Weaning off of prednisone & pain management
Last Tuesday, I went down from 7.5 mg of Prednisone down to 5 mgs. For the past 4 days my pain level has been a 12 out of 10. I could barely walk. Although I hate to take Advil, Motrin, etc., I took 2 Advil Gels and within 1 hour I felt better (not perfect, but a lot better). Hours later the pain started to come back but was maybe a 6 out of 10. The next morning I was crippled by the pain all over again. I forced myself to get moving, but could barely get around. Drank a lot of ice water, and before I went to bed, I raised the head part of my bed up and fell asleep. Woke up this morning with very little pain. Has anyone experienced any type of correlation between raising your head up vs laying flat, and the amount of pain you will experience? Had that slight change made that much of a difference in your pain level? I have found that drinking almost all my drinks with a lot of ice, definitely helps with internal inflammation. What are your experiences or thoughts regarding this matter? Thanks!
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I crashed and burned countless times at 7 mg of prednisone. After Actemra was tried, I parachuted down to 3 mg and hovered there for a while. After my cortisol level improved, I had a relatively soft landing. I still needed some recovery time after getting off prednisone.
I don’t want to play the PMR/prednisone taper game ever again! It was too stressful and my adrenals couldn’t handle it.
Thanks! You're always helpful.
It really is stressful!
For kidney health, wild lettuce is probably not a good option as it's high in oxalates, not good for kidney health. Some other things like turmeric are also high in oxalates. While we're trying to solve one health problem, we don't want to create others.
I agree that PMR and its complications can get worse after a flare, which is a good reason to try to avoid a flare and keep inflammation under control. When we have a flare the prednisone is increased and the total consumption of it is higher than a slower more cautious reduction under 10mg. Higher total consumption increases the problems, harms and side effects of prednisone. I'm on my second reduction, now with new post-flare complications like Morton's Neuroma pain in the balls of feet affecting walking, and new nodules on the joint of my big toes. Didn't have a problem with feet at all till after the flare.
Good luck to everyone as we try to deal with this all the best way we can.
My husband takes arthritis strength Tylenol. Recently had steroid injections in both hands which has helped. At some point he may try the aspercreme.. Trying one treatment at a time to see what helps the most.
Thank you! Maybe there is a light at the end of the tunnel after all.
Tapering now at 2.5, and based on the experience of another contributor, I tried and seem to be getting substantial relief from residual (non-PMR) lower back and shoulder pain from Tart Cherry capsules, an anti-oxidant. No theory on whether this is incidental, correlational, or cause and effect.
With the exception of an NSAID taken twice with Prilosec and with the doc’s permission, I have not tried any other remedies, so trying this or another anti-oxidant might be significant. Check with your doc. Good luck.
Fresh cherries are the only fruit I eat, for about a month a year while they're on my tree. I pick and eat them liberally without caring about carbohydrate/sugar content, the only exception to my low carb diet. Both sweet and tart cherries are said to be good for inflammation - that'll do me as a reason for hopping right into them, delicious with lots of plain yoghurt too. I can't say if they help with pain because last cherry season I had no pain at 7-8mg of prednisone anyway. If something is said to be good for us, I'd rather eat the natural food than take a supplement, but there are limitations to availability with seasonal foods of course.
Now I'm interested in Tart Cherry capsules. I have residual (non-PMR) lower back pain but I'm told that I need a lumbar fusion for that.
I'm off prednisone and on Actemra which works infinitely better for me. My rheumatologist is able to consider other causes of pain since I no longer take prednisone. When investigating why I had uric acid kidney stones, a rather high uric acid blood level was discovered. My rheumatologist thought that maybe gout was "contributing to my residual pain." My uric acid level was treated for a while but I said I didn't feel any different. The treatment for gout was stopped even though my kidney stones all but disappeared. My rheumatologist deferred to a urologist who subsequently said my uric acid level "probably" should be treated by my GP.
My uric acid level is rather high again but it isn't being treated. Maybe I should take Tart Cherry just to see what happens. They sound delicious. I love cherry pie but maybe I should stick with the capsules!