← Return to PMR and exercise: What helps you?

Discussion

PMR and exercise: What helps you?

Polymyalgia Rheumatica (PMR) | Last Active: Apr 26 1:16am | Replies (182)

Comment receiving replies
@deniseinca

Thank you John, i did have flare up i guess as i was titrating prednisone it would always occur day 4 after decrease and i would just battle through as i wanted to be off prednisone. Funny thing is evening, night time is much worse even when i felt great afternoons are when i would deteriorate and fatigue kicks in much different to original diagnosis which was all day everyday. i have been awake about 4 hours now and the pain is OK but the weakness is getting slowly worse. I recently retired as a Director of Health just too much throughout the COVID times so i am health literate but find this AI perplexing to say the least. I tend not to "google" too much as there is so much misinformation on most things. I am so happy to have found this group though! I am turning the big 60 this year! Thank you for your reply.

Jump to this post


Replies to "Thank you John, i did have flare up i guess as i was titrating prednisone it..."

Just a thought...do get enough vitamin D? I think one of the side effects is fatigue and it also impacts the autoimmune system. Just read this recent study which was kind of interesting.

Vitamin D and marine omega 3 fatty acid supplementation and incident autoimmune disease: VITAL randomized controlled trial: https://www.bmj.com/content/376/bmj-2021-066452