Connect
← Return to Polymyalgia Rheumatica (PMR): Meet others & Share Your Story
Discussion
Polymyalgia Rheumatica (PMR): Meet others & Share Your Story
Polymyalgia Rheumatica (PMR) | Last Active: Jan 27 8:38am | Replies (1879)Comment receiving replies
My Ortho is actually who recommended that I see a rheumatologist so some of them do have appropriate info. My insurance requires a referral to a specialist and my GP and I had to have several lengthy discussions before she ran some bloodwork. She didn’t make the referral until she saw my Sed rate and CRP which were extremely high. I probably would never have received the referral if those had been normal like others with PMR have reported. Education on PMR/autoimmune is likely needed for all of our medical professionals.
Replies to "My Ortho is actually who recommended that I see a rheumatologist so some of them do..."
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!
Connect
Glad to hear that your ortho recommended further testing. I totally agree that more education on these auto immune disorders is need for physicians across the board.