As some of you will have seen, Alice and I were the Anne Ford Cup (details at ataxia.org.uk/pages/awards.... for running Virtualataxia at the AtaxiaUK conference at the weekend. It was a total surprise and we were really shocked and honoured. There are two parts to Virtualataxia the email list and the twice weekly chat, details of both can be found at virtualataxia.org.uk. We get together for a chat on Tuesday evenings at 7pm and Sunday afternoons at 4.30pm (both UK time), these chats are held at virtualataxia.org.uk/chat.htm. It should work for you (he says hopefully) but if you do have troubles there is a 'help' section on the same website or email me at tim@spiveyworld.net I will try my best to help. The chats are very informal and we don't mind if you come late, leave early or are a slow typer. There are usually 4 or 5 chatters (sometimes more) and I'd like to think the chat provides a good, relaxing 'meet up'. I look forward to seeing a full chat room come Tuesday!
One last thing, I have just set up justgiving.com/vitrualataxia. Any money given will go straight to AtaxiaUK but they will see it has come via Virtualataxia.
Thank you all members for being a part of Virtualataxia and we look forward to seeing more new faces in chat! If you are not registered you can still partake in the chat sessions but will not receive any emails sent to the group.
Tim
Are you as fed up as me?
Ataxia with involuntary eye movements.
Should I go to an Ataxia UK branch or support group?
Ataxia Special Advice
