Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)

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Old 03-18-2011, 12:25 PM #1
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Quote:
Originally Posted by cndangel View Post
Just thought I would give you all a quick update. Last night was still a struggle. Pain meds helped take some of the edge off...but I found out the hard way if I don't take the next dosage right away the pain comes back even worse. It was around 4 am I found this out. I had slept through the time I was suppose to take another pain med. and I woke up to the stabbing pain in my head/back/arm again.
Take care,
Karen

You really should be on some type of extended release pain med, you do have a chronic pain condition correct?? Short acting meds for a long term condition just seem logical to me.

I think an extended release pain medicine makes sense and then a short acting med for break thru pain.

I know on the TOS forum that is pretty much the most of the long timers have, and usually a sleep med and /or antidepressant added too.
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cndangel (03-20-2011)
Old 03-18-2011, 06:00 PM #2
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Quote:
Originally Posted by Jo*mar View Post
You really should be on some type of extended release pain med, you do have a chronic pain condition correct?? Short acting meds for a long term condition just seem logical to me.

I think an extended release pain medicine makes sense and then a short acting med for break thru pain.

I know on the TOS forum that is pretty much the most of the long timers have, and usually a sleep med and /or antidepressant added too.
I agree! I really think my doctors need to rethink my pain management. Right now it seems they are giving me the quick band-aid fix and not managing my pain for chronic (long term) pain.

I am on Cymbalta (anti depressant) but I have not felt any difference what so ever since starting it (about 10 weeks ago) My doctors still want to give it a bit longer to see if it is going to work. In the meantime though i find myself feeling more and more depressed and the pain not decreasing at all.

I hope everyone (the doctors) start getting their act together soon. I know injections have been mentioned a few times...but nobody has even mentioned when I might start getting them.

Maybe on Thursday I will have some more answers regarding pain management, physio, therapy and what ever else i can think of to ask before then.

Take care,
Karen
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Old 03-19-2011, 10:53 PM #3
Lisa in Ohio Lisa in Ohio is offline
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Hi Karen, I am so sorry to hear how miserable you are right now. I have to PT several times and I am also a WC injury. I finally learned to just say no when they wanted me to do things that I knew would cause my pain to increase. I personally think that we let ourselves be intimidated by medical professionals, and for some reason do not think we can say NO to something that is not in our best interests. You went and tried it with devastating results, I think you can be justified in saying no more PT right now until your pain is more controllable. Lisa
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