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The Stem Cell Source
 News & Views from Cord Blood Registry

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Welcome to The Stem Cell Source:
unique perspectives, commentary and information about a unique source of stem cells. Newborn stem cells from umbilical cord blood are saving lives and changing medicine. As the global leader in the collection and preservation of newborn stem cells, Cord Blood Registry is playing a crucial role in advancing medical research using a child's own cord blood to treat conditions that have no cure today. Join our discussion, spread the word, and learn more at our Web site, www.CordBlood.com.



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June 2009 - Posts

  • Cord Blood Banking: The “Ultimate Biological Recycling” of Life-Saving Stem Cells

    Posted: Jun 26, 2009

    Pregnancy TodayWhen we think of recycling, it’s usually in terms of pizza boxes, soda cans and glass bottles, but RN Janine Henson has a different perspective. In a recent article posted at PregnancyToday.com, a popular education site for expectant moms, Henson describes cord blood banking as a form of biological recycling. “In this age of product recycling, it is exciting news that we now have the opportunity to recycle life-saving blood cells that have routinely been discarded with the placenta after childbirth,” Henson writes.

    In the article, Henson provides a comprehensive overview of cord blood stem cells, including the collection and banking process, public and private banking options, and current and potential uses of cord blood stem cells—from leukemia and lymphoma to diabetes. For Hansen, the value of cord blood stem cells is clear, particularly for the thousands of Americans with life-threatening conditions who are unable to find bone marrow matches through the public donor system. “Umbilical cord blood collection and banking can make the difference in life or death for those awaiting stem cell transplants,” Henson writes.

    Further Reading: The ABCs of Cord Blood Banking

  • North Carolina Latest State to Enact Cord Blood Education Law

    Posted: Jun 09, 2009

    North Carolina Governor Beverly Perdue signs cord blood education legislation with bill sponsor Representative Margaret Dickson and Matthew Farrow, who received the world’s first cord blood stem cell transplant in 1998 from cord blood provided by his sister, Dorothy (to left).This week North Carolina Governor Beverly Perdue signed a law that requires the state’s Department of Health and Human Services to provide free education about cord blood stem cells and the options for preserving them to parents and physicians. Sponsored by Representative Margaret Dickson, this law also encourages physicians to make the information available to expectant parents early enough in pregnancy so that the parents can make an informed decision about whether to participate in a public or private cord blood banking program.

    North Carolina is the 22nd state to institute legislation about cord blood education, guided by recommendations first issued by the Institute of Medicine (IOM) in 2004.  In a comprehensive report to Congress analyzing the issues involved with creating a national banking program, the IOM included two key recommendations highlighting the need for healthcare providers to help all expectant parents make an informed choice about the storage or disposal of their newborn's cord blood stem cells and to provide education on all cord blood banking options prior to labor and delivery:

    • Recommendation 5.2:  Informed Consent Should be Obtained Prior to Labor and Delivery.  Informed consent for the collection, storage and use of cord blood should be obtained before labor and delivery, and after the adequate disclosure of information.
    • Recommendation 5.3:  Donors Must Be Provided with Clear Information about their Options.  The information provided to a donor must include a balanced perspective on the different options for banking (family banking or public donation). The information disclosed for donation should not include language that gives the impression that the unit will be available to the family after donation.                                                                                      

    The importance of the IOM study in shaping health policy on cord blood banking was highlighted in a U.S. Senate Committee Report that accompanied The Stem Cell Therapeutic and Research Act of 2005, creating the national cord blood banking program:

    “The committee strongly supports the IOM report recommendation that women be provided with a balanced perspective and clear information in order to participate, actively and knowledgably, in the choice of whether or how to donate cord blood. Informed consent is likely to include, at least, consideration of the following options: public donation or private storage; and disposal.”

    Thanks to the work of the Institute of Medicine, federal and state health policy on cord blood is changing. With the passage of the North Carolina law, nearly 75 percent of the U.S. population now benefits from state-endorsed education on cord blood stem cells.

  • Every Voice Counts: Support the Family Cord Blood Banking Act!

    Posted: Jun 04, 2009

    A few months ago we wrote about the Family Cord Blood Banking Act (H.R. 1718), a new federal bill that would allow parents to use pre-tax dollars to pay for cord blood stem cells. Now we’re asking for your help in making sure the bill becomes law.


    Under current IRS regulations, you can use tax-free dollars to pay for everyday medical expenses like over-the-counter cough syrup or band aids, but not the cost of preserving your newborn’s stem cells. Enabling families to use tax-free dollars to pay for cord blood banking through flexible spending accounts (FSAs), health savings accounts (HSAs), or health reimbursement arrangements (HRAs) can reduce the cost of cord blood banking – a significant benefit for many families who are struggling due to current economic conditions.


    The Family Cord Blood Banking Act has solid bi-partisan support, but more co-sponsors are needed to accelerate the process and help ensure that the bill becomes law. You can support this effort by asking your Representative to become a co-sponsor of H.R. 1718 in three easy steps:


    1. Know what the bill says:  Read the content of H.R. 1718

    2. Draft an e-mail:  It’s important to use your own words, but you can use this sample template to get started. If you’ve banked your child’s cord blood, be sure to include the reasons why you chose to do so.

    3. Contact your U.S. Representative: Visit the U.S. House of Representatives “Write Your Representative” web site. 

    The Time is Now!


    Because Congress is actively discussing Healthcare Reform issues now, your e-mails will have the most impact in the next three weeks (before the July 4th Holiday).  And, because every voice counts, encourage your friends and family to write their U.S. Representatives, too.

    Thanks for supporting this important legislation to make cord blood banking more affordable for all American families!