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The idea for A Free Bird™ was born out of the creative energy experienced firsthand by singer/songwriter and makeup artist, Godni Amir, founder and president of the organization. When Godni’s voice teacher, Gail found out her husband had been diagnosed with cancer, she had to stop teaching and become his primary caregiver. Soon after, she was also diagnosed with cancer. Although she and her husband struggled to defeat the disease, she never gave up her passion for the arts! Deeply touched by Gail’s determination to continue teaching and pursuing her creative endeavors, Godni was inspired to write music and poetry that reflected her benevolent spirit, which lead to the creation of a poem called “A Free Bird.” After seeing how creative energy could provide solace and inspiration to cancer patients, Godni wanted to share the healing power of the arts with others. A Free Bird™ was then created, delivering the message that everyone should have the opportunity to express themselves and fly free.

As the first chapter in Virginia, we are looking to spread the word about our mission and welcome more members and more chapters across the region! Cancer research will lead to a possible cure or less difficult treatment for future generations. Let’s keep up the good fight, one step, one dollar, one year at a time!

The Jennie Goas Silverman Foundation was created with love by some of Jennie's closest friends to honor her spirit, sparkle and brilliance. Jennie was diagnosed with triple negative breast cancer in June of 2016 and fought a hard battle with this devastating disease until she passed away on May 20, 2017. Jennie was a special person who impacted the lives of the people she touched. First and foremost she was a daughter, sister, wife and friend, and she always took those roles seriously. Next, she was a teacher, a high school math teacher in the CPS system. She was beautiful inside and out, she was generous, she was brilliant, she was humble and she was kind. These qualities have inspired us to create this foundation and continue to help her spirit live on through philanthropy. The Jennie Goas Silverman Foundations fundraising efforts have a dual approach: 1) Raise funds to award a qualified senior year student(s) in the communities Jennie taught with a scholarship to attend a 4-year college. 2) Raise funds and awareness for Triple Negative Breast Cancer research. Through our mission we hope to give back to the community Jennie lived and worked in and continue to fight in her honor to find a cure for triple negative breast cancer.

The Peter J. Herchenbach Memorial Scholarship Fund is a recognized 501(c)(3) non-profit corporation that helps high school students that are fighting cancer or other life threatening diseases. We offer $5,000 college scholarships that support anyone whose high school experience is being overshadowed by their disease. We want to help these gallantly fighting young adults by investing in their college education.

HealthCode's mission is to empower people to live healthier lives, free from preventable diseases. We envision a future in which everyone can enjoy the benefits of a healthy life, free from preventable chronic diseases (heart disease, diabetes, obesity, certain forms of cancer). We see a future where, with awareness, education and motivation, everyone can live healthier and happier. https://healthcode.org/about-us/

Dynamo and Dash Charities believes in using the sport of soccer to support communities in the greater Houston area. We are committed to leveraging the passion of our players, our staff, and our fans to provide resources and education that positively impact lives in our community. We focus on 5 pillars of Impact in the city of Houston: 1-Youth development through education and soccer 2- Food Insecurity 3- Military and Veteran Support 4- Cancer support and awareness 5- Sustainability

Mission Statement: The Binaytara Foundation seeks to improve healthcare in resource poor communities and improve cancer care worldwide by collaborating with national and international organizations to: 1.) develop healthcare manpower in underserved areas 2.) improve access to cancer care by establishing direct care facilities and services 3.) promote the practice of evidence based medicine by providing research grants to young physicians and healthcare providers in training 4.) improve knowledge and competence of healthcare professionals by offering them continuing educational materials though live and virtual meetings, webinars, and other educational forums. Our Values: As individuals who grew up in Nepal, and were edified by higher education and professional training in their home countries and in the United States, BTF co-founders maintain a strong sense of responsibility towards helping improve healthcare in resource poor communities. BTF board members, volunteers, associates, and donors are individuals highly motivated to help the less privileged people around the world. Our philosophy is "Countries have man-made boundaries, humanity does not." We invite you to join hands with us in helping improve healthcare near and far.

At the Buck, we aim to end the threat of age-related diseases for this and future generations. We bring together the most capable and passionate scientists from a broad range of disciplines to study mechanisms of aging and to identify therapeutics that slow down aging. Our goal is to increase human health span, or the healthy years of life. Located just north of San Francisco, we are globally recognized as the pioneer and leader in efforts to target aging, the number one risk factor for serious diseases including Alzheimer’s, Parkinson’s, cancer, macular degeneration, heart disease, and diabetes. The Buck wants to help people live better longer. Our success will ultimately change healthcare.

Source Vive's mission is to bring support to families and relatives of children suffering leukemia and cancers in the greater Paris North area, at any stage of their disease. (each year, 2000 to 2500 children are declaring cancer or leucemia in France) Support consists of psychologist assistance (2 professionals), art-therapy sessions (1 professional), sport-health (1 professional) sessions and various activities (21 volunteers) such as gardening, cooking and games plays. All this is held in a dedicated 400 sqm+ location in the city of L'Isle Adam (North of Paris). The support is given in complement of and in coordination with the one local hospitals may be providing to the children and their families depending on the stage or importance of treatment. Hospitals may also call Source Vive directly for their support. Source Vive is as such supporting 75 families a year through a personalized and dedicated approach. This is a non-profit support; no financial participation is asked to families; this is free of charge and all financial resources come either from local and national subsidies or private donations. There is no limitation in time to the support provided to families (support length is average 3 years). The Source Vive location is mainly open on week-ends but many additional activities are created along the year to make sure children and families can benefit from a warm and dedicated attention through several experiences ( leisure park visits, horse riding, Christmas spectacle, etc...). Source Vive is also deeply developing in the support they can bring in the scholastic education of children who cannot go to school anymore due to treatments. They bring the support in coordination with local schools and can either bring the support in hospitals or at home for children where needed. Source Vive is also working closely with local other communities to make sure they can maximize synergies and join forces (sport associations, artistical associations, etc...). The association was founded in 1989 by Mrs Sylvie Brechenade who had to manage herself the leukemia of her 3 months children; she realized a lack of psychological support and excha,ge platform at that time and decided to create Source Vice as soon as her child had luckily recovered from the disease. 33 years after, she is still leading the way in the association, while making sure people will be ready to take over her action when time is needed.

The Italian League for the fight against tumours - Provincial Department of Milan, founded in 1948 thanks to a strong culture of solidarity and education of health, acts in Milan and hinterland with the aim of facing the cancer problem in its wholeness through various services in the area of prevention, precocious diagnosis and assistance with the support of well-prepared 700 volunteers and the sponsorship of the medical research. The intervention areas are: Prevention activities: programmes against smoking, prevention in schools, sensibility and medical information conferences just in order to educate people to a proper life-style, activities in the Antismoke Institutes of Milan and Monza that tend to eliminate smoke addiction and assistance for the application of "No smoking Policy " in companies. Activities of precocious Diagnosis: 16 Prevention Spaces, at disposal of people without bureaucratic procedures, where medical staff carry out examinations on sinus, cutis, oral cavity and prostate, and exams such as mammography, mammary ecography and pap-test. They also organize medical examinations requested by town councils and by Milan and hinterland companies. Assistance activities: in hospital and at home, socio-medical assistance, volunteers that see patient's home/hospital/home for therapies, hospitality in welcome homes for adults and children. Training School for Volunteers opened to other Associations. Sponsorship for oncology institutions - research: cash grants to the clinic research and to other institutions that work on oncology area, scholarships, conferences and training/ refresher courses for the medical staff.

Mission: Palliative Care Network is dedicated to alleviating the suffering of patients who are combating serious illnesses through open access education for professionals worldwide. Vision: Palliative Care for Everyone, Everywhere Chronic diseases are the leading cause of mortality in the world, representing 60% of all deaths. 35 million people died from chronic disease in 2005. These include heart disease, stroke, cancer, chronic respiratory diseases and diabetes. 80% of chronic disease deaths occur in low and middle income countries (1). Healthcare professionals lack appropriate training to care for patients as a "whole" and, in particular, fall short in skills to care for patients with diseases with poor prognosis. Quite often, patients receive poor end-of-life care, even in societies with technologically advanced healthcare. Ultimately, patients experience unnecessary pain and suffering during treatment of disease and at the end-of-life. Palliative Care Network (PCN) aims to address pain and suffering more effectively through education. PCN provides a FREE, online, educational platform for palliative care professionals. Registration on the website and access to materials remains free of charge allowing those who have limitations to remain abreast of palliative care trends. Expert interviews, lectures, presentations, posters, etc. are voluntarily shared on the PCN Community. Participants from Harvard share the same platform with palliative care providers from developing countries in Africa, landlocked Nepal and Mongolia, etc. PCN evens out the platform for palliative care professionals worldwide. The multiple projects initiated by PCN not only help the professional community in assisting patients and their families but allow palliative care providers to encourage each other. The PCN Directory lists professionals from around the globe interested in collaborating to exchange knowledge and information. For example, using the PCN Directory, an Indian physician connected with an American social worker to share cultural issues, myths, and norms about palliative care, grief, and loss. Additional success stories include collaborations with a professor of sociology, nurse, and a producer/director.

Every day more than 600 people in Bulgaria have a life-saving need for blood and blood products, because of accidents, emergency life-saving procedures, surgical interventions, childbirths, different cancers and many other diseases that need blood for treatment. Their lives are directly dependent on securing the necessary quantities of safe human blood which can be obtained ONLY through DONATION OF BLOOD because BLOOD has NO substitute! Unfortunately, Bulgaria is currently in one of the last places in Europe when it comes to donating blood. Most people donate blood only for relatives or friends who are in need and the true number of genuine voluntary blood donors is less than 25% of all blood donors. Due to the very limited amount of blood donors, hospitals force patients to find donors before they can have a required treatment (the so-called "replacement donor system", which poses significant problems to the patients and their families. Also, this highly questionable practice has led to the growth of an ugly black market for blood donors.). We hope that with our joint efforts we will be able to change this situation. BULGARIAN ORGANIZATION OF VOLUNTARY BLOOD DONATION is a non-profit association operating in public interest done by volunteers. We are the first Bulgarian association working entirely to encourage and promote regular, anonymous, voluntary, non-remunerated blood donation. We believe that blood donation is one of the most humane acts. We also believe that our cause is extremely important for every human being because the shortage of blood could affect everyone. In our daily activities we provide information about blood donation, answer questions and give support; help in cases of an urgent need for blood; organize blood drives and campaigns to educate and inspire people to donate. In 2013 BOVBD launched the first-of-its-kind for Bulgaria long-term project called "Donate Blood", aimed at promoting and facilitating voluntary blood donation and helping those in need of blood for themselves or their relatives. The core of this project lies with the "Donate Blood" system, entirely managed and administrated by BOVBD. The system is a sort of dual registry and has two main functionalities that are interlinked - on one side for the people who are voluntary blood donors or wish to become such and help, and on the other - for everyone who needs blood. The system is extremely useful for finding blood donors on time. It is an innovative and very effective tool to at least partially fulfil the need for blood in Bulgaria and to help when the need is urgent. "Donate blood" can be used completely free through our mobile phone applications for iPhone and Android. Every user has constant access to important and useful information about blood donation, offered through the BOVBD website - www.bgblood.org, including the prerequisites and contradictions for donating blood, addresses and contact details for blood centres in the country, blood collection campaigns that are ongoing or upcoming, etc. Our ambition is to upgrade the applications with additional functionalities when we have enough funding. By focusing the public attention on the problems that arise from the lack of information on blood donation and its importance, from the insufficient number of voluntary blood donors and the risks of paid donors, we are working together to resolve them. The World Health Organization proclaims voluntary blood donation as the safest method for collecting the necessary quantities of blood and blood products needed in everyday healthcare. We hope and work for so that one day there will be enough voluntary blood donors and we, our kids, our parents and everyone who needs blood or could find himself in need of blood to be sure that there is enough safe blood that would help to save his life.