I Hate Dialysis Message Board
Welcome, Guest. Please login or register.
November 27, 2024, 02:52:34 AM

Login with username, password and session length
Search:     Advanced search
532606 Posts in 33561 Topics by 12678 Members
Latest Member: astrobridge
* Home Help Search Login Register
+  I Hate Dialysis Message Board
|-+  Dialysis Discussion
| |-+  Dialysis: News Articles
| | |-+  Dear Abby: Child's kidney disease is topic for open discussion
0 Members and 2 Guests are viewing this topic. « previous next »
Pages: [1] Go Down Print
Author Topic: Dear Abby: Child's kidney disease is topic for open discussion  (Read 1310 times)
okarol
Administrator
Member for Life
*****
Offline Offline

Gender: Female
Posts: 100933


Photo is Jenna - after Disneyland - 1988

WWW
« on: October 15, 2011, 05:22:41 PM »


Dear Abby: Child's kidney disease is topic for open discussion

DEAR ABBY: I have two sons, 19 and 12. My younger boy has a rare form of kidney disease. His kidney function is currently normal, but his doctor says that in the future he may need a new kidney. At that point, his brother would be high on the list for compatibility and availability. I, sadly, would not.
How does one mention the possibility of being a donor to his older brother? Is it even fair to ask? If he doesn't offer, would I always resent it? Should we wait until there is a real need before asking?
Planning Ahead in California

DEAR PLANNING AHEAD: All families are different, and it's a credit to yours that you're thinking ahead regarding some of the difficult aspects related to donation. This subject can sometimes be fraught with the potential for perceived coercion. It can be offset by not framing it as a “request” from one family member, but as a general family discussion about the loved one's health situation.
Among the issues that should be raised: What does it mean for your younger son to have this rare kidney disease? What's the survival rate for an adolescent who receives a living donor transplant? What is involved in the donation process?
These questions should be raised as a family in conversation with a physician or other members of the kidney care team. Family members can then talk about how they feel about the issue, not as a response to a direct question. This provides a chance for better education about the condition as well as the process, and reduces fear.
The decision to be a living donor is a voluntary one and should be entered into free of pressure. Some people may not want to take the risk — and their rights should be respected. The evaluation process is very thorough. It's designed to minimize risk and also can uncover unexpected conditions in the potential donor that are important.
The National Kidney Foundation provides information on its website regarding this subject. Go to kidney.org to learn more.


http://newsok.com/dear-abby-childs-kidney-disease-is-topic-for-open-discussion/article/3611416
Logged


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
willowtreewren
Member for Life
******
Offline Offline

Gender: Female
Posts: 6928


My two beautifull granddaughters

WWW
« Reply #1 on: October 15, 2011, 06:09:12 PM »

Good advice!

 :2thumbsup;
Logged

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. :)
Pages: [1] Go Up Print 
« previous next »
 

Powered by MySQL Powered by PHP SMF 2.0.17 | SMF © 2019, Simple Machines | Terms and Policies Valid XHTML 1.0! Valid CSS!