Is it safe to get the Corona Virus (COVID-19) vaccine with PMR?
Just wondering if anyone has found out if it is okay to get the corona virus vaccine once it comes out. I'm 78, so past the 65+ age for early vaccinations, plus having the autoimmune diagnosis. I don't see my rheumatologist for another two months but guess I'll call him to find out if t comes to that. Just thought I'd see if anyone else has found out. I had no problem with the flu shot.
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@jenniferhunter- Hi. We haven't spoken for a while. I am so glad that your team was smart enough to send you to the ER and you got the appropriate meds. I hope that you're feeling much better today.
Have your doctors advised about your second shot? It must be concerning to you?
no but i am a believer in less rx the better.
@merpreb I did contact my doctor's office and they will schedule an appointment to discuss this. On the 2nd day after the shot when the initial steroid and anti histamine treatments wore off, I did have puffiness and some tingling in my face. After taking an antihistamine, that got better right away. Today, 5 days after, I don't have symptoms and my arm isn't sore anymore. I will see what the doctor thinks about the 2nd dose. Thanks for asking.
Jennifer, glad you got the aftercare! Sounds like an ordeal. I hope you get the answers from your MD. It would be interesting to see if after the one dose you create enough antibodies fir defense against the virus. Best of luck on this.
I had two shots weeks ago and nothing unusual happened.
I have PMR. Was on prednisone for almost a year. Slowly weaned off in December. No pain. Had my first vaccine shot about 3 weeks ago. Had a flare up about 2 weeks after the shot. Went on prednisone medral dose pack and finished last Friday. Getting 2nd shot his Friday and I’m hoping I don’t get another flare up. Won’t stop me from getting it though.
Hi @ssobx, Welcome to Connect. My PMR has been in remission since mid 2016. I got my first Pfizer COVID vaccine Feb 5th and only had a sore arm around where I received the shot. I'm also hoping things go well for the 2nd shot on Feb 26th. I'm hoping your PMR won't flare up also but like you if my PMR would have flared up I would still get the 2nd shot.
Did you register with the CDC to provide feedback (it's easy!) after you get the shot? - https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/vsafe.html#anchor_1607560764339
Hi. No I haven’t registered, but I will. Thanks for the link.
@johnbishop- I'm almost positive that I have PMR since my shingles shot in November. I speak with my PCP this Friday and I'm going to ask for blood work for sure. I also had discoid lupus years ago but I don't think that this is a flair up.
I'm a bit familiar with the symptoms. Mine flair up very often, like every week or so. Is there anything that you can recommend for me?
@merpreb - My experience with PMR when it's active is that the pain is always there unless I'm taking prednisone to control it. Then as I'm tapering, if I go too fast, the pain returns with different levels of intensity. The two big things that I believe help keep my PMR at bay are diet and exercise - not the cardio type but the just keep moving stuff, walking, stretching, etc.. PMR diagnosis usually involves Erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) blood tests to check the levels of inflammation in your body but they are just pointing to the possibility of PMR not a diagnosis if the levels are high. A physical exam by a rheumatologist is usually needed to confirm.
I've mostly focused on reducing or eliminating processed meats, sugar, fast food, and fried foods. Here is a good article on Medical News Today that offers some suggestions -- What to eat if you have polymyalgia rheumatica: https://www.medicalnewstoday.com/articles/321683