Buildings and landmarks around the world are joining us in raising some spectacular awareness by lighting up green tomorrow to bring a brilliant close to World Mito Week.
If you would like to know which buildings will be lit around the UK – and around the globe – see this map. Do you know any buildings or landmarks that may light up next year?
Please contact us.
Buildings and landmarks around the world are joining us in raising some spectacular awareness by lighting up green tomorrow to bring a brilliant close to World Mito Week.
If you would like to know which buildings will be lit around the UK – and around the globe – see this map. Do you know any buildings or landmarks that may light up next year?
Please contact us.
World Mitochondrial Disease Week starts today and ends on Saturday 24th September.
As part of our contribution, we are excited to quote experts from the worlds of medicine and science to confirm our key message that ‘Mito Research Matters to Millions.’
Please read the social media posts below to find out what these well respected experts have to say about the importance of mitochondrial research not solely for mitochondrial disease – but for MANY other conditions.
World Mitochondrial Disease Week starts today and ends on Saturday 24th September.
As part of our contribution, we are excited to quote experts from the worlds of medicine and science to confirm our key message that ‘Mito Research Matters to Millions.’
Please read the social media posts below to find out what these well respected experts have to say about the importance of mitochondrial research not solely for mitochondrial disease – but for many other conditions.
We have a new home!
My Mito Mission is now based in fabulous new offices KT Hydraulics Ltd in Elland, West Yorkshire. The facilities are a wonderful corporate donation, for which we are extremely grateful.
Our thanks to Richard, Roger and team for being our wonderful hosts, you are absolute ‘Mito Heroes’.
We have a fantastic new home!
My Mito Mission is now based in fabulous new offices KT Hydraulics Ltd in Elland, West Yorkshire. The facilities are a wonderful corporate donation, for which we are extremely grateful.
Our thanks to Richard, Roger and team for being our wonderful hosts, you are absolute ‘Mito Heroes’.
We are delighted to have just contributed a fantastic £40,000 to support two excellent research projects through our friends at The Lily Foundation …
1. Deoxynucleoside-based treatment for Mitochondrial DNA Depletion & Deletions Syndromes.
2. EMERALD Pilot study: Evaluating the Tolerability and Efficacy of a Remote Microphone (Assisted Listening Device) in Adult Patients with Mitochondrial Disease.
More information can be read here.
We are grateful to each and every one of our supporters who make grants like this possible.
We are delighted to have just contributed a fantastic £40,000 to support two excellent research projects through our friends at The Lily Foundation …
1. Deoxynucleoside-based treatment for Mitochondrial DNA Depletion & Deletions Syndromes.
2. EMERALD Pilot study: Evaluating the Tolerability and Efficacy of a Remote Microphone (Assisted Listening Device) in Adult Patients with Mitochondrial Disease.
More information can be read here.
We are grateful to each and every one of our supporters who make grants like this possible.
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.
Meet Louise, who we are thrilled has joined us this month – with a brand new Mito Mission based in Sheffield.
World Mitochondrial Disease Week is with us next month, 18th-25th September.
Our brilliant merchandise helps you to ‘Light Up For Mito’…. and raise a little awareness and funds at the same time.
Check out our brand new Light Up baseball caps and LED candles … along with all our other merchandise in our shop now!
World Mitochondrial Disease Week is with us next month, 18th-24th September.
Our brilliant Light Up merchandise helps you to ‘Light Up For Mito’…. and raise a little awareness and funds at the same time.
Check out our brand new Light Up Baseball Caps and LED Candles along with all our other merchandise in our shop now!
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.
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.
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.
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.
Many people with mitochondrial disease have no visible signs of being ill. Similarly, there are many other illnesses and disabilities which are hidden.
Our brand new ‘heat changing’ mugs are designed to get this message across – with their message becoming visible when filled with hot water.
This adds to our great range of merchandise available 24/7 in our online shop. Always worth checking out!
Many people with mitochondrial disease have no visible signs of being ill. Similarly, there are many other illnesses and disabilities which are hidden.
Our brand new ‘heat changing’ mugs are designed to get this across – with their message only becoming visible when filled with hot water.
This adds to our great range of merchandise available 24/7 in our online shop. Always worth checking out!
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
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
