Elizabeth's Hope was established as a way of Elizabeth's family to bring meaning to Elizabeth Minter's diagnosis. It's funding is focused to support research on rare tumors like Gliomatosis Cerebri. Here at Elizabeth’s Hope, we are deeply appreciative of our supporters, and we want to keep all of you updated.

The Joshua Bembo Project, Inc. is a non-profit organization created in memory of Joshua Bembo who lost his 15 month battle with Gliomatosis Cerebri on March 01, 2013. They are dedicated to providing hope to children diagnosed with rare and inoperable brain tumor such as the one that took Joshua’s life.

The association Izas, la princesa guisante (Izas, Princess Pea), has the solid objective of promoting research, encouraging tissue donation to forward this research, and raising awareness amongst the medical community, families, and society about this fatal children’s cancer. Click to learn more about us.

Created in 2010 by the family and friends of the young Franck, 14, died of a brain gliomatosis, the association is involved in favor of cancer research in children but also in supporting families affected by this disease. Our commitment is to donate 100% of donations collected to research,

AYJ Fund he mission of the AYJ Fund is to bring smiles to kids with cancer, to keep them connected to friends and school through technology, and to support the research of Gliomatosis Cerebri and other brain cancers to find the cures. The fund is dedicated in honor of the life of Anna Yan.

The Rudy A Menon Foundation has been set up to help fund research on Gliomatosis Cerebri and other rare brain cancers. They are working with ICR, London, UK, where Dr. Chris Jones and his team are doing groundbreaking research. It was set up to honor the memory Rudy Menon who lost his battle with GC on his 26th birthday.

Over The Moon is a group of dedicated family and friends. They’ve come together to honor the memory of TJ, one of our kids touched by Gliomatosis Cerebri. There main goal is to help other childhood cancer families by bringing joy and hope to children fighting cancer and their families.

To honor Sean’s Life his family has set up a fundraising campaign that assists families in their battle against this deadly disease. The campaign is dedicated to help fund the Dana-Farber Research whose sole mission is to conquer childhood cancer.

Remembering Chase Balay is a site dedicated in the memory of Chase Balay, another kid touched by Gliomatosis Cerebri. The site narrates the saga of a mother agonizing for his lost son. It also gives the reader some vivid walk to the life of Chase.

The Children’s Brain Tumor Family Foundation is built by families who have been united by tragedy. Frustrated by a lack of funding for research for inoperable brain tumors, these families have formed a foundation to support the research at the Children’s Brain Tumor Project at Weill Cornell.

Formed after three-year-old Allie "Little Owl" Fisher died of a rare brain cancer, Gliomatosis Cerebri, in 2013.  After Allie’s death, many of Allie’s family and friends felt compelled to lend a hand in the fight against these terrible pediatric brain tumors. Team Little Owl is an all-volunteer group committed to raising awareness and funds to brain cancer research.

Fe y Misericordia is a foundation inspired by the life of Patrick Bayly Mansano, a kid who had fought bravely against Gliomatosis Cerebri. Currently working on an agreement with Universidad Cayetano Heredia (UPCH), which has the best known Medicine Faculty in Peru, to implement the “Radiotherapy and Image diagnose Centre Patrick Bayly Marsano”.