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| | |-+  Here we go. I got a transplant
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Author Topic: Here we go. I got a transplant  (Read 12836 times)
American Airman
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« Reply #50 on: August 11, 2008, 11:30:06 AM »


Its weird, but I think my left side is more swollen than my right, but the left is where they put the kidney.  So I guess that's normal. 


I think some of you might have not quite understood what I ment.  When they put in the kidney... was the side they put it in more swollen than the other???
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pelagia
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« Reply #51 on: August 11, 2008, 01:03:20 PM »

Stephen stayed more swollen on the side where the kidney was placed for at least a month or two after the surgery.  In fact, his skin is still faintly discolored wherever he had bruising from the surgery, and he is just about to the three month anniversary.
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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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« Reply #52 on: August 11, 2008, 04:49:09 PM »


Its weird, but I think my left side is more swollen than my right, but the left is where they put the kidney.  So I guess that's normal. 


I think some of you might have not quite understood what I ment.  When they put in the kidney... was the side they put it in more swollen than the other???

Jenna had no swelling, her incision was flat and glued together, no staples, so very little trauma. It is possible to have fluid build up around the kidney and if this is the case they should see it on ultrasound. I hope you're doing better.
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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
Lori1851
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This is me Lori , Dustin's mom

« Reply #53 on: August 12, 2008, 07:16:54 AM »

 :yahoo; :yahoo; :2thumbsup;
Airman,
Praise the Lord you got your transplant!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! I am excited for you!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

Lori/Indiana
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vandie
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« Reply #54 on: August 12, 2008, 12:33:16 PM »

My new kidney is on the right side.   When I lie down, I can still see it and feel it.   It's not swollen.  It's just there.
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Life is the journey, not the destination.
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I received a kidney transplant on August 4, 2007.
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« Reply #55 on: August 12, 2008, 04:02:24 PM »

My new kidney is on the right side.   When I lie down, I can still see it and feel it.   It's not swollen.  It's just there.
Maybe it's just me or maybe other k/p tx recipients, but I can't tell mine is there and I am underweight. The doctors can feel it when they press down on it if I let them (I hate my abdomen pressed or touched). Might be because of a more intense surgery,don't know, but glad I don't see it.  I probably be to self conscious about it and the way it looks and then over protecting it.
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Diabetes -  age 7

Neuropathy in legs age 10

Eye impairments and blindness in one eye began in 95, major one during visit to the Indy 500 race of that year
   -glaucoma and surgery for that
     -cataract surgery twice on same eye (2000 - 2002). another one growing in good eye
     - vitrectomy in good eye post tx November 2003, totally blind for 4 months due to complications with meds and infection

Diagnosed with ESRD June 29, 1999
1st Dialysis - July 4, 1999
Last Dialysis - December 2, 2000

Kidney and Pancreas Transplant - December 3, 2000

Cataract Surgery on good eye - June 24, 2009
Knee Surgery 2010
2011/2012 in process of getting a guide dog
Guide Dog Training begins July 2, 2012 in NY
Guide Dog by end of July 2012
Next eye surgery late 2012 or 2013 if I feel like it
Home with Guide dog - July 27, 2012
Knee Surgery #2 - Oct 15, 2012
Eye Surgery - Nov 2012
Lifes Adventures -  Priceless

No two day's are the same, are they?
monrein
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Might as well smile

« Reply #56 on: August 12, 2008, 05:06:19 PM »

When I lie down I can see and feel mine too.  Actually I massage and "talk" to it regularly.  I think a little encouragement never hurt anyone or anything, even a kidney.  No one else would notice it though unless I pointed it out or let them feel it. 


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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
okarol
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Photo is Jenna - after Disneyland - 1988

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« Reply #57 on: September 17, 2008, 10:53:57 AM »


How are you doing Airman?
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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
American Airman
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« Reply #58 on: September 25, 2008, 12:16:12 PM »

Hi,

It's been a while since I've posted.  My computer went down.  very down. 

I'm using my wife's that her mom sent us from kentucky.

I got the pd cathiter out.  I for the life of me can't remember how to spell cathater...

doesn't matter now.  I'm doing very well.  I'm on 5 mg of Prograph and 1000 mg of cell cept
both two times a day.  The only downside I can see so far is um... not solid bowel movements...
They may switch me to the coated version of cellcept.

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willieandwinnie
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« Reply #59 on: September 25, 2008, 12:23:16 PM »

:waving; American Airman. Sorry about your computer. My husband is only on prograf because of all the bowel problems that Cellcept causes. Good to hear from you.  :cuddle;
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okarol
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« Reply #60 on: September 25, 2008, 02:40:22 PM »


Despite the bowel issue it sounds as if you're doing well - glad to hear it!  :clap;
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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
pelagia
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« Reply #61 on: September 25, 2008, 04:11:31 PM »

Thanks for giving us an update.  It's great to hear that you are doing well.   :bandance; :bandance; :bandance; :bandance;

Hopefully they will cut down on the meds a bit in the future.  Are you taking any prednisone?
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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
American Airman
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« Reply #62 on: September 28, 2008, 12:40:59 PM »

I started on 20 milligrams of prednisone, but was slowly taken off of it.  Good thing too, I'd be 300 lbs by now if they hadn't stopped.

Does anyone have any tips on how to work around the cellcept diarhea thing?  Would like any help.

What seems to work best for me is to not eat in the morning at all (I get up at 0400 or 4am for you non military types) and usually eat a bowl of cereal.  then I take my meds at 0800 or 8am.  I think I do better when I don't eat untill after I've taken the pills.

But when you're up at 0400, 5 hours is a long time to wait before you eat.

Any other suggestions?
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pelagia
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« Reply #63 on: September 28, 2008, 12:49:30 PM »

well, cheese and bagels are two foods that have the opposite effects on me, but of course I'm not on cellcept...

do you eat much fiber?  like whole grains?  could be that would help regulate your system a little bit.  maybe some oatmeal for breakfast, or whole grain toast (not the stuff that says "wheat bread, but the 100% whole wheat kind).

Stephen doesn't have any problems, but he is on 750 mg cellcept 2x a day, but also takes prograf and predinisone.
« Last Edit: September 28, 2008, 12:51:45 PM by pelagia » Logged

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
American Airman
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« Reply #64 on: September 28, 2008, 05:49:27 PM »

All,

Are there any military members who have retired due to kidney failure like myself?

I have several questions about the va and such.

Please send me a message here at the boards.

Thanks.

Please put this out there in the ihatedialysis boards.  I don't really know where else to post, so everyone please see that this gets around.

Thanks again.
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Romona
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« Reply #65 on: September 28, 2008, 05:57:37 PM »

You could try the BRAT diet that is recommended for kids with diarrhea Bananas, Rice, Apples and Toast.
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