Head & Neck Sweats

Posted , 5 users are following.

GCA on 35mg pred am getting head and neck sweats, could this be the Pred?

Thanks

Sue

0 likes, 6 replies

6 Replies

  • Posted

    well I don't know whether it's due to the predisolone but I too sweat a lot round my neck during the night - my hair around the nape of my neck is wringing wet!   I think it may be part of the PMR and GCA
  • Posted

    Both PMR/GCA and pred seem to cause sweats - some people have all-over sweats some just head and neck sweats. It is probably imbalances in the hormones secreted by the pituitary gland in the brain that make the entire body function - they affect the thyroid, the adrenal glands, pretty much everything. They do seem to get better as time goes on.
    • Posted

      Hello Eileen. I saw your instructions for coming off the steroids and I wanted to print it off but I just can't find it now. I seem to be loaded with e mails and I can't tell which one was the one I needed.  I don't think Ive got the hang of how to use this forum correctly or manage the e mail.

       

    • Posted

      Here you are:

      A group of us worked out reduction schemes individually that have allowed us to reduce far further than ever before but they are all basically the same - and they were based on a scheme a Swedish gentleman worked out when he simply couldn't get below 3mg without pain. Img at that level is 33%, 1/2mg is 17% - way above the 10% that has been recommended for years. So he used table to see the daily doses and took the new dose on one day, old dose for a few days and then proceeded by repeating that and then reducing the number of days of old dose - until he got to everyday new dose. It worked, he got off pred and has been off pred for at least 3 years (it could be longer). Something similar to mine is being tried by a consultant rheumatologist in the north of England and he too finds it works for every single patient he has given it to. As it did for several ladies beforehand.

      My reductions are VERY slow. I use the following pattern to reduce each 1mg:

      1 day new dose, 6 days old dose

      1 day new dose, 5 days old dose

      1 day new dose, 4 days old dose

      1 day new dose, 3 days old dose

      1 day new dose, 2 days old dose

      1 day new dose, 1 day old dose

      1 day old dose, 2 days new dose

      1 day old dose, 3 days new dose

      1 day old dose, 4 days new dose

      1 day old dose, 5 days new dose

      1 day old dose, 6 days new dose

      By that stage if I feel OK I feel safe to go all new dose. I suppose you might be OK starting and stopping at "1 day new, 4 days old" but I was terribly sensitive to steroid withdrawal pain so I err on the safe side. Once you get to the "everyday new dose" - if you feel OK you can start on the next reduction, no real need to spend a month at the new dose.

      This avoids steroid withdrawal pain - which is so similar to PMR pain that you often can't tell which is which and some of us suspect that many flares are NOT the PMR returning but problems with steroid withdrawal. Using a scheme like this also means you can stop immediately if you have any problems - you might be fine at one day old dose, 2 days new (lower) dose but not at a 3 day gap - but you have dropped your dose a lot and that is the idea. It also isn't as slow as you would think - you can reduce at a rate of about 1mg/month on a continual basis.

      The Bristol group start new patients with PMR with 6 weeks 15mg, 6 weeks at 12.5mg and then a year at 10mg before continuing the reduction and that achieves a far lower rate of flare (20% instead of 60%) and I suspect their flares then come below 10mg as they then do the 1mg at a time reduction. Just below 10mg is a common dose for people to get stuck at - and I (and others) believe it is because even 10% drops are too much for many patients. These patients are then labelled as "steroid resistant" or told they need methotrexate to help them reduce but we have seen this slow reduction work for those patients too. We believe that methotrexate (MTX) works for patients who have late onset rheumatoid arthritis (LORA) or LORA and PMR together. Very few patients get off pred altogether when taking the MTX - those who do are probably the mis-diagnosed LORA patients - or another arthritis that responds to MTX.

  • Posted

    I believe it's GCA that causes sweats.

    My husband had them badly before he was diagnosed with GCA . Now he's on pred he's better.

  • Posted

    Hi, I just wanted to say that I too have head sweats. I refer to mine as hot flushes. They are just in my head. I have been on Prednisolone now for 5 weeks, for PMR. My 

    GP has agreed that I should follow the Bristol plan so Ihope to be starting slow reduction in a weeks time. My head sweats happened quite a lot when I first started the Prednisolone. I never had them before taking the steroids so I just presume it is a side affect that I just have to put up with. Fortunately it is getting much better and some days I don't get them at all now. Hope it gets better for you.

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