Site Map

Home

• About Neuroblastoma & Research
• What is Neuroblastoma?
• How is Neuroblastoma Diagnosed?
• Treatment and Clinical Trials
• Understanding Clinical Trials
• Neuroblastoma Research

• Newly Diagnosed
• Coping with a Neuroblastoma Diagnosis
• Understanding the Treatment Options
• Preparing for Treatment
• Getting to Know Your Treatment Team
• Questions to Ask Your Doctor

• In Treatment
• Non–High-Risk (Low- or Intermediate-Risk Treatment)
• High-Risk Treatment

• Supportive Care
• Supportive Care Overview
• Nausea and Vomiting
• Constipation and Diarrhea
• Decreased Appetite and Nutrition
• Blood Counts
• Hair Loss
• Mouth Sores
• Pain

• Relapsed & Refractory
• What Is Relapsed/Refractory Neuroblastoma?

• After Treatment
• What Happens Next and When
• Late and Long Term Side Effects

• Stories of Hope
• Braving Neuroblastoma

• Support & Community
• Order Resources
• Downloadable Resources & Videos
• Neuroblastoma Support and Advocacy Groups
• Glossary of Terms
• Psychological Effects of Childhood Cancer
• Caring for the Caregiver

This website is intended for informational purposes and is not intended as treatment advice. It is not meant to replace conversations with your child's healthcare team. You should reach out to them with any questions you have regarding your child's treatment. Your child's healthcare team is your main source of information about your child's care and treatment.