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Hi I've just started on Toxilizumab which is fairly new, as the Rituximab I was on lowered my Immunoglobulin levels two low. I've opted to do the weekly injections at home rather than the monthly infusion at Rheumatology dept. But I'm finding the injections incredibly painful. I do weekly Methotrexate injections at home, with no problems at all. Is anyone else on Toxilizumab and have the same problems. I might have to swap to the infusion, but I'm feeling a bit of a wimp ha ha. I've had loads of ops, needles, injections etc but nothing felt as bad as this one
Is it just me
Thanks for reading
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