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Founded in 2011 with the mission to help families cope with the financial burdens of a colon cancer diagnosis and spread awareness of the symptoms of colon cancer and the importance of early detection.

We’re a non-profit organization on a mission to fund research to find a cure for brain tumors. We provide supportive and safe environments for patients, families, and caregivers to share experiences, learn about current therapies, and receive information about various aspects of a brain tumor diagnosis and treatment through monthly support group meetings.

ACCF helps alleviate the financial burden felt by patients who are struggling due to the costs associated with a cancer diagnosis and treatment. We provide fast, flexible, compassionate assistance with whatever their greatest financial need may be, so that they can focus on what matters most -- their treatment and recovery.

Bite Me Cancer's mission is to fight cancer through education, inspiration and research. The 2 main goals are to help teenagers with cancer across the country in their battle with support/inspiration and also raise research funds and awareness for thyroid cancer. We've been able to help almost 9,900 teenagers with cancer by giving them each a Teen Support Bag. These teens are in every state and DC and are given the bags through our 180 hospitals as of July 2022. The current cost is $85/bag to assemble and ship out.Bite Me Cancer has also directly funded 9 thyroid cancer research grants as of 06/30/2022. Funds this year will apply to our 10th grant (oversight/review is conducted in partnership with the American Thyroid Association)

To make Hepatoblastoma universally survivable by focusing on the pre-clinical gap in childhood cancer research.

Zcharia came to Kansas City in 2005. He soon became involved with the Kerala Association of Kansas City and became the sports coordinator. He became an active member of the volleyball community in Kansas City, participating in their Friday practices, local tournaments, and even the famous Jimmy George Volleyball Tournament held in New York. More than playing, he enjoyed connecting with people and introduced many people to volleyball. In 2010, he was diagnosed with stage 4 lung cancer. This put a damper on his ability to play the game he enjoyed. But soon after his first treatment of chemotherapy, he started playing volleyball with his friends again. This ended soon towards the middle of 2013 as his disease got worse. On December 21st, 2013, Zcharia Jose passed away.

To provide support for pediatric children and families who are faced with a life-threatening illness including ATRT, medulloblastoma, or similar brain tumors.

The mission of the Nevada Childhood CancerFoundation (NCCF) is to provide social, emotional, educational, andpsychological support services and programs to families of ALL children diagnosed with life threatening or critical illnesses such as cancer, HIV/AIDS, sickle cell, hemophilia, renal disorders, and immunologic diseases and provide healing arts and wellness programs to adults touched by cancer and to chronically ill children and their caregivers.

UBCF’s mission is to make a positive difference in the lives of those affected by breast cancer. We aid in providing screening, treatment, after-care, educational material, patient and family assistance and information. UBCF provides grants to hospitals and community health centers to benefit patients and families coping with breast cancer. We strive to alleviate the stress and strain that cancer can cause to patients and families and to foster health and well-being through both traditional and holistic treatments by never denying anyone service regardless of age, race, gender or income.

Abolish chronic lymphocytic leukemia (CLL) as a threat to the life and health of patients by accelerating CLL research.

Cool Kids Campaign is devoted to improving the quality of life for pediatric oncology patients and their families by focusing on the academic, social and emotional needs brought on by a cancer diagnosis.Cancer creates an instant crisis in a family. Fear and anxiety are the first emotions young people may feel after learning of their illness and what they are about to face. Kids with cancer are still normal kids! Our program's focus is guided by the direct feedback we receive from affected families and advice from the Cool Kids Advisory Committees.

In the fight for a DIPG/DMG cure, we help patients and families by funding game-changing research and providing navigation throughout their journey.