Love the idea but due to my limited ability to access most places, I doubt I would be able to do it. The range of electric wheelchair is also a factor. I've told my sister who has relapsing remitting MS, and lives in Leeds; about it and it's definitely something she needs as I'm the only other sufferer she knows with it. I hope its a successful event, as so many people with MS need advice on living with their condition, advice only those who have or live with an MS patient can provide. Fail to plan, is to plan to fail. As I told Debbie Purdy, there is life with MS but not without YOU. Her smile is deeply missed!