Childhood Leukemia
Chapter 24: End of Treatment and Beyond
“The best formula for longevity: have a chronic disease, and cure it.”
THE LAST DAY OF TREATMENT is a time of both celebration and fear. Families are thrilled that the days of pills and procedures have ended, but some fear a future without drugs to keep the disease away. Concerns about relapse are an almost universal worry at the end of treatment; but for the majority of families, the months and years roll by without recurrence of the leukemia.
However, while many children and teens quickly return to excellent physical and mental health, others have lingering or permanent effects from the treatment. This chapter covers the emotional and physical aspects of ending treatment and the need for excellent medical follow up.
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