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Author Topic: sitting g I. the ER  (Read 4071 times)
amanda100wilson
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« on: November 17, 2012, 10:19:14 AM »
having had my parathyroid glands removed on Wednesday, have been coughing g up a load of gunk and decided this morning to go to urgent care/ER as I was worried that I had a chest infection.  initially dismissive, the doc. is all of a sudden keeping me in as apparently there are some abnormalities on my EKG.  they haven't spelt it out but I think that they are suspecting a heart  attack as they have given me a baby aspirin and GTN. 
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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...
justme15
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« Reply #1 on: November 17, 2012, 11:44:30 AM »
Wow I hope it is nothing too serious! keep us posted, and let me know if you need anything!
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jeannea
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« Reply #2 on: November 17, 2012, 03:13:46 PM »
Sounds scary. I hope they figure it out soon.
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MaryJoe
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« Reply #3 on: November 17, 2012, 05:39:16 PM »
oh Amanda, I'm really sorry this complication has decided to rear it's ugly head.  I hope your docs figure it out in a hurry, and that you start felling much better soon.!

 :bestwishes;  Hang in there, we'll be thinking about you and waiting for good news   :boxing;
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Whether the glass is half empty or half full is not as important as being thankful there's a glass and grateful there's something in it.
boswife
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us and fam easter 2013
« Reply #4 on: November 17, 2012, 06:17:36 PM »
Please keep in touch   All the best
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im a california wife and cargiver to my hubby
He started dialysis April 09
We thank God for every day we are blessed to have together.
november 2010, patiently (ha!) waiting our turn for NxStage training
January 14,2011 home with NxStage
natnnnat
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« Reply #5 on: November 17, 2012, 11:24:26 PM »
Waiting for an update, hope you are okay.
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Natalya – Sydney, Australia
wife of Gregory, who is the kidney patient: 
1986: kidney failure at 19 years old, cause unknown
PD for a year, in-centre haemo for 4 years
Transplant 1 lasted 21 years (Lucy: 1991 - 2012), failed due to Transplant glomerulopathy
5 weeks Haemo 2012
Transplant 2 (Maggie) installed Feb 13, 2013, returned to work June 17, 2013 average crea was 130, now is 140.
Infections in June / July, hospital 1-4 Aug for infections.

Over the years:  skin cancer; thyroidectomy, pneumonia; CMV; BK; 14 surgeries
Generally glossy and happy.

2009 - 2013 PhD research student : How people make sense of renal failure in online discussion boards
Submitted February 2013 :: Graduated Sep 2013.   http://godbold.name/experiencingdialysis/
Heartfelt thanks to IHD, KK and ADB for your generosity and support.
billybags
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« Reply #6 on: November 18, 2012, 03:43:05 AM »
Hope every thing is going alright, they normally keep you in for 24 hours to redo the blood  test if they think it was your heart. Fingers crossed.
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willowtreewren
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My two beautifull granddaughters

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« Reply #7 on: November 18, 2012, 04:17:39 AM »
They always keep you if they suspect any heart issues. Happened to me last month.

I hope it is nothing serious.  :cuddle;

Aleta
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Wife to Carl, who has PKD.
Mother to Meagan, who has PKD.
Partner for NxStage HD August 2008 - February 2011.
Carl transplanted with cadaveric kidney, February 3, 2011. :)
Poppylicious
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« Reply #8 on: November 18, 2012, 10:38:39 AM »
Yikes.  I too hope it's nothing serious.  *huggles*
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- wife of kidney recepient (10/2011) -
venting myself online since 2003 (personal blog)
grumbles of a dialysis wife-y (kidney blog)
sometimes i take pictures (me, on flickr)

Everything was beautiful, and nothing hurt.
Deanne
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« Reply #9 on: November 20, 2012, 08:32:58 AM »
Amanda, are you ok? I've been watching for an update and worrying. I hope you're back home and just busy.   :flower;
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Deanne

1972: Diagnosed with "chronic kidney disease" (no specific diagnosis)
1994: Diagnosed with FSGS
September 2011: On transplant list with 15 - 20% function
September 2013: ~7% function. Started PD dialysis
February 11, 2014: Transplant from deceased donor. Creatinine 0.57 on 2/13/2014
amanda100wilson
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« Reply #10 on: November 21, 2012, 09:19:54 AM »
I am still in hospital but no longer in ICU.  they determined that I did not have a heart attack, even though elevated cardiac enzymes initially supported this possibility.  have been treated for a chest infection but have had some scary happenings during D.  the first day I was about an hour into treatment when my pulse rate shot up to about 200 and I had a heavy feeling to my chest.  they had to give me iv metoprolol to bring it down.  the next day I got to the last few minutes of D and it happened again.  two iv doses of metoprolol to bring it down this time.  thought that the doc was a bit blasé about sending me home on metaopralol to do D at home, only to discover today that he did not realise that I was doing home HD.  my home nurse was not impressed and essentially we have arranged my discharge care.  my neph. wants me to do in-center for a week which doesn't make me too happy but I do agree that it is for the best.

I am black and blue from my parathyroid surgery and my Hb has fallen to 8.2 and I feel like a wrung-out dishcloth so have reluctantly agreed to a blood transfusion.  never had one before but I really feel that on this occasion I do need one, particularly as I can already feel the depression monster rearing its ugly head.
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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...
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #11 on: November 21, 2012, 11:09:31 AM »
Poor girl, oh this sounds awful. Take care, I hope you can get home and rest.  :cuddle; :cuddle; :cuddle;
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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
Whamo
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« Reply #12 on: November 22, 2012, 08:26:59 AM »
Good Lord, I hope you feel better soon.  God bless you.
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amanda100wilson
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« Reply #13 on: November 22, 2012, 02:31:48 PM »
managed to escape from Hospital about 7.30 yesterday so managed to get a non-hospital version of Thanksgiving dinner.
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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...
cassandra
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When all else fails run in circles, shout loudly
« Reply #14 on: November 22, 2012, 03:47:07 PM »
Glad you've escaped, are you feeling a bit better after your real Thanksgiving dinner? Do they know something about your heart yet?

lots of love Cas
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I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
amanda100wilson
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« Reply #15 on: November 22, 2012, 09:30:41 PM »
my heart was fine.  they told me that the enzymes can be elevated in people with renal failure.
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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...
cassandra
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When all else fails run in circles, shout loudly
« Reply #16 on: November 23, 2012, 06:43:04 AM »
glad to hear that, I hope you feel completely better, with calcium under controle so you can really enjoy the Festive

Season at home.   :yahoo;

lots of love Cas

(thanx for info on those enzymes)
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I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
cdwbrooklyn
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Positive Thoughts equal Positive Energy
« Reply #17 on: November 26, 2012, 12:51:20 PM »
People all most always get better when they reach home.  Feel better.
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Dailysis patient for since 1999 and still kicking it strong.  I was called for a transplant but could not get it due to damage veins from extremely high blood pressure.  Have it under control now, on NxStage System but will receive dailysis for the rest of my life.  Does life sucks because of this.  ABOLUTELY NOT!  Life is what you make it good, bad, sick, or healthy.  Praise God I'm still functioning as a normal person just have to take extra steps.
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