Anyone from Wales....
Hello everyone, one of our volunteers is part of a steering group as part of the welsh neurological alliance. Next week they are meeting with the welsh minister, and they are sending a briefing paper close of play 24th September for her to look over. Are there any specific points you would want addressed in relation to NHS care in Wales for people with ataxia ? you can comment on this post, or email me on Jatkins@ataxia.org.uk