Hello and welcome to my blog.

My name is Kieron, I’m 45 years young and in February 2018, our son Alfie was diagnosed with Duchenne Muscular Dystrophy, a progressive muscle wasting disease that has no cure. As you can imagine our world was shattered.

Through this blog, my aim is to use this blog as a tool to ‘let everything out’. My coping mechanism. I will share my experiences both individually and as a family through the good times and the bad, in order to raise awareness of Duchenne Muscular Dystrophy.

Thank you for taking the time to read my posts.
Kieron #DuchDad

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