• I-MIBG Therapy for Neuroblastoma

    On August 26, 2009 Ken DeSantes , M.D. gave a presentation at the University of Wisconsin School of Medicine and Public Health on MIBG Therapy Although this presentation was not meant for parents of children with neuroblastoma or their caregivers it is...
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  • An overview of the Phase 1 Trial of TPI 287/Temozolomide in Neuroblastoma and Medulloblastoma

    Dr. Giselle Sholler, principal investigator and pediatric oncologist from Vermont Cancer Center, presented important information regarding the newly opened "Phase 1 Trial of TPI 287 as a Single Agent and in Combination with Temozolomide in Patients with Refractory or Recurrent Neuroblastoma or Medulloblastoma."  This presentation was intended for parents and caregivers of children with refractory or recurrent neuroblastoma and medulloblastoma.  Dr. Sholler provided an overview of the preclinical research leading up to the trial.  She also discussed the rationale behind the trial and the eligibility requirements.  Parents of children that have participated in this trial were also available to share their experiences.  The presentation was followed with a question and answer session. This presentation and question and answer session was originally published on Wednesday, August 26, 2009 at 12:00PM CST.

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  • Neuroblastoma and Hearing Loss

    UPDATE: STS is now available on study. See: Children's Oncology Group Study, "A Randomized Phase III Study of Sodium Thiosulfate for the Prevention of Cisplatin-Induced Ototoxicity in Children (ACCL0431)," View the video version of this...

There is nothing quite as devastating as hearing that word - neuroblastoma. In seconds your world is turned upside down and your normal life is but a distant memory. You are thrust into a confusing world full of fear. Your child has cancer.

We know. We have been there. The Neuroblastoma Foundation is here for you.

Welcome to our website. It is a place for you to find answers and ask questions. One of the primary goals of the Neuroblastoma Foundation is to ensure that parents, patients and health care professionals find the information they need to make the best treatment decisions possible for children and adults affected by neuroblastoma. There is a vast amount of information throughout the internet, much of which is encapsulated in medical jargon that is so complex that even many medical professionals have difficulty in interpreting its meaning. We are here to help to decipher this information and to make sure you (and your oncologist) understand exactly what it means to you. From treatment decisions to side effects we have parents and experts that have experienced it all and are willing to distill it for you.