Season’s Greetings

As we near the end of our third full year, here are our highlights festively themed on the 12 Days of Christmas:
Oh, the year 2020 it brought our charity …

• A wonderful new website
• Our highest ever donation
• Improved social media
• New ways to fundraise
• Awesome volunteering
• Several sponsored challenges
• Six-figure sum reached
• F-I-V-E N-E-W M-I-S-S-I-O-N-S!*
• Forty thousand granted
• Three patrons
• Too much support (to mention )
• … and a web-shop to sell our merchandise!

Everyone at My Mito Mission wishes you all the very best for the Christmas season and for 2021.

Thank you for your valued interest and support.

Seasons Greetings

Season's Greetings 2020As we near the end of our third full year, it’s a good time to look back and see what we’ve achieved this year despite the challenges it has brought. 

Here are our highlights festively themed on the 12 Days of Christmas:

Oh, the year 2020 it brought our charity …

 

  • A wonderful new website
  • Our highest ever donation
  • Improved social media
  • New ways to fundraise
  • Awesome volunteering
  • Several sponsored challenges
  • Six-figure sum reached
  • F-I-V-E   N-E-W   M-I-S-S-I-O-N-S!
  • Forty thousand granted
  • Three patrons
  • Too much support (to mention)
  • … and a web-shop to sell our merchandise!

 

Everyone at My Mito Mission wishes you all the very best for the Christmas season and for 2021.

Thank you for your valued interest and support.

Online Shop

We now have a shop!
Lots of great items from clothing to face masks to help you – to help us – raise awareness and a little bit of funds. Check it out … and maybe check something out too!

Online Shop

Shop Now OpenWe now have a shop!

Lots of great items from clothing to face masks to help you – to help us – raise awareness and a little bit of funds.

Check it out … and maybe check something out too!

Grants Update

Thanks to our fabulous supporters, we were delighted to grant funds this year towards enabling mitochondrial disease to be added to the Rudy Study. Check out more about this project on their website.
We’re also very excited to be able to contribute to research about mito and mental health which will begin next year. Both of these through our friends at The Lily Foundation

Our previous grant funding projects through Lily have been a 4-year gene editing research project and a support weekend for young adults affected by mitochondrial disease.
With your amazing help, we’ll continue to raise awareness and hopes of treatments and a cure for mitochondrial disease, and support for those affected.

Grants Update

Grants UpdateThanks to our fabulous supporters, we were delighted to grant funds this year towards enabling mitochondrial disease to be added to the Rudy Study. Check out more about this project on their website.

We’re also very excited to be able to contribute to research about mito and mental health which will begin next year. Both of these through our friends at The Lily Foundation

Our previous grant funding projects through Lily have been a 4-year gene editing research project and a support weekend for young adults affected by mitochondrial disease.

With your amazing help, we’ll continue to raise awareness and hopes of treatments and a cure for mitochondrial disease, and support for those affected.

Ronni & Freddi’s Mito Mission Launch

Delighted that this month is seeing us welcome a new mission – Ronni & Freddi’s.

Ronni & Freddi are brothers and have been affected in very different ways with mitochondrial disease. Ronni is eight and doing well, but tragically for little Freddi, it was severely
life limiting.

As part of Freddi’s legacy, his family have joined us with their own mission, based in King’s Lynn, Norfolk to help raise awareness, support and funds for research for everyone affected.
Please take a little time to read about the family’s journey with mito on Ronni & Freddi’s webpage

Ronni & Freddi's New Mito Mission Launch

Ronni & Freddi's Mission Launch Nov20Delighted that this month is seeing us welcome a new mission – Ronni & Freddi’s.

Ronni & Freddi are brothers and have been affected in very different ways with mitochondrial disease. Ronni is eight and doing well, but tragically for little Freddi, it was severely life limiting.

As part of Freddi’s legacy, his family have joined us with their own mission, based in King’s Lynn, Norfolk to help raise awareness, support and funds for research for everyone affected.

Please take a little time to read about the family’s journey with mito on Ronni & Freddi’s webpage

Steph & Jake’s Mito Mission Launch

Thrilled to introduce and welcome our first ‘twosome’ on a mission … Steph and Jake!

 

They’re mum and son and both live with different diagnosis and the varying symptoms of mitochondrial disease. Steph and Jake are keen to raise more awareness from their home in Bury St Edmonds where they are wonderfully supported by Steph’s husband and Jake’s dad, Paul.

 

By sharing their story locally and beyond, Steph, Jake and their family want to ensure that more people know about mito, and how important it is to find treatment and a cure.

 

Please read about their journey with mito on Steph & Jake’s webpage.

Steph & Jake's New Mito Mission Launch

Steph and Jake's MissionThrilled to introduce and welcome our first ‘twosome’ on a mission … Steph and Jake!

They’re mum and son and both live with different diagnosis and the varying symptoms of mitochondrial disease. Steph and Jake are keen to raise more awareness from their home in Bury St Edmonds where they are wonderfully supported by Steph’s husband and Jake’s dad, Paul.

By sharing their story locally and beyond, Steph, Jake and their family want to ensure that more people know about mito, and how important it is to find treatment and a cure.

Please read about their journey with mito on Steph & Jake’s webpage.