My advice to anybody newly diagnosed would be to carry on working and carry on doing the things you love. The first year of diagnosis was a nightmare until the meds kicked in but I managed to carry on with work ( bit slower than before!) and although I won't be playing the piano or dancing any time soon I try to do what I enjoy. I think if you decide you are disabled and can't carry on as normal you will get very depressed and my RA is better if I keep on the move , nice to see a positive post for a change!
When I was diagnosed I thought that’s it, I’ll have to cut my work hours, not do the Masters Degree I was planning on doing and just vegetate!
THEN - I thought “stuff” this - If I don’t do stuff now I never will and to be fair I am in agony what ever I do, my RA seems to progress what ever I do - so I may as well struggle and be in pain with what I want to do not be in pain and struggle with just existing.
Have I found THE treatment for me? Not yet but I’ve decided my life isn’t over yet so yes I struggle with everything (can’t even cut cheese at the moment) but I struggle with living life NOT struggle with RA
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