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.
Thanks so much. Do you find that, after a time, you are able to exercise longer?
Not sure I tried to exercise longer. My problem was more when I had to do extra work activities around the house.
I found that magnesium help my muscle pain a lot. But be sure to get one that has three ingredients and be sure to take D3 with it.
Magnesium Glycinate
Magnesium Citrate
Magnesium Malate
Vitamin D3
I have found chair yoga very helpful especially for my shoulders and arms.
After exercising over a period of time, did youcapasity to do more increase.?
Has the amount of exercise you are able to do increased?
As far as regular exercise, my capacity has increased some but not what I would consider a lot. At 79 going on 80, I still try to do 30 to 45 minutes a day on my Teeter FreeStep Cross Trainer which is similar to an elliptical bicycle plus 10 minutes or so on an inexpensive ride and row machine I bought a few months ago. It's a pretty intense machine for getting your heart rate up quickly and I think is better for my core muscles and leg strenghth as it's similar to doing squats combined with rowing - https://sunnyhealthfitness.com/products/squat-exercise-trainer-sf-a020052. On days where I have to shovel snow or other outside tasks I'm not particulary fond of I generally don't do the inside exercising.
I do feel like I can do more than a few years ago when my PMR was active. I think it's good to have a goal to slowly increase the exercise activity as it begins to get easier for you just because it's a challenge and I like the hope of losing less muscle mass or slowing it way down.
wow!
Hi everyone.I am 83 and have had PMR for 2 years. A bit of a background. Always active and was fine until 3 covid shots and one shingle shot,then developed PMR,in neck shoulders and arms.
I was placed on 20 mgs. 1 month.
15 mgs 1 month.
10 mgs 10 months,then reduce by 1 mg per month.
Reduced eventually to 0.Then had flare,am back on 5.
At 5 mgs am feeling great,have been told by Dr. This is most likely where I will be to eliminate the pain.
I do exercise with light weights,shoulder shrugs,meditation and walks.
I will eventually try dropping 1 mg but am not in a rush.
Please stop trying to get of Prednisone to fast and do not take ibuprofen with it.
Don't mean to rant.Cheers from Calgary.
These posts are so helpful. I have been off of prednisone now since January, and feeling really amazing. I wanted to strengthen up a bit and went to physical therapist who gave me some exercises to do. They helped for a week or two and then suddenly I went into a flareup. I backed off and things settled down so started back again, very gently, but went into a flare up. I had been doing some very gentle stretches before that with no negative affects so I went back to those and oh my, my body loves it! If I'm allowed to, I would like to suggest Justin Agustin (on FB and YouTube. He has been a lifesaver, especially for those of us of a certain age who want to stay "in the flow". When my body is feeling tight and scared, I put on Harry Styles and dance my little buns off around the house. 79 and caused the Amazon delivery man a few laughs!