Childhood Leukemia
Chapter 25: Relapse
“Hold fast to dreams for if dreams die Life is a broken winged bird that cannot fly.”
PARENTS FREQUENTLY DESCRIBE the return of their child’s cancer as more devastating than the original diagnosis. They may feel betrayed, guilty, and/or angry. They worry that if the previous treatments did not work, what will? Mostly, they are afraid. And their often unspoken but most crushing fear is: What if my child dies?
If your child’s cancer has returned, it is worth remembering that you now have several strengths you didn’t have before. You have already done this. You know the language, and you have a relationship with the medical team. You probably have friendships with other parents of children with cancer and you know they will be there for you. You can also hope that during the time your child’s cancer was in remission, researchers were able to develop newer and more effective treatments. You know that something that seems insurmountable can be endured, one day at a time.
This chapter describes signs and symptoms of relapse, what emotional responses you might experience, and how to set goals and decide on a treatment plan. It provides information about immunotherapy, which was recently approved to treat some children with leukemia who relapse or who never entered remission. In addition, several parents and survivors share stories about how they managed to cope.
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