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Brain Tumors, Part 3 — Implications for school

The presence of a brain tumor may result in significant implications for a child in school, and the management of a brain tumor at school has several facets. Educators must consider the physical, psychosocial and cognitive/educational issues of this diagnosis in order to ensure that the young person with a brain tumor is successful at school.

The physical aspects of a brain tumor must be addressed at school. The following accommodations and adaptations may be warranted for a child with a brain tumor:

  • Due to the possibility of fatigue, the child might need to rest during the school day. It is usually best to do this in the nurse’s office, or in a location away from the other students in order to not increase peers’ feelings that the child is different. 
  • Restroom privileges should be flexible and on an “as needed” basis.
  • Exercise may benefit the child with a brain tumor by helping to increasing muscle strength. The child should be encouraged to participate in all physical activities at school. From day to day, the child may be limited in how much he/she can do or the duration of time that he/she can participate in physical endeavors. There may be times, due to steroids, that the child has difficulty with movement as a result of weight gain and fluid retention. The child should be encouraged to do as much as possible, and allowed to set his/her own limits for physical activity. 
  • Balance and mobility should be evaluated by a physical therapist and any modifications or accommodations that are indicated should be incorporated into the student’s IEP.

Psychosocial concerns for the student may be significant. Due to frequent absences, frequent infections, limitations on physical activity, and possible changes in cogntive functioning, young people with a brain tumor struggle with issues of “fitting in”. They may feel left out by their peers, or struggle with keeping up socially as they flow in and out of school. In order to help facilitate healthy psychological, emotional and social adjustment, the school should consider:

  • Educating peers, with the consent of the child and parents, about a brain tumor. The hospital school teacher is a good resource for offering a presentation, suggesting materials, or assisting with the education of educators, peers or other interested community members.
  • Encourage peers to stay in contact with their friend when he/she is absent. Cards, letters and phone calls can serve to bridge the gap when youngsters with chronic illnesses must be away from school and activities.
  • This is a wonderful opportunity to teach peers about supporting a friend, how to show compassion and other essential life lessons.
  • Identify strong peers to mentor the student with a brain tumor when he/she returns after an absence. Having someone to “fill you in” on what you missed while hospitalized or home ill may make all the difference in facilitating a good reentry.
  • Help the student find areas of expertise and ways to excel in the school environment. Mentoring support could be included in the IEP to help the young person maintain or develop a strong self-concept.
  • Include social work or counseling services as part of the IEP. Having someone at school to talk to or act as an advocate for the youngster with a brain tumor can be a significant asset. The student may need the opportunity to discuss his/her fears about the future, keeping up in school, socialization issues, concerns about other family members, etc.

Finally, cognitive status and academic progress must be monitored on an on-going basis. The student is likely to experience some degree of cognitive or learning problems as a result of the tumor or the treatment. Usually, students with a brain tumor qualify for special education support as students who are other health impaired (OHI), learning disabled (LD), or developmentally delayed (DD) under the Individuals with Disabilities Education Act (IDEA). A comprehensive evaluation should be conducted to see if the student would qualify as a student with one of these special education areas of need.

Doctor visits, hospitalizations, radiation treatments and other medical requirements may result in excessive absences for the student. This may cause the child to feel concerned about keeping up academically. A student with a brain tumor is likely to miss a lot of school, and will need assistance and flexibility in completing assignments and work upon their return to school or home. Homebound education should be utilized ONLY if the child cannot possibly come to school. Otherwise, the child should be encouraged to attend school as much as possible.

In order to ensure that the student continues to progress, educators should:

  • Evaluate for potential classification as other health impaired, learning disabled, developmentally delayed or other special education category.
  • Create an IEP that allows for the possibility of on-going change and fluctuation in ability and physical stamina.
  • Identify areas of strength and help the student focus on the things he can still do, as opposed of the functions or skills that may have been negatively impacted by the diagnosis, surgery or treatment.
  • Provide for a great deal of flexibility when the child has been absent. Give plenty of time to complete make-up work.
  • Provide tutorial assistance if the student has been absent or if he/she is evidencing difficulty with specific learning material.
  • Provide careful monitoring to determine if student has declines in performance.
  • Notify the child’s parents and/or health care provider if a change in behavior, personality or school performance is observed.

Part 1 — Introduction, Incidence, and Symptoms

Part 2 — Treatment, Side effects and Restrictions

Part 3 — Implications for school

 


For more information, please contact:

Kathy Davis, MSEd, PhD
kdavis2@kumc.edu
(913) 588-6305