I was diagnosed with PMR in June 2014.
Over a period of about 7 years I managed to come off prednisone but after a time the PMR returned. Since 2022 I have managed to get down to 7mg daily and then have a flare. Back to 10 down to 8 and another flare.
I live in France and it seems PMR is not as common as in the UK and something the medical community are not as knowledgable about. I have seen, over this period, 3 rheumatologists who each in their own way has tried different treatments and dosages of prednisone. Over the last couple of years I have been managing it with the help of my GP.
We spent the month of October in the UK and whilst there I had a private consultation with a rheumatologist in Bristol. He was very thorough going through my past history and then explaining to me his thoughts.
His recommendation was
“have checked some blood tests today to look for rheumatoid factor and other antibodies that we sometimes see in this scenario. We could potentially consider x-rays and ultrasound scans of your hands and feet, but I think these would be unlikely to be helpful given that your symptoms are currently more settled on a slightly bigger dose of steroid.
My recommendation therefore, is to start methotrexate as an additional treatment. We use this quite commonly in difficult to treat polymyalgia, but it is also a standard treatment in rheumatoid arthritis. It would take two or three months to start working, so it would be necessary to continue your current dose of prednisolone for that period, with a view to weaning it down and then stopping it entirely.
The anti nuclear antibodies test was positive which I believe points to the diagnosis of RA.
I have, of course, to discuss this with my GP here and decide how to proceed. I’m very reluctant to start a new drug and wonder , at the age of 81 and in pretty good health apart from the PMR, if I seem to be stable on a dose of 10 mg which I can reduce from time to time if this is a way forward.