Muscular Dystrophy UK is the charity for the 110,000 children and adults living with muscle-wasting conditions in the UK. There's currently no cure, and it many cases, it limits lives. MDUK do vital work in funding pioneering research into treatments and cures as well as providing vital information, advice, resources and support for individuals and families living with these conditions.

Please take a minute to read Charlotte's story, I will be running with her in memory of her brother William

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"I will be running the marathon in my brother William’s memory. William was diagnosed with Duchenne Muscular Dystrophy at a very young age, 5 years ago at the age of just 15 we lost a beautiful soul far too early into his life. This charity and all it does has such a special place in my heart, endlessly researching into an illness that at the moment has no cure, and supporting the families and individuals effected. I’m hopeful that one day a cure will be found, but until then they need all the support we can offer."

All donations, big or small, are greatly appreciated. Thank you!!