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Hello everyone! So im not sure but does everyone gets all this like 8 or idk how many bloodtests done before picking their treatments? Because I did just to make sure of I was good for whichever I picked I was ok for and Today I got a result positive for Jcv ? What is this ? Is this related to MS An...

Hi All, I've been on Tysabri for almost 3 years and my JCV has always been negative but from having a negative result in February I've just had a medium to high positive result. Since being on Tysabri I haven't relapsed so I'm worried about having the treatment stopped. Do you think I would be bet...

I'm a little worried & confused . I got diagnosed earlier this year. My neurologist did blood work on me and results came back good BUT on my jcv test it says it's abnormal high index and I was exposed but I'm negative?? I told him what's going on?? That sounds confusing! He said you're negative so...

Hi. I've been on Tysabri for over 7 years. My jcv+ level is 3.5, which I'm told is high. I've been told I may have to come off Ty to go on a tablet, Gilena, I think it's possibly called. Has anyone had to do this and how effective it is in comparison? Thank you

So last year February upon getting my RRMS diagnosis I also found out that my JCV results were 2.14. On Tysabri for nearly 9 months now and my JCV results today is 0.84 🎉🎉🎉this is a definite win 🏆

Hiya! So, I had my appointment with my neurologist today - and I am now positive for the JCV virus!! Going from 4 weekly tysabri infusions to 6 weekly! Has anyone been through this process? And if so, how did you find the transition? Any information from anyone who’s been through this would be gre...

Hi w new to this site. Need some advice… i have been jv positive high titre levels for a year now, taking tysabri since 2017. I now have 3 monthly mri to monitor pml detection. I freak out everytime i have mri until i have mri results. Consultant recommends staying on tysabri, but i’m scared to stay...

Hi All, Went for my Tysabri infusion today and got the news I’m JCV positive. I know this doesn’t mean the end of Tysabri right now and the nurses tried to reassure me, but just feeling so disappointed about it, broke down in tears in the middle of the infusion unit 😔 I’ve been feeling so much more...

I got diagnosed with MS in October and started on Tysabri in December however, I tested positive for the JC Virus. Did any body else test positive at the start of their treatment and still continue with Tysabri?