MND awareness and support

Hi, I'm Scott Morris and I'm fundraising for MND.

What started as twitches in my arm and after nearly 12 months of tests, in June 2023 I was diagnosed with the ALS variant of MND.

Only after being diagnosed, I realised how little awareness of the condition was out there, so I'm taking this opportunity to do what I can to raise awareness with the help of my family and friends.

After careful consideration I have decided that any funds donated will be split, with the majority going to the MND association and some towards equipment I may need in the future to help with my independence and quality of life.

Please visit scottmorris.uk for further info, support and events.