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Author Topic: Moms hate dialysis too  (Read 2405 times)
lsavatski
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« on: December 20, 2010, 01:55:10 PM »

Hi group,  I'm a mom of a gorgeous 20 year old who was on dialysis since earlier this year.  Even though she's just gotten a transplant :bandance;, every day (especially MWF--that was her schedule) I think of all those bound to the chair.  Moms think dialysis sucks too.   :puke; 

For now we are dialysis free  :beer1; :yahoo;

And, wishing those still in treatment a fun and interesteing person along side of you   :yahoo; :flower;

Laura 
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boswife
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us and fam easter 2013

« Reply #1 on: December 20, 2010, 03:30:19 PM »

oh my goodness!!  what a great post!  I couldnt be happier for your daughter and wish her a life full of NO dialysis, and wonderful times.  Thank you for your great message :)   I really liked it, and wish you well...    :clap;
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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
Rerun
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Going through life tied to a chair!

« Reply #2 on: December 20, 2010, 08:17:36 PM »

Hi Isavatski, welcome to IHD.  I'm so glad you found us.  There are lots of young people on here and Moms too.  The Admin on this site Okarol has a daughter around 22 or 23 that now has a transplant.  You'll have to meet her.  I hope you can talk your daughter into joining.  This place has those on dialysis, those waiting for a transplant and those transplanted.  Seems like our members get a transplant once a month around here.  A good place to be.

Rerun, Moderator     :welcomesign;
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galvo
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« Reply #3 on: December 20, 2010, 08:57:29 PM »

G'day Isavatski and  :welcomesign;. Great news about your daughter.
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Galvo
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« Reply #4 on: December 20, 2010, 09:32:38 PM »

Welcome aboard.  Best wishes to you and your daughter.
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May you live as long as you want and never want as long as you live.
looneytunes
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Wishin' I was Fishin'

« Reply #5 on: December 21, 2010, 02:58:02 AM »

Hi Isavatski and I also welcome you to IHD.  It's a great place for anyone who has a connection to the world of renal failure.  I also hope you can get your daughter to spend some time reading the forums, I'm sure there is a lot of info there she can use.  She also could be a great help to some of our younger folks who are in the same situation as she.   :welcomesign;
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"The key to being patient is having something to do in the meantime" AU
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #6 on: December 21, 2010, 03:33:55 AM »

 :waving; Hi Laura,
Glad you joined us. I have a 25 year old daughter who did 3 years of in-center hemo and has now had a transplant for 4 years. My first post was I love/hate dialysis. We are grateful for it, but it sure is tough to watch your kid go through it. I look forward to your posts. Welcome!
 :welcomesign;
okarol/admin
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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
rsudock
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will of the healthy makes up the fate of the sick.

« Reply #7 on: December 23, 2010, 05:36:50 PM »

I'm a 26 year old living on dialysis....welcome!!

xo,
R
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Born with autosomal recessive polycystic kidney disease
1995 - AV Fistula placed
Dec 7, 1999 cadaver transplant saved me from childhood dialysis!
10 transplant years = spleenectomy, gall bladder removed, liver biopsy, bone marrow aspiration.
July 27, 2010 Started dialysis for the first time ever.
June 21, 2011 2nd kidney nonrelated living donor
September 2013 Liver Cancer tumor.
October 2013 Ablation of liver tumor.
Now scans every 3 months to watch for new tumors.
Now Status 7 on the wait list for a liver.
How about another decade of solid health?
kellyt
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« Reply #8 on: December 23, 2010, 05:44:39 PM »

How wonderful for your daughter that she's been given the gift of life and has a 2nd chance to get out there and live.  And so glad you found this site and joined!    :waving;
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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
Tysmom
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« Reply #9 on: December 30, 2010, 12:19:29 AM »

Hi I to am a mom of Kidney child who just joined today. I love the reference to the person sitting in the chair next to the dialysis patient. That is me now again as my child just turned 15 I look forward to your posts on how you stayed positive, I've given up on the grey hair and am going to dye!!!

I want to be that incredible person in the chair next to my son!


Welcome and continued well wishes to your daughter or did I forget already? Anyway Welcome! :shy;

























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