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I have been diagnosed with CP. My doctors currently are not doing much to help, although I do see someone soon about possibly getting a celiac plexus block. My doctors have put me on Creon and Phenegren for nausea. Nothing for pain. I find myself going to the ER once every 1-2 months because the pain and nausea get overwhelming. They do bloodwork, declare it's not a case of AP and send me home. I feel like an idiot everytime it happens, but I honestly do not know what else to do.
What I want to know is how does this compare with your CP experience? When do you feel it is time to go to the ER? Or do you? Are there any doctors out there who will treat the pain medicinally or have all the crackheads ruined it for everyone? I guess I am just looking for some help.
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