Our Story

My name is Mark, I was just 43 years old, when I was handed a death sentence. On October 10th 2023, I was diagnosed with Motor Neurone Disease (MND). This disease has turned my world upside down. I have four amazing children who I love more than anything. Two of them haven’t even started high school yet, and now, I’m faced with this devastating diagnosis.

The hardest part? It feels like there’s no help or support out there for people like me. Our government isn’t doing enough—in fact, they’re doing nothing to support those of us living with MND. The lack of action is frustrating and heartbreaking. People have my life in their hands, and they’re letting me down.

Our goal is to help support those with an MND diagnosis and their family and friends, from giving hope, to providing practical aid box that allows you to take on daily tasks with a bit more ease, the Mark Sommerville Foundation are on hand to provide a friendly ear, and support assistance to everyone that has an MND diagnosis.

Contacts us

Email:

Info@themarksommervillefoundation.org

Facebook:

The Mark Sommerville Foundation