Has anyone done a switch from Tysabri to Tyruko? What were your experiences?
Yes, some time ago. I made a conscious decision to not think about it, and so far so good.
This article was in The Guardian today.
‘It was awful for me’: one MS patient shares her experience with Tyruko | NHS | The Guardian
Thanks - I saw the Guardian article. It’s interesting, but I wonder about the broader context. After all, newspapers do not publish articles saying, “MS patients at hospital X started this new drug and they were fine.”
Indeed, the people using this forum are also more likely to be having issues than not - if life is fine, people are less likely to be on an MS forum looking for answers.
So I wonder whether there is a genuine issue here or whether the majority of people are fine with it. A cheaper drug might mean more willingness to prescribe on the NHS, so it would be a real shame if there are problems.
I have noticed a few posts on the MS Trust facebook page, but doubt it will provide the answers you need. Hopefully, the MSS will provide a news update with some firm evidence.