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Pain Management For RA

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Hi All.

I don't post as often as I used to, but I still try and get online to

read the posts from time to time. I have RA, Sjogren's Syndrome, and

was also diagnosed with Multiple Sclerosis this past December.

The issue I am having is with pain. I find that the more Prednisone

I take, the less swelling/pain I feel in my joints. But the more

Prednisone I take, the more weight I gain. It's this vicious cycle!

I have had to slowly taper down my Prednisone over the past few weeks

to prepare for some dental work that will be done next week. I will

also skip my MTX for that week as well. My Doc just wants to make

sure that everything heals up good and that I don't have any more

problems. I find with the Sjogren's that my teeth are literally

crumbling out of my mouth. This will be my second extraction in

about 8 months.

As my Prednisone is tapered down, I am noticing more and more of the

RA pain. I take my Tylenol 4's with Codeine, but they do little to

help with the pain. I have tried so many different pain meds, and I

now feel as though nothing works. I have tried the pain patch,

Oxycontin, Percocet, and even Morphine injections. I feel woozy or

dizzy, but I still have the physcial pain. I think the longer I take

pain meds, the less likely my body is to respond to them. Sometimes

I just take them because it makes me feel like I am doing " something "

to control the pain.

Just needed to vent. I am in Canada, and have a Rheumy that refuses

to prescribe pain meds. Fortunately, my GP is wonderful and has done

what he can to find the right med for me. We'll keep on trying!

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