This October, we will be lacing up our running shoes to take on the Manchester Half-Marathon! We're incredibly excited (and very nervous) to push ourselves and complete this challenge, while raising vital funds for Muscular Dystrophy UK.

We've chosen to support Muscular Dystrophy UK because of Luke's connection to muscle-wasting conditions. Luke lives with Charcot-Marie-Tooth (CMT) disease, a progressive condition that impacts his daily life.

Charcot-Marie-Tooth disease is a genetic neurological condition that affects the peripheral nerves – essentially, the nerves outside of your brain and spinal cord. In my case, it primarily impacts the nerves in my legs and feet, leading to muscle weakness and numbness. It's a progressive condition, meaning it can worsen over time.

For me, CMT means dealing with difficulty with balance and coordination as well as aching and pains every day. Simple things like walking any real distance, or even just standing for extended periods can be a challenge. I'm determined to take on this half though, even if it means adapting and pushing my limits in different ways!

Muscular Dystrophy UK is a fantastic charity that provides crucial support to individuals and families living with muscle-wasting conditions like CMT. They fund groundbreaking research to find treatments and cures, provide essential care and support services, and campaign for better access to healthcare.

All donations and support are greatly appreciated. Thank you!