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-   -   transplant donor backing out (http://forums.marrowforums.org/showthread.php?t=3583)

edithr Sat Apr 13, 2013 10:48 AM

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?

sstewart09 Sat Apr 13, 2013 01:45 PM

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.

Neil Cuadra Sun Apr 14, 2013 12:13 AM

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.

NLJabbari Mon Apr 15, 2013 01:10 AM

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.

KathyM Mon Apr 15, 2013 11:01 AM

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.

4bcsboys Tue Apr 16, 2013 03:32 PM

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.;)

Neil Cuadra Tue Apr 16, 2013 08:58 PM

Quote:

Originally Posted by 4bcsboys (Post 28070)
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.

pedro Mon Apr 22, 2013 09:35 PM

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.

Neil Cuadra Tue Apr 23, 2013 01:46 AM

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!


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