Hi all, I’ll try to keep this as short as possible!...
I’ve tried many medications over the 25 years since my RA/D was diagnosed & returned to Leflunamide about 4 years ago, when I couldn’t get along with infusions or self injections. I wasn’t seeing any improvement with them. I’ve had the occasional steroid injection into my hand & ankle (where the worse inflammation occurs) or just in my bum, when it’s a ‘general flare. I’m also taking 3mg daily prednisone & Palexia painkillers.
However, 18months ago, after huge amount of stress going on with Family in the U.K. Leflunamide coulcn’t seem to cope anymore. After several weeks of waiting (Rheumatologist left suddenly & my notes were ‘lost’ at the hospital) I eventually saw a new (very dishy!) Rheumatologist.
Between us we decided to give BARICITINIB a go. I’ve always had a skin test for TB before starting infusions etc. but this time I had to have a blood test. The results showed POSITIVE for TB, but the ‘preventive medicine doc’ said not to worry as it wasn’t serious!! But because I wasn’t ‘normal’ & with my low immunity with RA/D, I’d got to take ‘CEMIDON’ tablets for 6months as a precautionary measure. Rheumatologist said that I would be able to star BARICITINIB after 3/4 weeks of taking the CEMIDON.
Unfortunately after2 weeks I started to get awful side effects, sickness & diarrhoea my back went into spasm (that’s another story!) So, I was taken into hospital & they said that I had an infection but not sure where! I had cat scan, blood tests, & MRI scans etc. & stopped all meds when I went in hospital. As soon as they got my temperature down & put me on painkiller & antibiotics drip, I was allowed to start taking my meds again. The next day I was sick etc & Hubby & I wondered if CEMIDON had anything to do with it. Sure enough I’d had a toxic reaction to them & they had infected my liver!! I had to stay in for 8 days (& even had 2 visits from my dishy Rheumatologist!!)
The next TB blood test came back negative, but you have still have to finish the course.
Rheumatologist then put me on RIFAMPICINA for 4 months....but last week I started to get same symptoms with sickness etc. & I’ve stopped taking them. I see him on Dec. 10th. So not sure what next step will be. Taking meds to help you feel better is one thing, I don’t particularly want to take them to feel worse, throwing up & on the loo for 4 months!!!😩
Meanwhile the stress level is increasing, worrying about Family in U.K. & not being physically well enough to go over there & ‘do my Mum job!!!’ Obviously this isn’t helping at all!!!!! 😥
Sorry about the lengthy post! But I was wondering if anybody else was in a similar situation (not Family stress!!) but with medications!!?! 🤔🙄