Home         Forums  

Go Back   Marrowforums > Treatments > Transplants
Register FAQ Search Today's Posts Mark Forums Read

Transplants Bone marrow and stem cell transplantation

Reply
 
Thread Tools Search this Thread
  #1  
Old Sat Apr 13, 2013, 10:48 AM
edithr edithr is offline
Member
 
Join Date: Feb 2011
Location: 30 mi West of Cleveland
Posts: 86
transplant donor backing out

Bone marrow transplants are the only organ transplant situation (I believe, correct me if I'm wrong) where you are told there is a match before they ask the donor if they will donate. I've heard of several cases where a person in need of a transplant is told there is a perfect match, and then the donor backs out. This must be heart wrenching. So, do you think that Be The Match should change their policy to asking the donor before letting you know if you have a match?

Take Joe the Plumber. He needs a heart. There is a horrible car accident, and a heart becomes available. The transplant team asks the family if they can harvest the victims heart, they say no, and that it the end of it. Joe never knows that a life saving heart (a perfect match) was there, but for the families decision, he will not get it. Is that better for Joe? Is ignorance bliss?
__________________
Edith, mom to Eric, dx 2/11 at age 15 with SAA, began ATG/CsA 3/11, switched to Tacrolimis 8/11, off all meds 9/11 and is now considered to have bone marrow failure not otherwise specified.
Reply With Quote
  #2  
Old Sat Apr 13, 2013, 01:45 PM
sstewart09 sstewart09 is offline
Member
 
Join Date: Feb 2013
Posts: 65
Hmmm...that's an interesting question. Not sure what side I'd be on. It was devastating to find out that my husband's brothers were not a match, so finding out about all of his potential matches was the mental boost we needed. At the same time, we had a donor fall through and that was heartbreaking too. Not sure what the solution is.

I think a lot of people use Be the Match for testing for an individual person. People get signed up willing to be a match for that person and forget that they are now in the national donor registry. There are also a lot of active military in the registry. The military is where Be the Match started which is great, but when these people are deployed and end up being a match for someone, it can be disappointing as well.
__________________
Samantha, wife of Joe age 34; diagnosed vsaa 2012; MUD BMT February 2013
Reply With Quote
  #3  
Old Sun Apr 14, 2013, 12:13 AM
Neil Cuadra Neil Cuadra is offline
Owner
 
Join Date: Jul 2006
Location: Los Angeles, California
Posts: 2,556
As I understand it, the National Marrow Donor Program provides status information to your treatment center's transplant coordinator when donors are identified, contacted, and when they accept, decline, or (in the worst case) back out after initially agreeing. The transplant coordinator then informs the you (the patient) and your family. I assume that one reason they pass the information along promptly is that your treatment decisions can depend on it. For example, if you have a potential donor, even one that hasn't yet been contacted, you might hold off on a chemo treatment that you would otherwise choose to start.
Reply With Quote
  #4  
Old Mon Apr 15, 2013, 01:10 AM
NLJabbari NLJabbari is offline
Member
 
Join Date: Aug 2006
Location: San Jose, California
Posts: 139
Personally, I've always known that a "potential match" only means that the person is registered as a "Potential Donor" but that does not guarantee that they will be available or willing should they be called upon. I think most people who register do so with the intent to follow through if need be. But, sometimes for various reasons they're either not able to or not available. I can respect that...

I am thankful for the registry and for those who have willingly and voluntarily listed themselves as "Potential Donors". Bless them!

We were informed that my son had 2 potential 9/10 MUD's on the registry. They were not informed because we still had other options to explore before considering this route.
__________________
06/2004 my son was dx with SAA at the age of 10. No sibling BM match. He underwent ATG (H)/CsA. Relapsed 05/12 & dx'ed w/PNH. Currently in wait/see mode for Solaris as he is asymptomatic...
Reply With Quote
  #5  
Old Mon Apr 15, 2013, 11:01 AM
KathyM KathyM is offline
Member
 
Join Date: Mar 2013
Location: Philadelphia, PA
Posts: 23
Interesting question. It’s a tough one, for sure. My H was originally told there were 10 matches for him. Within days – 7 people declined. We weren’t bothered by that – I’d much rather someone make that decision right away rather than wait and provide false hope. And yes, who knows what the circumstances were – change in health, etc. I do believe that family members who agree to be tested should be told they are now in the registry and they should make a decision if they want to stay in the registry.

The worst thing is when the donor backs out, which is what happened with my husband. A donor was identified and contacted and tested. One week prior to the scheduled transplant he backed out. Can you even imagine the devastation? Believe me, I completely understand the need for anonymity now! Backing out at the 11th hour – oh my gosh – unbelievable. Thank goodness the 2nd donor has stepped up.
__________________
Kathy, wife of Dennis (58 yrs old) diagnosed October 2012 w/MDS; bone marrow biopsy confirmed significant fibrosis;blast cells of 5%-10% of total cells, high risk refractory anemia w/ excess blasts (RAEB1); 3 cytogenetic markers; +1, -7, and +21
http://www.caringbridge.org/visit/dennismolyneaux
Reply With Quote
  #6  
Old Tue Apr 16, 2013, 03:32 PM
4bcsboys 4bcsboys is offline
Member
 
Join Date: Jul 2008
Location: Lincoln, DE
Posts: 29
marrow versus PCSC

Some people may register, listing that they are willing to donate PCSC, but not wanting to have marrow collected in an OR. A family friend is registered this way. I don't know if all these potential donors show up on the preliminary search or not.

This is something I'm wondering about because I'm waiting on a match. My sister received the opposite genetic materia from BOTH parents. I'm trying to laugh over that one.
__________________
Wife and mother of three young boys, diagnosed at age 39 with AA 2007; treated with ATG and cyclosporine; progressed to MDS end of 2012; MUD on June 26, 2013.
Reply With Quote
  #7  
Old Tue Apr 16, 2013, 08:58 PM
Neil Cuadra Neil Cuadra is offline
Owner
 
Join Date: Jul 2006
Location: Los Angeles, California
Posts: 2,556
Quote:
Originally Posted by 4bcsboys View Post
This is something I'm wondering about because I'm waiting on a match. My sister received the opposite genetic materia from BOTH parents. I'm trying to laugh over that one.
Yeah, you have to laugh so you won't cry. My wife's brother and sister matched each other, but neither matched her.
Reply With Quote
  #8  
Old Mon Apr 22, 2013, 09:35 PM
pedro pedro is offline
Member
 
Join Date: Apr 2013
Location: london,ontario
Posts: 2
I was booked for "mud"bmt but found out the day before I was to have hospital tests that the donor was default for medical reasons . Thankfully the atgam treatment started to kick in and seven months later the cyclosporin is still working to keep my cell numbers up so that i am nine months since last transfusion. All the same it was a emotional time to go through from deciding to go though with bmt to finding out it was not going to happen,to having my cell numbers increase to a sustainable level.
Reply With Quote
  #9  
Old Tue Apr 23, 2013, 01:46 AM
Neil Cuadra Neil Cuadra is offline
Owner
 
Join Date: Jul 2006
Location: Los Angeles, California
Posts: 2,556
Pedro,

I'm very glad to hear that your immunosuppressant treatment is working. Things must have looked rather bad for you right after the transplant option was pulled out from under you. The way you've bounced back could give anyone hope!
Reply With Quote
Reply


Thread Tools Search this Thread
Search this Thread:

Advanced Search

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

vB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
No donor - Cord Blood Transplant? Sue&Dave Transplants 6 Tue Nov 22, 2016 01:15 PM
16 months past SCT and doing fairly well. The sage of my transplant, start to now rar MDS 7 Wed Nov 18, 2015 10:26 PM
From transplant to World Record in 6 years! squirrellypoo Transplants 4 Sat Sep 26, 2015 05:56 PM
New to site, Transplant Disappointment & Worries sveness Transplants 2 Sun Mar 4, 2012 11:05 AM
NMDP Provides Transplant Information Marrowforums Transplants 1 Tue May 8, 2007 04:00 AM


All times are GMT -4. The time now is 09:26 PM.


Powered by vBulletin® Version 3.6.7
Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.
Forum sites may contain non-authoritative and unverified information.
Medical decisions should be made in consultation with qualified medical professionals.
Site contents exclusive of member posts Copyright © 2006-2020 Marrowforums.org