My turn to Flare

[Chadwyck]

I've heard a lot of good things about Dr. Merkel and I live in Canada. I'm sure you're in good hands. My question is about Rituximab. What are the side effects compared to the old cyclophosphamide way of doing things? I'm in the clinical trial for Abatacept but if I flare out of control I was told that Rituximab would be where I go.

[Pete]

Although there are many listed possible side effects for rituximab, the most common are allergic reactions during the infusion and mild fatigue. The allergic reactions are usually well-managed by the treatment team. Fatigue generally lasts 24-48 hours and is generally mild enough to not interfere with normal activities. I've had six infusions, and the only side effect I've had is mild fatigue that lasts about a day.

[Alysia]

Sorry about the flare Victor. My wg dr. Says that I must get rtx every 6 months. Few months ago I was late and got it 6 weeks later and started to flare. Please update us. Sending prayers ☆

[blu4runner]

I have been very fortunate and have little effect from the infusions. 1 down and 3 more to go and we will be back in remission soon I hope. Thanks for all the support!!

[Jaha]

I glad that you got one down without any issues. I am wishing you all the best with the next three and that it puts you back in remission soon. Please keep us up on things and take good care of yourself.

[annekat]

Victor, sorry to hear about the flare, but we are learning more and more about managing this thing, and I'm sure you will get back on track with no problem! I'm glad you have a great doc like Dr. Merkel. Looking forward to hearing that things are improving as planned.