I’ve been doing a little bit of research, which in my vast medical experience [re:none] means I am doing the next best thing: screaming into the internet abyss.* Since this blog hits all of my social media accounts, consider this a super lazy post.

Any fellow Wegener’s Granulomatosis/GPA patients gone from Rituxan/Rituximab back to Imuran or methotrexate? I never did cyclophosphamide(s?) and don’t plan on going down that route ever, but I’m trying to weight my options between another round of Rituxan and its expenses/increasing side effects, or just going back to daily pills.

 

*For the record, I know that any final decision is between me and my doctor(s), but my new one doesn’t have the best bedside manor/patience and I don’t know the protocol on calling former doctors/doctors in another state. I also would rather hear experiences rather than data/stats.
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