‘Mini Miracle’ at My Mito Meet-Up!

Last weekend’s get together for our missionees, charity volunteers and top mitochondrial researcher Professor Kostas Tokatlidis truly showed the value of bringing patients and professionals together. Not only did it give those impacted by mitochondrial disease the chance to hear about developments in research, it also bought an unexpected and amazing result.

Professor Tokatlidis has studied a key mitochondrial protein (called GFER) for 15 years. GFER is one of almost 1500 genes linked to mitochondrial disease. The condition associated with GFER mutations is extremely rare, but one which potentially has wide implications for progress across mitochondrial function as a whole. Just a handful of families in the world are affected by this gene fault – with just one family in the UK to the scientist’s knowledge, none of whom were known to him.

Eddie Wall, who runs his Mito Mission in Leeds took the opportunity to speak with Professor Tokatlidis on Saturday evening. Through this chat, it was discovered that Eddie and his brother John are that very family.

‘It’s both an incredible coincidence and extremely exciting that I have connected with Eddie and his family’, said the Professor. ‘To be able to work directly with a patient has the potential to significantly advance our research and showcases how we can work together to maximise patient involvement and engagement in a very meaningful and impactful manner.’ Whilst Eddie added, ‘Research is hope to mito patients. I’ve wanted to play as big a role as I can for a long time and to have this opportunity occur is amazing. And on my birthday too!’

We are beyond thrilled that our first ever My Mito Meet-Up bought about this incredible connection which has the potential to advance mito research – something which brings hope to everyone impacted by mitochondrial disease.

First Ever My Mito Meet Up.

Kostas and Eddie - Mini MiracleLast weekend’s get together for our missionees, charity volunteers and top mitochondrial researcher Professor Kostas Tokatlidis truly showed the value of bringing patients and professionals together. Not only did it give those impacted by mitochondrial disease the chance to hear about developments in research, it also bought an unexpected and amazing result.

Professor Tokatlidis has studied a key mitochondrial protein called GFER for 15 years. GFER is one of almost 1500 genes linked to mitochondrial disease. The condition associated with GFER mutations is extremely rare, but one which potentially has wide implications for progress across mitochondrial function as a whole. Just a handful of families in the world are affected by this gene fault – with just one family in the UK to the scientist’s knowledge, none of whom were known to him.

Eddie Wall, who runs his Mito Mission in Leeds took the opportunity to speak with Professor Tokatlidis on Saturday evening. Through this chat, it was discovered that Eddie and his brother John are that very family.

‘It’s both an incredible coincidence and extremely exciting that I have connected with Eddie and his family’, said the Professor. ‘To be able to work directly with a patient has the potential to significantly advance our research and showcases how we can work together to maximise patient involvement and engagement in a very meaningful and impactful manner.’ Whilst Eddie added, ‘Research is hope to mito patients. I’ve wanted to play as big a role as I can for a long time and to have this opportunity occur is amazing. And on my birthday too!’

We are beyond thrilled that our first ever My Mito Meet-Up bought about this incredible connection which has the potential to advance mito research – something which brings hope to everyone impacted by mitochondrial disease.

Meet-Up Proves Magical

Our 1st My Mito Mission meet-up – a get together for our missionees around the UK – took place this weekend and was a huge success.

A visit to Cannon Hall Farm, Barnsley on Saturday was followed by a social on Saturday evening at the Cedar Court Hotel, Huddersfield featuring a talk by top mitochondrial researcher Professor Kostas Tokatlidis from Glasgow University.

Sunday saw everyone – including staff, trustees and volunteers – get some inspiration on how we can together raise even more vital awareness and funds for research.

“It was just magical to see so many of our missions able to get together in person”, says Christine Beal, Chair of Trustees and lead for Emma’s Mito Mission. “Some very precious memories were made and friendships forged to last a lifetime”.

We can safely say that the My Mito Meet-Up 2022 was a massive success. A huge thanks, as ever, goes to each and every supporter for making events like this possible.

First Ever My Mito Meet Up.

My Mito Meetup Cannon Hall Trip 2022Our first My Mito Mission meet-up – a get together for our missionees around the UK – took place this weekend and was a huge success.

A visit to Cannon Hall Farm, Barnsley on Saturday was followed by a social on Saturday evening at the Cedar Court Hotel, Huddersfield featuring a talk by top mitochondrial researcher Professor Kostas Tokatlidis from Glasgow University.

Sunday saw everyone – including staff, trustees and volunteers – get some inspiration on how we can together raise even more vital awareness and funds for research.

“It was just magical to see so many of our missions able to get together in person”, says Christine Beal, Chair of Trustees and lead for Emma’s Mito Mission. “Some very precious memories were made and friendships forged to last a lifetime”.

We can safely say that the My Mito Meet-Up 2022 was a massive success. A huge thanks, as ever, goes to each and every supporter for making events like this possible.

First Ever My Mito Meet Up!!

The My Mito Meet-Up 2022 is underway!!

For the first time since the charity’s inception in 2017, our missions from around the UK are getting together for a wonderful weekend of fun, socialising and above all, support and new friendships.

Just one of the support projects we have been able to complete thanks to our fabulous supporters. More news of the weekend to follow soon!

First Ever My Mito Meet Up.

My Mito Meetup 2022 WeekendThe My Mito Meet-Up 2022 is underway!!

For the first time since the charity’s inception in 2017, our missions from around the UK are getting together for a wonderful weekend of fun, socialising and above all, support and new friendships.

Just one of the support projects we have been able to complete thanks to our fabulous supporters. More news of the weekend to follow soon!

Louise’s Mito Mission is Launched

Meet Louise, who we are thrilled has joined us this month – with a brand new Mito Mission based in Sheffield.

Louise wants to increase people’s understanding of mitochondrial disease and how it impacts people differently. Louise also wants to raise funds for Mitochondrial research and hopes that this could bring treatments for common linked illness like cancer, as both have affected her family so much.

Read Louise’s journey with the illness and much more on her mission page here.

Louise's Mito Mission is Launched!

Louise's Mito Mission Launch 28 Aug 2022Meet Louise, who we are thrilled has joined us this month – with a brand new Mito Mission based in Sheffield. 

 
Louise wants to increase people’s understanding of mitochondrial disease and how it impacts people differently.  Louise also wants to raise funds for Mitochondrial research and hopes that this could bring treatments for common linked illness like cancer, as both have affected her family so much.
 
Read Louise’s journey with the illness and much more on her mission page here.

New Mito Mission – Welcome Susan!

Meet Susan, who we are thrilled has joined us this month – with a brand new Mito Mission based in Cumbernauld.

Susan wants to raise awareness, funds for research and hopes of a cure for everyone affected by Mitochondrial Disease. She is also keen to raise awareness of occasional wheelchair use.

Read Susan’s journey with the illness and much more on her mission page here.

New Mito Mission - Welcome Susan!

Susan's Mission Launch 2Aug22Meet Susan, who we are thrilled has joined us this month – with a brand new Mito Mission based in Cumbernauld.

Susan wants to raise awareness, funds for research and hopes of a cure for everyone affected by Mitochondrial Disease. She is also keen to raise awareness of occasional wheelchair use.

Read Susan’s journey with the illness and much more on her mission page here.

Emily’s Mito Mission is Launched

We are honoured to welcome Emily’s Mito Mission to our My Mito Mission family.

Incredibly sadly, Emily passed away in November 2021 aged just 5. Her loving family are launching her mission as a tribute and legacy to a very special little girl today, on what would have been Emily’s 6th birthday.

You can read Emily’s story with mitochondrial disease on her webpage or visit her JustGiving page.

Emily's New Mito Mission is Launched.

We are honoured to welcome Emily’s Mito Mission to our My Mito Mission family.

Incredibly sadly, Emily passed away in November 2021 aged just 5. Her loving family are launching her mission as a tribute and legacy to a very special little girl today, on what would have been Emily’s 6th birthday.

You can read Emily’s journey with a rare form of mitochondrial disease called Pearson Syndrome on her webpage or visit her JustGiving page.

Queen’s Baton Relay Honour

Our missionee Regan, who was tragically lost to mito in February aged 13, has been awarded a fabulous honour.

He was nominated by My Mito Mission to take part in The Queen’s Baton Relay for the Commonwealth Games. He was chosen for his bravery in the face of the illness.

Regan’s mum Melanie Lowe, will carry the baton in Birmingham on Monday 25th July on his behalf and in his honour.

What an amazing tribute to Regan and fabulous awareness raising for Mitochondrial Disease.

#QBR2022

Queen's Baton Relay Honour.

Mel - Queen's Baton Relay

Our missionee Regan, who was tragically lost to mito in February aged 13, has been awarded a fabulous honour.

He was nominated by My Mito Mission to take part in The Queen’s Baton Relay for the Commonwealth Games. He was chosen for his bravery in the face of the illness.

Regan’s mum Melanie Lowe, will carry the baton in Birmingham on Monday 25th July on his behalf and in his honour.

What an amazing tribute to Regan and fabulous awareness raising for Mitochondrial Disease.

#QBR2022

 

The Full Monty for Mito!!

When you are a Mito Mission based in Sheffield, what else are you going to do for your first big event but a Full Monty For Mito!

Lillia’s Dad Matt and his mates bared all at an event organised by mum, Emma which raised an amazing £4000 in funds for Lillia’s Mito Mission and priceless awareness. Including a terrific tweet supporting the event from Robert Caryle, currently filming a brand new series featuring the original cast.

Hats off to you all!!!

The Full Monty For Mito!

Lillia's Mito Mission - Full Monty for MitoWhen you are a Mito Mission based in Sheffield, what else are you going to do for your first big event but a Full Monty For Mito!

Lillia’s Dad Matt and his mates bared all at an event organised by mum, Emma which raised an amazing £4000 in funds for Lillia’s Mito Mission and priceless awareness. Including a terrific tweet supporting the event from Robert Caryle, currently filming a brand new series featuring the original cast.

Hats off to you all!!!

New Mito Mission – Welcome Brody!

A very warm welcome to Brody from Stockport, Greater Manchester who has joined us to raise awareness of mitochondrial disease by having his own mission.

Brody and his family live with the impact of mito every day and any support for his 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 Brody’s mission page.

New Mito Mission - Welcome Brody!

Brody's Mito Mission News ImageA very warm welcome to Brody from Stockport, Greater Manchester who has joined us to raise awareness of mitochondrial disease by having his own mission.

Brody and his family live with the impact of mito every day and any support for his 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 Brody’s mission page. 

 

My Mito Missionee Meet-Up 2022

A massive thank you to all of our amazing supporters and missionees, whose support means that for the first time, we are able to have a My Mito Missionee Meet Up!!

This will be a wonderful opportunity for our missionees to get together, socialise and get inspiration from each other.

It is going to be in West Yorkshire, in mid October and we plan to share lots of photos and news from this very special event.

My Mito Missionee Meet-Up!

My Mito Mission Meet up - NewsA massive thank you to all of our amazing supporters and missionees, whose support means that for the first time, we are able to have a My Mito Missionee Meet Up!!

This will be a wonderful opportunity for our missionees to get together, socialise and get inspiration from each other. It is going to be in West Yorkshire, in mid-October and we plan to share lots of photos and news from this very special event.