Elizabeth’s Hope has a unique mission: It will provide cutting-edge personalized medicine to children and adolescents with rare and operable brain cancers. Using a state-of-the-art gene sequencing machine and a team of scientists — including surgeons, molecular geneticists, pathologists, and bioinformatics researchers — the Weill Cornell Pediatric Brain and Spine Center will be able to identify the best treatment for each young patient, using methods that are currently either unavailable or cost-prohibitive for many families.
In a simultaneous effort, they’ll be testing innovative new delivery methods that bypass the blood-brain barrier and strike directly at tumors with the therapeutic agent identified as being most effective against that particular tumor.
Research funded by Elizabeth’s Hope will focus on rare tumors like gliomatosis
Inspired by Elizabeth’s courage and determination, Elizabeth’s Hope will accelerate finding a cure by becoming the country’s first pediatric cancer center to aggregate patient samples into a nationwide “genetic tissue bank,” accelerating and enabling this critical research.
Thanks to the work of Elizabeth’s Hope, the Weill Cornell Pediatric Brain and Spine Center will become New York City’s go-to center for rare and inoperable brain cancer in children, teens, and young adults, and will foster collaboration among leading medical institutions to efficiently focus research efforts to find better treatments and cures.
Join the advocacy and become part of the community that was established to support groundbreaking research in finding a cure for Gliomatosis Cerebri. Partners are either family touched by Gliomatosis Cerebri or foundations supporting the same cause. Click below to learn how to join the community.