Childhood Leukemia
Chapter 20: School
“Most of us had two feelings at the same time: wanting to go back to school and being scared of going back.”
CHILDREN AND TEENS WITH LEUKEMIA have disruptions in their education because of frequent hospitalizations and side effects from the disease or treatment. As their health improves and their treatment schedule allows, returning to school can be a relief or a challenge.
For many children, school is a refuge from the world of hospitals and procedures—a place for fun, friendship, and learning. School is the defining structure of children’s daily lives and returning to school can signal hope for the future and a return to normalcy. Some children and teens, however, may dread returning to school because of temporary or permanent changes to their appearance or concerns that prolonged absences may have changed their social standing with friends.
In addition, physical limitations caused by cancer treatment may prevent children from participating in games, physical education class, athletics, or other activities. These physical impairments sometimes require time out from the regular classroom for physical or occupational therapy. School can also become a major source of frustration for children who learn differently because of treatment.
Although educating children who have or had cancer can be a complex process, many challenges can be successfully managed through careful planning and good communication. This chapter covers ways to work with the school during and after treatment. It also includes information about avoiding communicable illnesses at school and getting any help your child needs to learn.
Table of Contents
All Guides- Introduction
- 1. Diagnosis
- 2. Overview of Childhood Leukemia
- 3. Acute Lymphoblastic Leukemia
- 4. Acute Myeloid Leukemia
- 5. Juvenile Myelomonocytic Leukemia
- 6. Chronic Myelogenous Leukemia
- 7. Telling Your Child and Others
- 8. Choosing a Treatment
- 9. Coping with Procedures
- 10. Forming a Partnership with the Medical Team
- 11. Hospitalization
- 12. Central Venous Catheters
- 13. Chemotherapy and Other Medications
- 14. Common Side Effects of Treatment
- 15. Radiation Therapy
- 16. Stem Cell Transplantation
- 17. Siblings
- 18. Family and Friends
- 19. Communication and Behavior
- 20. School
- 21. Sources of Support
- 22. Nutrition
- 23. Insurance, Record-keeping, and Financial Assistance
- 24. End of Treatment and Beyond
- 25. Relapse
- 26. Death and Bereavement
- Appendix A. Blood Tests and What They Mean
- Appendix B. Resource Organizations
- Appendix C. Books, Websites, and Support Groups