The Rheumatologist that diagnosed me with seronegative RA said there were 3 tiers of medications. She was going to start me out with a rier two however after discussing it she started me out with tier one which was plaquenel (sp). That was 2 years ago.
Have any of you heard about these tiers? I am not asking for medication advice. My Rheumatologist and I will discuss that. I was curious as to an example of tier 2 meds.
My Rheumatologist said humira would be a 3 tier medication.
I do go to a different Rheumatologist in another week that I have seen 3-4 times through video.
My first Rheumatologist was great but retired. rx me with chronic myofascial pain syndrome and malagia. My second one got done as coming to my state from SC every 6 weeks was yoo much. She RX me with seronegative RA, small fiber neuropathy, polyneuropathy, and discovered I don't absorb vitamin D or B 12 like I should.so on supplements for that.
My new Rheumatologist who is 2 states away and comes up every 6 weeks for a week seem good so far. We have our first face to face in person in a couple weeks.
So I'm curious about the tiers and a bit about my journey.