Emma was just like you and me. A devoted cob owner and new Mum to an absolutely amazing little girl who is just 2. Last year Emma received a devastating diagnosis of Motor Neurone Disease.

Like most people, I knew nothing about MND until it came into my life via my best friend. There’s no cure for MND, it’s a terminal, devastating, horrible disease and something that can affect anyone. I didn’t know any of that.

Emma and her family now need help to make wheel chair adaptions to their home to enable her to lead as normal a family life as possible.

Emma has had to give up so much already, including her beloved cob Olivia, that we would like to raise some funds to add to the home adaptions fund, and help her to live her best life.