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#1 |
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Countyfemme,
I'm glad you're there with Clay. Thanks for keeping us posted. She still has a long journey ahead but you're there to help. |
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#2 |
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feeling pretty darned blissful right now! Join Date: Aug 2011
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#3 |
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Rough night, wheww poor Clay fluid buldup in her stomach couldn't get a good breath and they didn't tube her till this morning after the doc saw her...once the tube was in she felt soooo much better...she is finally resting and we hope she is moved to a private room today. Her pain lvl is great she hasn't had to "hit" the little extra button, they still have her on the epiy and it is working really well for her. I feel so bad for her and there's not much I can do but keep watch and hold her hand when she needs it I really feel kinda useless
Will update later! Thanks so much for all the support! |
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#4 | |
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I had a hospital stay once, I was in the most incredible abdominal pain I could imagine, the docs could find nothing to pinpoint the why, so I just suffered. My partner at the time was a nurse, for God sake. She could not bring herself there to visit at all during the 5 days I was there. I should have known by that, yanno? |
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#5 |
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Ok the nurses are going to be soooo ready to be rid of my ass, I rode them HARD today....but if i don't feel things are as they should be I'm going to speak up! I had them in here three times before they finally admitted the N/G wasn't pulling the fluid that it is mean to do and fixed it.
And can I say that Clay is one stubborn butch! Has taken all my fem wiles to get her to do what she needs to do lol I really hope tonight is better for her...lord I hope so. |
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#6 | |
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You keep riding their butts!!!! Clay can't speak for herself (we'll she could but...is loopy from meds). And someone needs to be her advocate. I'm glad you're there! |
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#7 | |
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#8 | |
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They decided to leave the epi in one more day, I'm glad of that as her bowels are still not responding. Longer they can keep her off the narcotics the better. She rarely hits the pain meds, which is good, but I fear that will change once the epi is gone. They are going to get her up and back in a chair today,I'm hoping she'll get to moving around more, that's what she needs to be doing to stimulate the bowel activity. Hurts like hell but I keep telling her she has to work thru it and it'll get better. |
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#9 | |
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![]() I watched my best buddy go through something similar, and you being at the bedside and observant is a blessing for Clay, and rough on you. ![]() ![]() |
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#10 |
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Hi everyone,
The new TPN pump has been figured out, after 4 calls to the nurse and a few panic moments. She's on it 12 hours a day now rather than 24 because they're trying to "stimulate her appetite". I got her to eat 5 times yesterday but quantities are very, very small. And, I'm in a bit of an internal tussle because the thing she seems to handle the best is greek yogurt....right when I have concerns about dairy products. Joy. She has napped a few times...slept 12 hours last night...and is much more comfortable in the warmth of south Florida...so that's all good. Her first appointment with the new doctor is this afternoon...so it'll be interesting to see what's said. I am now inserting myself into all doctor visits....enough of this being in the dark.
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#11 | |
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#12 |
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It was a rough afternoon.
Took Mom to see the new doctor...who was more honest and clear than her previous doctors have been. He was very supportive, but also frank that this type of cancer doesn't get better. They can keep her alive on chemo...but as soon as the chemo stops...the cancer will keep coming back. If the chemo stops, she probably has a few months.
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#13 |
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So...I just got my hands on the results of my mother's last CT scan....holy cow.
![]() She's been keeping way too many secrets.
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#14 |
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Great night, almost 6 hours sleep! Walking the halls has commenced, pain is managed. She's starting to feel froggy again!
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#15 |
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{{{{Jo}}}}} Oh dear
![]() YAY CLAY!!! |
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#16 | |
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#17 |
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"cancer free" has such a MAGICAL ring to it, doesn't it!!!!!!
bless bless bless~~~ |
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