Navigating Your Child'sCancer Journey
We're here to help you explore clinical trial options for your child, find support, and take control of this journey together.
Discover clinical trial options for you
Find Personalized Clinical Trial Options
We match you with clinical trial options that may be right for you.
Financial & Community Support
Programs and grants to help pediatric cancer patients and their families manage costs and find community.
Travel For Care for Pediatric Cancer Travel | Alex’s Lemonade Stand Foundation (ALSF)
Family Support for Travel and Emergency Costs | National Children’s Cancer Society (NCCS)
Peer Support for Childhood Cancer Caregivers | Momcology
Good Days | Copay Assistance
Camp Kesem
Guides That Make Things Easier
Helpful articles and guides to support your journey.
How Neuroblastoma Is Diagnosed: A Step-by-Step Guide for Parents
Neuroblastoma Treatment and Management
Understanding Neuroblastoma: A Guide for Families
How is Neuroblastoma Diagnosed?
Frequently Asked Questions
Take a breath.
Then ask the care team:
What type of cancer does my child have?
What stage or risk group is it?
What does the first month of treatment look like for my child specifically?
Should we get a second opinion?
It's okay to ask questions, and to ask them again until things feel clear.
Children usually go through diagnostic testing in steps, not all at once. Depending on the type of cancer suspected, the care team may recommend imaging, lab work and biomarker testing, and often a biopsy to confirm the cancer type and understand its biology. Our How Neuroblastoma Is Diagnosed: A Step-by-Step Guide for Parents walks through what each test is for and what the results help doctors decide.
Treatment for children is different from treatment for adults, and is often more structured and specialized, typically delivered through dedicated pediatric cancer centers and cooperative research groups. Our Neuroblastoma Treatment and Management guide breaks down what a typical treatment plan can look like, so you can compare options with confidence.
Pediatric clinical trials are carefully designed research studies that test new treatments or new ways of using existing treatments for childhood cancers. They follow strict safety and ethical review, often with additional oversight because they involve children, and are monitored closely by medical experts throughout. Clinical trials are always optional, and participation depends on your child's diagnosis, stage, and your family's comfort level. WeTrials helps you explore relevant trials, understand eligibility, and prepare questions so you can decide with confidence alongside your child's care team.
There is no single right way to talk with a child about cancer, and it often depends on their age and how they process hard news. Helpful steps may include using simple, honest language, giving them space to ask questions, and leaning on your care team for guidance on what to share and when. Our Understanding Neuroblastoma: A Guide for Families is written to help the whole family learn together and feel less alone.
Childhood cancer affects the whole family, emotionally, financially, and practically, and you do not have to manage it alone. Support options may include patient assistance and medication support programs, insurance and financial navigation resources, counseling and peer support groups, and resources built specifically for siblings and caregivers. WeTrials connects you to trusted information and organizations that support your whole family, not just the diagnosis.
Navigating Your Child'sCancer Journey
We're here to help you explore clinical trial options for your child, find support, and take control of this journey together.
Discover clinical trial options for you
Find Personalized Clinical Trial Options
We match you with clinical trial options that may be right for you.
Financial & Community Support
Programs and grants to help pediatric cancer patients and their families manage costs and find community.
Travel For Care for Pediatric Cancer Travel | Alex’s Lemonade Stand Foundation (ALSF)
Family Support for Travel and Emergency Costs | National Children’s Cancer Society (NCCS)
Peer Support for Childhood Cancer Caregivers | Momcology
Good Days | Copay Assistance
Camp Kesem
Guides That Make Things Easier
Helpful articles and guides to support your journey.
How Neuroblastoma Is Diagnosed: A Step-by-Step Guide for Parents
Neuroblastoma Treatment and Management
Understanding Neuroblastoma: A Guide for Families
How is Neuroblastoma Diagnosed?
Frequently Asked Questions
Take a breath.
Then ask the care team:
What type of cancer does my child have?
What stage or risk group is it?
What does the first month of treatment look like for my child specifically?
Should we get a second opinion?
It's okay to ask questions, and to ask them again until things feel clear.
Children usually go through diagnostic testing in steps, not all at once. Depending on the type of cancer suspected, the care team may recommend imaging, lab work and biomarker testing, and often a biopsy to confirm the cancer type and understand its biology. Our How Neuroblastoma Is Diagnosed: A Step-by-Step Guide for Parents walks through what each test is for and what the results help doctors decide.
Treatment for children is different from treatment for adults, and is often more structured and specialized, typically delivered through dedicated pediatric cancer centers and cooperative research groups. Our Neuroblastoma Treatment and Management guide breaks down what a typical treatment plan can look like, so you can compare options with confidence.
Pediatric clinical trials are carefully designed research studies that test new treatments or new ways of using existing treatments for childhood cancers. They follow strict safety and ethical review, often with additional oversight because they involve children, and are monitored closely by medical experts throughout. Clinical trials are always optional, and participation depends on your child's diagnosis, stage, and your family's comfort level. WeTrials helps you explore relevant trials, understand eligibility, and prepare questions so you can decide with confidence alongside your child's care team.
There is no single right way to talk with a child about cancer, and it often depends on their age and how they process hard news. Helpful steps may include using simple, honest language, giving them space to ask questions, and leaning on your care team for guidance on what to share and when. Our Understanding Neuroblastoma: A Guide for Families is written to help the whole family learn together and feel less alone.
Childhood cancer affects the whole family, emotionally, financially, and practically, and you do not have to manage it alone. Support options may include patient assistance and medication support programs, insurance and financial navigation resources, counseling and peer support groups, and resources built specifically for siblings and caregivers. WeTrials connects you to trusted information and organizations that support your whole family, not just the diagnosis.