Working out with PMR

Posted by mwarrior @mwarrior, Feb 9, 2025

I'm a newbie to PMR and glad I found this forum. I have so many questions. I'm around the corner from 69 years old and was diagnosed on Dec 17, 2024. For months I kept thinking, I'm not stretching enough, I need to whip this by working out a little harder. My inner Rocky Balboa has always kept me in reasonably good shape through other geezerly challenges. Before tapering I was feeling great but now it seems whenever I have a great workout, later that day the pain ratchets up. My wife tells me to moderate but that's not in my psyche. Am I damaging things more by enjoying a good hard workout? Should I back down? Will I be sorry I push too hard?

Interested in more discussions like this? Go to the Polymyalgia Rheumatica (PMR) Support Group.

Profile picture for tuckerp @tuckerp

At least for me, the longer term effects of prednisone are worth the short term "over thinking". The quicker you can understand this disease and the effects prednisone has your system or the disease the better. Your doing a great job. Keep after it.

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Thanks for the encouragement! I needed that.

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I am relatively new to PMR. I was diagnosed by my PCP just 3 months ago. I started with prednisone 10mg and and tapering now, down to 8mg. I have some stiffness in my legs and soreness in my arms but it’s not unbearable. I have been reading comments and am somewhat confused, trying to figure out what I’m really up against at almost 73 yrs. I don’t want to be on prednisone forever, I not sure what it’s doing to my body and brain at this age. It has helped so far but the thought of being dependent on thie drug is scary to say the least. I exercise regularly and just push through the soreness. I take vitamins and try to eat healthy. I welcome any advice members can offer. Thanks, this group is a lifesaver

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I was diagnosed with PMR in Oct., 2023. Started me on 20 mg. prednisone in Nov. 2023 thru Dec. 2024 Every time I tried to wean down to six mg., I would relapse (weaning was 1 mg every 4 weeks). Rheumatologist talked me into Actemra infusion, along with prednisone - which allowed me to wean down faster. I could wean down 1 mg every 2 weeks, instead of 4 weeks. I am off the prednisone (which my rheumatologist encouraged - as it is a steriod) as of Dec. 2024. Now, just on Actemra infusion once a month for 12 months....could be longer....we do not know. No side effects for me. Takes about one hour. Actemra is not a steriod. I believe the prednisone and the PMR compromises the joints/muscles. I have taken two big falls since Dec. 2024 and now, March 5, 2025. I feel strong and okay when I walk.....I just don't have the strength to recover from tripping/off balance....and fall. I am in PT, which I am hoping it will help with strength. Judy - age 81

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Profile picture for Howdy! @kereno

John @johnbishop, Thank you so much for those links! I am learning a lot about PMR through them and through this and other discussion threads. I spoke with my PT yesterday about my confusion regarding what to attribute my soreness to and when to back off or push through exercising, or when to give it a day's rest. Other symptoms for me include morning stiffness, afternoon/evening light headedness and feeling increasingly flushed, foggy and wiped out as the day progresses as well as generalized anxiety (which I attribute to prednisone). I am trying to figure out what is going on. Of my symptoms, what is attributable to the flare? What is over-extending my limits? Am I tapering too fast or too slow? (It sometimes feels like just too much prednisone in my body.)

The PTs response was that we could slow things way down to isolate factors as in a scientific experiment (do everything the same except modulate one factor over time). But the patience that would require and the unintended consequences of say, stopping making any gains in the gym, would extend a person's prednisone duration for months or years and take down our general health and well-being--bringing on a secondary "illness." Avoiding over-use of prednisone is my number one priority. Of course, we're all eager to get out from under prednisone's side-effects.

So I'm trying to clear the fog somehow. Maybe I'm making this harder than it needs to be and am trying to be overly analytical when an easy-going exploratory, intuitive approach may be better. Straddling these ideas, I've decided to add dietary supplements for pain control. I am currently trying PEA (Palmitoylethanolamide) for "Discomfort Relief." I purchased some SPM (a fish oil concentrate that is designed to "target root causes of soreness by supporting the body’s natural ability to soothe and minimize discomfort.") These aren't my ideas--I am working with a naturopathic health practitioner to oversee this. I can't say I'm into meditation, but I am trying to soothe my nervous system in ways that may have some resemblance to meditation.

So I am with you guys. Thankful and really interested in learning from your experiences, all the while recognizing that this is an individualized experience. We each have to find our own way through it.

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@kereno new to this forum and I'm specifically looking for feedback on Palmitoylethanolamide (PEA) - just curious to know if it has helped you? I have horrid reaction to prednisone so I can't take it.

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Profile picture for leeta @leetaanderson

Before PMR, I was riding my bike for some good distances, two or three hours out on the road, a hard hour + on my indoor trainer. My stamina has gotten knocked back with this condition: I can’t generate the watts I used to, and I haven’t been able to ride with my usual Saturday group. I’ve become aware of a lower limit where pushing myself feels more like injury than training.
But my PMR seems to be subsiding after a year, and I’m feeling stronger again! Hoping to join that group ride again this spring. I agree with the others that exercise is critical, but you do need to be aware of your limits.
One last observation I’ve had reading comments in this forum: so many of us come from very active lives, and great fitness, into this unfortunate condition. I haven’t seen any studies, but I do find it curious.

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@leetaanderson Wow.....your story sounds like mine! Before PMR I was a very active 70 year old competitive cyclist winning gold medals both for state and national championships. Three years ago I had a very serious bike crash that put me into the hospital for 3 weeks but my attitude and physical condition was able to recover from major pelvis surgery, total hip replacement and total knee replacement. Despite the major surgeries I was able to recover and get back to cycling joining the local A rides in my neighborhood,........Then out of nowhere I woke up one morning with PMR! Fortunately I did not listen to my GP doc who said I did not have PMR.....I had some pred. on hand that I refused to take in the past for a ear infection so I tested as per my online research and I went from level 9 pain to 0 within hours.........I knew then I had PMR. Fortunately I was able to get more pred. to hold me over until I saw a Rumy doc who also confirmed I had PMR. I started with 20 mg and quickly tapered to 10 mg and have been tapering down with 1 mg. per every three weeks..........I'm now down to 5 mg with a goal to be off pred. within a total of 6-8 months. This has been quite the journey but with the help of this forum, and with lots of careful research I'm doing quite well, so far. I plan on getting back to the physical level I was at before my crash and I do get a lot of resistance and defiance from non athletic friends on that statement. This is what I learned so far after almost 4 months: It's imperative to adhere to a very strict non inflammatory diet, try to exercise everyday for at least 30 min. at a time such as a walk, stationary diet.....light weight lifting......lots of supplements to counter the pred. side effects, saunas, if possible hyperberic chamber, no or very little if any alcohol, no gluten..........I have broken these rules about once per month :)). I wanted to share my journey to help give some uplifting advise to those just getting started on this journey. Hope this helps someone.

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Profile picture for ds1 @ds1

@leetaanderson Wow.....your story sounds like mine! Before PMR I was a very active 70 year old competitive cyclist winning gold medals both for state and national championships. Three years ago I had a very serious bike crash that put me into the hospital for 3 weeks but my attitude and physical condition was able to recover from major pelvis surgery, total hip replacement and total knee replacement. Despite the major surgeries I was able to recover and get back to cycling joining the local A rides in my neighborhood,........Then out of nowhere I woke up one morning with PMR! Fortunately I did not listen to my GP doc who said I did not have PMR.....I had some pred. on hand that I refused to take in the past for a ear infection so I tested as per my online research and I went from level 9 pain to 0 within hours.........I knew then I had PMR. Fortunately I was able to get more pred. to hold me over until I saw a Rumy doc who also confirmed I had PMR. I started with 20 mg and quickly tapered to 10 mg and have been tapering down with 1 mg. per every three weeks..........I'm now down to 5 mg with a goal to be off pred. within a total of 6-8 months. This has been quite the journey but with the help of this forum, and with lots of careful research I'm doing quite well, so far. I plan on getting back to the physical level I was at before my crash and I do get a lot of resistance and defiance from non athletic friends on that statement. This is what I learned so far after almost 4 months: It's imperative to adhere to a very strict non inflammatory diet, try to exercise everyday for at least 30 min. at a time such as a walk, stationary diet.....light weight lifting......lots of supplements to counter the pred. side effects, saunas, if possible hyperberic chamber, no or very little if any alcohol, no gluten..........I have broken these rules about once per month :)). I wanted to share my journey to help give some uplifting advise to those just getting started on this journey. Hope this helps someone.

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@ds1 great work…. I too had bike accident and similar path issues f diagnosis and recovery.
And am now drug free, pain free and awaiting next blood work in 2 months.
Keep up the good work..
lemons turned to lemonade.

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New PMR Diagnosis, took my first dose of steroids today. Although since my Father and his Brother had it, I initially diagnosed myself.
Thanks for talking about exercise. I’m also interested in benefits of anti-inflammatory diet.

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I don’t know how much about diet in respect to PMR, but I can tell you the more sports I do daily the better I feel.

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Profile picture for ds1 @ds1

@leetaanderson Wow.....your story sounds like mine! Before PMR I was a very active 70 year old competitive cyclist winning gold medals both for state and national championships. Three years ago I had a very serious bike crash that put me into the hospital for 3 weeks but my attitude and physical condition was able to recover from major pelvis surgery, total hip replacement and total knee replacement. Despite the major surgeries I was able to recover and get back to cycling joining the local A rides in my neighborhood,........Then out of nowhere I woke up one morning with PMR! Fortunately I did not listen to my GP doc who said I did not have PMR.....I had some pred. on hand that I refused to take in the past for a ear infection so I tested as per my online research and I went from level 9 pain to 0 within hours.........I knew then I had PMR. Fortunately I was able to get more pred. to hold me over until I saw a Rumy doc who also confirmed I had PMR. I started with 20 mg and quickly tapered to 10 mg and have been tapering down with 1 mg. per every three weeks..........I'm now down to 5 mg with a goal to be off pred. within a total of 6-8 months. This has been quite the journey but with the help of this forum, and with lots of careful research I'm doing quite well, so far. I plan on getting back to the physical level I was at before my crash and I do get a lot of resistance and defiance from non athletic friends on that statement. This is what I learned so far after almost 4 months: It's imperative to adhere to a very strict non inflammatory diet, try to exercise everyday for at least 30 min. at a time such as a walk, stationary diet.....light weight lifting......lots of supplements to counter the pred. side effects, saunas, if possible hyperberic chamber, no or very little if any alcohol, no gluten..........I have broken these rules about once per month :)). I wanted to share my journey to help give some uplifting advise to those just getting started on this journey. Hope this helps someone.

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@ds1 I diagnosed myself, also. My orthopedist told me to come back in 6 months and we would talk about hip replacement surgery (no imaging had been done on my hips to indicate a problem). I convinced my PCP to test me, she recognized the signs and started treatment while I waited for a rheumatologist. She admitted she had never dealt with PMR but shared that she had “personal not professional” knowledge of RA. She must have researched the same protocol for PMR as I had because she did exactly what I would have done but I didn’t have prednisone hanging around. Actually, a quick response to prednisone is one sign that confirms the diagnosis of PMR.

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You didn’t mention your pred dosage…
I’m 72, 12 yrs on pred for PMR. Current dosage 5 mg.
Recently retired and started routine trips to the gym to improve overall strength. I can tell the difference btw muscle soreness and PMR pain. Can you? If a moderate workout actually causes PMR pain, you probably aren’t taking an adequate dosage of pred. Try increasing 1-2 mgs and see if that makes a difference.

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