This handbook has been prepared for you by parents of children who are or have been in treatment for neuroblastoma. We understand that there is no pain like hearing the word “cancer” used in connection with your child. Each of us has struggled to understand what it means to have our child diagnosed with a disease we had never heard of before, and to obtain the information we needed to manage our child’s treatment. Having been there, we want to offer you hope and tools to make this journey easier. ...

The purpose of this blog is to help families that have been touched by neuroblastoma. Our goal is to provide unbiased information for families interested in making treatment decisions for their family members. We view no topic as taboo and we are willing to tackle any subject. We encourage feedback and comments. Please let us know what you are interested in and we will do our best to come back with fair, balanced, and medically reviewed information. ...

Did you want to more about what is going on the Neuroblastoma Research World? Everyday the top 50 newest articles to the U.S. National Library of Medicine can be found here. There is no where else you will find more information.

Did you miss the last CNCF Neuroblastoma Conference? Well, not to worry, now you can watch all of the videos from the conference in the comfort of your own home. The CNCF's 2007 Neuroblastoma Conference videos are now online! They are also available through Google video so you can download them to your iPod. We hope you find all of the information that you are looking for. Please take a moment to leave comments or feedback on each video you watch so that we can make them even better next year. ...