Sorry dear, this is an old thread and I doubt Kaceygrace is still active in our community. Please feel free to begin a new thread so others can see your comments. You'll have better visibility and may obtain more responses.
Thanks,
~Tuck
Kaceygrace, I have PMR, and i am on Prednisone 10 mg daily along with Methotrexate 25 mg weekly this seems to handle 90% of my sysptoms. if it is relieving his pain, i would say think in terms of quality of life rather than lenght. yes prednisone is bad, but so is a bullet to the head. you have to ask yourself what is worse. being in so much pain that a bullet to the head is a legitimate option or a drug that will kill the pain but cause bone damage over the long term.. personally if the prednisone delays the need to take the bullet then so be it. hate to sound harsh but i went undiagnosed for 3 months and in so much pain that i could barely get out of bed let alone work or even walk for that matter. I am 62 and it gave me a clear understanding of why old people (people older than me) walk like they are in extreme pain. it is because they are.
You're welcome. :) 10 mg of prednisone isn't too high of a dose, however if that's the only thing that works for you my advice would be to get a baseline DXA (dexa) scan to measure your bone density, and have it repeated once a year to make sure you're not slipping into osteopenia/osteoporosis. Also get x-rays of your hips and shoulders; long-term use of prednisone can cause what's called avascular necrosis, or bone death, which usually affects the largest joints first. Not to scare you, just so you're aware so you don't end up like me, on Fosamax and with two hips that had to be replaced. (I probably would have had to have them replaced at some point anyway, but AVN accellerated the timeline a few years.)
Hang in there!
Thank you for the information, I appreciate you passing it along! So far, I like my doctor, but I may decide it's time for a second opinion at some point.
Thank you for your information. Yes, I was tested for everything before being diagnosed with PMR. And, I agree, although I think that was the last resort diagnosis, I do truly believe I fit the symptoms. I am still on prednisone, nothing else seems to work. The highest dose has only been 10 mg and right now the lowest I can seem to get to is 7.5 mg. But, I definitely have some days that are better than others. Good luck to your dad!! He's had it a long time, I'm hoping for this to go away soon!!
This information on the Mayo Clinic site might be helpful. http://www.mayoclinic.com/health/polymyalgia-rheumatica/DS00441
As with most auto-immune disorders, it is not well understood, there is no known cure, there is only long-term management of symptoms. It may go into remission on its own but there is no guarantee. Sorry I can't be more optimistic about it going away, but there is help for the symptoms. Sometimes it takes finding the right doctor.
My dad was diagnosed with PMR March of 2006- he still has it... They tested him for everything... finally I think they just picked PMR because nothing else made sense... I don't think that is really infact what he has... Is this what happened with you?
He has been on Prendisone since 06, so so so bad to take that every day... are you on it as well?
I'd love to know how you are feeling, and if you've found anything to relieve the pain so I could pass it along to my dad.. let me know.. hope you are feeling better!!