Me and my muscles!

Twenty years ago, on February 14th, I was diagnosed with a rare muscle-wasting condition called Dermatomyositis. Fresh out of university, this unexpected Valentine's present left me scared and uncertain about my future.

While I could detail symptoms, treatments, and flares, I prefer to focus on the positive impact this chronic illness has had on me. It has turned me into a resilient individual, with a zest for life, and someone who appreciates life's small joys. When you've struggled to put on your own socks, the moments of jetting off to explore a new country are gold!

I thought about setting myself a challenge, but a marathon is out of the question, my hip wouldn’t survive a swimming challenge, and let’s be honest, I’m unlikely to complete a 24-hour silence! However, I can offer hugs, a phone call, or send you a postcard of my face for any donations you’re able to give to the charity Muscular Dystrophy UK

Muscular Dystrophy UK is the charity for 111,000 people living with muscle-wasting conditions. They are making a difference today, providing vital information and support to help people live as independently as possible. They are making a difference for tomorrow, accelerating progress in research and driving the campaign for access to emerging treatments.

Thank you for your donations, however big or small - together we are stronger!

Photo credit: Jonathan Howard