With my first, I was almost sold on the cord blood banking, and we had a family member willing to pay for it. Then at almost the last second I didn't do it because I wanted to delay cord clamping with DS, which wouldn't have worked. Now that I'm on my second, I am thinking about it more because 1. the cord blood stem cells are more likely to be compatible with a sibling and 2. there are more and more developments in the medical community in regards to stem cells. My own good friend is working on a study in her lab which will (hopefully) reverse MS with the use of stem cells. Oh, and 3. my children have a very unlikely genetic makeup (I am Russian, DH is is afro-Carribean with Indian and British ancestry...), which makes me think that if God forbid they ever needed a transplant it would be hard to find a donor who is compatible.
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Has anyone researched private banking? What made you decide for or against it?
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My mom, who is a phd research biologist seems to think I am better off doing delayed cord clamping again to benefit my child immediately, as opposed to planning for the "what ifs". But she was totally of the other opinion with my first.
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I would love any advice on how to approach this decision. Oh, and it IS a very expensive one for us. I don't want to make it sound as if money isn't an issue.....It IS!








