I've posted on the main forum asking for some advice but though I'd say a quick hello here.
I'm Vicki, 42, and I live in North Wales (although I'm originally from the NE) and I was diagnosed with PsA 10 years ago. I'm currently on Leflunomide, having previously been on Sulfasalazine and Methotraxate; but I have had a really bad flare up and am now going onto another tyoe of meds as well to add to the Leflunomide. (My inflam markers went from 11 to 90 in one month).
I've always tried to manage the condition and for the most part have succeeded, but recently have been really down and feel worried for the future and my ability to have a decent life, stay working etc.
So hello all, and I hope I can get some advice/support/friendship or whatever here. Feels like no one irl 'gets it' at all most of the time. My husband tries but don't think you can truly understand unless you go through it.