Company!

Order yours now on our website – just scroll to the bottom of the page to find the order form, and fill in your details.

Project 1000 Strong gets its first Business Supporter!

Our scheme to sign 1,000 people and businesses up to donate regularly has its first business supporter.

Project 1000 Strong has had 73 people sign up so far to give us a donation every month and our good friend, Raj Beadle – managing director of a company which sells iconic Italian coffee machines throughout the UK – is now giving us an amazing £50 a month.

Raj runs Gaggia UK which is less than a mile from us on the other side of Elland on the Lowfields Business Park.

Raj has supported My Mito Mission many times in the past by providing free coffee and machines for our coffee mornings, making donations and providing coffee machines as raffle prizes.

Here’s what he says about signing up to Project 1000 Strong: “When we learned My Mito Mission had set up Project 1000 Strong it was the logical step for us to take that support to another level by making a regular £50 a month donation.

“Times are tough for charities to fundraise or apply for grants so regular giving helps them to budget for the months and years ahead, knowing what’s coming in and what they can then afford to do to help support people with mitochondrial disease or to put into medical research.”

Our co-founder and chair of trustees Christine Beal adds: “Regular donations are the most powerful way to support our vital work, allowing us as a small, high-energy charity to plan and build from a strong foundation.

“We need a 1000 strong team of amazing people to donate any amount from just £2 a month. Yes, 1000 is a lot but, one by one, we know we can reach it and strengthen the future of Mito awareness, support and research.”

When it comes to donations, just £2 can buy some small tombola prizes and £5 covers a My Mito Mission collecting can while £50 pays for vital counselling appointments for someone impacted by mitochondrial disease and £200 equips a family or individual with their own mission, a ready-made ‘charity in a box’ enabling them to raise awareness and reduce isolation.

To find out more and to sign up go to https://www.mymitomission.uk/project-1000-strong

To read more about Gaggia UK’s charity work go to https://www.gaggiadirect.com/supporting-charities.html

'PROJECT 1000 STRONG's First Business Supporter!

P1000S Gaggia news storyOur scheme to sign 1,000 people and businesses up to donate regularly has its first business supporter.

Project 1000 Strong has had 73 wonderful people sign up so far to give us a donation every month and our good friend, Raj Beadle – managing director of a company which sells iconic Italian coffee machines throughout the UK – is now giving us an amazing £50 a month.

Raj runs Gaggia UK which is less than a mile from us on the other side of Elland on the Lowfields Business Park.

Raj has supported My Mito Mission many times in the past by providing free coffee and machines for our coffee mornings, making donations and providing coffee machines as raffle prizes.

Here’s what he says about signing up to Project 1000 Strong: “When we learned My Mito Mission had set up Project 1000 Strong it was the logical step for us to take that support to another level by making a regular £50 a month donation.

“Times are tough for charities to fundraise or apply for grants so regular giving helps them to budget for the months and years ahead, knowing what’s coming in and what they can then afford to do to help support people with mitochondrial disease or to put into medical research.”

Our co-founder and chair of trustees Christine Beal adds: “Regular donations are the most powerful way to support our vital work, allowing us as a small, high-energy charity to plan and build from a strong foundation.

“We need a 1000 strong team of amazing people to donate any amount from just £2 a month. Yes, 1000 is a lot but, one by one, we know we can reach it and strengthen the future of Mito awareness, support and research.”

When it comes to donations, just £2 can buy some small tombola prizes and £5 covers a My Mito Mission collecting can while £50 pays for vital counselling appointments for someone impacted by mitochondrial disease and £200 equips a family or individual with their own mission, a ready-made ‘charity in a box’ enabling them to raise awareness and reduce isolation.

Click here to find out more about Project 1000 Strong. 

You can read more about Gaggia UK’s charity work and to see Raj’s interview with Christine here.

Christine and Raj clinking mugs       Raj & Christine with certificate

Warmly Welcoming Callie’s Mito Mission!

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.

Warmly Welcoming Callie's Mito Mission!

Callie news imageWe 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.

The Energy Ball 2025

We are thrilled to announce that on Saturday 10th May 2025 we will be holding our annual charity ball, The Energy Ball sponsored by KT Hydraulics. This is our flagship event to raise vital mito awareness and funds for mitochondrial research and support for families impacted.

The ball will take place at Cedar Court Hotel Bradford, 6.30pm till late. Tickets are now on sale at the early bird price which includes a welcome drink and a 3 course meal.

You can click here for more information.

This year we three exciting sponsorship packages available for your company or workplace to purchase, each having different perks.

If you would still like to support our event but you can’t make it on the night, please get in touch!

The Energy Ball 2025

Energy Ball news

We are thrilled to announce that on Saturday 10th May 2025 we will be holding our annual charity ball, The Energy Ball sponsored by KT Hydraulics.

This is our annual flagship event to raise vital mito awareness and funds for mitochondrial research and support for families impacted.

The ball will take place at Cedar Court Hotel Bradford, 6.30pm till late. Tickets are now on sale at the early bird price which includes a welcome drink and a 3 course meal.

You can click here for more information and here to buy your tickets.

This year we have three exciting sponsorship packages available for your company or workplace to purchase, each with different perks, including marketing, CSR and a great night out!  Contact us to purchase your package, or to discuss bespoke sponsorship opportunities.

If you would still like to support our event but you can’t make it on the night, please get in touch!  

We hope to see you there for a magical night of powering support, awareness and research for mitochondrial disease!

My Mito Mission on the Airwaves!

We’re pleased to announce that our Medical Alert Wristbands are now available to order, free of charge for anybody with a mito diagnosis.
Providing the kind of support those affected by mito want and need is at the very core of what we do.
Time after time, we have heard that people are worried about whether they will get appropriate medical care where mitochondrial disease will be taken into account, either for themselves or a loved one – especially in an emergency situation, or where communication is difficult for any reason.

My Mito Mission on the Airwaves!

We were fortunate recently to have been invited to speak on both BBC Radio Leeds and BBC Radio Sheffield!

Our co-founder & chair Christine Beal was on BBC Radio Leeds earlier this month with the lovely Gayle Lofthouse to talk about all things mitochondrial disease and My Mito Mission!

Emma Sheppard, Lillia’s mum from Lillia’s Mito Mission also took to the airwaves this month, this time on BBC Radio Sheffield, with Ellie Colton. 

We appreciate any opportunity to raise awareness of mitochondrial disease, and are very grateful to both BBC Radios Sheffield and Leeds for their time and consideration.

Santa Dash 2024 – A Huge Success!

Our festive Green Santa Dash took place on Sunday, raising vital awareness and funds for mitochondrial disease!

The event at Stainland Cricket Club featured 1.5k and 5k courses, refreshments and stalls, and a whole lot of green Santa hats!

A gorgeous rainbow even appeared as our runners set off – what a view!

Thank you to Addev Materials for their kind sponsorship, and to our wonderful volunteers who helped out in organising and on the day.

We especially want to thank our 30 amazing dashers, both kids and adults, who braved the cold, wind and rain to take part in our first ever Santa Dash and we hope to now turn it into an annual event – look out for next year’s in December 2025!

Santa Dash 2024 - A Huge Success!

Santa dash roundup Our festive Green Santa Dash took place on Sunday, raising vital awareness and funds for mitochondrial disease!

The event at Stainland Cricket Club featured 1.5k and 5k courses, refreshments and stalls, and a whole lot of green Santa hats!

Santa dash dashers

A gorgeous rainbow even appeared as our runners set off – what a view!

Rainbow

Thank you to Addev Materials for their kind sponsorship, and to our wonderful volunteers who helped out in organising and on the day.

green santa with bellsAmanda Caldwell Elf    

We especially want to thank our 30 amazing dashers, both kids and adults, who braved the cold, wind and rain to take part in our first ever Santa Dash and we hope to now turn it into an annual event – look out for next year’s in December 2025!

Group photo

dashers in a bar

Santa running

Runners after the run

Red santa and green hat

Elf & Safety

Child running

Welcoming Justine’s Mito Mission!

We are honoured to welcome Justine’s Mito Mission, based in Stoke, Staffordshire. This mission is being led by her loving husband Jason, following Justine’s passing earlier this year.

You can read Justine’s story on our webpage where her story highlights the devastation that mito brings and the complex care issues that can arise for those impacted.

Any support for Justine’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.

Welcoming Justine's Mito Mission!

Justine news imageWe are honoured to welcome Justine’s Mito Mission, based in Stoke, Staffordshire. This mission is being led by her loving husband Jason, following Justine’s passing earlier this year.

You can read Justine’s story on our webpage where her story highlights the devastation that mito brings and the complex care issues that can arise for those impacted.

Any support for Justine’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.

Welcome to Gordon’s Mito Mission

We’re delighted to be welcoming another new mission to our growing team- Gordon’s Mito Mission, based in Oldham, Greater Manchester!

Gordon’s mission was launched by his loving partner Dot at his funeral and celebration of life on 2nd December 2024. Gordon was diagnosed with MELAS and had heart attacks aged 42 and 50 with a stroke in between.

Just before Gordon’s 56th birthday, he suffered a devastating heart attack which unfortunately he couldn’t recover from.

Dot ‘implores anyone with mito to never delay personal plans, excursions or celebrations because the illness is cruel and steals time, plans and futures.’

Gordon’s mission is to help others affected
by mito and to create a lasting and meaningful legacy for a special person who faced too many challenges.

Welcome to Gordon's Mito Mission!

Gordon news imageWe’re delighted to be welcoming another new mission to our growing team- Gordon’s Mito Mission, based in Oldham, Greater Manchester.

Gordon’s mission is launched by his loving partner Dot at his funeral and celebration of life  today (2nd December 2024). 

Please read Gordon’s story and discover why Dot ‘implores anyone with mito to never delay personal plans, excursions or celebrations because the illness is cruel and steals time, plans and futures.’ 

Any support for Gordon’s mission will be greatly appreciated.

Welcoming The Singh Family’s Mito Mission

Today we officially welcome The Singh Family from Perth, Perthshire to our My Mito community!

Jacqui is joined by her mum Ruby, her daughter Shishi (22) and her sons Jaeden (19) and Rubyn (10) for their family mission – a first of its kind for our charity.

All the family is impacted by mitochondrial disease and you can read their story on their webpage and about how the illness has tragically impacted their wider family too.

Their mission is to help increase awareness and understanding about the condition within their local communities and to gain more opportunities to meet with other affected individuals and families.

Welcome The Singh Family's Mito Mission

Singh Family's Mito Mission newsToday we officially welcome The Singh Family from Perth, Perthshire to our My Mito community!

Jacqui is joined by her mum Ruby, her daughter Shishi and her sons Jaeden and Rubyn (10) for their family mission – a first of its kind for our charity.

As mito is a genetic condition, all five of them are impacted by mitochondrial disease. You can read their story on their webpage and about how the illness has tragically impacted their wider family too.

Their mission is to help increase awareness and understanding about the condition within their local communities and to gain more opportunities to meet with other affected individuals and families. 

Art Sale Now Available Online!

We’re very pleased to announce that all remaining pieces from our Art Sale fundraiser are now available in our online shop!
All funds raised through the sale of art generously donated by local artists and those impacted by mito will go to our cause and Leigh Network, another mitochondrial disease.
Esteemed Huddersfield born artist Darren Baker, celebrated as the official portrait artist for Her Majesty The Queen in 2011, presents a rare opportunity to own a personalised piece.
Known for his hyper-realistic portraits, Baker’s impressive portfolio graces distinguished collections worldwide, including Downing Street, The House of Lords, St James’ Palace and The Bahrain Royal Household. His works continue to attract art collectors globally, solidifying his reputation as one of the most sought after artists of our time.
Featured also are pieces by local artists Carol Banks, Matthew Evans and Barbara Place. Artist Paul Jorden, who has mito, is selling limited edition prints of his gorgeous ‘Tree of Life’, and there are some remaining pieces by Faye Wylie, who we sadly lost to mito aged just 34 this year.
Have a browse through our varied selection, available til the end of November only, here.

Art Sale Now Available Online!

Art Sale online newsWe’re very pleased to announce that all remaining pieces from our Art Sale fundraiser are now available in our online shop!

All funds raised through the sale of art generously donated by local artists and those impacted by mito will go to our cause and Leigh Network, another mitochondrial disease. Esteemed Huddersfield born artist Darren Baker, celebrated as the official portrait artist for Her Majesty The Queen in 2011, presents a rare opportunity to own a personalised piece.

Known for his hyper-realistic portraits, Baker’s impressive portfolio graces distinguished collections worldwide, including Downing Street, The House of Lords, St James’ Palace and The Bahrain Royal Household. His works continue to attract art collectors globally, solidifying his reputation as one of the most sought after artists of our time.

Featured also are pieces by local artists Carol Banks, Matthew Evans and Barbara Place. Artist Paul Jorden, who has mito, is selling limited edition prints of his gorgeous ‘Tree of Life’, and there are some remaining pieces by Faye Wylie, who we sadly lost to mito aged just 34 this year.