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@josiemc24

HI! I am new to the board. I am 71 and I was diagnosed last June 2nd with PMR.
I had no idea what happened. I woke up that morning and couldn't move my arms or legs. After a struggle and with help from my husband, I was able to get out of bed and took 800 mg of ibuprofen. I tried getting hold of my Dr. but because of Covid, I could only schedule a virtual appt., he sent me for bloodwork and put me on 40 mg of prednisone. When the results came back my SED Rate was 40. He suggested that I see a rheumatologist. Two weeks later I saw a rheumatologist and she weaned me down to 20mg. The pain was gone. I didn't want to do it. I didn't understand the ramifications of the high dosage of prednisone. I was feeling great! I was up at 4am cleaning, washing windows, cleaning out closets, etc. I was scaterbrained, never able to finish a Sentence, it was as if I was high! She (my Dr.) brought me gradually down to 10mg. I have been able to drop it lower to 6mg at present. On January 1st I developed Covid. I received the monoclonal antibody infusion on the 4th. It kept my symptoms to aches and pains. My problem is that I can't stop the aches and pains. It is mostly in my arms, back of my legs, wrists and sometimes fingers. I dont want to up the prednisone. Has anyone had Covid with this PMR? Has it brought back the pain? I am also loosing my hair. I am trying to find out if this a side effect of the PMR, COVID OR THE INFUSION I HAD. I am scheduled to get my first vaccine on April 6th but I am hesitant to do so because I feel I am in antibody overload now. MY rheumatologist never heard of anyone loosing their hair from PMR or steroids. As I am reading through the posts, it looks as if others are having ups and downs with their symptoms.
Do I have to resign myself to the fact that I will always have some form of pain? Thank you for any comments!

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Replies to "HI! I am new to the board. I am 71 and I was diagnosed last June..."

Hi @josiemc24, Welcome to Mayo Clinic Connect. I'm glad you were able to see a rheumatologist. Both occurrences I've had of PMR I was started at 20 mg prednisone and the pain went away within a few hours of taking the first dose. Then it was a tapering process to get off. The first occurrence took me 3-1/2 years to taper off, the second time 1-1/2 years to taper off. Hoping someone else may have had COVID and recovered that can share their experience with you. I've had both Pfizer COVID vaccine shots but have never tested positive for COVID thankfully. The pain symptoms can come back if you try to taper off of prednisone too fast. I've never heard of PMR causing hair loss either but did find this statement in a search...

"Symptoms of polymyalgia rheumatica - Fatigue can be another characteristic symptom. People suffering from this disease have more and more difficulty getting out of bed and starting their daily activities. Other symptoms include: Hair loss that has happened because of a loss of appetite." - Polymyalgia rheumatica (pmr): what is it, symptoms, causes ...: https://www.topdoctors.co.uk/medical-dictionary/polymyalgia-rheumatica-pmr#

Giant Cell Arteritis is a related condition to PMR and one of the symptoms is facial swelling and hair loss - "headache, symptoms of polymyalgia rheumatica, low-grade fever, fever of unknown origin, loss of appetite, depression, joint pains, weight loss, hair loss, and ..."
- Giant cell arteritis presenting as facial swelling - Pub Med: https://pubmed.ncbi.nlm.nih.gov/18926062/

Did your rheumatologist mention anything about Giant Cell Arteritis (GCA) or ask about pain around your temples or scalp?