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Children’s Brain Tumor Foundation,

a non-profit organization, was founded in 1988 by dedicated parents, physicians and friends. Our mission is to improve the treatment, quality of life and the long term outlook for children with brain and spinal cord tumors through research, support, education, and advocacy to families and survivors.

We Need Your Support

The Children's Brain Tumor Foundation depends upon individuals and companies to continue its crucial programs for children with brain and spinal cord tumors and their families. You can help


CBTF Blog

By: Kayla Giacin  |  Wednesday, February 22, 2012
CBTF’s teen survivors seem to be taking New York City by storm as we continue our adventures with our new teen photography class, led by professional photographer Annie Levy and her assistant, Paul White.  The class has been meeting since the beginning of January and with only two months in; we already have a few adventures under our belt!
By: Catherine Blotner  |  Wednesday, February 15, 2012
Dating can be awkward for anyone. On top of the typical worries that most teenagers have when it comes to dating like wondering what to wear, or simply what to talk about when on a date, tumor/cancer patients have an extra layer of questions to think about. For many patients and survivors this layer includes figuring out how to hide ports underneath clothing, cover up scars, take pills when no...
Today,
  • 11 families across America will learn their child has a brain or spinal cord tumor
  • A mother will grieve that her instincts about her child’s health were right.
  • A father will allow himself to cry, but only alone in the shower.
  • 3 families across America will mourn the loss of their child to a brain or spinal cord tumor
  • Friends, family and community will try to make sense of an untimely death and the unfulfilled promise of a life.
  • 6 families across America will transition to survivorship.
  • A mother will be too exhausted from providing constant care to her child to simply write checks to pay bills.
  • A father will again adapt his day, family and life to a new definition of normal, unlike any he had previously envisioned.
  • A survivor on the brink of adulthood will wonder if he’ll ever date, marry or have a family.
 
Today, Children’s Brain Tumor Foundation will be there with insight, support, respite and hope.

Today, we invite you to join us!

Please support Children’s Brain Tumor Foundation. Make a donation to childhood cancer. Thank you!

Knowledge is critical for families and patients facing the diagnosis of a childhood brain tumor. Our website provides an array of information and resources for the newly diagnosed and long-term survivors.




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