Ocrevus infusion
I had an appointment with my MS nurse yesterday who said that come New Year they’re looking at changing the infusion. I know there’s been talks about this as a single injection but the way it works is you will still have to go into hospital and they will put a syringe drive into your tummy which will last for about 30 minutes and then you have to sit for an hour afterwards . I did ask if I still have to have the steroids to be told yes but this will be oral not IV hope this helps people who has been worrying how it will work
You can refuse this change if you want to it's your decision and not there's if Uk Nhs.
I asked this question at my yearly check up and the way he explained it, was that the infusion was a more pleasant experience and thw injection would leave lumps on the skin etc. By the way, I had my infusion last week and always get sore throats and ulcers on my mouth followed by a heavy cold..anyone else?