Childhood Brain and Spinal Cord Tumors
Chapter 20: Nutrition
Let your food be your medicine and your medicine be your food.
— Hippocrates
NOW, MORE THAN EVER, it is important for your sick child to eat balanced, healthful, and energy-packed meals. Yet, the reality is that the eating habits of children with brain or spinal cord tumors go haywire. Although, your child’s body needs added energy to metabolize medications and repair the damage to healthy cells caused by chemotherapy and radiation, those same treatments can wreak havoc on your child’s appetite and taste sensations. This chapter discusses eating problems, explains good nutrition, suggests ways to pack extra calories into small servings, and offers tips about how to make food more appealing to children undergoing treatment.
Table of Contents
All Guides- Introduction
- 1. Diagnosis
- 2. The Brain and Spinal Cord
- 3. Types of Tumors
- 4. Telling Your Child and Others
- 5. Choosing a Treatment
- 6. Coping with Procedures
- 7. Forming a Partnership with the Treatment Team
- 8. Hospitalization
- 9. Venous Catheters
- 10. Surgery
- 11. Chemotherapy
- 12. Common Side Effects of Chemotherapy
- 13. Radiation Therapy
- 14. Peripheral Blood Stem Cell Transplantation
- 15. Siblings
- 16. Family and Friends
- 17. Communication and Behavior
- 18. School
- 19. Sources of Support
- 20. Nutrition
- 21. Medical and Financial Record-keeping
- 22. End of Treatment and Beyond
- 23. Recurrence
- 24. Death and Bereavement
- 25. Looking Forward
- Appendix A. Blood Tests and What They Mean
- Appendix C. Books and Websites