I had a really good visit to the hospital, actually saw my consultant rather than one of her team. She is good, she listens.
First though, I am amazed at the MRI scan I had on my left hand. That technology is awesome, the lady who did it was excited about the capability of it and chatted throughout explaining the images. It seems that I have severe inflammation and some sponginess and erosion but not much, thankfully. Apparently, it was only necessary to scan one part of me as that gives a clear picture overall.
I had a steroid injection and already feel better. I slept without pain.
My mouth ulcer infection is getting better. Apparently I am on a hiding to nowhere with these. high levels of inflammation in the body prevents healing, but so do many of the medications we take including biologics. It is a balancing act.
No more Methotrexate, a medication that causes depression in me is no more acceptable to the Rheumy than it is to me.
There was a trainee in the consult, (ARI is aligned with the university). My blood works can cause confusion it seems CRP & ESR are never high despite the obvious (now) inflammation. My last CRP a week ago came back at 6, Dr said she would expect it to be very much higher than that, so advised the trainee that bloods alone are never to be used. Though it is unusual.
Tocilizumab to start as soon as can be arranged, but probably a month. Meantime, I need to have a chest Xray my breathing is not quite as it was, also will need to have video chat with the biologics nurse.
Anyway, thank you all for your feedback and support.
It is a bright but frosty morning and I have a mountain of jobs to do, while I can.
Go gently through the day and stay safe.