Reclast and RA
Has anyone with RA had a Reclast infusion? If so, did you do okay with it; have side effects; have a way to mitigate side effects? I had a 6 week flare after my first Evenity, but was able to continue. Would prefer not to repeat that experience though. Thank you.
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@aspirecreative
I just want to say I'm surprised you haven't had any comments on your thread. It's exactly what I'm wondering. I really trust my rheumatologist, he's gotten me through 12 years of RA with no progression of the disease. Reclast is one of the 3 meds he asked me to consider. I am already at an infusion center. But one thing I read is that side effects were harder or people with autoimmune illness.
Have you tried searching for Reclast Infusion on the first page for this support group?
I think I'll try it too.
Let me know what you find. I know I read about others on Reclast, I'm still starting to sort out all of the information for osteoporosis.
@jw9 I put the question to the Women with RA FB group. Only a couple of responses, as I recall they were women who did ok with it.
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Thanks for asking about it. I read that, but don't find any stories of women who had problems with Reclast and autoimmune. Onward!
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