I'm 73 and just diagnosed yesterday, although I've been dealing with it undiagnosed since October. It's very depressing when you have to change or eliminate the things you do or change how you have to do things. I was on 15 mg prednisone for 3 weeks because my rheumatologist suspected this when my blood work started coming back. It didn't make much of a difference at that dose. I'm now up to 25 mg and I worry that maybe prednisone isn't going to work for me. I've been retired since covid started in 2020. My incentive to keep going (besides my wife) is we have a daughter who will be 6 in the next week and a half. I can't take her to the park or play with her like I used to doing. I'm always tired and sore now. I feel like I'm a burden when I can't do things that I used to do. That's where I am as of today.