Muscles for Mitchell
Support us: Donate to Muscles for Mitchell here
In the summer of 2014, our son Mitchell, then 5 1/2, took part in school sports day with the rest of his reception class. I noticed how he struggled to run short distances, fell down a lot and was out of breath after just a short run. He had large calves and my friend commented that ‘you’d expect him to run really fast with those calf muscles’. That comment stayed with me and I casually Googled, large calves in boys, frequent falls. I was faced with pages on muscular dystrophy and it began to dawn on me that my beautiful boy could have this condition. Lots of things started to make sense. Why he used to hold the rail so tight to get up the nursery steps. Why he disliked snow. And why he complained of walking even short distances. I’d never heard of Duchenne muscular dystrophy and there’s no history of the condition in my family. We were referred to a specialist and I hoped that I would be told that I was an overbearing mother and that all was well. The look on the consultant’s face, told me that all was not well. Mitchell received his official diagnosis, following genetic testing on the 9th September 2014. Four days after my 40th birthday. At the time, we were just devastated. It’s such a cruel disease and to learn that there are limited treatments and no cure is very difficult to come to terms with. Our little family felt changed forever and the future that we had imagined was fading away.
Over the next few months, as we processed the news, we got to know other families living with the condition through social media and became aware of the numerous charities doing great work to accelerate research and hunting for better treatments for our boys. Fundraising became our hope. On 1st February 2015, we launched Muscles for Mitchell to support Duchenne charities on their mission to find potential treatments for the condition.
Duchenne UK has proven to be a driving force in accelerating research opportunities and changing the landscape in the UK for clinical trials. Although we have accepted Duchenne as part of our lives now, we will continue to fight for better treatments and hope for a cure for our special boy and all the children living with Duchenne. This is why we have set up Muscles for Mitchell as a family fund with Duchenne UK.
Family Tinkler (Kate, Steven, Ellie and Mitch.)
(Credit to Tracy Kidd photography for the photo of Mitchell)
Donate to Muscles for Mitchell here