Today I’ve launched our fundraising for the MNDA. Georgina will start this by doing a 10k in June and her training for this has just begun.
When I was diagnosed with this wicked disease, after getting over the emotional days this was what we decided to do. I want us to raise awareness and funds for the only charity in England, The Motor Neurone Disease Association.
This is what I want to do for the rest of my life and I’m sure Georgina and the rest off my family will carry this on when I leave this world.
Making sure that I let a lot of people know how this disease affects me and the people I care about is the only way that I can deal with it. It’s the only way to go.
Please join us in our journey and let the world know!