PMR - possible diagnosis
I have developed what my PCP theorizes is PMR. First available appointment with a Rheumatologist is in February. Meanwhile, it has been a huge and painful life altering experience. My shoulders have been immobile some mornings and my hips don't want to function either. A couple of hours into the morning I feel better and can move. I was given Prednisone (game changer) dosed at 30mg every other day. I've researched the negative aspects - but it really does help. I'm trying acupuncture, PT, and I've cleaned my diet up drastically. No sugar, refined foods, red meat, processed food, etc. Nothing that can be considered inflammatory passes my lips! I just turned 70, am fit, did Yoga everyday for 4 years prior to this malady striking me. I take Turmeric with black pepper 3 times a day. Light exercise seems to help a bit. Thanks for listening, this has been a very scary 2 months. Any other anecdotal suggestions for symptom control? Thankful I found this support group, My body can't do much, but my brain can!
Interested in more discussions like this? Go to the Polymyalgia Rheumatica (PMR) Support Group.
"I hope to be on Prednisone for a short time, and will gladly trade the consequences of it for the pain relief."
This is the sad part about being in pain. It wasn't that I wanted to "feel good" --- I just could NOT endure all of the pain! Most of the pain wasn't even PMR. However, PMR ushered in a state of "systemic inflammation."
I was willing to do anything to make the pain stop no matter what the consequences were. Realistically, I don't think I had any other choice at the time. If I could do it all over again ... I would probably still take prednisone even knowing what I know now. Even though I don't understand much of anything.
The pain is incredible.
The only time I've ever experienced anything remotely severe was during childbirth. That only lasted 8 hours and I had a wonderful reward for it!
@nancy53
If you’re adding K2 to protect against atherosclerosis make sure it’s MK7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238900/.
Thank you.
I have had PMR for 30 years off and on and now on. I have not heard about " low dose statins for mitigating the atherosclerosis with autoimmunity". Any references? I have an odd adverse reaction to statins so I am on Praluent.
How do you cope best mentally?
I’ve seen references online to this immune-modulating property. In a sample of one, I’m RA with moderate to severe disease status and since a year ago. also on low statin for arteriosclerosis. I don’t think it’s changed anything in my case.
Sounds like you're on top of it.
I've just begun as you But not nearly as healthy. Working toward that. Good luck and wish you well.
Work is the right term for it. It's hard and I'm afraid I'm impatient.
This magnitude of pain would have been unfathomable 3 months ago. Still is.
Good luck to you as well. This support group has been a lifeline.
Regarding diet, my rheumatologist recommended gluten free and that has helped. I’m still on prednisone (finally down to 2.5 mg) and find that daily exercise is a must. It’s counter-intuitive when we’re in pain to exercise, but whether just walking or an exercise bike, the benefits can be significant. My rheumatologist also teaches his clients tai chi and you could explore that online if there are no groups near you. Best to you! I’m also grateful for this group❤️