We at Leigh Network are delighted to hold our annual mito family days, which we fundraise for throughout the year. These are a wonderful opportunity for our amazing mito warriors and their families to meet, share experiences and learn from each other, as well as the specialist Drs. and researchers who often give talks. Our…
Throughout the pandemic, we have been running a virtual art exhibition on our social media pages. This is a celebration to show how creative our mito families have been and continue to bravely endure the lockdown period. This is to showcase mitochondrial disease in a positive light and to highlight the abilities people with mitochondrial…
At the start of lockdown Faye set herself a challenge to pedal 10 hours across 5 days 2 hours a day, to raise funds for Leigh Network. Although 2 hours a day may not sound much to a healthy person, to someone with mitochondrial disease who has dystonia, fatigue and mobility problems this was a…
