Hi all,
I'm new to this forum but I've been finding it really helpful to hear from people going through similar situations. I've been diagnosed with UC in Sep 2021, was prescribed Mesalazine tablets which got me into remission for about 6 months. I flared again in March and haven't really been able to get it under control since. I got prescribed a course of steroids (prednisolone) in addition to max Mesalazine dose which still hasn't done it, so now I'm moving to Adalimumab. Reading on side effects and disclosures of the medication are a bit scary (so are immunosuppressants in general which I've never been on), mainly referring to the increased chance of lymphoma and so on.
Is anyone else here on Adalimumab? Has it worked for you or given you any bad side effects?