Anyone donate bone ...
 

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[Closed] Anyone donate bone marrow?

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Just given blood and was asked if I’d consider joining the bone marrow register. Before I say yes, has anyone done it? Is it as unpleasant as I suspect it will be?


 
Posted : 16/04/2018 7:02 pm
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Yes. It was one of the best things I have done in my life and a honour.

It'snot pleasant, but it is not that bad either. I donated on a  Wednesday was back on the bike gently on Sunday and work on Monday.


 
Posted : 16/04/2018 7:11 pm
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P.s. most people do not donate marrow but stem cells via  dialysis type method where you sit in a chair for 4 hours. I have done this too. Feel a bit weak forb24 hours but fine after.


 
Posted : 16/04/2018 7:15 pm
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Thanks TheBrick.

Anyone else?


 
Posted : 17/04/2018 10:55 am
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Can't do it sadly, too old 🙁

But I would if I could, wouldn't think twice.


 
Posted : 17/04/2018 11:29 am
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I'm on the Anthony Nolan register. Have been for about 5 years and one day may hear something if I'm a potential match for someone.


 
Posted : 17/04/2018 11:42 am
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I was recently identified as a possible donor. I registered over 20 years ago, back when I was a student. I've had the blood tests and the results have indicated that I am compatible. The last I heard was back in February when I was told that the transplant centre had not issued any instructions and they would be in touch as and when. I don't know if they line up several potential donors or just the one!

BTW apparently if your weight is below 50 kg (not a problem I have) the stem cell method is not suitable and they have to take the marrow from the pelvic area!


 
Posted : 17/04/2018 12:11 pm
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It will be only one person Hells, but the donation is tightly coupled to their treatment. So their treatment maybe better or worse than planned.... . Your match is is usually someone with a common ancestor aparently.


 
Posted : 17/04/2018 12:25 pm
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Interesting!! If they're related to me they have my sympathies!!!


 
Posted : 17/04/2018 12:28 pm
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Also been on the Anthony Nolan register for the last 20 years, ever since my brother became ill(A-plastic anaemia) and one of the potential treatments at the time was a bone marrow transplant(fortunately he didnt need it in the end).

Have been called up twice as a potential match in the early years but nothing for over 15years now.


 
Posted : 17/04/2018 4:24 pm
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I had bone marrow removed from my pelvis to cultivate my own stem cells, they froze the area, took a hammer to the crown of my pelvis and sucked out some marrow, only thing I felt was a wierd feeling as they were sucking it out, it was literally nothing to be worried about at all

Im sure as a donor they would be nice to you


 
Posted : 17/04/2018 5:13 pm
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They knocked me out when they took the bone marrow from my pelvis. Super easy.

If you are black or Asian (or I think any ethnic minority) you should double  definitely as the odds of a match for BME is massively lower. You should say yes anyway but we need more BME registered as it can be so tough to find a match for patients.


 
Posted : 17/04/2018 7:10 pm
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Received a letter today from Anthony Nolan Trust. Apparently the person I was matched with is not a suitable candidate for stem cell transplant!

Not sure what to make of it!! The letter says that the transplant centre have not indicated that the person has improved or deteriorated! 😕


 
Posted : 26/05/2018 5:53 pm

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