How to address PMR pain while decreasing prednisone
I have been diagnosed w poly myalgia rheumatica (pmr). Am taking 5 mg of predisone, was taking 10mg.
Every time I go on a low dose, symptoms come back. I can't take pain meds, but do drink wine to ease pain, although I'm told no alcohol w prednisone. Anything you can share as far as info
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The bottom line is each of us is different and her rheumatologist are different and PMR pain is absolutely no fun!!!! I started prednisone at 10 mg in April now I am down to 1 mg for three weeks and then my rheumatologist said she does not believe in medication unless the pain is intolerable!!! The mornings are the worst I can hardly move every joint hurts as the day goes on and improves a little but not good. I am going to take one day at a time and see how things work out with the pain.
When I got down to 8mg some tolerable pain in the previously painfree joints came back. On John's pain scale, I had moved from 1/10 pain with zero pain in shoulders, elbows, wrists, hands and back of the knees (the only pain which never went away was base of thumbs), to 3/10 pain returning in some joints. I sat on the 8mg for 4wks hoping it would resolve by itself but it got no better. The new pain was tolerable but to me was a warning that a further reduction could only make things worse.
Whenever I reduce, some slight aches usually come back in the first week but are gone by week 2-3. Faster reductions wouldn't give enough time to see if the body is able to adjust to the new dose.
Edit: To directly answer your question about pain level after the slight dose increase, yes, I mean zero pain in all joints, apart from occasional aching twinges in the base of the thumbs and the odd finger. I have no problem with that at all.
I’ve had PMR for a year. I’m on my 2nd attempt at tapering and stalled out at 7.5 mg again this time. Gave it two weeks but had such limited functioning that I’ve now gone back up to 8 mg. I’ll give myself the respite of less pain for a week or two and then try alternating days of 8 and 7.5.
Dear @alissahe
Have you and your Dr. thought about combining your prednisone with Low dose Naltrexone (LDN)4.5
I believe that it's been helpful for me.
I was diagnosed with PMR eight months ago.
Was put on 20 mg of prednisone by my GP. The prednisone started taking my pain away within days to a tolerable level But I struggled with lots of side effects.
Two weeks after that my functional doctor included LDN.
After reading some articles about
Splitting prednisone I got permission to take most of my prednisone in the morning with my breakfast. Then 1 mg of prednisone at night before I went to sleep so that I could wake up without much pain and get a good sleep.
Today I'm down to 6mg of pred 5+ LDN in the am and 1 at night bf bed.
My functional doctor also said that if I had pain anywhere I could take Traumeel ( an analgesic) as needed. So far the journey has been tolerable and my moon face has slowly disappeared.
Good luck to you in your PMR journey.
What are the possible side effects of LDN?
I’m reluctant to take another med but I have an appointment w/ my rheumatologist in about 3 weeks and will try to learn a bit about this option before they
Look it up but I don't think that there are any.
In higher doses Naltrexone is used for a lot of other things.
I have been splitting my 5mg in half as well. Seems to work well. Going from 20 - 15 was causing too much pain but when I went to 17.5, it was good and kept pain tolerable. After a month, I went to 15, then another month later down to 12.5. I will go to 10 after Thanksgiving so we shall see how that goes. She gave me 1 mg tablets so if dropping 2.5 is too much, I can drop just 1.5.