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 2024 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.
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