FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
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) |
|
Thread Tools | Display Modes |
![]() |
#1 | ||
|
|||
Junior Member
|
AJ is in the hospital 300 miles from home. Her dad is with her.
The doctors have cut her oxy in half, and are giving her slightly over the equivalent of her oral dose of Dilaudid in the pump, if I read the online conversion charts correctly. She's in great pain, worse than before, so bad she can barely talk. The doctors won't be in until late this evening. DH called the doctor this afternoon to let him know her pain is so bad. The doctor told him that she has to get out from the comfort level of her oral meds (comfort? Does 2 years of not being able to sleep for the pain and being stuck in a wheelchair, count as comfort?), that she is getting more than her oral dose in her pump (true, of the oral dilaudid she was taking, but her oral oxy dose has been cut from 960 mg a day to 480), and that they would increase her meds tonight, but they wouldn't give her enough to kill her. He said it's her last chance and there's nothing else. He is supposed to be one of the pioneers, the best in RSD treatment. Then he said that she is a very anxious young woman, that he knows it's hard for parents to see their child in pain, that maybe her dad should go home, and that if we persist in meddling, they will not proceed any further. We really don't want to meddle, but we don't know what's going on. AJ is ready to crawl out of the hospital. I thought they would get the pump working before they cur her oral meds so much. We don't know what to do. Is she going through withdrawal? Is the RSD spreading? She's begging us to listen to her. What do we tell her? |
||
![]() |
![]() |
|
|