Do we actually “recover”?
Will there be a time when the PMR actually goes away, or is this a lifetime diagnosis? I have to taper off prednisone rather quickly, preferably 1mg/wk do to the effects on my heart and kidneys. My fifth referral to Rheumatology has been sent. I only have three choices within 200 miles, two are a year out, one isn’t accepting at this time. You would think since it’s causing heart and kidney failure, and the cardiologist sent the referral, they’d consider a faster appointment! Sigh… I know I’m not special and there are people hurting who have also been waiting.
I guess I just want to know that there will be a time with no prednisone or pain somewhere in my future!
Interested in more discussions like this? Go to the Polymyalgia Rheumatica (PMR) Support Group.
I also live in Portland and was diagnosed by my PCP who is also a geriatric specialist (I’m 73). She is very knowledgeable and I don’t have to worry about being marginalized. The long wait times for specialist is so frustrating.
Are you by any chance with Kaiser? I'm trying to find a new PCP that is better than the one I have
I'm not. Providence
I am 74 and had PMR in 2020. After 10 months on Prednisone (decreasing 1 mg per month) I am fully recovered. My rheumatologist said that because I had no relapses for the last 5 years I am basically “cured” but as with many autoimmune diseases there is always a chance it could return.