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Author Topic: NEW KIDNEY YAYYYYYYYYYYYYYY  (Read 6978 times)
RichardMEL
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« Reply #25 on: October 26, 2008, 10:34:56 PM »

LMAO @ cute doctor....

yep, Claudia is feeling 110% for sure!!!!!!

 :grouphug;
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
Bajanne
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Goofynina and Epoman - Gone But Not Forgotten

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« Reply #26 on: October 26, 2008, 11:52:31 PM »

 :yahoo; :yahoo;  Great news, Claudia  :2thumbsup; :2thumbsup;

Please continue to keep us updated - we are so happy for you!  :grouphug;

 :flower; :flower; :flower; :flower; :flower;
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"To be found in Him, not having a righteousness of my own ...but that which is based on faith"



I LOVE  my IHD family! :grouphug;
circleNthedrain
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« Reply #27 on: October 27, 2008, 12:12:50 AM »

Great news!!  Keep us posted on your high flying adventures.
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1979 Diagnosed with kidney failure
1979 Right arm fistula
1979 Start hemodialysis
1980 CAPD catheter
1980 Start CAPD
1989 Cadaveric kidney transplant
1995 2nd cadaveric  kidney transplant
2007 Start hemodialysis
2010 Still drawin' wind
Lori1851
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This is me Lori , Dustin's mom

« Reply #28 on: October 27, 2008, 02:48:31 AM »

Claudia,
 :yahoo; :bandance; :beer1;
Congrats! I am soooooo happy for you hon!!!!

Lori/Indiana
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lola
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I can fly!!!

« Reply #29 on: October 27, 2008, 04:32:36 AM »

 :bandance; :bandance; :flower; :flower;
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willieandwinnie
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« Reply #30 on: October 27, 2008, 04:40:20 AM »

:flower; Claudia. Please get plenty of rest and drinks loads of water, and remember to keep us updated.  :cuddle;
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"I know there's nothing to it, but I want to know what it is there's nothing to"
pelagia
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« Reply #31 on: October 27, 2008, 05:44:47 AM »

yep, do it!  :cheer:
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As for me, I'll borrow this thought: "Having never experienced kidney disease, I had no idea how crucial kidney function is to the rest of the body." - KD
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #32 on: October 27, 2008, 07:06:27 AM »

 :clap; Good to hear you're smiling!
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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
kellyt
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« Reply #33 on: October 27, 2008, 07:44:24 AM »

Fabulous story!  I read it really, really fast, as that's the way I felt it was going through her brain and out her mouth (through her hands, of course).  :)

I couldn't be happier for you and your cats!   :beer1;
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1993 diagnosed with glomerulonephritis.
Oct 41, 2007 - Got fistula placed.
Feb 13, 2008 - Activated on "the list".
Nov 5, 2008 - Received living donor transplant from my sister-in-law, Etta.
Nov 5, 2011 - THREE YEARS POST TRANSPLANT!  :D
Deanne
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« Reply #34 on: October 27, 2008, 08:52:07 AM »

Congratulations!!!!!!!!!!!!!!!!!!!!!!!
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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
Claudia30
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« Reply #35 on: October 28, 2008, 06:36:56 PM »

went to the clinic on monday...my creatine was 1.8!!!!!!!!!!!! wow what a number. Amazing. Today has been a roller coaster kind of day...i went out tonite to go food shopping, and what an adventure...lol. i didn't realize food shopping could be so fun. The things we take for granted. Every moment is special no matter what you are doing. at times i feeling like  :boxing; the walls of my apt as i am so sick of looking at them. And by the way...pple need to teach children better manners..actually there are plenty of adults who need a lesson in manners. Didn't anyone ever tell them that it is not right to stare.  :Kit n Stik; i also got to go to the bookstore and load up on my books...which is great since there is nothing on tv...800 channels and still nothing lol. and i swear if i watch another 'judge something" show i am gonna scream. I still have some pain and need to remind myself to slow down at times as i feel like i am ready to face the world straight on. I go in on nov 21st for surgery to take out my PD cath...i am gonna miss that little guy...lol. it has been part of me for so long. gonna be strange when it comes out as i'm so careful about it now and no pulling on it and such. i was reading pples stories about their cath sites and i thank god that mine didn't come out. My doctors are so pleased at my recovery and how well i am doing. Sorry my thoughts are all over the place tonight. Thanks again for all your thoughts as they help tremendously. Have a great day/nite and take care.
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A little Consideration, a little Thought for Others, makes all the difference. ~ Eeyore
Wattle
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« Reply #36 on: October 28, 2008, 07:39:06 PM »

 :cheer: :cheer: :cheer:  Great news.

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PKD
June 2005 Commenced PD Dialysis
July 13th 2009 Cadaveric 5/6 Antigen Match Transplant from my Special Angel
RichardMEL
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« Reply #37 on: October 28, 2008, 08:17:41 PM »

Your progress gives us all hope for those of us still waiting that we, too, can have a fantastic transplant and recovery!!

Hope the pain eases soon...

and you know the kids and people are staring because you're so glowing with energy and happiness now they, like the chick in "when Harry met Sally" want "what she's having" !!!! They're jealous!!!

 :cuddle; :bow; :beer1; :grouphug;
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
Claudia30
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« Reply #38 on: October 29, 2008, 10:45:38 PM »

hmmm question...i go in on oct 21st to have the pd clath removed and to have the stent they used in the transplant removed. This may be a dumb question but that means that the scar that is finally healing will have to be oppened up again to take the stent out right? Am worried about it. Also has anyone had a pd cath removed, i know i have to go under but do they open me up to take it out or just kind of pull? The cath i know is in deep in me in my adbomen. Silly questions and i know that i shouldnt be so worried esp since i have already been through the major surgery. Will this procedure put me back a bit as i will have to recover from being opened again?  ???
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A little Consideration, a little Thought for Others, makes all the difference. ~ Eeyore
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #39 on: October 29, 2008, 11:02:37 PM »


Jenna's stent was removed using a small instrument that was inserted through the urethra. There's was a little tug and it was out. She was uncomfortable for about 3 minutes total, and said it wasn't too bad. She was awake the whole time.
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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
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