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.
37 likes, 145 replies
jan52617 Emis_Moderator
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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.
celia14153 jan52617
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BettyE celia14153
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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.
jennybshaw Emis_Moderator
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erika59785 jennybshaw
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randy79521 jennybshaw
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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
jennybshaw randy79521
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g.95482 jennybshaw
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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.
Anhaga jennybshaw
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I'd give up some of the housework and do one of the fun things instead.
Anhaga
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MR._BELLA Anhaga
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Anhaga MR._BELLA
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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.
MR._BELLA Anhaga
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connie28112 jennybshaw
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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!!
jennybshaw connie28112
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connie28112 jennybshaw
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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.
lois41428 connie28112
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margot34956 jennybshaw
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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.
jennybshaw connie28112
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connie28112 jennybshaw
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