Why does injections just have to be for a cure, if it works for pain management go for it! I liked them until it stopped working. I am on the morphine ER and it works but sometimes I need more. As for the worker's comp wish they could all just kiss our butts! They definitely give me more anxiety that makes me worse. I took some great advice (thanks by the way) and am getting an atty.
Hope all turns out well for you with the chair. Quality of life is also important not just moving all the time!!!!
Jennelle
Quote:
Originally Posted by Dew58
Well, again I was told by my PM doc that I will never be cured of RSD/CRPSI. I KNOW!!!
PM Doc also told me that blocks would not help me..would probably harm me at my stage of the disease.He stated, WC made you wait too long to have remission as a possibility. (too far gone)
Wheel Chair: I have to have lawyer deal with this issue. Doc wants me to stay as mobile as possible. Doc said the electric chairs can not be scripted for my condition,as in my current disease status. ( not far enough gone)
Also,PM doc added a new med in my already bountiful cocktail glass:
OPANA ER 10 mg. tablets taken twice a day..along with my other meds!
In Morphine family. I will see him again in 4 weeks, at which time he will bump up the mg. on the OPANA ER ( Oxymorphone;Time released).
Also, all my other meds will be scripted for 3 months and I will most likely be MMI. My maintenance schedule is to see him every 3 months..indefinitely.
I feel  nausea and  drowsy at the moment...at the same time 
Are/Have any of you taking/taken Opana ER? If yes..what is your opinion on this pain med?
Talk to you all later.
Dew |