PMR - What do you wish you had known . . .
Each of us has been on a journey with a disease that is not well understood, common but not identical symptoms and the steroid treatment is scary and problematic with its own side effects.
What is the one or two things you wish you had known early on that helped you put the pieces together and helped you better understand what is going on with you and your body.
Please share so we can learn from each other.
Interested in more discussions like this? Go to the Polymyalgia Rheumatica (PMR) Support Group.
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@pmrnew I was diagnosed April 2024. Started with 20 mg prednisone which worked like magic and brought my CRP and SED numbers back to normal. I was treated by my primary care doc as he had experience with PMR and no rheumatologist in my area. I stayed at 20 a month and then started tapering in 5 mg increments. All went well until I got down to 5 mg and had a big flare. Went back up to 10 mg and came down using a much slower taper until I got down to 3 mg - another big flare. At this point my doc referred me to a rheumatologist in another city, thinking I might need a biologic. It took a long time (several months) to get an appointment. In the meantime I read on this site about the slow taper method for use with low doses that I shared here. I discussed it with my doc and we agreed that I would try it, monitoring and adjusting the dosage myself, and just keeping him updated periodically on my progress until I could see the rheumatologist. By the time my appointment came I was doing well and at 3.5 mg - rheumatologist said I should stick with this taper schedule as it’s obviously working for me. Had new bloodwork recently and my CRP and SED levels were normal. I asked the rheumatologist if I could just stop the prednisone since I’m at such a low dose, and he said no - that I should follow it out to the end. I’m at .5 mg now - will stay here a week and then start the steps down to zero if all goes well. I give my primary care doc a progress update every time I get down by another mg. I wish you the best of luck with your taper. I never realized that these last few mg would be so challenging and was very surprised when I flared again (with high blood numbers) at 3 mg!
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1 Reaction@dadcue indeed everything you say make s so much more sense with the nuance. And with what you just said, maybe, just maybe the worst is behind me. And yes I am and just 2 weeks ago was in Zeist visiting family.
@cyndip wow, so you have been on pred over 2 years. When you tapered below 3mg and had a flare, that immediately reflected in CRP and ESR? Yes, so the last little bit, very slowly.