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Author Topic: Got our call!  (Read 9522 times)
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #25 on: June 02, 2011, 03:11:21 PM »

It could be a leak with fluid squeezing the new kidney.
Praying here.  :pray;
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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
Sluff
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« Reply #26 on: June 02, 2011, 04:08:54 PM »

Hoping and praying they can fix the problem.
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boswife
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us and fam easter 2013

« Reply #27 on: June 02, 2011, 05:52:48 PM »

Any news Lost?
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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
jbeany
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« Reply #28 on: June 02, 2011, 06:26:39 PM »

 :grouphug;
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"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

LostWife
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« Reply #29 on: June 02, 2011, 07:04:45 PM »

All tests coming back negative:

No rejection
No obstruction
U/S look GREAT
No urine collecting in the abdomen
No repeating IGA in the new kidney


They said this started after giving him the initial dose of Prograf.  They are hoping the kidney is "asleep" - it is still producing SOME urine just only a small amount.  Anyone ever hear of this?  They said that they have seen it before.
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LostWife
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« Reply #30 on: June 06, 2011, 07:24:08 AM »

Hi All,

Kidney is producing more (MUCH more).  the fear now is that he had undiagnosed fsgs or simplified change disease.  Treating with predisone (which we were hoping to avoid) but hopefully we can get our little kidney in a good spot and can take it home soon!
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boswife
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us and fam easter 2013

« Reply #31 on: June 06, 2011, 08:06:24 AM »

Glad to hear it's producing MORE now, and truly pray for continued success on all health...  And thats for the both of you.  Tough spot to be in i know.  Sending more prayers and  :cuddle;
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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
rsudock
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will of the healthy makes up the fate of the sick.

« Reply #32 on: June 06, 2011, 11:10:20 AM »

Hoping things continue to improve!!

Keep us updated!

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?
LostWife
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« Reply #33 on: June 06, 2011, 04:16:13 PM »

I feel the need to confess something.  They kept talking about how many CCs the kidney was producing.  I had no frame of reference for this!  So...I ate a bunch of that hospital ice (great stuff btw, like a snow cone), waited til I had to go REALLY bad, and then peed into one of those containers with 1000 CCs measured! 

LOL.  I can't believe I did that.  But I thought I'd fill it up and instead put out only about 350 CCs.   My husband produced about 450 over a three hour period.  This made me feel better.   Crazy things we do for those we love, huh?

Glad to have an anonymous outlet for these confessions!!  hope you enjoy the sentiment...

:shy;
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rsudock
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will of the healthy makes up the fate of the sick.

« Reply #34 on: June 06, 2011, 04:17:34 PM »

I feel the need to confess something.  They kept talking about how many CCs the kidney was producing.  I had no frame of reference for this!  So...I ate a bunch of that hospital ice (great stuff btw, like a snow cone), waited til I had to go REALLY bad, and then peed into one of those containers with 1000 CCs measured! 

LOL.  I can't believe I did that.  But I thought I'd fill it up and instead put out only about 350 CCs.   My husband produced about 450 over a three hour period.  This made me feel better.   Crazy things we do for those we love, huh?

Glad to have an anonymous outlet for these confessions!!  hope you enjoy the sentiment...

:shy;


what a trooper!!!

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?
willowtreewren
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My two beautifull granddaughters

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« Reply #35 on: June 06, 2011, 04:54:28 PM »

I'm so glad to hear this good news!  :cheer:

When Carl got his kidney and they said there was significant necrosis, they didn't bother to tell us that since the blood flow was good, the kidney would likely regenerate. Oh, the anguish that we could have avoided.

Health care workers forget that we lay people don't know what they are talking about!

So, I do understand wanting to get an understanding of how much 450cc's really is!  :2thumbsup;
Very clever of you!

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. :)
boswife
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us and fam easter 2013

« Reply #36 on: June 06, 2011, 08:17:43 PM »

oh my gosh lostW.... that is definatly something i would do...lol............ So glad it helped ya out and eased your worries some...
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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
LostWife
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« Reply #37 on: June 07, 2011, 05:22:41 AM »

I know I could've just looked on the cup at where 450 CCs was, but I had no reference point as to what a normal output was!  I would've sworn it would be like 1000, I had to pee so bad.  I was alone in the bathroom blushing as I did it!!    :rofl;

I feel like a nut.  The things we do for love I guess.

He's having a really rough time and is EXHAUSTED.  Poor guy.  But we're making lots of pee jokes.  Hope this continues.
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willowtreewren
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My two beautifull granddaughters

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« Reply #38 on: June 07, 2011, 05:42:48 PM »

They would not let Carl out of the hospital until he pooped. So the pee jokes can switch to poop jokes, too. It was really hard for him to do that because he just did not feel like eating after the surgery. There was nothing TO poop!

 :rofl; :rofl; :rofl;
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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. :)
LostWife
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« Reply #39 on: June 16, 2011, 04:23:06 AM »

So the wild ride continues.  I'd like to get off now, please!

Kidney function has picked up again and we're home from the hospital.  However the biopsy shows what looks like either minimal change disease or FSGS.  He's spilling about 10g of protein right now.  All other numbers are looking great.

He has (supposedly) IGaN.  So how?  how? how? is this happening?  Well his doc tracked down his original biopsy from 2000 and there is a note written on there about possible FSGS but his doc at the time did/said NOTHING about that.  NOTHING.  I could spit nails. 

I don't really know anything about FSGS.  Web searches are freaking me out.  They are giving him phresis and hoping for the best.   They have to do a more intense biopsy to really figure out what is going on.

I'm so worried that this means we'll have to be right back on dialysis in a few years?  Whatever he has it is slow to progress - his childhood doc said he always had protein spilling, but then didn't progress to failure until 2008 (he's 35).
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okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #40 on: June 16, 2011, 10:12:54 AM »

It's good you're home - hopefully things will settle down - best wishes to you both!
I added your hubby here http://ihatedialysis.com/forum/index.php?topic=4927.0
 :yahoo;
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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
LostWife
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« Reply #41 on: August 03, 2011, 07:26:08 AM »

Back with an update.  :)

Hubby is home and back at work.  Prednisone being used for the protein problem, and it is now down to 700mg a day.  So we are so hopeful that will stay put and not come back to haunt us.  For now they are not doing a biopsy, since the number dipped - leaving well enough alone.  Which I could not be happier about.

Outside of that the kidney is doing really well.  He got a great kidney, really.  Creatinine is well below 1 (0.7 I think?) and all other numbers look phenomenal.

He had his catheter removed (he had just stopped PD in April, had a catheter in his chest and was about to get a fistula when the call came) and can possibly swim in a few weeks.  We are looking forward to that.

Ended up coming home from the hospital with 40 pounds of excess fluid, which took about 2-3 weeks to pee off, even with lasix.  Now he has some residual foot pain.  His feet took the brunt of the fluid, just looked awful.  He's doing PT and taking lyrica, so we're hoping that all helps.

We didn't get to meet our donor (he didn't come to the party they had for the exchange) so we are trying to craft a letter to him.  It seems he did this just to do a good deed.  I am so amazed and thankful.

Anyway, just dropping in to say hi!  Thanks to you all for everything. 
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boswife
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us and fam easter 2013

« Reply #42 on: August 03, 2011, 07:34:04 AM »

amazing!!  so good to hear and glad you droped in to let us know..  It's amazing so short ago you were in such a different situation.. Happy things are going good for ya and wish you continued wellness  :flower;
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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
RichardMEL
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« Reply #43 on: August 03, 2011, 06:03:08 PM »

wow.. 0.7. I have creatanine envy!!!

Such good news!!!

 :yahoo; :yahoo; :yahoo; :yahoo; :yahoo;
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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!
jbeany
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« Reply #44 on: August 03, 2011, 07:08:28 PM »

 :bandance; :bandance; :bandance; :bandance;
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"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #45 on: August 13, 2011, 06:21:19 PM »

 :waving; Just thinking of you!
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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
LostWife
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« Reply #46 on: September 11, 2011, 09:19:30 AM »

Thanks okarol. 

Protein NEGATIVE the past few checks!  could have possibly been simplified change disease, but we won't know unless kidney function changes to the point of needing a biopsy.

Wanted to share with you all a poster I had made for him....ironically, hanging by our hall bathroom.  :)
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The Noob
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« Reply #47 on: September 11, 2011, 09:30:46 AM »

sister! this is awesome news!!!!! many hugs and PRAYERS for you both!  :cuddle; :cuddle; :cuddle;
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Poppylicious
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« Reply #48 on: September 11, 2011, 02:24:42 PM »

Love the poster, LostWife.  So sweet!

 ;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.
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