Regan’s Mito Mission Launch

A huge welcome to Regan Nash and his family who’ve joined us to raise awareness of mitochondrial disease from their home in the West Midlands.  This lovely family sadly lives with the impact of mito every day and any support for their mission will be very welcome.

Regan's Mito Mission Launch.

Regan Nash, New Mito Mission launchedA huge welcome to Regan Nash and his family who’ve joined us to raise awareness of mitochondrial disease from their home in the West Midlands.  This lovely family sadly lives with the impact of mito every day and any support for their 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 Regan’s mission page.

Kiss Campaign

Our #KissGoodbyeToMito campaign 2019 has been a huge success and raised some fantastic awareness for mitochondrial disease.

Kiss Campaign 2019.

Kiss Campaign 2019Our #KissGoodbyeToMito campaign 2019 has been a huge success and raised some fantastic awareness for mitochondrial disease.

Celebrities from the world of comedy, acting, musical theatre and sport got their green lips on and joined the promotion to highlight Global Mitochondrial Disease Awareness Week. Social media was filled with green lips thanks to our fantastic supporters.

Check out the video on the ‘Our Story’ page.

Valuable Research Into Treatments

Thanks to everyone’s incredible support, My Mito Mission is thrilled to announce that we have been able to grant an amazing £42,500 to The Lily Foundation.  The money will help fund three projects – research into treatment, research into a cure and the first ever support weekend for young adults with mitochondrial disease in November.

Research Into Treatments.

Research PercentageThanks to everyone’s incredible support, My Mito Mission is thrilled to announce that we have been able to grant an amazing £42,500 to The Lily Foundation.  The money will help fund three projects – research into treatment, research into a cure and the first ever support weekend for young adults with mitochondrial disease in November.