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Author Topic: In hospital  (Read 3486 times)
amanda100wilson
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« on: December 10, 2013, 07:38:47 PM »
I started with a sore throat that didn't develop into a cold but went down further and I had difficulty drawing a full breath.  I went to the ER and they diagnosed a slight case of pneumonia.  They gave me a broncho-dilator and rather than being discharged with antibiotics, I ended up getting admitted because the broncho-dilator initiated atrial fibrillation.  They were going to give me levaquin as an antibiotic, but then consulted an infectious disease 'specialist' for an alternative ad I have a prolonged Q-T interval on EKG.  I then find out from the cardiologist that I shouldn't gave had this particular one as it has the same action!  He argued away with me for a while and I just told him to go speak with the cardiologist if he had a problem.  I had the impression by the end, that he was trying to save face but I had no faith in him.  (Didn't help that the person next door must have had a bowel movement At about the time that he was there and .i was convinced that smell was coming from him! :)). Due to this issue I then  have to stay in  until tomorrow.  I am going to get dialysis before I leave but have already specified that I put in my own needles and I will determine how much they pull.
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ESRD 22 years
  -PD for 18 months
  -Transplant 10 years
  -PD for 8 years
  -NxStage since October 2011
Healthy people may look upon me as weak because of my illness, but my illness has given me strength that they can't begin to imagine.

Always look on the bright side of life...
MooseMom
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« Reply #1 on: December 10, 2013, 09:59:12 PM »
What?  In hospital?  What a shock! I hope your docs will learn to talk to each other!  And they had better listen to and obey you when it comes to your D treatment!   :Kit n Stik;
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"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #2 on: December 11, 2013, 01:07:40 AM »
 :grouphug; Hope you get out soon and are feeling better.
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
jeannea
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« Reply #3 on: December 11, 2013, 08:16:15 AM »
Good for you for standing up for yourself. Feel better soon!
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Jean
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« Reply #4 on: December 11, 2013, 12:06:51 PM »
Hope you are soon feeling better. Is this fibrillation new to you?
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One day at a time, thats all I can do.
Rerun
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Going through life tied to a chair!
« Reply #5 on: December 11, 2013, 12:51:07 PM »
Hope you are home soon and feeling yourself again soon.

     :flower;
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galvo
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« Reply #6 on: December 11, 2013, 08:25:44 PM »
Best wishes!  :bestwishes;
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Galvo
kitkatz
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« Reply #7 on: December 11, 2013, 10:03:33 PM »
Get out soon!!!!
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lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
amanda100wilson
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« Reply #8 on: December 12, 2013, 08:15:14 AM »
Home from hospital and feeling better.  Of course while I was in there I had the question 'where do you dialyze and what days do you dialyze?'  Of course as soon as I did home dialysis they assumed PD and were all surprised when I said home hemo.  I also met a really nice nephrologist, but
I asked what dialysis units they used.  There were only two and one I have used and didn't like, and to my disappointment I said this, she didn't bother to ask why.  Nonetheless, I may keep her up my sleeve in case I need to find another nephrologist, although I would research the other dialysis first. 

Dialyzed in their dialysis unit before I came home.  Nice little unit, but in-patients only.  Decided I would have a little respite day but did of course cannulate myself which impressed them.  One of the nurses expressed an interest in becoming a Home patient trainer.

Jean, the A. fib is newly diagnosed but I suspect that I have had it a few times without realizing what it was.
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ESRD 22 years
  -PD for 18 months
  -Transplant 10 years
  -PD for 8 years
  -NxStage since October 2011
Healthy people may look upon me as weak because of my illness, but my illness has given me strength that they can't begin to imagine.

Always look on the bright side of life...
MooseMom
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« Reply #9 on: December 12, 2013, 08:26:35 AM »
It's always good when a home hemo patient has the chance to educate other healthcare providers about this modality!  Good for you!
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"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
obsidianom
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« Reply #10 on: December 12, 2013, 09:52:04 AM »
Quote from: amanda100wilson on December 12, 2013, 08:15:14 AM
Home from hospital and feeling better.  Of course while I was in there I had the question 'where do you dialyze and what days do you dialyze?'  Of course as soon as I did home dialysis they assumed PD and were all surprised when I said home hemo.  I also met a really nice nephrologist, but
I asked what dialysis units they used.  There were only two and one I have used and didn't like, and to my disappointment I said this, she didn't bother to ask why.  Nonetheless, I may keep her up my sleeve in case I need to find another nephrologist, although I would research the other dialysis first. 

Dialyzed in their dialysis unit before I came home.  Nice little unit, but in-patients only.  Decided I would have a little respite day but did of course cannulate myself which impressed them.  One of the nurses expressed an interest in becoming a Home patient trainer.

Jean, the A. fib is newly diagnosed but I suspect that I have had it a few times without realizing what it was.
What are you being treated with for the Afib?   I have it too and have kept in under control for several years with a low dose beta blocker(nadolol).
I can always feel it when it gets going. It feels like a vibrator in my chest. Its very uncomfortable.
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My wife is the most important person in my life. Dialysis is an honor to do for her.
NxStage since June 2012 .
When not doing dialysis I am a physician ,for over 25 years now(not a nephrologist)

Any posting here should be used for informational purposes only . Talk to your own doctor about treatment decisions.
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