So... I've looked into it and gotten a basic idea of what it costs to bank and store and what it can treat. However, I'd love to get a better idea of how practical it is to get it out and use it, should a need for it arise. Do most doctors have the ability to use it as a treatment? Would insurance cover the use of cord blood stem cells as a treatment? Would you need to live near an ongoing clinical trial in order to use it? Would it cost an additional arm and leg to use it?
My mother in law currently has breast cancer in liver. I'm wondering if we could use it for her? Unfortunately, she is an irrational person who will probably say no without even asking her doctor or hearing us out...

Anyone got any info on how to approach that? I guess we would need to start with her doctor?
If not for her, I'm interested in it for all family members. DH has a family history of cancer, and I have a family history of autoimmune diseases. If not that, I definitely want to donate it.
What are you guys doing?
Re: Talk to me about cord blood banking
And I'm so sorry that you're going through that with your mom, @strickland8052. Both my mom and grandma were/are breast cancer survivors. I know how shitty and scary it can be.
BFP #1: 7/15/15, SB: 11/14/15
Rainbow baby DS born 9/29/16!!
BFP #3 3/26/18 | Due 12/3/18
I think donating it makes sense if it's something that you care about. There's a whole lot more research that needs to be done. I really view private banking as a money making scheme with very little practical use or benefit for the vast, vast, vast majority of people. Not to mention the fact that cord blood is only usable for about 10 years.
From what I do remember tho is that it is pretty
expensive bank it. The chances of your baby needing its own cord blood the road are extremely slim.
I would look into the cancers that run in your family and see if any can be treated with cord blood. I would also talk to some doctors in those fields. They might have some expierence and insight.
But I did read that donating is a great choice because there's a great chance that they would find someone it would benefit.
Fell in love: Dec 2005 // Married: Feb 9, 2013
Little Miss Rosalie Harper--Born Jan 9th, 2014
I knew nothing about this with my first two at all, just recently heard about it.
HOWEVER stem cells are SO SO SO important for research and have more uses every day so I definitely recommend donating!!
Also, I have never heard that you can't do delayed cord clamping and donate. I already talked to my doctor about it and will be doing both.
DS#2 due 25 April 2019
We banked our son's. We wanted to donate, but we didn't qualify as my husband is a cancer survivor. It was expensive, but given my husband's history, it was no question for us.
I think they said the chances of us getting our own back in the event we needed it if donated, was high, but I'm not sure if that's the norm for all donation banks.
We plan to bank our twins as well.
I encourage you to call your local donation center. That helped us decide for sure.
BFP #1: 7/15/15, SB: 11/14/15
Rainbow baby DS born 9/29/16!!
BFP #3 3/26/18 | Due 12/3/18
This is a biased blog post for delayed clamping from a midwife, but it contains good facts as well as some visual representation to see what you're actually working with (blood wise) after you've done delayed clamping.
It's obviously a very personal decision, and should require some research as with anything else.
However I bolded the above because I would remind people that donation centers like viacord (etc) are a business, and as such they are in it to make money. So if you contact them they are going to try to sell you on it.
I agree, please do your research on whatever method you choose.