Bone Marrow Donors Needed

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sygyzy

Lifer
Oct 21, 2000
14,001
4
76
I wanted to help after watching an episode of House M.D. (don't laugh). But after I read more about it, it kind of turned me off. From what I understand, you have to pay for the sample to be taken and stored in a DB. Then if you get called, you have to fly out and take off work on your own time and money. Then when you get there, you have to undergo a bunch of tests to check if you are compatible (apparently more extensive tests than they can get from the original sample). Then if you are chosen, the extract. If not, you go home. Again, all of this is on your time and money. Does anyone realize how expensive a hospital stay and procedures are? And regardless of the outcome, even if yuo donate, you never get to meet the recipient.

Does anyone have any real world experience to counter this?
 

Fritzo

Lifer
Jan 3, 2001
41,920
2,161
126
Originally posted by: Mizugori
how do they determine who can donate... im surprised they haven't found a donor yet, does donating marrow have harmful side effects?

Unfortunately it's fairly painful :(

How are bone marrow stem cells donated?

Donations are made in one of two ways: surgically or peripherally.

The vast majority of unrelated donors go through the surgical procedure, which is considered a minor procedure. Donors who are related to patients often undergo the peripheral method.

If a donor has a stroke history but otherwise is healthy, we would use the surgical procedure because the peripheral procedure involves using a drug that is contraindicated for stroke.

What does the surgical procedure involve?

The week prior to surgery, a donor would give blood to be re-infused during surgery. The surgery itself, which is considered a day procedure, is two hours long.

While under general anesthesia, donors lay on their stomachs and surgeons insert a large hollow needle through the hip bones in the small of the back. There will be two to four puncture sites.

The needle is attached to a syringe that is used to draw blood containing stem cells up through the bone marrow.

How much pain does surgery cause?

The following day you can walk, but you?ll feel like you have a pretty bad bruise in the small of your back for about a week. The older the patient, the more difficult the procedure.

What does a peripheral donation involve?

Once donors pass their physical, they begin a series of injections of a drug called filgrastim (Neupogen®), which causes stem cells to concentrate in the bloodstream. They take two injections for four days.

What are the side effects of Neupogen?

Neupogen can cause:

Headaches
Bone pain
Backaches
Electrolyte imbalances
Fatigue
Some people experience the bone pain to a great degree, and others say they never had the bone pain. We treat it with pain pills and make sure there is someone looking after the donor.

To monitor side effects, the donor is required to stay in Houston seven to 10 days and has clinic visits with lab tests. As soon as donors stop taking injections, side effects start to diminish within 24 hours.

How are stem cells collected peripherally?

During up to three procedures, called apheresis, an intravenous (IV) line is inserted in each arm. A machine circulates blood out of the body from one IV, through the machine, where it is processed, then returns it to the other arm.

Only about 100ccs (half of a soft drink can) are outside the body at any given time.

What are the side effects of apheresis?

People feel cold, but we give them warm blankets. There?s some pain related to the IV. There also might be a drop in blood pressure, but donors lie in bed and their vital signs are monitored.

What care is needed after apheresis?

At the end of each collection, donors return to their home or hotel for the day. The following morning, doctors check the results of the previous day?s collection and check the donor?s blood count and electrolyte levels.

 

Mike2002

Senior member
Jan 11, 2004
290
0
0
Originally posted by: sygyzy
I wanted to help after watching an episode of House M.D. (don't laugh). But after I read more about it, it kind of turned me off. From what I understand, you have to pay for the sample to be taken and stored in a DB. Then if you get called, you have to fly out and take off work on your own time and money. Then when you get there, you have to undergo a bunch of tests to check if you are compatible (apparently more extensive tests than they can get from the original sample). Then if you are chosen, the extract. If not, you go home. Again, all of this is on your time and money. Does anyone realize how expensive a hospital stay and procedures are? And regardless of the outcome, even if yuo donate, you never get to meet the recipient.

Does anyone have any real world experience to counter this?

Most of the time the person's insurance that is receiving the transplant will cover the costs of the donation process. They will also harvest the marrow in a location closest to the donor and then transport the marrow to the transplant center in a little red cooler.

 

SacrosanctFiend

Diamond Member
Oct 2, 2004
4,269
0
0
Originally posted by: Mike2002
Originally posted by: illusion88
Originally posted by: Xanis
Originally posted by: akshatp
Originally posted by: illusion88
well what blood type do they need?

Its not blood they need. Its bone marrow.

IIRC, a compatible blood type is needed for a successful transplant.

True statement. A compatible blood type is needed for all transplants I believe.

This acutally isn't the case. The donor and recipient do not need to match blood types. But the Marrow Registry is definitely a great thing. I just had my bone marrow transplant 3 months ago and searched through this registry since no one in my family was a match.

So to anyone on the registry or to anyone that donates blood you're a big help to everyone. :D

The donor and the recipient do need to have the HLA and the MLC match. Family members are best, as there is a greater chance of mismatch when using an unrelated donor.
 

Turin39789

Lifer
Nov 21, 2000
12,218
8
81
im still interested in the difference between the drives listed on the friends site and the donation centers listed on the nmdp homepage, and the merits of each. if anyone knows.
 

OutHouse

Lifer
Jun 5, 2000
36,410
616
126
that sucks dude. my dad had AML but was too old to be considered for a transplant.
 

Mxylplyx

Diamond Member
Mar 21, 2007
4,197
101
106
Donating bone marrow seems like more than a casual procedure. I think I would only have the will to do this if I knew the person who was in need.
 

Mizugori

Senior member
May 3, 2007
496
0
0
I saw on their site there's a meeting or whatever tomorrow at 5-9pm in flushing. i'll try to be there.

it said on some literature that ethnicity is a big factor, will my marrow be useless because I'm white?
 

jaybert

Diamond Member
Mar 6, 2001
3,523
0
0
what happens when you go to one of these? does you get put into the national registry? or just for the people that these drives are for?
 

jman19

Lifer
Nov 3, 2000
11,225
664
126
After reading all of this, I am highly considering donating... I doubt I will be able to help these guys (I'm white, of British and Eastern Europe decent) but maybe I can help someone else down the road... I pray that these guys get the help they need to beat off this terrible affliction. Sad to see people so young suffer from this disease.

Out of curiosity, can you have your own stem cells harvested for a later time in case you need a transplant at some point in the future?
 

NissanGurl

Golden Member
Sep 4, 2003
1,111
0
0
I've been registered for a few years. Signed up during a blood drive at the school. I actually matched someone and was in the process of getting all the screening done, but before they could take the marrow the person unfortunately passed away. I didn't qualify for the type of donation where they screen the cells out of the blood. I was getting scheduled for the two holes in your hip bone donation. It still makes me sad that I couldn't donate in time to help that woman. Do you have to renew your registration or is it along the lines of once you are registered, you are registered for life? I'd like to be sure I'm still in the registry.
 

akshatp

Diamond Member
Oct 15, 1999
8,349
0
76
Originally posted by: Mizugori
I saw on their site there's a meeting or whatever tomorrow at 5-9pm in flushing. i'll try to be there.

it said on some literature that ethnicity is a big factor, will my marrow be useless because I'm white?

Thanks not only to you but also the others that have showed support in other posts;

The chances of the donor being South Asian are significantly better, but you never know, it isnt impossible for someone not to be a match purely based on race.

Any like I said before, you might be helping someone else down the road.

Thanks again to everyone for the continued bumps and general discussion. I, myself, am learning alot more about it thanks to the replies.
 

akshatp

Diamond Member
Oct 15, 1999
8,349
0
76
Originally posted by: jaybert
what happens when you go to one of these? does you get put into the national registry? or just for the people that these drives are for?

You get put on the national registry. If you cant help the people that the drive is for, they put you on the list and if you are a match in the future, they will contact you.
 

RearAdmiral

Platinum Member
Jun 24, 2004
2,280
135
106
I actually signed up for this when a drive came to penn state. I have my card and everything :)
 

jaybert

Diamond Member
Mar 6, 2001
3,523
0
0
bump. just went earlier today to the one in dallas (well, in richardson). im chinese, so prolly not a match, but figured it was as good time as any to get put into the registry.
 

DanTMWTMP

Lifer
Oct 7, 2001
15,908
19
81
I have to bump this. I just got a phone call that I AM A MATCH for a leukemia patient.
The side effects and stuff posted above is nothing compared to how much the patient goes through. I sincerely hope that I can save this person's life. And much luck for the OP.



for people who live in SD
Originally posted by: DanTMWTMP
Originally posted by: JulesMaximus
Nothing in San Diego County?

this is where I registered:
http://www.sandiegobloodbank.org/bone_marrow/

actually, they came to UCSD often, so that's how I got registered. When I was a student at UCSD, they had blood drives and bone marrow registering drives.

 

ngvepforever2

Golden Member
Oct 19, 2003
1,269
0
0
Originally posted by: DanTMWTMP
I have to bump this. I just got a phone call that I AM A MATCH for a leukemia patient.
The side effects and stuff posted above is nothing compared to how much the patient goes through. I sincerely hope that I can save this person's life. And much luck for the OP.



for people who live in SD
Originally posted by: DanTMWTMP
Originally posted by: JulesMaximus
Nothing in San Diego County?

this is where I registered:
http://www.sandiegobloodbank.org/bone_marrow/

actually, they came to UCSD often, so that's how I got registered. When I was a student at UCSD, they had blood drives and bone marrow registering drives.

You my friend, deserve a :beer: and a :cookie:

Good luck!

ng
 

akshatp

Diamond Member
Oct 15, 1999
8,349
0
76
Originally posted by: DanTMWTMP
I have to bump this. I just got a phone call that I AM A MATCH for a leukemia patient.
The side effects and stuff posted above is nothing compared to how much the patient goes through. I sincerely hope that I can save this person's life. And much luck for the OP.



for people who live in SD
Originally posted by: DanTMWTMP
Originally posted by: JulesMaximus
Nothing in San Diego County?

this is where I registered:
http://www.sandiegobloodbank.org/bone_marrow/

actually, they came to UCSD often, so that's how I got registered. When I was a student at UCSD, they had blood drives and bone marrow registering drives.

I would like to personally thank you and anyone else that even made the effort to sign up. My friends are still without any possible matches, and we had some huge drives here in NJ over the last month.