Reducing pred: dead slow and nearly stop method

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Copied from Eileen's post in another discussion.

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."

Further comment from Eileen in original discussion:

Can I add a codicil to the very slow reduction plan in the above post:

When you are at doses below 5mg it is a good idea to rest at each new dose for a month at least before trying the next reduction. At this point you risk overshooting the dose that is controlling the inflammation so waiting a short time to see if symptoms reappear is helpful. If you just continue there is a possibility that you get to very slightly below the "right dose" and inflammation will start to reappear very slowly. The blood tests will lag even further behind the dose reduction - there must be enough inflammation to increases the proteins being measured for the blood tests to rise.

Someone has asked this question:

"I'm at 7mg going down to 6mg, and I'm at the point where I'm starting to shift from more 6mg than 7mg, but I can tell the pain is returning. So...do I jump up big to say 10mg, or try 7mg or 8mg? I hate the very idea of going up at all, but it is what it is."

My reply was:

No - you go back to the last dose that worked well immediately and stop the reduction. This isn't a "flare", this is your body telling you that you have got to the dose you are looking for: the LOWEST DOSE THAT MANAGES THE SYMPTOMS. It doesn't mean you won't get lower, it just means not yet. However slowly you reduce, whatever scheme you use, you will not get below that dose without a return of symptoms because of left-over inflammation that hasn't been removed by the amount of pred you took. It is if you ignore these warnings that you will allow a build-up of the inflammation to the stage where you will have a flare on your hands.

To comment on something someone else said - you have differentiated between steroid withdrawal and a return of symptoms by using DSNS. If you were going to suffer with steroid withdrawal you will notice it the first day you use the new lower dose. That is the idea of DSNS - you go back to the dose your body is happy at for a few days and then show the new dose to your body again. For me it usually takes about 3 times for my body to accept the new lower dose and stop complaining.

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  • Posted

    I'm brand new here so I'm probably not following the correct protocol.  I have been on prednisone for 3 years starting I think on 50 mg and was until today on just 2 mg with no pain UNTIL my son died 2 weeks ago, and today I'm in pain ALL OVER.  I have a regularly scheduled doctor's visit in a couple of weeks, but I believe I've figured out that prednisone is in my case due to stress.  When I first began prednisone because of all-over pain, my son had just been diagnosed with a terminal disease.  Now, as I said, I am way down to just 2 mg a day and today the all-over pain came back and - guess what - most extreme stress ever in my life now with my precious son dying. I had taken 2 mg this morning and with the pain this afternoon just took an additional 2 mg.  We'll see,  Thanks.

     

    • Posted

      You are absolutely right to up the Pred when you are in the middle of this shattering experience of the loss of your most precious son. Take what you need until you feel less numbed and shocked. You can do without the increase in physical pain whilst dealing with all that’s happening at the moment. I’m pretty sure emotional stress impacts on our symptoms and thank goodness treatment helps. My heart goes out to you and I am sending you the biggest warmest hug, Celia
    • Posted

      What celia says is absolutely what we have all found in times of stress and yours is extreme. My sincere condolences.

      Not sure where you are; I'm in UK and we can leave a message at our surgery for GP to 'phone us. Would that be a reassurance for you if you are worried about what you are doing is right.? Two weeks is a long time and sadly typical these days but I think urgent cases are treated sympathetically.

  • Posted

    I am down to 12.5 mg of Prednisone.  My pain is not too bad but I have never in my life felt such tiredness.  Could someone please tell me if they have suffered these symptoms.  I don’t see anywhere where people are complaining of abject tiredness.  Please help if you can because this is a living death and I am taking care of my husband who is also ill.
    • Posted

      Yes, fatigue can be a real problem with PMR.  Pacing helps me, and taking breaks ever so often.  This is especially tough being the caretaker for your ill husband.  My heart goes out to you.
    • Posted

      Jenny, sorry to hear about the tiredness. Fortunately, my tiredness disappeared after the diagnosis and I began taking 20mg/day of Prednisone. I was so tired for the previous 2 months before diagnosis,I could not exercise. One morning, I could not move literally. I was paralyzed and lying in bed. 

      After a visit to the doctor and 11 blood test for everything from , Rocky Mountain Spotted Fever, PMR was diagnosed by my doctor.

      He put me on 20mg and said to call him in 3 hours, if the pain was subsiding quite a bit he had made the correct diagnosis.The regimen was 20 mg for a month, then to 15mg. After seeing a RA specialist here in the US, she reduce me  to 10 mg/day for a month then 9 and now on 8mg/day for a month. Her plan is to reduce me by 1mg/ month until I can hopefully come of the Prednisone completely. Blood test are taken on every monthly visit. Coming off Prednisone at a faster rate can cause problems unrelated to PMR.

       

      I have a bit of stiffness in my left hand, but that is all. I am still playing golf and back to the YMCA daily.

      I hope this helps. It has been an interesting battle that at 60, and very active, did not expect to see.

      best of luck

      USA

    • Posted

      Thank you for this Randy.  I am on a similar reduction to yours and just hope that with the reduction the tiredness will go away.  I too used to be so active, swimming, walking and gym every day but now have trouble just doing my housework.  I hope you continue in the way you are going on now.
    • Posted

      I'm over 75 and started over a year ago for pains from my shoulders to my knees. I was put on 60mg/day. I'm now down to 2mg/day. I made it to 1/mg, but the pains returned in both my wrists, so I'm slowly trying again.

      Sorry to hear about your tiredness Jenny, but that's not one of the symptoms I encountered. Hope you're feeling better soon.

    • Posted

      I'd give up some of the housework and do one of the fun things instead.  twisted

    • Posted

      In fact I have... One reason my poor home is a bit of a tip these days is because I absolutely MUST have my daily walk(s).  
    • Posted

      I started daily walks on my treadmill about 7 days ago. I was on pain when i started and still have pain but the pain is not any worse. I walk 1 1/2 miles on a incline of 3 to 6 % grade. I have made up my mine to do this every day no matter how bad the pain is that day. Am i wrong or right to do this? I have osteoporosis and i am not taking any drugs for it and i am not going to.
    • Posted

      It sounds like a plan.  I find when I use a treadmill it's so crashingly boring I tend to go too fast just to get my distance in quicker!  Just pace yourself.  I'd hate to think you might be injuring yourself by going a bit too fast.  Better to start slow and easy and work up gradually as you get used to it,  All the best - I'm sure you are doing the right thing with this resolve.  

    • Posted

      Thank you, I walk at a rate of 2 miles per hour and walk 30 to 50 minutes.
    • Posted

      Jenny-

      I experience fatigue - you are not alone in this.  Caring for your husband must be very stressful and can trigger many aspects of the disease to be sure. I am 55 and up until my PMR diagnosis & symptoms, I had so much energy. I can’t keep up with my friends and when I try, I have a setback of pain and fatigue.  Pacing myself is an experience of trial & error but so necessary... at least for some of us!! 

    • Posted

      Connie, thank you for this.  I did get down to 7mg but started to experience terrible pain and abject exhaustion.  I went back to 9mg and for the first few days felt a lot better but since have been very tired and very painful.  I will not go up any further.  Have also been suffering with some bad intestinal problems.  Anyone else had this?  Boy I am sick of whining.  It is not me.  Wouldn’t it be great if we could have a huge meeting in one of our countries where we could all get together and talk about it then have fun.  I’m sick and tired of being sick and tired and I want fun!  Anyone else?
    • Posted

      Jenny - I too have intestinal issues.  I was on 6 mg but recently increased to 8mg due to pain and severe dryness in many areas- eyes, throat, skin, sinuses. I have difficulty with my bowel movements - it comes and goes. From diarrhea to the opposite!  I take care in what I eat to try to promote regularity: I have added flaxseeds, flaxseed oil, avocado, dried prunes, even Laxaday & senna tea.  I was diagnosed with collagenous colitis a couple of years ago.  I have apts with a variety of specialists to see if we can figure out what is going on or if it’s a “flare” of some sort and I’m seeing my Rheumy for follow up in 2 weeks... I will let you know if I get any additional info or insight. 

    • Posted

      Could the ‘dryness’ symptoms be due to Sjorgen’s syndrome?  - another auto immune complication.
    • Posted

      Hi Jenny, Exactly what I said too, sick and tired of being sick and tired. Also love your idea of a huge meeting to talk and have fun!

      All the best to you, it's quite nice to know you are not alone.

    • Posted

      Thanks Connie.  Glad I’m not alone in this.  Me too up and down with intestinal problems.  Had tests , no infection or anything so we will see what comes next.  We’ll keep up to date.
    • Posted

      Yes I too had lots of tests ... even my inflammation markers are low despite the fact that we can see inflammation in many areas of my body, eyes, etc. Oh well, we need a good Doctor who will listen and keep on believing us when we say something’s wrong!

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