PMR and exercise: What helps you?
We are told that we have to stay active but what does that mean? This issue became very real for me when I attempted to swim the crawl stroke in the swimming pool. I was feeling pretty good at the time. The prednisone had kicked in and I swam the equivalent of two laps. The next day my shoulders were on fire and I was suffering a full flare; my first. Maybe everyone reading this will say that I was foolish to do any exercise that involve my shoulders and that I should limit my exercise to other parts of the body like walking or maybe biking. Let’s start a dialogue and find out what exercises work for all of us.
Interested in more discussions like this? Go to the Polymyalgia Rheumatica (PMR) Support Group.
Oh my gosh - I didn't know the on-going inflammation can trigger GCA. That is scary! However, my inflammatory markers were well within the low-normal range when I decided to taper off Prednisone, but I am still experiencing pain and stiffness, although not nearly as bad as it was when I was first diagnosed. If anyone can enlighten me more about triggering CGA I would love to hear from them. Regards to all. Also, does PMR every just go away?
Just for your information my husband is an Ophthalmologist. He treats many patients with this condition and GCA and neither condition causes glaucoma. Hope you feel better.
Yes, I am aware that these conditions do not cause glaucoma but prednisone does increase eye pressure in those that have it. So the use of it is a balance. Thanks for reaching out. (My opthomalogist was sure at first that my rheumatologist could give me something else, we had several discussions about it.)
I've read that GCA can result from uncontrolled inflammation resulting from untreated PMR. Have also read that it occurs in 10% of people with PMR. As to the "how and why?" I don't remember enough of it. Sorry, I know that doesn't explain much at all.
If your inflammatory markers were good I'd consider that to be showing one was at the correct prednisone dosage and it was keeping the inflammation under control.
Has anyone any experience with accupuncture and/or dry needling for PMR pain. I have been doing this once a week for the last month and it provides relief. I am unsure however if it may have negative consequences. Any experience out there? Thank you.
@mary4, There is another discussion where a few members have posted about acupuncture. Never tried it myself for my PMR as prednisone was all I needed. My mother had rheumatoid arthritis and severe pain in her hands and got some relief from acupuncture but from my memories she still seemed to be in pain afterwards.
--- Acupuncture and PMR:
https://connect.mayoclinic.org/discussion/acupuncture-and-pmr/
I used a (activator) chiropractor and responded well, also used a Fitbit and tried (not always successful) to walk 10,000 steps per day. Before bed 25 lateral leg lifts each side while on the bed. Everyone is an individual, I have been off steroids for a year.
The day after exercise my inflammation and pain gets worse. Does this get better after a period of exercising.?
This is what I experience as well. Any kind of unusual activity too causes a lot more pain the next day-for example up and down the ladder. But then again, some days I wake up and remain in much more pain then the day before for no obvious reason. Strange disease it is.
Hi @paelwell, You will notice that we moved your post to an existing discussion - PMR and exercise: What helps you?: https://connect.mayoclinic.org/discussion/pmr-and-exercise/ so that you can learn what other members have shared. It's good to see that you already have a response from @froehlich22. I too have experienced the "next day" effect after over doing it with exercise or activing when my PMR was active. The key for me was how much activity is too much and I'm not sure I ever figured that out 🙂