hi is anyone jcv positive and receiving tysabri my partner has been on tysabri for 2years this april and has to decide wether to carry on or change treatment what is frightening him more than anything is that a member of his group has now got pml which as we all know is devastating would like to know if anyone has any experience of this obviously we understand its his decision at the end of the day but have a lot of questions he needs answering and his neuro team not helping
thankyou in advance