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Author Topic: vein too small....  (Read 3307 times)
angela515
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« on: November 27, 2006, 10:02:23 AM »

So last year when i lived in vegas, my brother wanted to be tested as a possible donor. So they sent him to the mayo clinic in AZ for testing. His blood tests came back good, he matched me very well, and so on to the next step, 24 urine collection and ultra sound of the kidneys. Ultra sound of the kidneys was not good... thats what got the transplant turned down. The dr explained it like this... his left kidney the vien that would connect his kidney to me, was too small.. they wouldnt be able to connect it to me. So they looked at his right kidney, his vien is wrapped around a main artery so no doctor will go near it because of the risk of cuting the main artery.

My brother was upset about the whole thing more than I was, he wanted to help out, and felt he didn't. I assured him it was a great thing he did just trying and I appreciate it. 

Now I live in Iowa, and he was asking me if he could be tested here. His thoughts are a different doctor may think the vien is long enough to hook it up to me, as different dr's have different qualifications and do things differently then each other.


Any thoughts?



EDITED:  Fixed spelling error in title -  Goofynina/Moderator
« Last Edit: November 27, 2006, 10:24:10 PM by goofynina » Logged

Live Donor Transplant From My Mom 12/14/1999
Perfect Match (6 of 6) Cadaver Transplant On 1/14/2007
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« Reply #1 on: November 27, 2006, 11:45:32 AM »

I think I would if I were in your position, I'd want a second opinion.
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Lorelle

Husband Mike Diagnosed with PKD Fall of 2004
Fistula Surgery  1/06
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okarol
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« Reply #2 on: November 27, 2006, 12:47:12 PM »

I have heard of something similar happening before. What one center sees
as a problem is nothing to another.
This would be a good question to post on www.livingdonorsonline.org
as many living donors have had good luck when they've gone to a new hospital.

~Karol
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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 -
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« Reply #3 on: November 27, 2006, 03:03:11 PM »

I think I would if I were in your position, I'd want a second opinion.

I would certainly ask for a second opinion, just to be sure. But what if the new doctors say no problem and then the kidney actually can't be connected properly (meaning the Vegas doctors were right)? I don't want to discourage you, if you're brother is still willing (and  by the looks of it he is not only willing but insisting!), I would definitely run another series of tests. It can't hurt.
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Fox_nc
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« Reply #4 on: November 27, 2006, 08:01:24 PM »

Oh YES!  Go for it!  The worst thing they can tell you is no (again) but at least you would know and not always wonder "what if"  Good luck!
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Rerun
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« Reply #5 on: November 27, 2006, 08:04:31 PM »

I think you have a wonderful brother.
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