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Spina Bifida: How to Protect Yourself and Your Baby

By: Jennifer Wider, MD
October 25, 2010

October marks National Spina Bifida Awareness Month, a condition that affects thousands of American babies each year.

Spina Bifida is a birth defect caused by the incomplete closing of the neural tube during embryonic development. The neural tube is a structure that ultimately forms the baby’s brain and spinal cord and their surrounding tissues. In normal fetal development, the neural tube forms early on in pregnancy and closes several weeks thereafter. In babies with Spina Bifida, a portion of the tube fails to close properly, which can lead to defects in the back bone and spinal cord.

According to statistics from the Spina Bifida Association of America (SBAA), Spina Bifida is the most common, permanently disabling birth defect in the United States. Every day, roughly eight babies are born with Spina Bifida or a related birth defect in this country.

While the exact cause of Spina Bifida is not entirely known, there are several recognized risk factors. According to information from the Mayo Clinic’s Foundation for Education and Research, the following are the most common risk factors:

  • Family history: Women who have given birth to one child with a neural tube abnormality seem to have a higher risk of occurrence in subsequent children.
  • Race: Spina Bifida seems to more common in Caucasian and Hispanic populations.
  • Folic Acid deficiency: A nutritional deficiency of folate (or folic acid), vitamin B9, increases the risk of Spina Bifida and many other neural tube defects.
  • Certain medications: Research studies have shown that certain drugs including anti-seizure medications may interfere in the body’s ability to utilize folic acid and can lead to an increase in neural tube problems.
  • Obesity: Women who are obese prior to and during their pregnancies have a higher risk for Spina Bifida and other known neural tube deformities.

While some of the risk factors cannot be controlled, others including diet and vitamin supplements clearly make a difference. “Folic acid dietary supplementation appears to reduce the occurrence of Spina Bifida and other neural tube defects,” explains William Graf, MD, Director of the Yale/New Haven Hospital Spina Bifida Program in Connecticut. “Clinicians in the United States should advise women without a family history of NTDs (neural tube defects), who anticipate a pregnancy to take .4-.8 mg (400-800 micrograms) of folic acid daily.”

According to data from the SBAA, “if all women who could possibly become pregnant were to take a multivitamin with folic acid, the risk of neural tube defects like Spina Bifida could be reduced by up to 70 percent.” Because many pregnancies are unplanned, most experts recommend women in their childbearing years to take the recommended dose of 400 micrograms of folic acid. Folic acid can be found in foods including: dark, green leafy vegetables, whole wheat products, nuts and seeds, oranges, grapefruits and fortified cereals and grains.

It is important for women to realize the cause of Spina Bifida is not clearly understood and most likely results from an interplay of many factors, including: nutritional, environmental and genetic. According to Dr. Graf, “there has been a slight miscommunication that folic acid will completely prevent this very complex, early neurodevelopmental disorder.” Thus, if a woman has a family or personal history of neural tube defects, it is important she speaks to her health care provider about how to further reduce the risk for her offspring.

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For more information on the Society for Women’s Health Research please contact Rachel Griffith at 202-496-5001 or Rachel@swhr.org.

 

Havoc Reigns in DC

Provocative new documentary premieres in DC

Washington, DC (September 29, 2010) — On September 28, in front of a packed house at the Burke Theatre in the United States Navy Memorial, the provocative documentary Hot Flash Havoc premiered to an audience of prominent Washingtonians as well as out of town guests.

Hosted by the Society for Women’s Health Research (SWHR), the film, which was both informative and entertaining, received thunderous applause at the curtain’s call. Following the screening, a panel moderated by SWHR president and CEO Phyllis Greenberger, MSW, and featuring distinguished physicians Alan Altman, MD, Pamela Peeke, MD, and Susan Wysocki, RNC, NP took questions from the audience on this important rite of passage.

“We are very happy with the turnout and reactions the documentary is receiving,” said Greenberger. “Producer Heidi Houston will be taking her film on a cross-country major market tour de force. The film is a must-see!”

The partnership between Hot Flash Havoc and SWHR will continue to raise awareness on menopause and available treatments. To order a copy of the DVD, please visit www.swhr.org and watch for the announcement of the DVD’s availability; a portion of the proceeds benefit SWHR and women’s health research.

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For more information on the Society for Women’s Health Research please contact Rachel Griffith at 202-496-5001 or Rachel@swhr.org.

The Society for Women’s Health Research (SWHR), a national non-profit organization based in Washington D.C., is widely recognized as the thought leader in women’s health research, particularly how sex differences impact health. SWHR’s mission is to improve the health of all women through advocacy, education and research. Visit SWHR’s website at www.swhr.org for more information.

 

SWHR Applauds House Passage of the HEART for Women Act

Washington, DC (September 30, 2010) — Important legislation to improve the diagnosis, treatment and prevention of the leading killers of American women — heart disease, stroke and other cardiovascular diseases passed the House of Representatives late last night, Septemeber 29, marking a huge victory for women’s health advocates everywhere.

The Heart Disease Education, Analysis and Research and Treatment (HEART) for Women Act raises awareness among women and their health care providers about their risk for heart disease and stroke. The bill provides greater oversight of Food and Drug Administration requirements for reporting sex and race-based data about new medicines and devices and authorizes the expansion of the Centers for Disease Control and Prevention’s WISEWOMAN screening program for low-income, uninsured women to additional states.

“Cardiovascular disease is the number one killer of women and the HEART for Women Act will raise awareness, improve treatment options and educate women on prevention and care. SWHR is pleased with the House’s vote today,” said Phyllis Greenberger, M.S.W., president and CEO of the Society for Women’s Health Research.

Every minute in this country, someone's mother, sister, wife or friend will die from heart disease, stroke or other cardiovascular diseases. These diseases claim the lives of more than 432,000 American women each year — more than the next four causes of death combined. Nearly half of all African-American women have some form of cardiovascular disease, compared to 35 percent of Caucasian women. More than 90 percent of primary care physicians do not know that more women die each year from cardiovascular disease than men, according to an American Heart Association survey.

The legislation was introduced by Representatives Lois Capps (D-CA) and Mary Bono Mack (R-CA) and Senators Debbie Stabenow (D-MI) and Lisa Murkowski (R-AK).

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For more information on the Society for Women’s Health Research please contact Rachel Griffith at 202-496-5001 or Rachel@swhr.org.

The Society for Women’s Health Research (SWHR), a national non-profit organization based in Washington D.C., is widely recognized as the thought leader in women’s health research, particularly how sex differences impact health. SWHR’s mission is to improve the health of all women through advocacy, education and research. Visit SWHR’s website at swhr.org for more information.

 
 
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