I have my 10th ocrezilumab infusion and I was asked what 3 things i take to make it better and I thought I should share this on shiftms, so 1. a travel neck cushion. One that’s good neck support. You never know if you’ll fall asleep 2. Sheath catheter and box. Though you can get up to use the toilet, as urinary urgency is one of my main symptoms and moving disturbs the cannula infusion site, wearing a sheath means I can go to wee whilst being infused. I use a night bag through a my catheter leg bag which I empty at the end of my infusion. The boxes the sheaths come in make excellent boxes to put the night bags in for integrity and infection control issues the hospital have. 3. Adhesive remover spray. This reduces the pain from the cannula when it’s removed as it sticks to hair on your arm Hope this post others with their next infusion, good luck 😀