George Joins Us as Our 30th Mission!

Today My Mito Mission reaches a new milestone by welcoming our 30th mission George’s Mito Mission, from Knaresborough in North Yorkshire to our My Mito Mission family.

George’s story tells of how their mum was badly affected with mitochondrial disease and how that impacted on the family in many different ways. You can find out much more on George’s webpage.

Unfortunately George’s mum’s journey with mito ended when she passed away in April 2022 not long after their dad died unexpectedly. Now George wants to be a part of raising awareness as a legacy to their mum and dad.

Welcome to our My Mito Mission family George, we are delighted to have you on board.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.

George Joins Us as Our 30th Mission!

George's Mito Mission news imageToday My Mito Mission reaches a new milestone by welcoming our 30th mission George’s Mito Mission, from Knaresborough in North Yorkshire to our My Mito Mission family.

George’s story tells of how their mum was badly affected with mitochondrial disease and how that impacted on the family in many different ways.  Unfortunately George’s mum’s journey with mito ended when she passed away in April 2022 not long after their dad died unexpectedly.

Now George wants to be a part of raising awareness as a legacy to their mum and dad.  You can find out much more on George’s webpage.

Welcome to our My Mito Mission family George, we are delighted to have you on board.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.

Light Up For Mito Glow Walk

We are excited to announce our upcoming Glow Walk, an event aimed at raising awareness for mitochondrial disease as part of the Light Up For Mito campaign during World Mitochondrial Disease Week (16-22nd Sept). The concept behind Glow Walk is simple: walk from point A to point B with as many or as few people as you’d like, using our glow wands to shine a light on mito awareness.
If you’re in the Elland area, don’t miss our local Glow Walk on Saturday, September 21st! We’ll start at MMM HQ in Elland once night falls and walk to Wainhouse Tower, which will be illuminated in green to honor mito. Bring your glow wands and join us! Stay tuned for more details and sign-up information. We would love to see Glow Walks happening all over the country, with your help!
If you’d like to organize a Glow Walk in your local area, here’s a simple guide:
Choose Your Route: Select two points in your area and gather your friends, family, and supporters! The route can be any length, and you can have as many or as few participants as you’d like, whether it’s just your family or a large group.
Gather Your Glow Gear: Once you’ve settled on your route and gathered your walkers, contact us to let us know how many glow sticks you’ll need, and we’ll send them to you free of charge. You can also wear your MMM tops, bring Light Up candles, or any other glowing items to enhance the experience!
Make It Extra Fun (optional): Not keen on just walking? Add a costume theme, turn it into a run, make it a pub crawl, or hand out mito awareness leaflets in your neighborhood. The goal is simply to participate in the campaign and raise awareness in any way you can. If you wish to fundraise, consider creating a JustGiving page for your event. However, please note that street collections require a special license, so we recommend avoiding donation buckets. That said, you are welcome to accept any donations offered! This event is primarily focused on raising awareness, so fundraising is entirely optional.
Keep an eye out for updates and sign-up sheets for our Glow Walk in Elland! We look forward to seeing your Glow Walks light up the night in support of World Mitochondrial Disease Week!

Light Up for Mito Glow Walk.

Glow walk news imageWe’re excited to announce our upcoming Glow Walk, part of the Light Up For Mito campaign during World Mitochondrial Disease Week (Sept 16-22). The idea is simple: walk from point A to B with your glow wands, with as many or as few people as you like, to raise awareness for mitochondrial disease!

If you’re near Elland, join us on Saturday 21st September! We’ll start at MMM HQ after dark and walk to Wainhouse Tower, which will be glowing green for mito. Stay tuned for more details and sign-up info!

We’d love to see Mito Glow Walks happening all over the country, and here’s how you can organise your own:

  • Pick Your Route: Choose two points in your area and invite friends, family, or anyone who wants to join. It can be a short or long walk with a few people or a big group.
  • Get Your Glow Gear: Let us know how many glow wands you need, and we’ll send them to you for free. Don’t forget to wear your MMM tops and bring anything else that glows!
  • Add Some Fun: Make it more exciting by adding a costume theme, turning it into a fun run, or handing out mito awareness leaflets. Fundraising is optional, but spreading awareness is the main goal!

Keep an eye out for updates and sign-up sheets for our Elland to Halifax Mito Glow Walk. We can’t wait to see your Mito Glow Walks light up the night in support of World Mitochondrial Disease Week!

Welcoming Emily’s Mito Mission!

Big welcome to Emily, from Sunderland, Tyne & Wear, whose mission starts today.

Emily’s Mito Mission is our first to be based in the North East of the country. Her story shows how mitochondrial disease symptoms can emerge at any age but also how is it possible for some, like Emily, to fight back against those symptoms.

Welcome to our My Mito Mission family Emily, we are thrilled to have you on board.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.

Welcoming Emily's Mito Mission.

Emily's Mito Mission Sunderland news imageBig welcome to Emily, from Sunderland, Tyne & Wear, whose mission starts today.

Emily’s Mito Mission is our first to be based in the North East of the country. Her story shows how mitochondrial disease symptoms can emerge at any age but also how is it possible for some, like Emily, to fight back against those symptoms.

Welcome to our My Mito Mission family Emily, we are thrilled to have you on board.

If you are impacted by mitochondrial disease you can get more information about starting your very own Mito Mission here.

New Clothing Range Available Now!

Raising awareness of mitochondrial disease is what we are all about. Our fabulous merchandise is a great way for anybody to support us in spreading the word and we are pleased to be able to offer a new range of black clothing.

This brand new merchandise consists of black long and short sleeve shirts for both men and women, as well as polo and t shirts. All of these items are available to be made to reflect the mission of your choice (or the charity as a whole) and come in smaller and larger sizes

You can check out all our new and existing products here.

New Clothing Range Available Now!

New black merchandise news image

Raising awareness of mitochondrial disease is what we are all about.

Our fabulous merchandise is a great way for anybody to support us in spreading the word and we are pleased to be able to offer a new range of black clothing.

This brand new merchandise consists of black long and short sleeve shirts for both men and women, as well as polo and t shirts. All of these items are available to be made to reflect the mission of your choice (or the charity as a whole) and come in smaller and larger sizes.

You can check out all our new and existing products here.

Out and About Summer Fundraising!

Some of our missions have been out and about doing some summer fundraising, and of course awareness raising.

Eddie’s Mito Mission held an awareness stall at Shepley First School with welly wanging and a tombola.

Emily’s Mito Mission had their annual fishing competition and raised lots of awareness and £1057 for mito research! A huge thank you to Waterfront Fisheries and Colin Pang.

Lillia’s Mito Mission held a charity football match in Sheffield with 28 local men taking part. A whopping total of £1836 was raised on the day!

Lucas’s Mito Mission held an awareness stall at Middleton Market in Leeds and had a tombola.

Emma’s Mito Mission held awareness and fundraising stalls at Brodstock Festival and Brighouse Gala with welly wanging, a teddy tombola and a parade.

And finally Aiman’s Mito Mission held a awareness and fundraising stall at Broadway Shopping Centre, Bradford with the help from Rotary Club of Adventurers, Rotary Bradford West and Rotary Community Corps. They had face painting, crafts, henna, origami and a tombola.

Well done to all involved.

Out and About Summer Fundraising

Our missions have been out and about doing some summer fundraising and vital awareness raising!


Eddie’s Mito Mission held an awareness stall at Shepley First School, Huddersfield with welly wanging and a tombola, and Lucas’s Mito Mission held an awareness stall at Middleton Market in Leeds with a tombola too.

Eddie's school fair news image  Middleton market news image

Emily’s Mito Mission had their annual fishing competition and raised lots of awareness and a huge £1057! A huge thank you to Waterfront Fisheries and Colin Pang for facilitating the event, and their ongoing support.

Emily's fishing comp news pic

Lillia’s Mito Mission held a charity football match and community fun day in Sheffield with 28 local men taking part. A whopping total of £1836 was raised on the day!

Lillia's football match news image

Emma’s Mito Mission held awareness and fundraising stalls at Brodstock Festival and Brighouse Gala with welly wanging and a teddy tombola.  They also joined the Brighouse Gala parade and made it to the front page of The Brighouse Echo sporting their bright green mito merch! 

Brodstock festival news image 

And last but not least, Aiman’s Mito Mission held an awareness and fundraising stall at Broadway Shopping Centre, Bradford with help from Rotary Club of Adventurers, Rotary Bradford West and Rotary Community Corps. They had face painting, crafts, henna, origami and a tombola.

A massive well done to all involved.  If you would like to host a stall or event for a mission or the charity as a whole, get in touch and we can provide you with support gear.

My Mito Mission Receives National Lottery Community Fund Grant!

We are thrilled to be able to announce that My Mito Mission have been granted £18,000 by the National Lottery Community Fund.

This money has been granted for the My Mito Meet Up, taking place in October, and will then free up other money for vital mito awareness, research and support.

The My Mito Meet Up is a vital weekend for our missionees to get much needed support from each other.

We would like to say a huge thank you to the National Lottery Community Fund from all at My Mito Mission!

My Mito Mission Receives National Lottery Community Fund Grant!

National Lottery news imageWe are thrilled to be able to announce that My Mito Mission have been granted £18,000, a National Lottery award from the National Lottery Community Fund.

This funding is for our Mito Meet Up in October, and will allow us to free up extra funds for vital mito awareness, research and support.

The Mito Meet Up is a vital weekend for our missionees to build connections with others who understand the unique struggles of mito and attend various workshops and activities.

We would like to say a huge thank you to the National Lottery Community Fund and to all National Lottery players!

 

Our Next Yorkshire 3 Peaks Challenge

Following from the huge success of our first Yorkshire 3 Peaks Challenge, we will be holding our second one on Saturday 7th September.

This time, you have the option of doing all three peaks, Pen-Y-Ghent, Whernside and Ingleborough, or just the one (Ingleborough).

The 3 Peaks challenge is open to adults only, but should you choose to do one peak, young people aged 14 and over can participate accompanied by an adult.

Join us on the day to raise priceless mito awareness and vital funds for mitochondrial research!

Our Next Yorkshire 3 Peaks Challenge!

Y3P news imageFollowing from the huge success of our first Yorkshire 3 Peaks Challenge, we will be holding our second one on Saturday 7th September.

This time, you have the option of doing all three peaks, Pen-Y-Ghent, Whernside and Ingleborough, or just the one (Ingleborough).

The 3 Peaks challenge is open to adults only, but should you choose to do one peak, young people aged 14 and over can participate accompanied by an adult.

Join us on the day to raise priceless mito awareness and vital funds for mitochondrial research!

Find out more here!

Y3P view
My MitoTed at Y3P
refreshment stop at y3p challenge
Y3P finisher with medal for news
Y3P finisher for news
Ash and Mia with certificate and medal
Y3P refreshment stop
Y3P participants
Y3P 2 finishers for news

NEW: Project 1000 Strong!

We are very excited and proud to announce our new fundraising campaign: PROJECT 1000 STRONG!

PROJECT 1000 STRONG is our brand new campaign aimed at building a team of 1000 regular donors.

Regular donations are the lifeline of any small charity and one of the most powerful ways that you can support us.

This enables us to strengthen the future of mito awareness, support and research.

We know that people kindly support our cause without expecting anything in return other than helping our charity thrive; however, we want to make sure they know how important they are to us with some small but heartfelt gifts. Those who sign up will receive:
A welcome letter
A membership card:
A code for 5% off our merch
Early access to MMM event tickets
An online ‘pack’ of images you can post to social media, or put in your email signature showing that you are supporting us:

Can you help us and be a part of PROJECT 1000 STRONG?

NEW: PROJECT 1000 STRONG!

P1000Strong news imageWe are very excited and proud to announce our new fundraising campaign: PROJECT 1000 STRONG!

PROJECT 1000 STRONG is our brand new campaign aimed at building a team of 1000 regular donors.

Regular donations are the lifeline of any small charity and one of the most powerful ways that you can support us.

This enables us to strengthen the future of mito awareness, support and research.

We know that people kindly support our cause without expecting anything in return other than helping our charity thrive; however, we want to make sure they know how important they are to us with some small but heartfelt gifts. Those who sign up will receive:

  • A welcome letter
  • A membership card:

Project 1000 Strong membership card

  • A code for 5% off our merch
  • Early access to MMM event tickets
  • An online ‘pack’ of images you can post to social media, or put in your email signature showing that you are supporting us:
    P1000S image

P1000S banner tilted

1000 is a lot, but – one by one – we know that we can reach it.

Can you help us and be a part of PROJECT 1000 STRONG?

Yorkshire 3 Peaks Challenge Success!

An 24 amazing people joined us to climb the Yorkshire Three Peaks on Friday 17th May, and we’re so incredibly proud of them all!

As well as raising lots of funds through sponsorships, we have raised valuable awareness of mitochondrial disease on the day (and on social media) sporting our stylish neon tops!

The day was a huge success, and we’re looking forward to organising similar events in the near future, so keep an eye out for details…

Amanda, Chris, Howard and Teresa did a fabulous job at keeping us motivated and energised, providing water, plasters and even homemade flapjacks at pit stops along the way.

Yorkshire 3 Peaks Challenge Success!

Y3P challenge news image24 amazing people joined us to climb the Yorkshire Three Peaks on Friday 17th May, and we’re so incredibly proud of them all!

As well as raising a huge £9,380 through sponsorships, we have raised valuable awareness of mitochondrial disease on the day (and on social media) sporting our stylish neon tops!

The day was a huge success with Emma’s and Ronni & Freddi’s missions both represented!  We’re looking forward to organising similar events in the near future, so keep an eye out for details…

Amanda, Chris, Howard and Teresa did a fabulous job at keeping us motivated and energised, providing water, plasters and even homemade flapjacks at pit stops along the way.

Y3P view
My MitoTed at Y3P
refreshment stop at y3p challenge
Y3P finisher with medal for news
Y3P finisher for news
Ash and Mia with certificate and medal
Y3P refreshment stop
Y3P participants
Y3P 2 finishers for news

Welcome John’s Mito Mission!

Big welcome to John whose mission starts today.
John lives in Batley, West Yorkshire and joins his younger brother Eddie in having a Mito Mission.
John’s story is one of disbelief among medical professionals as a child to finally getting his mitochondrial disease diagnosis as a young adult.
John is very keen to raise mito awareness in the general public but also medical professionals. He believes that the more people who know about mito, the more chance that those impacted will get a diagnosis, and feel much less isolated as a result.
Welcome to our My Mito Mission family John, we are delighted to have you on board.

Welcome John's Mito Mission.

John's Mito Mission news imageBig welcome to John whose mission starts today.

John lives in Batley, West Yorkshire and joins his younger brother Eddie in having a Mito Mission.

John’s story is one of disbelief among medical professionals as a child to finally getting his mitochondrial disease diagnosis as a young adult. John is very keen to raise mito awareness in the general public but also medical professionals. He believes that the more people who know about mito, the more chance that those impacted will get a diagnosis, and feel much less isolated as a result.

Welcome to our My Mito Mission family John, we are delighted to have you on board.