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@fam8284

I was recently diagnosed with
PMR and received a prescription of 5mg prednisone to be taken daily.
I’m 75 yrs old and have been reluctant to start the meds. I’m always concerned about side affects. I’ve alway tried to take natural remedies but due to pain and this diagnosis I’m thinking I may have to take the prednisone. I’m glad I found this support group and I’m hoping to find the best solution for myself by hearing others experiences.

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Replies to "I was recently diagnosed with PMR and received a prescription of 5mg prednisone to be taken..."

79 here. Have osteoporosis, but didn't see any real choice because the PMR could get worse, and I was in a lot of pain. Was also afraid of Giant Cell Whatever. Started with 15mg end June, which was increased to 25mg after a week because change was minimal. A few days after that, improvement was very noticeable. Now I'm down to 10mg, entirely functional and almost without discomfort other than minor shoulder and arm aches. Most of the day, I don't think about having PMR. Now I mow the lawn vs. the earlier time when it was a struggle to put on clothes.

Are you only supposed to take 5mg as your starting dosage?

It took over 4 months to diagnose my PMR. I could barely walk. I was so sedentary and in bed for extended periods of time. I even developed a decubitus on my back side. My rheumatologist missed my PMR. It was my PCP who diagnosed my PMR and started me on 15 mg of prednisone a day. Within 36 hours, my pain was reduced by 90%. I took it for 4 months, than began a slow taper off of it. That was 3 years ago. I have not had any signs or symptoms of PMR since then.

The prednisone was not fun, and I developed a ‘double’ colon infection which required a 3 day hospitalization. Even with that, the prednisone was so very helpful and worth the side effects.

I hope you are able to get your PMR under control quickly.

Hi Fam, I was recently diagnosed (May 2023) and am/was a very healthy 76 year old. I too was reluctant to take medication (prednisone) but the pain was so unbearable and limiting I had no choice. I started at 30 mg with a slow taper. Fast forward and now I am at 8 mg. I have experienced no pain or flares and can almost forget I have PMR…haha. I see my rheumatologist once every 6 weeks and get blood work done for that visit. Her goal is to reduce prednisone to 0 mg. I am tapering 1 mg per month. We shall see. Because of the possible side effects of prednisone I am taking calcium, vit D, vit K, pepcid and fozamax. So far I haven’t noticed side effects. Am also following a modified Mediterranean Diet with little or no salt or sugar. Good Luck and have patience. Liz Ward

Hi @fam8284, I understand your reluctance to take Prednisone, but most people who suffer from PMR experience a dramatic relief from symptoms after taking it. 5 mg sounds like a low dose - I think the usual for PMR is 15 -10 mg.
I had PMR, then GCA for a year, undiagnosed, so no prednisone, just constant pain and other strange symptoms. Was diagnosed with GCA after a temporal artery biopsy and put on 40 mg, with tapering down every two weeks. I was on it a year and a half, and have been off prednisone now for nearly a year.
My mother-in-law had GCA as well and didn't want to take the prednisone, but was told she could go blind or have a stroke if she didn't. She took the Prednisone and was cured of GCA eventually with no flareups,. She lived to be nearly 100.
I hope our stories help you make a decision.