I have been on Prednisone for a year and a half. Started at 15 mg and am now still at 7 mg. This winter I did a four month experiment with a Humira biosimilar and saw no improvement, actually a bit worse with the PMR. I am now in my third month of Kevzara with 7 mg of Prednisone. My condition seems to be getting worse, not the typical sick and wrong pain of PMR, but numerous other issues: Weaker, balance issues, lots of extreme hand pain and strangely, skin breaking out on my back and itching like mad. I am trying to muscle through this new four month experiment but it is getting tiring and frustrating. This disease is truly a nasty and life-changing problem. Yes, it is not cancer but we still are having our lives turned upside down and as far as I can see with no real hope of ever getting better. I am 79 so be it I guess. Thank all of you for this chat room as most folks have no idea of what we are going through.