SPINA BIFIDA

Fact Sheet Number 12 (FS12), 1997
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NICHCY
National Information Center for Children and Youth with Disabilities
P.O. Box 1492
Washington, DC 20013
E-Mail: nichcy@aed.org
URL: http://www.nichcy.org
1-800-695-0285 (Voice/TT)
______________

DEFINITION OF SPINA BIFIDA

Spina Bifida means cleft spine, which is an incomplete closure in the
spinal column. In general, the three types of spina bifida (from mild to
severe) are:

1. Spina Bifida Occulta: There is an opening in one or more of the
vertebrae (bones) of the spinal column without apparent damage to the
spinal cord.

2. Meningocele: The meninges, or protective covering around the spinal
cord, has pushed out through the opening in the vertebrae in a sac called
the "meningocele." However, the spinal cord remains intact. This form can
be repaired with little or no damage to the nerve pathways.

3. Myelomeningocele: This is the most severe form of spina bifida, in which
a portion of the spinal cord itself protrudes through the back. In some
cases, sacs are covered with skin; in others, tissue and nerves are
exposed. Generally, people use the terms "spina bifida" and
"myelomeningocele" interchangeably.

INCIDENCE

Approximately 40% of all Americans may have spina bifida occulta, but
because they experience little or no symptoms, very few of them ever know
that they have it. The other two types of spina bifida, meningocele and
myelomeningocele, are known collectively as "spina bifida manifesta," and
occur in approximately one out of every thousand births. Of these infants
born with "spina bifida manifesta," about 4% have the meningocele form,
while about 96% have myelomeningocele form.

CHARACTERISTICS

The effects of myelomeningocele, the most serious form of spina bifida, may
include muscle weakness or paralysis below the area of the spine where the
incomplete closure (or cleft) occurs, loss of sensation below the cleft,
and loss of bowel and bladder control. In addition, fluid may build up and
cause an accumulation of fluid in the brain (a condition known as
hydrocephalus). A large percentage (70%-90%) of children born with
myelomeningocele have hydrocephalus. Hydrocephalus is controlled by a
surgical procedure called "shunting," which relieves the fluid buildup in
the brain. If a drain (shunt) is not implanted, the pressure buildup can
cause brain damage, seizures or blindness. Hydrocephalus may occur without
spina bifida, but the two conditions often occur together.

EDUCATIONAL IMPLICATIONS

Although spina bifida is relatively common, until recently most children
born with a myelomeningocele died shortly after birth. Now that surgery to
drain spinal fluid and protect children against hydrocephalus can be
performed in the first 48 hours of life, children with myelomeningocele are
much more likely to live. Quite often, however, they must have a series of
operations throughout their childhood. School programs should be flexible
to accommodate these special needs.

Many children with myelomeningocele need training to learn to manage their
bowel and bladder functions. Some require catheterization, or the insertion
of a tube to permit passage of urine.

The courts have held that clean, intermittent catheterization is necessary
to help the child benefit from and have access to special education and
related services. Many children learn to catheterize themselves at a very
early age.

A successful bladder management program can be incorporated into the
regular school day.

In some cases, children with spina bifida who also have a history of
hydrocephalus experience learning problems. They may have difficulty with
paying attention, expressing or understanding language, and grasping
reading and math. Early intervention with children who experience learning
problems can help considerably to prepare them for school.

Mainstreaming, or successful integration of a child with spina bifida into
a school attended by nondisabled young people, sometimes requires changes
in school equipment or the curriculum. Although student placement should be
in the least restrictive environment the day-to-day school pattern also
should be as "normal" as possible. In adapting the school setting for the
child with spina bifida, architectural factors should be considered.
Section 504 of the Rehabilitation Act of 1973 requires that programs
receiving federal funds make their facilities accessible. This can occur
through structural changes (for example, adding elevators or ramps) or
through schedule or location changes (for example, offering a course on the
ground floor).

Children with myelomeningocele need to learn mobility skills, and often
require the aid of crutches, braces, or wheelchairs. It is important that
all members of the school team and the parents understand the child's
physical capabilities and limitations. Physical disabilities like spina
bifida can have profound effects on a child's emotional and social
development. To promote personal growth, families and teachers should
encourage children, within the limits of safety and health, to be
independent and to participate in activities with their nondisabled
classmates.

RESOURCES

Bloom, B.A., &: Seljeskog, E.S. (1988). A parent's guide to spina bifida.
Minneapolis, MN: University of Minnesota Press. (Telephone:
612-627-1970.)

Lutkenhoff M. & Oppenheimer, S. (1996). SPINAbilities: A young person's
guide to spina bifida. Bethesda, MD: Woodbine. (Telephone: 1-800-843-7323.)

McLone, D. (1994). An introduction to spina bifida. Washington, DC: Spina
Bifida Association of America. (See address below.)

Rowley-Kelly, F.L., & Reigel, D.H. (Eds.). (1993). Teaching the student
with spina bifida. Baltimore, MD: Paul H. Brookes. (Telephone:
1-800-638-3775.)

Spina Bifida Association of America. (1996). Publications list. Washington,
DC: Author. (See address below.)

ORGANIZATIONS

Spina Bifida Association of America
4590 MacArthur Boulevard, Suite 250
Washington, D.C. 20007
(202) 944-3285; (1-800) 621-3141 (Toll Free)
E-mail: spinabifda@aol.com
Web Address: http://www.infohiway.com/spinabifida

March of Dimes Birth Defects Foundation
1275 Mamaroneck Avenue
White Plains, NY 10605
(914) 428-7100
E-Mail: resourcecenter@modimes.org
Web Address: http://www.modimes.org

National Center for Education in Maternal and Child Health
2070 Chain Bridge Road, Suite 450
Vienna, VA 22182
(703) 821-8955, Ext. 254 or 265

National Easter Seal Society
230 West Monroe Street, Suite 1800
Chicago, IL 60606
(312) 726-6200; (1-800) 221-6827 (Toll Free)
E-mail: nessinfo@iseals.com
Web Address: http://www.seals.com

National Rehabilitation Information Center (NARIC)
8455 Colesville Road, Suite 935
Silver Spring, MD 20910-3319
(301) 588-9284; (1-800) 227-0216 (Toll Free)
Web Address: http://www.naric.com/naric

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Update June 1997

This fact sheet is made possible through Cooperative Agreement #H030A30003
between the Academy for Educational Development and the Office of Special
Education Programs. The contents of this publication do not necessarily
reflect the views or policies of the Department of Education, nor does
mention of trade names, commercial products or organizations imply
endorsement by the U. S. Government.

This information is in the public domain unless otherwise indicated.
Readers are encouraged to copy and share it, but please credit the National
Information Center for Children and Youth with Disabilities (NICHCY).


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