marie09
Hello, my Rheumatologist wants to put me on rituxan infusions. I am a little scared. I was wondering how rituxan has worked for other people and how do they like it.
Amanda Osowski Moderator & Contributor
Hi
I have not personally been on Rituxan, so I'm hoping some of other community members will weigh in. I wanted to share these articles with you incase they're helpful!
https://rheumatoidarthritis.net/treatment/rituxan-reviews-how-well-does-it-work
https://rheumatoidarthritis.net/living/rituxan-rituximab-side-effects
Thinking of you!
Warmly,
Amanda (RheumatoidArthritis.net Team Member)
L rick Phillips Moderator & Contributor
rick - moderator
Joanie16 Member
Wow! What a wonderful surprise! Thank you for responding! It's nice to meet you! I feel welcome already! 😊 I appreciate the link you provided, so hopefully I
Janellen Member
The first 6 months I had Humira, it did nothing. My RA was out of control and I was constantly in and out of hospital.
Next I was given Rituximab. This had an amazing affect on my RA, it's been a game changer.
I've been having Rituximab every 6 months since the research.
Yes, I still have flare ups but nowhere near as bad as before having Rituximab.
Joanie16 Member
Hello Rick,
Thanks for your quick and friendly reply. I was a bit worried that I asked you too many questions...
I wrote back to Christine and I hope you will read what I wrote her. I didn't want to copy and paste the same thing to you that I wrote to her.😊
But, just in case you don't read it... I do want to personally thank you for responding back to me. I meant it when I said your post on the good response you had to the Rituxan really inspired me to try the medication and to take the risk and write to someone in this community. So, thank you.
Christine sent me a link, so, I will definitely write my story and post it. I have always enjoyed writing but the RA has really gotten in my way; fatigue and pain... so, as I told her, I think I will write a little at a time so that I don't scare off everyone (or bore them) and so I won't physically overextend myself. At 64 years old, and living with RA for 63 of those years, I do have a loooong and involved story. 😁
Oh, yes, I do need some help from you... Can you explain if
Alright...I will post this now and look forward to becoming more involved in this community. I feel that I really NEED to participate..because I usually stay disconnected from groups. I was involved in different groups many years ago and then I stopped. But, now, I realize that I don't want to feel so alone and that I don't HAVE to. By belonging to a group, I can really help myself feel better just by participating. So, fingers crossed...I will read some more posts and then post something about myself. Thanks for "listening" and
RHall Community Admin
kentuck2a Member
pommum Member
I have been on Rituximab now for seven years, with very few side effects, after trying all other biologics. ( I am unable to take JAK inhibitors because of Factor
V Leiden, which makes me a high blood clot risk.) Rituxan was the first drug that allowed me to discontinue prednisone, after taking it for over twenty years, sometimes at high doses for vasculitis, episcleritis and rheumatoid lung. The first two conditions have been stable now for a number of years, but recent X-rays have shown I have rheumatoid nodules in my lungs, which I had many years before starting Rituxan. These lung nodules have caused pleural effusions in the past, (when the nodules have ruptured) but I have not had this problem since taking Rituxan. I am currently waiting for a CT scan of my lungs.
Effie Koliopoulos Moderator & Contributor