Sarah Lannie

I am extremely honoured to be a trustee for the Ian Pratt MND Foundation.

I had to sit in a room with my lovely husband and 2 doctors as they gave us the devastating news that Steve had Motor Neurone Disease. That day I can honestly say I felt like my life had ended as I knew it. All of our dreams were wiped out like a tsunami had hit.

Steve fought a remarkable battle but we lost him in 2013. I made him many promises during his illness and one was to always help others in ways that perhaps we didn’t get or knew how to get.

So here I am, now promising you…….I will do everything I possibly can to help you to get what you need.