Can PMR (Polymyalgia Rheumatica) be induced by vaccine?
Good evening, I’ve recently been diagnosed with PMR. It came on a week after my flu shot October 23, 2020.
Has anyone experienced the same diagnosis after a flu shot?
Interested in more discussions like this? Go to the Polymyalgia Rheumatica (PMR) Support Group.
Oops. PMR diagnosed in April 2021 NOT 2001. I’ve been in remission since 2019 NOT 2029! Sorry about the typos. Don’t know how to go back & edit a post…
Hey John-
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Hi Dave, I retired from IBM after 30+ years and then retired from a local telephone company where I was the Internet helpdesk and computer fixer for 20+ years. I also maintain a few volunteer websites for our church and a missionary in Tanzania plus my Navy ship's reunion website (ussmckeanreunion.org, fccwc.org and wwechurch.org). It's a full time job being retired 😁
My PMR started within 2 weeks after my pneumonia shot
Hello @mark1udxemail, Welcome to Connect, an online community where patients and caregivers share their experiences, find support and exchange information with others. You mentioned that your PMR started within two weeks after your pneumonia shot. Did you see a doctor or rheumatologist who diagnosed it? Did they start you on prednisone?
I received the flue vaccine 4 years ago and 2 days later went to work sat down and 10 min later could not stand up. I had to pull on the desk to get myself in and upright position and my knees would not hold me, I did a duck walk down the hallway to my bosses office to tell her I was heading to the urgent care. I have had 2 remissions and am currently on 3mgs of prednisone and it is tolerable but I still do not get much done and have to take a nap every day. Now i am starting to swell in my ankles and have pain in my two knuckles, first IP joint on the right hand middle and finger to the right of it. I had to retire last last year as I still cant walk the long hallways and am worn-out by mid- week and ran out of sick leave and vacation time, but had to keep my health insurance.
What treatments other than prednisone are you doing? I have been doing physical therapy and he has been doing ultrasound on my muscles which has been helpful when they feel thick, and has strengthened the portion of the muscle just above my knee that helps one to stand (so I'm not duck walking-butt close to the floor. Has anyone done platelet therapy, which before covid, clinical trials were underway with some autoimmune disorders. I take care of my 96 yr old Dad and I don't have a doc in town that will anything other than prednisone.
Hello @quilterdar, Welcome to Connect, an online community where patients and caregivers share their experiences, find support and exchange information with others. I have never heard of platelet therapy done for PMR. I have heard of it for knee osteoarthritis and other specific joints just not for something as pervasive as PMR. My rheumatologist summed it up for me as arthritis all over the body. There is another discussion you might find helpful.
PMR initial diagnosis: Can there be an underlying disease?: https://connect.mayoclinic.org/discussion/pmr-initial-diagnosis-1/
After my second occurrence of PMR I decided to see if I could make some changes that would help with the PMR and started eating healthier and trying to get more exercise daily. Here's some information that you might find helpful if it's something you are considering or maybe have already done -- Diet and Supplements for Polymyalgia Rheumatica (PMR): https://www.arthritis-health.com/blog/diet-and-supplements-polymyalgia-rheumatica-pmr
Have you tried making any diet or lifestyle changes to help your PMR?
YES! 20 years ago the first time I had PMR pain was the day after a flu shot. I've been on and off prednisone since then. Over the years I continued to get better and then would relapse around vaccine time or shortly after. All my doctors told me it could not be the vaccine... The last time I had a flu vaccine was in 2014 and within hours I could barely walk. That was the worst one! No more vaccines for me. 🙂
My original post was related to this topic. I got J&J and two weeks later symptoms started and became at unbearable. Diagnosed with PMR at 4 weeks and started 10mg prednisone - better in 3 days. Now on 5mg. Friends and family were/are sceptible of getting a Covid shot after seeing me - a healthy, active 74 year old decline so rapidly. Still think there is a connection. Next follow up in October.