Find your favorite nonprofit or choose one that inspires you from our database of over 2 million charitable organizations.
Displaying 217–228 of 604
The mission of The Foundation is to empower lives for a brighter future by facilitating projects and partnerships that enhance the welfare, education, health, and artistic and athletic abilities of individuals with Down syndrome. The vision of The Foundation is to create an environment where people with Down syndrome are included in every facet of the community. We believe that every person has something to offer regardless of their abilities. It is our hope to enable people with Down syndrome to become integrated into all areas of their lives beginning with school, through college and meaningful employment.
Impact Network is a U.S.-based charitable organization that provides successful technology based education solutions in rural Africa. We believe every child deserves access to a quality education. By empowering local teachers with tablets loaded with activity-based lessons and intensive training on the use of the technology, we make this possible. We developed the eSchool 360 system as a way to sustain high-quality education for less than $5 a month per student. Our solution is currently operating in over 40 schools in rural Zambia, serving over 6,000 students in the primary grades.
Israel Friends is a testament to unwavering support and humanitarian action. Operating under the wing of Worldwide Friends, a distinguished U.S.-based 501c3 organization, we were born from the collective determination of visionary entrepreneurs. Our origin was an emergency response to Russia's unjustified aggression against Ukraine, sparking our commitment to deliver critical aid on the ground. In resolute solidarity with Israel, our mission is clear: to provide essential humanitarian aid and tactical support exactly where it's needed most. Our approach is marked by thoughtfulness and deliberate action, ensuring that we adapt swiftly as the needs of those we serve evolve. Transparency is paramount to us as we believe it's the cornerstone of trust in our collaboration with donors.
#HalftheStory's mission to empower the next generation’s relationship with social media, through advocacy, education, and providing access to resources for youth. We believe in digital wellbeing. In the digital age we have the freedom to filter out our lives however we choose. Hiding behind our social media identities, we mask the truth behind partial realities we post everyday. #HalftheStory is a global community that encourages individuals to share parts of their lives that exist outside of the standard social media story— Life unfiltered. #HalftheStory celebrates hidden human talents, passions, beliefs and struggles that connect us on a deeper level. By sharing a part of our identity that is not regularly revealed through social media, we restore human connection.
Alex’s Lemonade Stand Foundation (ALSF) is changing the lives of children with cancer by funding impactful research, raising awareness, supporting families and empowering everyone to help cure childhood cancer. When Alex, who was diagnosed with childhood cancer just before her first birthday, was 4, she told her parents she wanted to set up a front yard lemonade stand. Her plan: to give the money to doctors to help them find a cure. Her first “Alex’s Lemonade Stand,” held with the help of her older brother Patrick, raised an astonishing $2,000 in one day. While bravely fighting her own cancer, Alex continued to set up lemonade stands every year. As news spread of the remarkable girl so dedicated to helping other sick children, people everywhere were inspired to start their own lemonade stands — donating the proceeds to her cause. In 2004 when Alex passed away at the age of 8 — her stand and inspiration had raised more than $1 million towards finding a cure for the disease that took her life. Alex’s Lemonade Stand Foundation (ALSF) was started by her parents in 2005 to continue the work that Alex began. Our mission is simple: to change the lives of children with cancer through funding impactful research, raising awareness, supporting families and empowering everyone to help cure childhood cancer. Since Alex set up her first lemonade stand in 2000 — truly exemplifying the saying “When life hands you lemons, make lemonade” — we have raised more than $250 million. That money has helped to: - Fund more than 1,000 cutting-edge research projects at nearly 150 institutions. - Create a Travel For Care program to help support families of children receiving treatment and develop resources, such as our SuperSibs program to help people everywhere affected by childhood cancer. Alex’s Lemonade Stand Foundation is the living embodiment of Alex’s spirit of determination and hope. Like Alex, we believe that every person can make a difference. Together, we can bring about a cure. Please join us in “making lemons into lemonade” today!
The core mission of the IRSF is to fund research for treatments and a cure for Rett syndrome while enhancing the overall quality of life for those living with Rett syndrome by providing information, programs, and services. In 1983, a small dedicated group of parents whose children had Rett syndrome formed the first non-profit to focus exclusively on Rett syndrome – International Rett Syndrome Association (IRSA). In 2007, IRSA and Rett Syndrome Research Foundation (RSRF) consolidated resources to better serve families and maximize research investments toward a cure. The International Rett Syndrome Foundation (IRSF) emerged with a mission to accelerate research and empower families that builds upon these foundations’ pioneering work toward care and cure. We are walking this journey with you. IRSF is comprised of parents and friends of those diagnosed with Rett syndrome. We are dedicated to empowering families with the latest medical information, offering meaningful support and resources, and advocating for all those living with Rett syndrome. Our strategy is simple but powerful: improve care today and create treatments for tomorrow. IRSF is committed to a full-spectrum approach, providing solutions for everyone living with Rett syndrome. We do this by investing in innovative research, working to build a robust treatment pipeline, and removing barriers to ensure clinical trial success.
OUR MISSION LUNGevity Foundation is firmly committed to making an immediate impact on increasing quality of life and survivorship of people with lung cancer by accelerating research into early detection and more effective treatments, as well as providing community, support, and education for all those affected by the disease. OUR VISION A world where no one dies of lung cancer. OUR VALUES We believe it's important for our board, our staff, and our constituents to know the values that drive all our actions. We are: FOCUSED ON SURVIVORSHIP 100% dedicated to increasing and improving lung cancer survivorship RESULTS-ORIENTED Always challenging the status quo and seeking a more efficient and effective way Rigorously measuring our performance to ensure maximum impact COMPASSIONATE AND RESPECTFUL Building and sustaining a community for all those affected by lung cancer Respectful of all people with lung cancer, caregivers, loved ones, medical professionals, donors, board members, and employees COLLABORATIVE Committed to being good partners and strategic collaborators to enable us to reach our goal more quickly and efficiently, including through our scientific endeavors TRANSPARENT Fiscally responsible and holding ourselves to the highest ethical standards
“Maanavseva" (Service to Humans) is a Registered Non-Profit with a mission to fight malignancies including breast cancer among rural women in Indian villages. The mission is achieved through activities such as educating, creating awareness, conducting preventive examinations and mammogram screenings and facilitating the hand-holding of rural women with necessary follow-up and treatment.Maanavseva intends to implement this mission by adopting one village at a time and conducting 100% screening of all village women as per the health guidelines and implement follow-up on a sustained basis. The short term focus is to create a successful process for a cluster of villages that is replicable and sustainable. Maanavseva will achieve this goal through conducting pilot studies in villages, identify, resolve and document the challenges involved and arrive at a workable and sustainable model. The long term focus is to expand the model to several clusters of villages through sponsorship of corporations, local bodies and other Governmental Schemes. Most prevalent cancers for rural women can be cured by early detection and appropriate treatment. If these cancers are detected early, the cost is less, treatment is less invasive, survival rates are higher and the quality of life is better. Therefore we believe that by creating awareness about these cancers and early detection through mammogram and other screenings is extremely important and is the only way to win the war on breast cancer.
THE CROODS, DESPICABLE ME, THE LORAX… Ask any child to name their favorite movie and one of these titles might pop up. There’s nothing like seeing a child’s face light up as the previews end and the movie that he/she has been anticipating for weeks is finally about to begin! But what about the children who are battling life-threatening illnesses who are unable to visit a movie theater? LOLLIPOP makes it possible for hospitalized children around the nation to see the season’s biggest blockbuster movies* at the same time as their friends and siblings. Our desire is to create a fun escape from the daily reality of the illnesses and medical treatments these children face. And in the process, LOLLIPOP hopes to deliver a “normal” experience for the entire family. We believe hope and laughter are the key ingredients in having the strength to fight and to cope with hospitalization. Most of these pediatric patients – ranging in age from 2-20 years – are normally deprived of the movie-going experience, as they are unable to leave the hospital for weeks or months on end, if ever. Since LOLLIPOP’s first screening in 2002, we have screened over 300 films and now reach hospitalized children in over 18 states nationwide. In 2005, we expanded the program to include other entertainment mediums like TV movies, shows, and our Rhythm of Hope® music program, as well as collaborations with other organizations to provide movie-themed arts and crafts pre-show activities.