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To make all who are touched by invasive lobular breast cancer (also referred to as invasive lobular carcinoma or “ILC”) aware of its unique characteristics and the critical need for more ILC research; to be the go-to source for information on ILC studies, clinical trials and educational tools; to foster partnerships among patients, scientists, clinicians, and breast cancer organizations to increase dialogue about ILC and research advocacy; and to fund vital ILC research. We envision a world in which lobular breast cancer is found early, treated effectively, and eradicated permanently.
A joint commitment to raise money for research and patient care with the mission of finding a cure for, or the means to control, cancer.
Cancer for College provides need-based college scholarships and educational experiences to cancer survivors.
The Jonsson Cancer Center Foundation (JCCF) was founded in 1945 by a group of volunteers dedicated to cancer research at UCLA. Their idea, using funds raised from private sources to invest in the work of promising young cancer researchers, resulted in the Seed Grant Program, which has helped the Jonsson Comprehensive Cancer Center (JCCC) break new ground in the quest to defeat cancer.
Supports compassionate care and refuge for those suffering in body and soul.
Money raised through the Coronavirus Relief Fund will be split evenly amongst CDC Foundation, International Medical Corps and Direct Relief to support first responders & medical professionals working on the coronavirus globally. CDC Foundation EIN: 58-2106707 Funds raised by the CDC Foundation through their Emergency Response Fund will be used to meet fast-emerging needs identified by CDC to help respond to the public health threat posed by this virus. These include additional support for state and local health departments, support for the global response, logistics, communications, data management, personal protective equipment, critical response supplies and more. International Medical Corps EIN: 95-3949646 International Medical Corps is taking an agency-wide approach to their response, providing their 7,000+ staff members in more than 30 countries with clinical guidance and planning documents designed to help them screen patients, enhance infection prevention and control (IPC), and protect health providers. They also have developed specific training materials to help staff and healthcare providers better respond to the virus. Direct Relief EIN: 95-1831116 Direct Relief is coordinating with public health authorities, nonprofit organizations and businesses in China and the U.S. to provide personal protective equipment and other items to health workers responding to coronavirus (COVID-19). Direct Relief is also staging personal protective equipment with regional response agencies across the world, including in the Caribbean and South America through the Pan American Health Organization. For most recent updates on the spread of the disease, please visit the CDC's website: https://www.cdc.gov/coronavirus/2019-ncov/index.html
The P.U.N.T. Pediatric Cancer Collaborative is a nonprofit 501(C)(3). The mission of P.U.N.T. is to provide critical and comprehensive financial, emotional and practical support to families facing a pediatric cancer diagnosis and to serve as a source of hope and healing for the bereaved.
Positively affecting the lives of pediatric cancer patients and their siblings through the writing, recording and sharing of their original songs.
CHOSA (Children of South Africa) identifies and supports community-based organizations that care for orphans and other vulnerable children in South Africa. The charity provides mostly unrestricted grants plus capacity-building, after‑school programs, and local networking to help communities run and sustain child‑care and development services.
The Cornelia de Lange Syndrome (CDLS) foundation is a family support organization which exists to ensure early and accurate diagnosis of CDLS, promote research into the causes and manifestations of the syndrome, and help people with a diagnosis of CDLS and others with similar characteristics make informed decisions throughout their lives. Reaching out, providing help and giving hope.
Myasthenia Gravis Foundation of America (MGFA) is committed to finding a cure for Myasthenia Gravis and closely related disorders, improving treatment options, and providing information and support to people with Myasthenia Gravis through research, education, community programs and advocacy.
To increase positive awareness of Down syndrome through national campaigns, educational programs, and by empowering individuals with Down syndrome, their families and the community.