Founded in 1973, the American Brain Tumor Association (ABTA) was the first national advocacy organization committed to funding brain tumor research and providing information and education to patients, caregivers, and their loved ones. For 50 years, the ABTA has been providing comprehensive resources that support the complex needs of brain tumor patients and caregivers, as well as the critical funding of research in the pursuit of breakthroughs in brain tumor diagnosis, treatment and care.

Brain Cancer Canada is a national charity that funds research and neurosurgical technologies, and advocates for effective treatment of primary malignant brain tumours, pediatric and adult. Through the extraordinary contributions of our sponsors and donors, we accelerate advancements in science, advocate for patient access to drugs, multiple forms of treatment, and increased availability of neuro-surgical technologies and care, and transform the power in community to change the experience of brain cancer patients and their caregivers.

A brain tumor diagnosis can feel overwhelming. Whether you’re navigating watch-and-wait (WW), preparing for surgery, or adjusting to life post-treatment, the journey can often feel isolating. At Brain Tumor Companion (BTC), we’re here to help. Our weekly online peer support groups provide a welcoming space to connect with others who truly understand your experience.To learn more about Brain Tumor Companion, listen to their organization spotlight on the Rewired Minds Podcast at this link.

The Brain Tumor Network, Inc. (BTN) is a nonprofit organization serving patients with primary brain tumors and their caregivers nationwide. Our multidisciplinary team includes clinical and social work navigators plus professionals in data, medical records, research, and operations. BTN provides free, individualized navigation so people facing a primary brain tumor can understand their options, overcome barriers, and access high-quality care aligned with their goals and values. To learn more about the Brain Tumor Network, listen to their organization spotlight on the Rewired Minds Podcast at this link.

Brain Tumour Alliance Australia (BTAA) was established in 2008 and is a non-profit, volunteer-run organisation. BTAA's mission is to unite and strengthen the voices of the brain tumor community to drive better outcomes for all affected. As Australia's peak brain tumour advocacy body, they support, inform, and represent people living with brain tumours, their families, care givers, and the professionals who care for them. They connect people, organisations, and government to foster collaboration and build awareness; educate the community; and inform decision-makers to shape policy and better outcomes. By uniting lived experience with expertise, BTAA champions the needs of the brain tumour community to achieve lasting improvements in research, clinical care and support.

Brain Tumour Foundation of Canada is the only national charity offering information and support to Canadians affected by any kind of brain tumour—malignant, non-malignant or metastatic. Since its inception in 1982, the organization has allocated millions of dollars to fund crucial research projects that advance brain tumour treatment and patient care. Every day, the organization strives to bring HOPE to all those affected by a brain tumour. HOPE through support. HOPE through information and education. HOPE through research. HOPE for a cure. Brain Tumour Foundation of Canada is funded solely through generous contributions from individuals, corporations, organizations, employee groups and special events.

Brain Tumour Society Singapore (BTSS) has become the local point of support, information, practical and financial assistance, and advocacy for brain tumour patients, caregivers and their families in Singapore.

brainstrust - a charity offering practical and emotional support to those given the devastating news that they have a brain tumour To learn more about brainstrust, listen to their organization spotlight on the Rewired Minds Podcast at this link.

The Central Brain Tumor Registry of the United States (CBTRUS) is a not-for-profit research corporation, recognized by the international research community as the premier resource for annual histology-specific statistical information for all primary brain and other CNS tumors in the United States. The CBTRUS analytic database has been developed by compiling data from central (state) cancer registries, the District of Columbia, and Puerto Rico that include information on both malignant and non-malignant primary brain and other CNS tumors.

DIPG is the deadliest form of pediatric cancer and has a <1% survival rate. In the fight for a DIPG/DMG cure, ChadTough helps patients and families by funding game-changing research and providing navigation throughout their journey. They provide resources and insight, from a team of Nurse Navigators, to families who are working through a diagnosis and treatment plans. In addition, they fund grants for those researching a cure for the disease. They see a world where kids diagnosed with DIPG/DMG can have bright futures and can live out their dreams. To donate to ChadTough, visit this link: https://chadtough.org/ways-to-give/

The Children’s Brain Tumor Foundation (CBTF) was founded in 1988 by a group of dedicated parents, physicians, and friends 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. In addition to providing funds to research a cure, the organization is the nation’s leader in quality of life programs for families impacted by brain and spinal cord tumors. We support families from the day of diagnosis and throughout the brain tumor journey. Our mission is dedicated to improving the treatment, quality of life and the long-term outlook for children and families affected by a brain or spinal cord tumor.

Established in 2006, the CERN Foundation is now a designated program of the National Brain Tumor Society dedicated to improving the lives of those affected with ependymoma. Thanks to the efforts of an international network of collaborators, the CERN Foundation has been responsible for the publication of over 50 peer-reviewed papers in leading medical journals. This body of research has greatly advanced our understanding of ependymoma and has left a lasting legacy for future investigators to build upon.

The Ghana Brain Tumor Foundation (GBTF), founded in 2024, aims to be the leading association dedicated to funding brain tumor surgeries for underprivileged individuals and advancing cutting-edge surgical technology in the field of brain surgery within the Ghanaian community.

Gray for Glioblastoma is a 501 (c) 3 created to raise awareness for and funds to support Glioblastoma Multiforme research by accepting donations and donating to cancer care and research facilities. Our organization has gifted over $200,000 to support GBM research projects at renowned cancer centers including Dana Farber Cancer Institute, Children’s Hospital LA/Saban Research Institute and The Preston Robert Tisch Brain Tumor Center at Duke. We accomplish this while simultaneously creating a hopeful and positive space and providing resources and a space of community through our social media and events.

Humor to Fight the Tumor is dedicated to funding research and patient services that will improve the lives of brain tumor patients. We do this by raising awareness, providing support and encouragement, and offering uplifting events that provide a sense of community and hope to affected individuals and families. Humor can strengthen resilience, hope, and build connection during this journey. Laughter doesn't deny reality -- it makes reality more survivable.

Beyond the physical and emotional distress that comes with a brain cancer diagnosis, the financial challenges can be significant. Love Goes Further grant recipients receive assistance with immediate expenses. This is offered along with gifts of comfort and encouragement designed to make waiting rooms and treatment days a bit more tolerable. These gifts come with our assurance to patients and families that they are not alone. They have a team behind them—our team. No matter how far we go our love goes further. To learn more about the Kendall Nicole Eich Foundation, listen to their organization spotlight on the Rewired Minds Podcast at this link.

The Medulloblastoma Initiative (MBI) is a non-profit organization that raises and channels donations to accelerate research and develop a cure for pediatric medulloblastoma. Bringing together leading scientists worldwide, MBI fosters a transparent, synergistic, and silo-free research environment that enables faster progress toward a cure. In record time, two MBI-funded studies have been approved by the FDA, with one already advancing to patient recruitment and clinical testing — a testament to the urgency, collaboration, and innovation that define MBI’s mission, described by MIT as “a new playbook for curing rare childhood diseases.

The Musella Foundation for Brain Tumor Research & Information, Inc. is a 501(c)(3) nonprofit public charity devoted to empowering brain tumor patients and their families. We provide emotional and financial support, facilitate educational resources, advocate for patients' needs, and strive to raise funds for groundbreaking brain tumor research. Together, we aim to make a difference in the lives of those affected by brain tumors and contribute to the advancement of effective treatments.

As one of the world’s leading brain tumor centers, the Northwestern Medicine Malnati Brain Tumor Institute (MBTI) constantly works to develop and deliver the most advanced treatment options to patients across the Chicago area. Our experts offer brain and spine tumor care at Northwestern Memorial Hospital, nationally ranked in cancer, neurology and neurosurgery by U.S. News & World Report. To learn more about MBTI, listen to their organization spotlight on the Rewired Minds Podcast at this link.

OurBrainBank is a patient-led movement designed to move glioblastoma from terminal to treatable, powered by patients. They focus on GBM -- one of the most complex and aggressive brain cancers -- because overcoming one of the toughest cancers may be the key to cracking them all. They collect data to share the truth. Their Glioblastoma Bill of Rights empowers patients to demand better and equitable care.

The Pediatric Brain Tumor Foundation® is committed to leading the way toward a future without childhood cancer. Because of supporters’ generosity, advocacy, and encouragement, thousands of families turn to us each year and find the resources and community support they need on their cancer journey.

StacheStrong is a 501(c)3 nonprofit devoted to raising funds and awareness for brain cancer research. Defeating brain cancer and improving the quality of patients’ lives is our daily focus. StacheStrong was started by two brothers following GJ’s diagnosis of Glioblastoma Multiforme (GBM). After a 25-month battle, he passed away in 2019 at only 30 years old. StacheStrong continues to fight in his memory and for all those facing a similar diagnosis.To learn more about StacheStrong, listen to their organization spotlight on the Rewired Minds Podcast at this link.

Team Schladt Foundation is a 501(c)(3) nonprofit organization dedicated to spreading awareness of glioblastoma and other brain cancers; providing education, resources, and support for the brave warriors and their loved ones battling such diagnoses; and funding research to find new, life-changing treatments and ultimately a cure for glioblastoma. To learn more about the Team Schladt Foundation, listen to their organization spotlight on the Rewired Minds Podcast at this link.

The Brain Tumour Charity is the world’s leading brain tumour charity and the largest dedicated funder of research into brain tumours globally. Committed to saving and improving lives, we’re moving further, faster to help every single person affected by a brain tumour. We’re set on finding new treatments, offering the highest level of support and driving urgent change. And we’re doing it right now. Because we understand that when you, or someone you love, is diagnosed with a brain tumour – a cure really can’t wait.

The Sontag Foundation is dedicated to advancing brain cancer research by investing in brilliant scientists who are committed to the pursuit of bold, innovative, and transformative ideas.

Tough2gether Foundation is committed to transforming the future for children and young adults facing DIPG and DMG, some of the most aggressive pediatric brain cancers. Born from the lived experience and advocacy of Jace Ward and his family, their mission is to ensure that no family faces this diagnosis alone and that every patient has access to the knowledge, resources, and support they need. They work to accelerate research, expand equitable access to innovative clinical trials, and break down barriers within the pediatric brain cancer landscape. Through collaboration with scientists, clinicians, foundations, and families across the world, Tough2gether pushes for faster translation of discoveries and greater sharing of data — because progress must move at the speed families need.

The Ty Louis Campbell Foundation is a nonprofit organization that funds innovative research and clinical trials specifically geared toward the treatment of the most aggressive childhood cancers with a strong focus on brain tumors. Our mission is to help fund the intelligence and technology that will improve long-term survival rates and minimize side-effects for children diagnosed with the deadliest cancers, while helping to care for families when their child is in treatment by providing financial assistance and uplifting experiences.