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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: Stacia Wagner  |  Tuesday, September 25, 2012
During survivor discussions, the topics of how does a having a brain tumor fit into my life, how has it changed me, and how do I talk about it to others frequently arises. There are no right or wrong answers and no right or wrong approaches. Each situation, every personality and figuring out how to incorporate something which was out of your control into your life is different for every...
By: Kayla Giacin  |  Wednesday, September 19, 2012
As more and more is learned about teen and young adult survivors in the brain tumor and cancer world, a lot is also learned about coping mechanisms for this age group.  Self-help books and support groups are great but let’s face it, patients and survivors in their teens and 20’s are more interested in what most other teens and 20 year olds are interested in. 
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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