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Author Topic: Have Any Tips on Patient Resource Info?  (Read 2043 times)
virrat
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« on: November 17, 2007, 01:58:56 PM »

Hello Everyone

I am interested in hearing from members about information resources that they've found helpful. This could be anything including books, video or audio tapes/cd's/dvd's, websites, blogs, brochures, etc.

My husband Virrat passed away earlier this year and I've been thinking about creating a patient resource centre in his memory. We're both librarians and very interested in consumer health issues and patient self-management.

I appreciate any feedback you're interested in providing. Feel free to reply on the message board or contact me directly: sjmiller@magma.ca

Cheers,  :thx;
Sandra

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Carpe Diem Chris
http://carpediemchris.blogspot.com/
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paris
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« Reply #1 on: November 17, 2007, 02:28:59 PM »

What a wonderful idea and such a meaningful way to honor his memory.    How are you doing now?  Keep us updated on your project.  :grouphug;
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It's not what you gather, but what you scatter that tells what kind of life you have lived.
tamara
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WOO HOO NEW KIDNEY PEEING !!!(Transplant 23/10/07)

« Reply #2 on: November 17, 2007, 03:28:00 PM »

Sandra,

What a thoughtful thing to do. May his memory live on by helping others  :grouphug;  :cuddle;
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ABO Incompatible Transplant from my loving Partner 23/10/07
after over four years on the D Machine 

                                                                                                                  
Dialysis Sucks and Transplants Don't.................So Far Anyway !!!!!
Sluff
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« Reply #3 on: November 17, 2007, 04:05:22 PM »

What a great idea.  :2thumbsup;
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paddbear0000
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Dogs & IHDer's are always glad to see you!

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« Reply #4 on: November 18, 2007, 01:48:21 PM »

You're in luck! I just did a website for a class project on chronic kidney disease. There is a page on the site with a list of resources. Feel free to use them. Here's the link - http://www.yourbadkidneys.com/resources.html. Be warned though, the site will only be up until November 30th, so get the info as soon as possible. As I said, it was a class final project and I don't plan on leaving it up forever!

Good luck!
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okarol
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« Reply #5 on: November 18, 2007, 03:52:55 PM »

Kitkatz started a thread that has some good internet resources here http://ihatedialysis.com/forum/index.php?topic=858.0

I would have to say IHD is the best dialysis forum I have seen. I like this site regarding transplantation http://www.organtransplants.org/

Personal blogs regarding dialysis that I found helpful are Gil's http://gil1.home.pipeline.com/esrd/ and Sandra's mom http://kidneytransplantforkyliesmom.blogspot.com/

I know I have more, also some books, I will post later.

I admire you for taking on this project!
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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
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