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Glad to hear she is being admitted, so they can keep a watch on her. They can rehydrate her fairly quick.
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They've already gotten 2 quarts or liters (whichever it is they use) of fluid into her, and the TPN to be started shortly. I'm sure that will help a lot.
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My every other week blood draws were taken from my arm (not port). There shouldn't be any hormone treatments afterwards (for the standard colon cancer chemo tx). Quote:
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Preliminary info says that she'll be in the hospital at least until early in the week, then going home with the TPN and IV fluids....I'm guessing done through the port (?)....but long term. And they'll set up nursing services for her at home when she does go home, too. The thing that may come into play is the tests being done to determine why she still has pain in her abdomen....and whatever those show. When we spoke last night, she was glad to be back in the hospital...and I'm relieved that she's there too so they can get a handle on this weight loss and dehydration.
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![]() intervention~ When you don't feel well, and you live alone, the last thing you want to do is eat. Sometimes fatigue is greater than hunger, and walking to the kitchen to get a box of cereal, to eat dry, just isn't worth it. Dehydration can occur from the obvious manners...sweating (fever), diabetes, Diarrhea...and even what a patient under going chemo thinks is *just from the chemo*, lots of fluid gets lost. Vomiting (?) Nausea can come from dehydration and or the chemo. The inability to eat or drink will bring about weakness. Eating, well, foods contain water. It's all pretty cicular, as much as it makes sense Jo, it doesn't make sense. Because it's cancer. And as I've seen it written many times. It sucks. Dehydration goes hand in hand with the electrolytes and she is in the right place to get everything balanced out. Here, since Mrs. Jo is stoic, and won't admit pain...they will know, pain makes the heart race faster. Usually, when the pulse goes up, the blood pressure goes down. And the opposite, if the BP goes up, the pulse comes down. Mrs. Jo and her *Oh, I'm ok* has made it a little harder for them to treat her. This way,she will be monitored, and with the help of the fantastic advancements in science and medicine. They'll be able to help her much better. Sux that it took all of this, to get to this point. Patients have rights. Hello Hippa. Enough from me. Thinking about you Jo. Last edited by Dominique; 09-03-2011 at 10:05 AM. Reason: typo |
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You're so right Yellow Band...thank you. Having the iliostomy (and no more colon) makes the dehydration issues so much harder, too.
She hates asking for help, and the only place she seems to be willing to take it is (literally) in the hospital. I think having the doctor order at-home nurse care will help too....the whole "doctor's orders" thing is easier for her to swallow.
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