Tracy's brother Jeremy is raising money for the MNDA by participating in MOvember, which if you don't know, involves growing a moustache throughout November . Hopefully apart from raising money for the MNDA we can look forward to some amusing facial topiary!
He told me if he hits £1000 he will sport a Village People design (ok, he didn't but we can hope).
If you would like to support Jeremy visit
http://www.justgiving.com/jeremyalter
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About Me
- Steve Evans
- OK, should have done this two years ago when I was first diagnosed with Motor Neurone Disease but better late than never. I thought it would be a good way of keeping anyone who was interested up to date with what's going on with us. Communication is getting harder and whilst I want to keep texting, emailing and chatting to everybody this seemed a good way of saying more things to more people more easily. Typing is a slow process (this has taken 20 minutes so far) so a once to many approach seemed good. I hope to keep it up to date with various stuff including whinges about things MND related as despite trying to "keep positive" it does affect (in a generally f**ks it up kinda way)almost everything I do! For those of you who really want to, you can check out my "status" on my web link. Finally, PLEASE leave comments, even if brief as its the only way I know its being read!!
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