I have tapered from 15mg to 9mg but could not get down to 8mg, so back to 9mg for the last month. Visited my GP yesterday and he says to stay at 9mg until March! It won't do me any harm! I was hoping/planning to reduce to 8mg very slowly next month and if successful carry on that way, so now I do not know whether to follow his instructions or go my own way! I suppose I could try and see, or do as I am told! Any thoughts?
To taper or not?: I have tapered from 15mg to 9mg... - PMRGCAuk
Bearing in mind how many PMR sufferers experience difficulties tapering below 10 mg, including myself, my inclination would be to follow your GP's advice, even though you might not wish to do this.
You may get away with the reduction you describe, but in the long run, what is a few weeks if it saves you a flare with all that that means.Sounds to me you have good GP!
Good luck whatever you decide to do.
PS: for sure others will be along with their advice.
Good advice from your GP - what a sensible person!
Stick at 9mg, it will help you stabilise nicely, help you through the “excitement” of Christmas, and the worst of the winter weather. And probably help you in the long run.
As we’re always saying - there’s no rush - your PMR’s not going anywhere soon!
And hang on to that GP!
I think you have a very sensible GP. There are rheumies who say not to reduce over the winter - cold weather doesn't help.Nor the stress of the holiday season.
It took me over 4 years to get below 9mg - with a lot of mini-flares in the meantime. I have never let anything get out of hand since.
The guy I saw 2 years ago when I had what eventually turned out to be just a flare told me not to worry and try to get back from 15 to 8mg by the end of the summer. I did - it is a lowish dose that should do little harm. And 1mg here or there really isn't much in the great scheme of things! If you have a flare and have to go back to a higher dose then the "advantage" your forced reduction gained you is wiped out in just a few weeks.
That’s natural, but you have to remember that so long as you have PMR you are going to need some pills, or course the doses gets smaller (hopefully) as you go along.
But it’s the PMR that decides when it’s time to go, not much anyone can do about that, except live with it, and manage it rather than let it manage you.
It different to most illnesses, and that’s what many people find difficult at the beginning, but once you accept it not going anywhere fast life becomes a lot easier.
Hello Kathleen, Yes tapering is very much personal trial. It appears once a person has started down a test path and reached a point where it flares again, that is your rock bottom. So back up again to a dosage which works. Looking at many personal trials on here, the longer a person can keep away from a flare up, the better the chance of a return to normal, eventually.
That agrees with my rheumatologist 'silver recommendations. When I get to 8mgs in Feb or March I am to stay on that dose for 6 months. The thinking behind it is that this condition is not going to go away any time soon, so appease it till you reach a reasonable time frame to lower your dose further.
This seems to me to be a realistic approach to a disease that is not going to go away any time soon!!!!!
This is all so reassuring. I think that, like others, I did not really believe that I had a long term condition and that it would all be over in a few weeks. I am now beginning to accept the longer term situation and understand how it all works and to live accordingly with regular resting and pacing life generally. I suppose it is a good thing that I am constantly being told how well I look! All down to the pills! I must now learn to be a patient patient!
P.S. I like the Welsh name!