Spina Bifida Association Serving people living with spina bifida, the most frequently occurring permanently disabling birth defect. SBANC is a tax-exempt, non-profit 501 (c)(3) charity organization serving people living with spina bifida and their families. All donations are tax-deductible. |
sbanc@mindspring.com 1-800-847-2262 3915 Grace Court Indian Trail, NC 28079 |
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Frequently Asked Questions
How do I get the SBANC newsletter?
The condition can result in varying degrees of paralysis, loss of sensation in the lower limbs, and in bowel and bladder complications. Spina bifida is often accompanied by hydrocephalus, the accumulation of fluid in the brain. Hydrocephalus is controlled by a surgical procedure called "shunting".
Therefore, the US Public Health Service recommends "that all women of childbearing age in the United States should consume 0.4 mg of folic acid daily to reduce the risk of having a pregnancy affected by a neural tube defect." The Spina Bifida Association of North Carolina is open to people in North Carolina living with spina bifida, and their family members. There is no cost to join. Just send your name, why you are interested in joining SBANC (e.g. have spina bifida, family member, etc.) your mailing address and e-mail address to: sbanc@mindspring.com
The SBANC newsletter may be of interest to members, teachers, health care professionals, donors, volunteers, etc. To receive a copy, please send your name, why you are interested in getting the newsletter (member, donor, volunteer, teacher, etc.), mailing address and e-mail address to sbanc@mindspring.com
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