Hello and welcome to my blog.
My name is Kieron, i’m 44 years young and in February 2018, our son Alfie was diagnosed with Duchenne Muscular Dystrophy, a progressive muscle wasting disease that has no treatment or cure. As you can imagine our world was shattered.
Through this blog, my aim is to use this 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.