Hi all, New here and hoping for some advice from fellow RA’ers! I’m mid 30s and was diagnosed a few years ago, have been on methotrexate tablets (made me ill), went on to Metaject and (not able to tolerate more than 15ml), and take hydrocloxi - still don’t know how to spell or say it! - every other day. My next option is…
Hi Community - I have been on Imraldi for 2.5 years now (PSA) and it’s changed my life. Today I received a letter from the NHS stating they are moving everyone to a BioSimilar (Yuflyma) - assuming due to cost. I am going to contact my consultant but wondered if anyone has any experience of changing from one to another? I’m…
I've had PsA for about 8 years. 2 years ago, I started on Adalimumab injections. Since starting on Adalimumab, it's like a don't have arthritis. Most days I forget I have arthritis, that's how good Adalimumab has been for me. But, I've never quite understood how immune suppressed I am. My PsA is in my toes, feet, ankles…
Hello everyone, I start Amegevita today. The nurse is coming this morning to do my first dose. I knew the side effect info on the Versus Arthritis and NHS sites and had made my peace, knowing that it was needed and the benefits outweighed the risks. However, I have just read the info leaflet, and it has scared the life out…
Hi everyone, I'm relatively new on here and have never posted but I'm having a wobble. What are peoples thoughts or experiences on Adalimumab? I was diagnosed with PsA at 29 I'm now 34. I've tried sulphazaline, methotrexate and leflunomide. All of which knock my liver off pretty good. I've had to have 2 big steroid…
My knee replacement was cancelled on the day of the operation last month due to a flare up of Psoriasis on my legs and feet and the surgeon was worried about infection. After a dermatology appointment last week the suspicion is that this was most likely caused by the bi-weekly Adalimumab injections I have been taking for…
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