Polymyalgia Rheumatica (PMR): Meet others & Share Your Story
Welcome to the Polymyalgia Rheumatica (PMR) group on Mayo Clinic Connect.
Meet other members who are dealing with PMR. Let’s learn from each other and share stories about living well with PMR, coping with the challenges and offering tips.We look forward to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Grab a cup of coffee or beverage of choice and let’s chat. Why not start by introducing yourself? What's your experience with PMR? How are you doing today?
Interested in more discussions like this? Go to the Polymyalgia Rheumatica (PMR) Support Group.
When I was first diagnosed with PMR my hands swelled to the point where I wasn’t able to hold on to a pen. After being on 20mg of prednisone for several months the swelling disappeared. My doctor assured me that I did not have rheumatoid arthritis but that it was related to the PMR. Hopefully you’re situation will improve with time as well.
I can’t tell you how thankful I am for this group. I’ve learned so much by hearing others stories. In early 2022 I was initially diagnosed as having Trapezius muscle strain. A week of Prednisone knocked out the pain but the pain came right back. In addition I had hip pain. Couldn’t get out of bed. Couldn’t get off the toilet. Can’t put on my socks, etc. Take an Advil in the morning and eventually I could function ok for the rest of the day. Finally blood tests confirmed that I had PMR as I had all the classic symptoms. I started on 15mg of Prednisone in April 2022 and I taper 1mg each month. I will be tapering down to 8mg this week. I am starting to understand my moods and why I am so pooped at night. I didn’t think in my early 70’s that I would have to temper my exercise. I’ve managed my weight, but the osteoporosis side effect is my main concern. Thanks to everyone for all of the information.
I developed PMR after my Pfizer booster shot for Covid. I had never reacted to immunisation before. I had instant results with 10 mg prednisone and decreased by 1 mg per month. I am down to 1 mg tomorrow and have to decide whether to get another Covid booster and/or flu shot. Any experiences to share out there? Thank you.
I also developed PMR seven days after my 2nd Moderna booster. No doctor will say that there was a connection but neither will they rule it out. I decided against a flu shot or another Covid booster at present. I started 15 mg of Prednisone in September and am currently at 9 mg. I will see what my rheumatologist says in March. Meanwhile I’m being careful with crowds and wearing a mask when necessary. I’m just nervous that vaccines right now will cause a flare up.
I don’t know about a connection between vaccinations and PMR, but interestingly PAXLOVID removed all of my PMR symptoms for the short time I took it after contracting Covid. I reported this outcome to my rheumatologist. It will be interesting to see if PAXLOVID at some point replaces, or supplements, steroids.
Thank you for your helpful reply. Both my rheumatologist and family doctor suggested Novavax as a possibility for consideration for my booster. At this time it isn't bivalent as yet for the new strains like the other vaccines. I haven't decided. I'm nervous about a flareup too. Prednisone did give almost instant relief.
I'm Paul 79 and pretty healthy. At the beginning of the month I suddenly had pain and stiffness in my upper arms and upper thighs. After 4 days it disappeared. But then a few days later, the arm pains returned, sometimes to my shoulder, but not to my pelvis, neck or anywhere else. My CRP was 18.6, sedimentation normal. PCP diagnosed PMR and I will start on prednisone in a day or so. My question is, does PMR get worse--that is, more painful and stiff, progressively, and is it likely to return to my pelvis, or am I lucky to have a relatively mild case? I' very glad I found this helpful group!
That is very interesting! I tried to get Paxlovid because of my age and being on prednisone when I contracted Covid last April. Had I been on 20 mg I may have gotten it but my dosage didn't qualify. Fortunately I wasn't very sick with it. In Canada it is doled out very scarcely.
When I was on long-term dexamethasone (not for PMR) I took weekly Fosamax, a bisphosphonate medicine that alters bone formation and breakdown in the body. See if your doctor thinks that's a good idea.
Thank you for your reply. It is very helpful to me. Doctors suggested Novavax could be an alternative altho it doesn't include the bivalent as yet. I am encouraged to hear of your experience and will most definitely consider it in making my decision. Thank you and continued good health!