PMR or PREDNISONE

It's really hard to tell which is which when you are at a higher dose of Prednisone. It also depends on how long you have been on the higher dose. I started Prednisone in August, 2023 and have been weaning down slowly ever since. I found when I was at 7.5 mgs and weaned down to 5 mgs, that's when my symptoms started breaking through again, so I thought. Muscle pain, joint pain, neck and shoulder pain, tingling in legs and arms, etc. Could not tell if it was a reaction to the Prednisone or PMR returning. I tried to hang in there for 4 very long days of severe pain to wait it out, but gave in and took 2 Advil (my doctor just told me it's okay to take it once in a while). My symptoms subsided very quickly, and then I waited for the storm to hit again, but it never did. That was the only way that I could tell that it was a reaction to the Prednisone. Same thing happened when I weaned down from 5 to 4, and 4 to 3 mgs. Now I am at 2 mgs every other day with 3 mgs in between. Able to do more and sleep a little longer but still have insomnia, but I'll take that over the pain any day. Was very excited that I was able to give both of my dogs a really good bath yesterday; they are pretty big dogs but were so happy when I was done. However, my German Shepherd had to rub the clean off of her on the grass for about 10 minutes, lol. I probably did too much but the benefits outweighed the aftermath so I went for it. Although I'm in a bit of pain today, I plan to get moving and unclutter my house. I just had knee surgery for a meniscus root detachment in mid-March which involved a fracture and ACL issue, but so it feels good to be able to move around and get things done. Promised myself not to overdue, and to be careful.

I have had PMR for a year and a half and have never taken prednisone or any other steroid, so my experience might help: I have never had insomnia or brain fog or shaking anywhere. I have had pain in my hands but not swelling.