I have had MS for thirty years - since I was at school, so no wonder I am feeling pretty battered by it. I saw my MS nurse this week and she said that the reason why I have been feeling progressively worse these recent years, is because I now have ataxia. I had never even heard of this, but she says that many people with MS develop it bad enough to warrant action. But what surprised me even more, was to hear that there are treatments for this. Is anyone else on the forum having to put up with ataxia, and if so can they recommend or warn against any of the medication that might be offered for this? Thank you for any ideas.