Integrating Stem Cell Banking into Maternity Care

Diving deeper into

Kathryn Cross, CEO of Anja Health, on the future of stem cell therapy

Interview
About 2% of parents in the US today bank their stem cells, whereas in certain areas of China, it's as high as 10%, and in Singapore it’s reported to be around 30%.
Analyzed 4 sources

The real signal is that stem cell banking is not constrained by science alone, it is constrained by how each country packages it into maternity care. In the U.S., banking is still a niche out of pocket add on that many parents first hear about late in pregnancy. In parts of Asia, higher uptake has come from stronger hospital distribution, more normalized physician education, and banking models that sit closer to the healthcare system rather than outside it.

  • Europe is not broadly ahead of the U.S. on private banking uptake. The stronger European pattern is public donation infrastructure, with organizations like Eurocord, Netcord FACT, and JACIE shaping a system that has emphasized donor registries and transplant access more than consumer paid storage.
  • China looks different because cord blood is tied more directly to actual treatment demand. One 2024 comparison estimated both China and the U.S. at about 3% banking penetration overall, but China was doing about 10,000 cord blood therapies per year versus roughly 450 in the U.S., helped by transplant heavy use cases like thalassemia and province level hybrid public private banks.
  • Singapore became an early leader in private family banking because the category was commercialized as a mainstream birth decision. A 2012 Cordlife prospectus described Singapore private banking penetration at about 30%, showing how far adoption can rise when obstetric channels, consumer marketing, and family banking contracts are tightly integrated.

The next step in the U.S. is to move stem cell banking from a specialty purchase into a standard part of prenatal workflow. If education shifts upstream to OBs, doulas, and hospital birth programs, and if more therapies move from experimental use into routine care, U.S. adoption can climb meaningfully without needing any breakthrough in collection technology.