Information. When a child is diagnosed with neuroblastoma, getting access to the information and resources you need to make the best possible decisions for your child is an important first step. CNCF has assembled a comprehensive list of resources to support you through every phase of your journey with neuroblastoma – from diagnosis to treatment, late effects and beyond. Here you will find information on the latest neuroblastoma research, educational information and a reading list for parents and patients. If you haven’t already, be sure to download the NB Parent Handbook, which also has a wealth of useful information and is written by parents just like you.
We continue to add to this list of critical resources on an ongoing basis. If you have suggestions for additional items, please feel free to drop us a note at firstname.lastname@example.org