Hi Carole,
I am a newby to the site but had my second infusion of Ritiximub last Tuesday so hope I can be of some help. Over the past three years I tried the various tablets and injections. The first session was quite daunting as I didn't know what to expect and the second was easier. I was told not to drive after the infusion and must say I felt quite 'wobbly' but nothing untoward. After each session I felt very tired and although I took a day off work after the first dose, I took 2 off after the second. My downfall. like many, is not taking it easy, I have too much to do. A week after I feel fine, just a few niggly pains in toes and feet but not for prolonged periods and at a level I can easily cope with.
For me it has been a positive experience and the nursing staff were great, I couldn't fault them. The info I received from my rheumy nurse was lacking a bit as I didn't know it took 6 - 7 hours for each infusion but it was great being able to read for so long and then play games on my Kindle. A whole day when when I couldn't do anything else. So far it seems to be working for me and I am one who will try anything that is offered, even though some people are against the bio medicines, to reduce a flare up.
So from me it's a
for now. Just hope it continues. Good luck with whatever you decide.
Val
