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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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May 2009 - Posts

  • Safety Mom Helps Parents Get Smart about Cord Blood Banking

    Posted: May 21, 2009

    Safety Mom Alison Rhodes has been an active proponent of child health and safety issues ever since her first child died from Sudden Infant Death Syndrome (SIDS) in 1997. A fervent believer that parents are the best advocates for their children, Alison maintains a website and blog, and travels the country speaking on topics about children’s health and well-being, including cord blood banking.

    Alison recently appeared on ABC San Francisco’s The View from the Bay television program, where she discussed emerging research involving cord blood stem cells as well as the cost of preserving a child’s own cord blood for future use – approximately $18 per month for the first 18 years of a child’s life.  “Things are being done with cord blood that are absolutely amazing,” Alison stated.  Given the tremendous pace of medical research, “it’s insurance for the future.”

    View Safety Mom Alison Rhodes on The View from the Bay

    Visit the Safety Mom online

  • A Physician’s Perspective: Two Purchases That Can Be Lifesaving for Your Newborn

    Posted: May 15, 2009

    Increasingly, physicians and researchers are studying the use of a child’s own cord blood stem cells to help repair specific tissue or organs in the body damaged by disease or injury.  Referred to as regenerative medicine, this field of study has the potential to change the treatment of conditions that have no cure today. 

    Dr. Marra Francis, a board-certified obstetrician-gynecologist and former Chair of Obstetrics and Gynecology at Memorial Hermann Hospital in Texas is a strong believer in the value of cord blood stem cells, as well as the importance of educating expectant mothers about the ability to preserve this important medical resource.

    Recently Dr. Francis’ shared her perspectives with us:

    What do you tell your patients about cord blood banking?
    From my perspective, there are only two things you can buy for your unborn child that are lifesaving: a good car seat and cord blood banking.  I educate every one of my patients on the options for preserving cord blood. 

    How did you first become involved with cord blood banking?
    I was introduced to cord blood banking during my residency. We collected cord blood for private storage, public donation and for a study using cord blood to research the impact of toxins from the World Trade Center disaster to unborn children. During my chief year of residency, I became pregnant and knew from my experience and education of cord blood banking that I wanted to have this valuable medical resource for my child.

    How do you incorporate cord blood education into your practice?
    This is an important topic, so I begin cord blood education on the first visit by handing out educational materials.   I check at the both 16-week visit as well as the 20-week visit during the ultrasound to see if the patient has any questions. By this time the parents, and usually the grandparents, are a very captive audience as they first see the baby. My final discussion with the patient is at the 36th week, so the decision on whether to store, donate or discard their child’s cord blood is made well before the newborn arrives. 

    What do you tell your patients when they ask about the cost of banking?
    I believe the cost of banking should be incorporated into a baby budget established at the very beginning of pregnancy.  A newborn does not know – or care – if the crib bedding matches the curtains, or if they have on a designer “onesie.”  But the ability to provide your child a treatment option for a life-threatening illness or injury is absolutely priceless. I often compare the cost of banking to the cost of a flat-screen television.  The price may be the same, but the value to your family is very different.  All of my children have their cord blood banked, and we still use the television from my husband’s college fraternity house.

    What do most patients ask about cord blood banking?
    I often get asked about the likelihood of using banked cord blood stem cells.  I point to the published data that suggests 1 in 200 individuals will need a stem cell transplant at some point in life.  I also explain that the odds of using cord blood will increase with advancements in regenerative treatments for tissue and organ damage. I truly envision a day when patients arriving at the ER will be routinely questioned by the triage nurse, “Do you have your cord blood banked?”  That answer will determine the course of treatment for the patient.

  • A Horse? Of Course! Using Cord Blood Stem Cells to Treat Race Horse Injuries

    Posted: May 07, 2009

    We may not be the only ones to benefit from banking cord blood. In a recent blog entry published at the Huffington Post, nurse practitioner Barb Dehn describes how the latest advances in regenerative medicine may have exciting implications for thoroughbred horses. For example, the stem cells of race horses may someday be used by veterinarians to safely treat what could otherwise be career-ending injuries.

    In her blog entry, Barb points out that many researchers are now recommending that owners and breeders of prize-winning thoroughbreds bank their umbilical cord blood. “If it’s a good idea for a race horse, then you can bet it’s probably a great idea for humans,” Barb writes in her blog post. We couldn’t agree more. You can read Barb’s blog entry in its entirety here.

  • Every Parent Has the Right to Know

    Posted: May 01, 2009

    Congresswoman Jackie Speier, a longtime champion of women’s and children’s health issues, introduced landmark legislation on the floor of the U.S. House of Representatives this week that advocates for the right of every parent to understand the value of cord blood stem cells and the ability to preserve them. 

    Designated the Cord Blood Education and Awareness Act (H.R. 2107), this landmark legislation takes a much-needed step forward in addressing a fundamental problem: expectant parents are poorly informed about cord blood banking.  In fact, a comprehensive study of obstetric patients’ knowledge of cord blood banking published in the Journal of Reproductive Health found that only 14 percent of patients were educated about cord blood banking by their nurse or obstetrician.  Of those patients that indicated some familiarity of the topic, 74 percent described themselves as “minimally informed!”

    Given what we now know about the many available uses of cord blood stem cells, plus the great potential they hold for future regenerative medicine therapies targeting conditions that have no cure today, Representative Speier understands that providing better education and resources is a public health priority. 

    The Act includes several provisions intended to provide much-needed information about cord blood banking, including:
    • A public education campaign that highlights the value of cord blood stem cells, provides details of public and private banking options, and average costs associated with cord blood banking.
    • Creation of a patient informed consent document enabling expectant mothers to acknowledge in writing that they’ve received balanced information about cord blood banking options from their healthcare professional.
    • Development of professional materials aimed at educating healthcare providers who offer prenatal services to pregnant women.
    • Grants for targeted education about cord blood banking, particularly for people with certain conditions who may benefit from new stem cell therapies and minorities who may have trouble finding available public cord blood samples.

    We believe this legislation will ultimately save lives and help further the remarkable progress we’re already seeing in the use of cord blood stem cells for regenerative medicine purposes. While cord blood legislation has been enacted in 21 states, specifics vary from state to state. The Cord Blood Education and Awareness Act would ensure that every pregnant mother in America has the same level of support to make an informed decision about whether to preserve her child’s cord blood for family use, donate the cells for public use or consent to allowing them to be disposed of as medical waste.

    We encourage everyone to show their support.  Contact your Representative of Congress and encourage them to support the Cord Blood Education and Awareness Act of 2009!  For information on how to contact your Congressperson, visit the U.S. House of Representatives “Write Your Representative” site or call 202-224-3121.
     
    CBR press release in support of the Cord Blood Education and Awareness Act of 2009

    Rep. Speier’s official statement on the Cord Blood Education and Awareness Act of 2009