I’ve had my first Tysabri infusion today, after the initial nerves, it went really well.
I have a slight headache and i’m so tired.
I have a blog about HSCT but I’ll be regularly posting about my MS experiences if anyone is interested in having a read, please do 
Hi Had a little read, hope all goes well.
I am JCV+ and assumed I would not be able to have Tysabri, as from reading some people on Tysabri and are JCV+ are changing DMT. May be going on Tysabri short term is ok if JCV+.
Hi, if you are positive you can still have Tysabri. I’m only planning on being on it 18 months at the most, I did meet a guy at the infusion centre who is JC + and been taking Tysabri for 8 years! He didn’t say what his risk was but he had no intention of stopping!
It is supposed to be very good time will tell.
It was Ty or Lemtrada were my options, or nothing. I’m trying the Ty for now
Hi thanks, the Barts blog has details about Tysabri.
http://www.clinicspeak.com/understanding-pml-risk-on-tysabri/
Hopefully I can see my neuro in next few weeks as need to change DMT.
I have had 7 infusions so far.
I was JC positive from the start. I always feel tired for a day or two after my infusion.
Tysabri has kept me stable so I am happy at the moment on it.
I have a MRI scan every 3 months. So I am well looked after.
Hope it works well for you.