For those taking or who have taken adalimumab (Humira) for PsA — questions about antibodies and diagnosis
Hey everyone! I have a couple of questions for people living with psoriatic arthritis, especially those with axial PsA.
How long were you on adalimumab (Humira) before developing anti-drug antibodies, if you developed them at all?
Did it stop working for you, and were you able to switch to another biologic successfully?
How long did you have symptoms before you were finally diagnosed with PsA? I’m particularly interested in hearing from people with axial PsA. How long did you suffer before getting your diagnosis?
I have axial PsA and am considering starting adalimumab. Honestly, I’m feeling quite anxious because I’ve read so many Reddit comments about people developing antibodies or losing their response to Humira. It’s made me worry that it might only work for a year or so before becoming ineffective.
I’d really appreciate hearing about your personal experiences, including people who have been on Humira for several years and are still doing well.
I know everyone’s experience is different, but hearing from people who have been taking it long-term would really help me put things into perspective.
Thank you! ❤️