← Return to Polymyalgia Rheumatica (PMR): Meet others & Share Your Story

Discussion
Comment receiving replies
@vjs

Interestingly, my GP was the one who tested me first for PMR. I think she was tired of me going back repeatedly over the past year about the pain which was increasing. She tried to get me into a rheumatologist but no one would add an extra patient. Something needs to be done about that!! I’m in Saskatchewan Canada. So I suggested my husband’s internist. She has been a godsend!! It has been a bit of a learning curve as well as trying to accept this diagnosis. But one foot in front of the other, as they say! Who ever they are!!😁Im just relieved to have some respite from the pain, not looking forward to all the side effects of prednisone, but am happy to be able to move again!

Jump to this post


Replies to "Interestingly, my GP was the one who tested me first for PMR. I think she was..."

@vjs May I ask did you have the hallmarks of PMR - Bilateral stiffness in shoulders and hips ? Sudden onset , Pain is worse in morning , after waking ( what I call the "Ground Hog Day" feeling - think of Bill Murray waking up over and over again in same situation. It is 2023! Pre-Dx, when I googled bilateral pain "polymyalgia rheumatica popped up! I was already familiar with the term when I first saw PCP. Please look at the info in pmrandyou.com and PMRandIL6.com. NASAIDs are not going to help, there is immune cell-mediated pathway that needs blocking. The conversations on this site are very helpful and others have had uncannily similar experiences with Prednisone dosing and others are trying KEVZARA. European clinicians
/researchers seem to have more interest in "fast tracking" PMR Dx. I do not (yet) know who are the Key Opinion Leaders in the USA, besides Dr Callabrese of the Clevland Clinic.