Fellow PMR sufferer

Posted , 17 users are following.

I went to a party last night and by accident sitting outside to cool down because of sweating, one of the male guests said he was on Steroids ( Predisolone) funny  i am also on the same drug, I have PMR he said he did, but for a year he was told he had Lupus, when he was not getting better he paid to see a Rhmy  consultant who said you don’t have Lupus because over 70 you are too old. Hence he was properly diagnosed with PMR. He was put on 15mg and is now tapering down 1mg every 2 months, he is on 7mg and is feeling great except for the normal sweating tiredness etc. The interesting thing was he was told he would be cured in 2yrs I was told my adrenal glands would wake up but to be patient. Is it known that PMR does  only last two years. 

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  • Posted

    Many, about 50% go into "permanent" remission in <3 years.  Many do not.  I've had it for 8.... ugh

    Hope you are in the remission group!

    • Posted

      No not in the remission group, on 13mg tapering slowely. It makes me feel better just reading what every one  else’s journey has been, I  think I am lucky that I do not have any real life threatening illness. We may all hate PMR but we are still managing to live our lives through Pred. I am loving seeing my 7 week old Grandaughter every day and taking her for a walk in her pram. I feel blessed most of the time.

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