I check back to the site all the time for advice but I don't usually comment. I was in ICU 6 weeks ago with Sepsis I'm doing a lot better now and am going to ring my Dr. Tomorrow as I want to take 10mg instead of 5mg for 4-5 days and then go back down to 5mg. I can't remember the initials of inflammation markers I think it's CPR and letters beginning with E. Can you help me please?
I can't remember inflammation markers CPR and E - PMRGCAuk
I can't remember inflammation markers CPR and E
CRP and ESR
C-Reactive Protein and
Erythrocyte Sedimentation Rate (
Why if you want to go up? Are you having a flare?
I am pretty sore my lower back etc and I was thinking of the sick day rules x
Okay….sorry to hear that… but if you aren’t flaring just wondering if ordinary painkillers might be better if the pain isn’t caused by PMR [which it my or my not be] or have already tried that? But guess you have to see what GP thinks/says…
Pain killers and heat pad aren't doing much x
In that case then perhaps you need to treat as a flare -this includes advice -
healthunlocked.com/pmrgcauk...
Read yr advice. I couldn't remember if it was 4-5 days or 7 days that you could take double steroids and then go back to previous dose but I think maybe I should do 14 days and taper as I don't know if I was getting steroids while in ICU and resus. Thank you very much
As you’ve been out of hospital for a while….and are having issues I’d treat it as a flare [SDR are slightly different] - so you can stay on the extra 5mg for up to 14 days [so as you say 10mg] without having to worry about the tapering back down .
I think if I were in your shoes rather than going back down in one step, I’d try stepping down to say 8mg for 5-7 days then to 6mg - always better to be just above previous dose.
When you are sure 6mg is okay, then you can recommence your previous taper as and when you feel it’s right.
Sorry to hear you've been ill. Glad things are improving.
But why do you want to take more now? Did they up the pred dose when you were in hospital in line with Sick Day Rules?
No they didn't as I was in recus. and ICU for 2weeks (I'm only guessing as I don't rem.) Then I was in ward In Ulster hosp for another 2 weeks. Apparently I nearly died a few times and they sent me to ward to wake up or die, but I'm a stubborn wee coot it seems and I woke up the first week in ward it was still touch and go. I'm in a wee nursing home for a few weeks respite and because my back is really sore I remembered sick day rules but couldn't remember ESR to ring the Dr tomorrow x
You were a very lucky bunny! I would hope they noticed but part of the problem could have been you needed more corticosteroid. People who travel via Resus and ICU often don't get a second chance.
I had Sepsis so I've been very lucky x
I have recently had blood tests for GCA and the two that were raised for me was
Erythrocyte Sedimentation Rate - Sed Rate
C - reactive Protein test - CRP
Hope this help and best of luck for tomorrow
Welcome back. What a terrifying time you have had! Sending you good wishes and a warm gentle hug 😘
What was the cause of the sepsis?
Oftentimes steroids are given IV, in hospital, because of the inflammatory response to the infection.
Your body had a great stress.
I was supposed to have a haemorriodectomy (not spelt right) op. on the Tues after I ended up in A+E. The Haemorrhoids had caused a bowel prolapse front and back. I have bowel incontinence so some faeces had got where it shouldn't be, that's my understanding. Yes very big stress I'm just so grateful to be alive
I hope conversation with Dr went well. Best wishes to you for a good recovery. Do what you need to feel well again. 💗🍀
I tried yesterday but the phone lines closed early (I rang at 9.30am the same has happened today so I will have to ring back at 2pm)
I finally got through to Drs they have agreed to me going up to 10mg for 1-2 weeks, then down to 8mg for 1 week, then down to 6mg then down to 5mg when I'm ready. Dr asked me where I got this taper and I told her PMR/ GCA site that the Dr. had told me about when I first was diagnosed. She said "It sounded safe to her" so thank you Dorset Lady x
Brilliant!
I'm getting home tomorrow yippee I have a Benign Brain tumour which was found in June. The neurologist rang me today and assured me I didn't need any more MRIs as they think I've already had it for 10 years as it's well calcified and it shouldn't give me any trouble ( I had thought I would have 10 years before it would grow big enough to cause any symptoms) so that is brilliant news. I also have a numbness in my face and food doesn't taste right and she says I had Bells Palsy in 2015 and they believe it's from that, like a scar on a nerve, it's so good to finally have an answer. I Told her after having purried food in hosp. Everything now tastes lovely to me lol. Thank you all for listening to me and for all the advice I've been given over the past few days and years since I was recommended PMR/GCA site. I will continue to read posts etc even if I don't post xxx
Just take it easy - being well enough to go home isn't the same as fully recovered! Take some time to get back into the daily routine you haven't had for umpteen weeks!