Just a post to say hi as I’m new on here I was diagnosed with RRMS 11 years ago, started on rebif straight away but it didn’t work for me so I was started on tysabri and that has been great for me unfortunately I tested Jc positive recently so infusions have been put to 6 weekly and my treatment will be changed after this covid pandemic.
Anyway, look forward you chatting with you all! Xx
ThisIsMS is the most popular MS forum on the planet cause it's an amazing source of information.
So here is an other advice: Of course, it's better to keep an eye on differents MS sites (like I do) but, if I were you, I wouldn't want to run too far away:)