Has anyone actually had Ocrevus infusion cancelled or delayed? MS trust talks about having the treatment delayed however after speaking to the appointments team at my hospital Monday I am still planned to receive treatment at beginning of April. The hospital talked about speaking to consultants due to the information on MS trust website and will aim to get back to me however have not yet. I was thinking about stoping this treatment anyway due to having bad anxiety and depression after each infusion (however it’s important to say am not 100% sure this is linked and everyone reacts differently) I was diagnosed in December 2017 at the age of 20 with RRMS and luckily no episodes since initial diagnosis . Am I been ungrateful for wanting to stop treatment and just see how my body reacts without treatment? as I feel well mentally and in my MS with the exception of the symptoms that are not reversible from my first and only relapse Thanks in advance everyone I feel I get better information on here than my MS nurses