North Florida Nesties
Dear Community,

Our tech team has launched updates to The Nest today. As a result of these updates, members of the Nest Community will need to change their password in order to continue participating in the community. In addition, The Nest community member's avatars will be replaced with generic default avatars. If you wish to revert to your original avatar, you will need to re-upload it via The Nest.

If you have questions about this, please email help@theknot.com.

Thank you.

Note: This only affects The Nest's community members and will not affect members on The Bump or The Knot.

s/o Bone Marrow

Are you on the bone marrow registry? Would you join and donate marrow to a complete stanger if you were a match? Why or why not?
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Re: s/o Bone Marrow

  • I joined the registry 1 1/2 years ago & if they called and said I was a match for someone, anyone, I would donate. I know they say it can be painful & like any procedure there are a few risks, but I can make more bone marrow. I actually look forward to the possibility of them calling me one day.
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  • I've heard this brought up in a few different circles recently and it's something I'm considering. I am a total pansy so I'm afraid of the pain aspect but I think it would be a wonderful thing to do.
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  • I am not on the registry currently, but I may consider it later in life.
  • I didn't know that you could just join the registry. I'll have to look into that. I would have to research the risks more but I don't think I would have an issue donating marrow to a person I know or to a stranger.
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  • imagejodippls:
    I didn't know that you could just join the registry. I'll have to look into that. I would have to research the risks more but I don't think I would have an issue donating marrow to a person I know or to a stranger.

    Well you can either stop by a facility or have them send you a packet in the mail. I had one sent in the mail and they give you all of the supplies and instructions. Joining is easy. It's simply four swabs on the inside of your cheek. I guess they get all the info they need from your cells and then only if you're a match do you actually have to have a more invasive procedure.

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  • imageclseale13:

    imagejodippls:
    I didn't know that you could just join the registry. I'll have to look into that. I would have to research the risks more but I don't think I would have an issue donating marrow to a person I know or to a stranger.

    Well you can either stop by a facility or have them send you a packet in the mail. I had one sent in the mail and they give you all of the supplies and instructions. Joining is easy. It's simply four swabs on the inside of your cheek. I guess they get all the info they need from your cells and then only if you're a match do you actually have to have a more invasive procedure.

    That is easy. Thanks for the info, I'm going to look into it.
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  • No I'm not and I don't see myself joining the registry any time soon.  I don't know enough information to know all about the procedure/risks/details, etc.  At this point I also don't care enough to do the research for it apparently.
  • imageMadisen:
    No I'm not and I don't see myself joining the registry any time soon.  I don't know enough information to know all about the procedure/risks/details, etc.  At this point I also don't care enough to do the research for it apparently.

    Haha. Well doing some work for the Leukemia & Lymphoma society was what prompted me to finallly join. Plus, my mom has been an Oncology nurse practitioner for the last 15 yrs and does bone marrow biopsies all of the time. She's also on the registry. I was able to ask her any questions & I guess after seeing how routine she really felt it was it eased any concerns I had.

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  • I didn't eve know there's a registry. I'll look into it now!
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  • imageclseale13:

    imageMadisen:
    No I'm not and I don't see myself joining the registry any time soon.  I don't know enough information to know all about the procedure/risks/details, etc.  At this point I also don't care enough to do the research for it apparently.

    Haha. Well doing some work for the Leukemia & Lymphoma society was what prompted me to finallly join. Plus, my mom has been an Oncology nurse practitioner for the last 15 yrs and does bone marrow biopsies all of the time. She's also on the registry. I was able to ask her any questions & I guess after seeing how routine she really felt it was it eased any concerns I had.

    Good to know.  There's been talk on MM about the registry and when I read about it it pique's my interest, but I'm too chicken (or lazy) to follow through on finding out more about it.

  • A girl on my month board posted about the registry recently b/c her nephew has leukemia. I looked into it then, but then honestly it slipped my mind. I would certainly consider it.
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  • No because I'm selfish and am a pansy when it comes to anything painful especially if it involves needles.  Just being honest.
  • imageLucille Bluth:
    No because I'm selfish and am a pansy when it comes to anything painful especially if it involves needles.  Just being honest.

    Yes Nothing wrong with that, LB.

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  • I didn't know there was a registry. It is something I would like to look into now.
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  • imageMadisen:
    No I'm not and I don't see myself joining the registry any time soon.  I don't know enough information to know all about the procedure/risks/details, etc.  At this point I also don't care enough to do the research for it apparently.

    I agree with Madisen on this one.  Maybe sometime later I will take the time to sit down and do some research on this and then make an informed decision.

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  • imageluckyinlove11902:
    I've heard this brought up in a few different circles recently and it's something I'm considering. I am a total pansy so I'm afraid of the pain aspect but I think it would be a wonderful thing to do.

    This. 

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  • I've thought about it, but I've never actually taken the steps to sign up for it.
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