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cozmic555
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« on: November 06, 2011, 06:34:56 AM »

my name is Scott , I'm 24 live in England and found this site looking for infomation concerning my future dialysis treatments

i got 13% of my kidneys working and yesterday i saw the dialysis nurses to decide what type of dialysis i wanted i haven't chosen yet but i think I'm heading towards Peritoneal dialysis

my story starts when i was 18moths old i got a bug that eat away at my kidneys i was on Peritoneal dialysis for 6 months then i started urinating nurses say it was a miracle :) from then on Ive had around 20-18% working renal function all my life growing up ,with doctors saying i will need dialysis or transplant when i reach my early teens then when I'm 16 then 18 then 20 now all the way to 24 , i see my renal doctor now every 6 weeks but it used to be every 6 months then 3 months then 2 then now down to 6 weeks , doctor says my kidneys will never get better and dialysis is inevitable ,to tell you the truth i dont think too much into it as with me the more i know the more i worry ,

so I'm gonna look through all the forum and see if others have asked some of the questions i wanted to know, looks like a great site and am glad to be a part of it ,thanks again
« Last Edit: November 06, 2011, 06:36:34 AM by cozmic555 » Logged
boswife
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us and fam easter 2013

« Reply #1 on: November 06, 2011, 06:45:27 AM »

welcome  :welcomesign; Scott  :flower;  So glad you found your way here and i hope it eases some of your fears.  Great place, great friends and lots of information. Sounds like you can share some of that yourself  ;)  I wish you well, and even if you see questions already asked, go ahead and ask again... Mabie some new answers will come in..   :welcomesign;
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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
willowtreewren
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My two beautifull granddaughters

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« Reply #2 on: November 06, 2011, 12:27:52 PM »

Hi, Scott!

If you don't find the answers you are seeking, just ask away. There are so many knowledgeable and kind folks here!

 :welcomesign;

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. :)
lmunchkin
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"There Is No Place Like Home!"

« Reply #3 on: November 06, 2011, 02:11:04 PM »

Welcome Scott & glad you found us!

lmunch
 :kickstart;
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11/2004 Hubby diag. ESRD, Diabeties, Vascular Disease & High BP
12/2004 to 6/2009 Home PD
6/2009 Peritonitis , PD Cath removed
7/2009 Hemo Dialysis In-Center
2/2010 BKA rt leg & lt foot (all toes) amputated
6/2010 to present.  NxStage at home
Poppylicious
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« Reply #4 on: November 07, 2011, 05:03:15 AM »

 :welcomesign; Scott, from another England-er!

 ;D
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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.
Ang
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« Reply #5 on: November 07, 2011, 03:29:17 PM »

 :welcomesign;
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live  life  to  the  full  and you won't  die  wondering
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