CEREBRAL PALSY



Fact Sheet Number 2 (FS2), 1997

___________________



NICHCY

National Information Center for Children and Youth with Disabilities

P.O. Box 1492

Washington, DC 20013

E-Mail: aed@nichcy.org

URL: http://www.nichcy.org

1-800-695-0285 (V/TT)



This information is copyright free, unless otherwise indicated. Readers are

encouraged to copy and share it but please credit the National Information

Center for Children and Youth with Disabilities.

_____________



DEFINITION OF CEREBRAL PALSY



Cerebral palsy is a condition caused by damage to the brain, usually

occurring before, during or shortly following birth. "Cerebral" refers to

the brain and "palsy" to a disorder of movement or posture. It is neither

progressive nor communicable. It is also not "curable" in the accepted

sense, although education, therapy and applied technology can help persons

with cerebral palsy lead productive lives. It is not a disease and should

never be referred to as such. It can range from mild to severe.



The causes of cerebral palsy include illness during pregnancy, premature

delivery, or lack of oxygen supply to the baby; or it may occur early in

life as a result of an accident, lead poisoning, viral infection, child

abuse, or other factors. Chief among the causes is an insufficient amount

of oxygen or poor flow of blood reaching the fetal or newborn brain. This

can be caused by premature separation of the placenta, an awkward birth

position, labor that goes on too long or is too abrupt, or interference

with the umbilical cord. Other causes may be associated with premature

birth, RH or A-B-O blood type incompatibility between parents, infection of

the mother with German measles or other viral diseases in early pregnancy,

and microorganisms that attack the newborn s central nervous system. Lack

of good prenatal care may also be a factor. A less common type is acquired

cerebral palsy: head injury is the most frequent cause, usually the result

of motor vehicle accidents, falls, or child abuse.



INCIDENCE



Between 500,000 - 700,000 Americans have some degree of cerebral palsy.

About 3,000 babies are born with the disorder each year, and another 500 or

so acquire it in the early years of life.



CHARACTERISTICS



There are three main types of cerebral palsy: spastic -- stiff and

difficult movement; athetoid -- involuntary and uncontrolled movement; and

ataxic -- disturbed sense of balance and depth perception. There may be a

combination of these types for any one individual. Other types do occur,

although infrequently.



Cerebral palsy is characterized by an inability to fully control motor

function. Depending on which part of the brain has been damaged and the

degree of involvement of the central nervous system, one or more of the

following may occur: spasms; tonal problems; involuntary movement;

disturbance in gait and mobility; seizures; abnormal sensation and

perception; impairment of sight, hearing or speech; and mental retardation.



DEVELOPMENTAL, EDUCATIONAL, AND EMPLOYMENT IMPLICATIONS



Early identification of cerebral palsy can lessen developmental problems

and lead to appropriate intervention when it helps the most. Early

intervention programs are family-centered in which professionals and

families work together with the child in specific activities. Educators,

physical and occupational therapists, social workers, speech- language

pathologists, psychologists and physicians can assist families by providing

information and education.



Activities for children with cerebral palsy may include:

-- speech and language therapy;

-- occupational therapy;

-- physical therapy;

-- medical intervention;

-- family support services;

-- early education; and

-- assistive technology.



As a child gets older and begins formal schooling, the intensity of

services will vary from individual to individual. Persons with cerebral

palsy are usually able to attain a substantial degree of independence but,

in some cases, may need considerable assistance. Services for the school

age child may include continuing therapy, regular or special education,

counseling, technical support, community integration opportunities,

recreation and possible personal attendants. A key factor seems to be a

supportive family. People extensively affected by cerebral palsy can still

be highly functional and independent. The HEATH Resource Center, the

clearinghouse on postsecondary education for individuals with disabilities,

states that a significant number of students with cerebral palsy are

enrolled in colleges and universities.



Important advances have taken place in the last 15 years which have had a

great effect on the long-term well-being of children born with cerebral

palsy. Advanced technology, including computers and engineering devices,

has been applied to the needs of persons with cerebral palsy. Technological

innovations have been developed in the areas of speech and communication,

self-care, and adapting living arrangements and work sites. The future may

bring even more significant applications.



Another important development has been the increased ability of persons

with disabilities, including those who have cerebral palsy and other severe

disabilities, to live independently in the community. Adults with cerebral

palsy are now living, with or without assistance, in their own apartments

or townhouses. Independent Living Centers have also proven to be important

resources for persons with disabilities.



RESOURCES



Geralis, E. (1991). Children with Cerebral Palsy, A Parent's Guide.

Rockville, MD: Woodbine House. (Telephone: 1-800-843-732.)



Metzger, L. (1993). Barry's Sister. New York: Puffin. (A book for children

ages 10 and up. The story line is about a child with cerebral palsy and his

sister.) (Telephone: 1-800-253-6476.)



Weiss, S. (1993). Each of Us Remembers: Parents of Children with Cerebral

Palsy Answer Your Questions. Washington, DC: United Cerebral Palsy

Associations, Inc. (See address and telephone number below.)



ORGANIZATIONS



United Cerebral Palsy Associations, Inc.

1660 L Street N.W., Suite 700

Washington, D.C. 20036

(202)776-0406; (202) 973-7197 (TT)

(800) 872-5827 (V/TT)

E-mail: ucpanatl@ucpa.org

Web Address: http://www.ucpa.org



Independent Living Research Utilization Project (ILRU)

The Institute for Rehabilitation and Research

2323 South Sheppard, Suite 1000

Houston, TX 77019

(713) 520-0232; (713) 520-5136 (TT)

E-mail: ilru@bcm.tmc.edu

Web address: www.bcm.tmc.edu/ilru



National Easter Seal Society, Inc.

230 West Monroe Street, Suite 1800

Chicago, IL 60606

(312) 726-6200; (312) 726-4258 (TT)

(800) 221-6827

E-mail: nessinfo@seals.con

Web address: http://www.seals.com



National Rehabilitation Information Center (NARIC)

8455 Colesville Road

Suite 935

Silver Spring, MD 20910-3319

(301) 588-9284 (TT/Voice); (800) 346-2742

Web address: http://www.naric.com/naric

_________________



Updated 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).





Back To Special Education Articles Page