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National Council on Folic Acid

National Council on Folic Acid

A Coalition to Promote the Vitamin Folic Acid for the Prevention of Birth Defects

Mission | Goal | Strategies | What is the Council? | How was the Council formed? | Where is the Council now? | Members

Mission

To reduce birth defects by promoting the consumption of folic acid among reproductive-age women.

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Goal

The goal of NCFA is to reduce the number of neural tube defect affected pregnancies by recommending that women of childbearing age take 400 micrograms of synthetic folic acid daily, from fortified foods and/or supplements, in addition to consuming food folate from a varied diet.

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Strategies

1.  Increase the proportion of women who understand that consuming folic acid daily can help prevent birth defects.

  • Conduct broad-based public health education campaigns through all available media.

  • Partner with corporations to increase exposure for the folic acid message.

  • Develop, demonstrate and evaluate model programs to reach reproductive age women of various social and economic groups.

  • Conduct behavioral research to identify barriers to use of supplements.

2.  Make folic acid awareness a routine and standard part of the delivery of preventive health care services to women.

  • Work with national and state professional organizations to encourage physicians, nurses, nutritionists and other health professionals to counsel women to consume a supplement containing folic acid daily.

  • Work with managed care organizations, government programs, and nonprofit organizations to incorporate folic acid educational interventions into their existing programs and services.

  • Develop, demonstrate and evaluate model programs to teach health care providers how to educate their patients about the need for folic acid supplements.

3. Increase the level and availability of folic acid in food.

  • Conduct research and convene experts to determine most effective, safe level of folic acid fortification.

  • Conduct research and monitor medical literature to identify other health benefits of folic acid fortification (cleft lip, cleft palate, heart defects, heart disease, stroke).

  • Conduct and monitor research to assess any adverse effects of folic acid consumption on adult health.

  • Build relationships with administration and congressional officials to share new knowledge relative to folic acid fortification benefits and appropriate levels.

4. Evaluate the effectiveness of folic acid projects and programs and share lessons learned.

  • Conduct public opinion surveys to assess awareness of folic acid and use of supplements among women of childbearing potential.

  • Evaluate methods and build capacity for blood folate survey research.

  • Conduct birth defects surveillance to measure incidence of spina bifida and anencephaly.

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What is the Council?

The Council is a coalition of organizations committed to promoting the consumption of the B vitamin folic acid for the prevention of birth defects.

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How was the Council formed?

The staff of the Division of Birth Defects and Developmental Disabilities at CDC recognized the need to involve as many organizations as possible in the effort to educate the American public about the Public Health Service recommendation that all women consume 400 mcg of folic acid daily to prevent the serious birth defects of spina bifida and anencephaly. Discussions began with CDC, the March of Dimes, the Spina Bifida Association of America, the American Academy of Pediatrics, the American College of Obstetricians and Gynecologists, and a state health department representative. The idea was received with enthusiasm and the fledgling organization expanded quickly.

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Where is the Council now?

National Healthy Mothers, Healthy Babies Coalition has assumed leadership of the National Council on Folic Acid in 2002. The Council meets quarterly to coordinate educational activities related to the national campaign. The Council launched its education campaign in January, 1999. The campaign is based on messages and materials developed and tested by market research experts contracted by CDC. In order to maximize the reach of the campaign, the Council will share materials and implementation plans with many other groups from the fields of health care, public health, and business. Toward this end, the Council is expanding to include representatives from other organizations with activities and a commitment to increasing folic acid consumption for the prevention of NTDs. The current members of the Council, as of December 31, 1998, will serve as the Steering Committee of this alliance. If your organization is interested in joining the National Council on Folic Acid, please contact:

Donna Gentry
NCFA Program Manager
National Healthy Mothers, Healthy Babies Coalition
121 N. Washington Street, Suite 300
Alexandria, VA 22314
Phone: (703) 836-6110, Fax: (703) 836-3470, dgentry@hmhb.org

Web site:  http://folicacidinfo.org/

 

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Member organizations of the Council:

  • Alabama Folic Acid Council

  • Alliance of Genetic Support Groups

  • American Academy of Family Physicians

  • American Academy of Pediatrics 

  • American Academy of Physician Assistants

  • American Association of Health Plans

  • American College of Medical Genetics

  • American College of Nurse Practitioners

  • American College of Nurse-Midwives

  • American College of Obstetricians and Gynecologists

  • American College of Physicians – American Society of Internal Medicine

  • American College of Preventive Medicine

  • American Dietetic Association

  • American Medical Association

  • American Medical Student Association

  • American Medical Women’s Association

  • American Pharmaceutical Association

  • American Society for Reproductive Medicine

  • The Arc of the United States

  • Association of Maternal and Child Health Programs

  • Association of Reproductive Health Professionals

  • Association of State and Territorial Health Office

  • Association of State and Territorial Public Health Nutrition Directors

  • Association of Women’s Health, Obstetric and Neonatal Nurses

  • Centers for Disease Control and Prevention

  • Council for Responsible Nutrition

  • Health Resources and Services Administration

  • March of Dimes Birth Defects Foundation

  • National Association of Hispanic Nurses

  • National Association of Neonatal Nurses

  • National Association of Nurse Practitioners in Women’s Health

  • National Association of Pediatric Nurse Associates & Practitioners

  • National Association of School Nurses, Inc.

  • National Association of WIC Directors

  • National Birth Defects Prevention Network

  • National Black Nurses Association

  • National Alliance of Hispanic Health

  • National Council on La Raza

  • National Healthy Mothers, Healthy Babies Coalition

  • National Perinatal Association

  • National Society of Genetic Counselors

  • Pan American Health Organization

  • Robert Wood Johnson Foundation

  • Shriners Hospitals for Children

  • Spina Bifida Association of America

  • The Teratology Society

  • University of North Carolina, Chapel Hill

  • USA Dry Pea & Lentil Council

  • Wheat Foods Council

  • Organizations in bold comprise the Steering Committee 
    Member list as of March 13, 2003

    We appreciate your support and efforts in raising awareness about the importance of folic acid!

    Ask Flo!

    Sorry, we can't give you medical advice. Please talk with your doctor for questions about yourself. For other information, please contact:

    Division of Birth Defects and Pediatric Genetics 
    NCBDDD, CDC
    1600 Clifton Rd., NE, MS E-86
    Atlanta, GA 30333
    404-498-3800
    888-232-5929
    FAX: 404-498-3550
    flo@cdc.gov


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    Date last reviewed: 09/19/2003
    Content source:  National Center On Birth Defects and Developmental Disabilities (NCBDDD) 
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