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.
Connect

@naples3
I'm sorry to hear you haven't had better results with prednisone treatment. I was very fortunate that I felt the help within hours and continued to improve. I tapered off after the first month. It took almost a year to do so. So far no symptoms of PRM have returned. I'll be 89 in a few weeks. Good luck and good health. Hugs, smj
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3 Reactions@smj
Happy Early birthday. I will be 80 in a few weeks and had a good experience too.
I’ll 🥂 you at my birthday.
Reminder, is the pain PMR pain or adrenal suppression pain, or something else.?Any discomfort while on prednisone was supplemented with Tylenol for Arthritis, as per my Dr.s suggestion. My prednisone roadblock came at not being able to taper past 8mg. Not an uncommon problem. I was put on the biologic Kevzara and it was clear sailing. Off Prednisone after 3.5 months and now off Kevzara after 11 months.
Good luck everyone
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1 Reaction@tweetypie13
Thank you for the birthday greetings. Happy birthday to you too! Stay well!
@johnbishop did you have many flares
in that time? I’m getting close to 4 years and it’s hard to stay under 7 mg. And when I flare I have to go to 12mg. Drs now are not sure what it is and why it’s lasting so long. Did any other meds help you get off. I tried methotrexate in the beginning but it didn’t help, maybe because stupid Dr didn’t think it was PMR and he tried to ween me off in 3 months. Any suggestions?
@sharon44r You mentioned in an earlier post that you also have Hashimoto's. @lblauvel mentioned in another discussion having Hashimoto's and also being diagnosed with PMR, and may have some thoughts or suggestions - https://connect.mayoclinic.org/discussion/can-hashimotos-be-caused-by-pmr/.
I did have a lot more flareups my first time with PMR and I think for me it was a combination of things, sometimes triggered by diet, sometimes by overdoing exercise/activity the previous day or possibly tapering too fast or too much. If you haven't already seen it, you might find this discussion started by Mike @dadcue helpful:
-- How to Slowly and Safely Taper Off Prednisone but ... no set rules.
https://connect.mayoclinic.org/discussion/how-to-slowly-and-safely-taper-off-prednisone-but-no-set-rules/
@johnbishop thx. I’ve tried the alternating too! I’ll just keep trying 🥴 how any times did it come back?
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1 Reaction@sharon44r I've had 2 instances of PMR. The first one lasted 3 and half years followed by 6 years of remission. The second instance of PMR lasted 1 and half years and I have now been in remission for almost 7 years so hoping it is never coming back. I attribute the shorter second time with eating healthier, less inflammatory foods and more exercise along with losing some weight. Can't really say it will never come back and I do have aches and pains from degenerative arthritis and a few other old guy issues.
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2 Reactions@johnbishop one more question… were your inflammatories high while on prednisone ? Mine are normsal on 7 mg, but still have flares and not totally pain free. My new rheumatologist isn’t sure what I have, but I know it was PMR when it started. All the drs says is long for PMR
@sharon44r my CRP and ESR labs were elevated when I was first diagnosed but I remember them being normal for yearly follow up tests when my PMR was active. There are quite a few members that have posted about PMR symptoms/flare ups with normal labs. Here's a search of Connect that lists the comments and discussions from members about normal labs with PMR - https://connect.mayoclinic.org/search/.
There are other conditions with symptoms similar to PMR. I'm not sure I understand what you mean by "all the doctors says is long for PMR". Are they saying your time having PMR is too long?