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Author Topic: Cellcept sucks  (Read 11338 times)
monrein
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Might as well smile

« Reply #25 on: January 27, 2009, 02:37:42 PM »

I have everything, including my eyes, crossed for you Traci girl, and I'm three weeks behind you.   :flower;
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
kidney4traci
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« Reply #26 on: January 27, 2009, 02:44:56 PM »

I know, I said prayers for you last night.  I decided anytime I get anxious, I will just pray for you and take my mind off me!  So you will get lots of prayers!!  Ha Ha!
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Married - three children.
Alports female, diagnosed ESRD 10/04
11/04  Hemo in clinic
6/07 hemo at HOME! 
2/3/09 - Transplant from an angel of a friend!!!
willieandwinnie
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« Reply #27 on: January 27, 2009, 02:49:43 PM »

 :cuddle; I'm going to pray for both of you.  :grouphug;
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"I know there's nothing to it, but I want to know what it is there's nothing to"
kidney4traci
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« Reply #28 on: January 27, 2009, 02:55:03 PM »

Aaawwe!  Thanks!!!!!!
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Married - three children.
Alports female, diagnosed ESRD 10/04
11/04  Hemo in clinic
6/07 hemo at HOME! 
2/3/09 - Transplant from an angel of a friend!!!
pelagia
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« Reply #29 on: January 27, 2009, 03:13:25 PM »

Traci - only one week to go?!?  :yahoo;

P.S. Stephen never takes his any of his meds on an empty stomach, always takes pepcid (famotidine) and has had no stomach problems at all, even in the beginning when he was on the highest doses. 
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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
monrein
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Might as well smile

« Reply #30 on: January 27, 2009, 03:19:07 PM »

Thanks so much Traci and Kathy.  It means a lot to me.   :cuddle; :cuddle;
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
kellyt
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« Reply #31 on: January 28, 2009, 11:27:14 AM »

I'm so excited for you both!  I wish I could drive up to Houston to see you, Traci.  Take a laptop so you can keep us up-to-date on your progress.

Monrein, I'd love to be able to go to Canada to see you!  It's so beautiful there!  You know the process already, so does it make you any more or less nervous or excited?  You need to plan on coming to Vegas in Oct!  That would be so much fun!
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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
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