Connected Kansas Kids

Skip Navigation LinksHome » Diagnoses » Leukemia » Leukemia, Part 3 — Restrictions and implications for school
Connected Kansas Kids -- The place for special kids and their parents.

Leukemia — Part 3

Physical/dietary/other restrictions

Physical restrictions will vary from person-to-person. The doctor and health care team will let the person know what, if any, physical restrictions they should observe. If the patient has a central line, or intravenous catheter, precautions should be taken to ensure that it does not become dislodged or kinked. When platelets are low, the health care team may recommend restricted physical education and recess activities. Other limitations may be suggested to help prevent catching an infection, such as staying away from large crowds, using good hand washing techniques, and others. However, it is important for young people with leukemia to do as much as possible throughout their treatment.

It is important for a person on treatment for leukemia to try to eat well during the cancer therapy. They will need enough calories to maintain a good weight and enough protein to keep up strength. Good nutrition can help the person feel stronger and more energetic. However, it is sometimes difficult to eat well during treatment due to the side effects of medications. The doctor or dietitian may be able to offer suggestions to help maintain a healthy diet. If a person receives a stem cell transplant, some foods may be restricted to control exposure to bacteria. Again, the doctor is your best source for more information.

Implications for school

The presence of a leukemia may result in significant implications for a child in school, and the management of leukemia 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 leukemia is successful at school.

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

  • Due to the possibility of fatigue, a child with a brain tumor may 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 leukemia by helping to increasing muscle strength. The child with leukemia 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.
  • Physical stamina should be evaluated by the school nurse, and any modifications or accommodations that are indicated should be incorporated into the student’s IEP.

Psychosocial concerns for the student with leukemia may be significant. Due to frequent absences, frequent infections and limitations on physical activity, young people with leukemia 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 leukemia. 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 leukemia 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.
  • Including 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 leukemia can be a significant asset. The student may need the opportunity to discuss his/her fears about dying or about the future in general, keeping up in school, socialization issues, concerns about other family members, etc.

Part 1 — Introduction, incidence, symptoms, and treatment

Part 2 — Chemotherapy, stem cell transplants, and possible side effects

Part 3 — Restrictions and implications for school

 


For more information, please contact:

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