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Prednisone Taper Stories

Polymyalgia Rheumatica (PMR) | Last Active: Mar 5 11:55pm | Replies (101)

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Profile picture for oldflaguy69 @oldflaguy69

I was diagnosed with PMR in 2024, for a year I was treated with prednisone and initially had good luck with relieving pain. After about a year, one morning I woke up and the pain never went away, went to a rheumatologist and then was diagnosed with RA. I’ve been receiving treatment with Humira and trying to taper the prednisone. I’m currently down to 7 mg a day, from a high of 20mg/day with occasional flareups. Now dealing with an insurance plan that won’t cover Humira all of a sudden and wants me to use a biosimilar drug. My doctor and I have identified several drugs that seem to be very similar to Humira, however we can’t get them approved through the insurance. Overall, a very difficult situation and difficult at times to keep a good attitude, especially when dealing with insurance companies that just deny, deny, deny.

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Replies to "I was diagnosed with PMR in 2024, for a year I was treated with prednisone and..."

@oldflaguy69
I am 79 and just developed PMR last March. I absolutely detest prednisone, sure it helps with pain, but the side effects, in my case are destroying my life. I am at 7 mg a day now and receiving twice monthly injections of a biosimilar. So far I am worse off with discomfort and trying to reduce the Prednisone a mg every two weeks. No one seems to talk much about the attitude one develops with this disease but I, for one, feel that it is destroying my otherwise great life. Hang in there and check with local hospitals, as some have programs to make injections affordable.