Hi everyone! After months of saying to my Rheumy that my DMARDS aren’t really doing the job (currently sulfasalazine and hydroxychloroquine), yesterday I had scans and, after a crappy flare last week (hands, wrists, knees, left big toe), I am being moved to Adalimubab. Yay! Here’s hoping it does the job, as i’m so bored of propping up Nurofen’s profits, haha.
If anyone has any positive success stories, tips or things to be aware of, please do let me know!
Mxx
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TheMarfs
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Hi there, it’s me again! I am delighted for you - adalimumab has changed my life and taken away all my stiffness (as long as I avoid jumpy aerobic exercise). It’s been a total game-changer and sounds just what you need. Hope you get access to it soon.
Hellooooo! Thanks! I am looking forward to trying something new! I remembered you saying it had been a game changer and you had similar issues with the sulfasalazine. Will keep you posted! Xxx
I hadn't realised that I just ignored the constant pain and difficulties until I started adalumimab and it went away. Even my daughter noticed the lack of swelling in my hands which she had assumed was permanent. I hope you do as well.
I’ve been on Amgevita for 9 months & it’s made a big difference to me. My fingers are still stiff, don’t bend easily. But my pain levels are way down 😊 And, for me, it worked very quickly, noticed an improvement almost straight away 😊
3 years ago adalimumab changed/improved everything for me and is still working well alongside my methotrexate. Retired from work now at 62 but I’m at the gym two or three times a week and no flares at all 👍👍
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