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The National Kidney Foundation (NKF), a major voluntary nonprofit health organization, is dedicated to preventing kidney and urinary tract diseases, improving the health and well-being of individuals and families affected by kidney disease and increasing the availability of all organs for transplantation. The NKF is ranked in the top 1% of socially responsible brands and meets the standards of the Wise Giving Alliance of the Better Business Bureau where 80% of every dollar raised goes directly to programs and services. 

New Directions believes that people who have disabilities deserve the same opportunities in life that others expect and enjoy. Our profoundly enriching travel programs expand the self-esteem of every traveler. Whole new worlds of understanding open for both participants and the general population. Through these unique programs, people with disabilities are increasingly understood, appreciated and accepted as important and contributing members of our world. Changing the way the world views disability— one adventure at a time.

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.

The Multiple Myeloma Research Foundation, Inc. mission is to: relentlessly pursue innovative means that accelerate the development of next-generation multiple myeloma treatments to extend the lives of patients and lead to a cure. To achieve this purpose, four goals are pursued: Funding research in the field of multiple myeloma, building collaborations among researchers and industry, providing disease and treatment related information to patients and family members while advocating for optimal patient care, and raising awareness of multiple myeloma.

The Multiple Sclerosis Association of America (MSAA) is a leading resource for the entire MS community, improving lives today through vital services and support.

The mission of the Lung Cancer Research Foundation is to support national research studies and activities focused on developing innovative strategies for better treatments, screening, and prevention of all cancers of the lung. New knowledge gained by funding scientific and clinical research initiatives will lead to more positive outcomes and improved quality of life for all lung cancer patients.

The Fisher Center for Alzheimer’s Research Foundation is an organization that provides millions of dollars for novel Alzheimer’s research all over the world to investigate the latest, most promising research available. Our mission is to understand the causes of Alzheimer’s disease, improve the care of people living with it, and find a cure. A majority of our funding goes to the Fisher Center Lab at The Rockefeller University that was under the direction of the late Nobel laureate Dr. Paul Greengard, which is now under the leadership of Dr. Nathaniel Heintz. The Center has provided researchers around the globe with a conceptual framework for understanding the disease process and continues to be at the forefront of one day finding a cure for Alzheimer’s disease. We also fund research at NYU Langone, where a handful of clinical trials are taking place. The Foundation’s national comprehensive Alzheimer’s Information Program, the heart of which is the Foundation’s website, www.ALZinfo.org continues to spearhead efforts to increase awareness of and education about Alzheimer’s disease to the general public. The website provides in-depth information on the most current research studies, treatments, and disease management approaches. We also publish a magazine (Preserving Your Memory®) that provides readers with information about Alzheimer’s and how to take the necessary steps to prepare adequately if they or a loved one fall victim to the disease. Another facet of our Information Program is the e-newsletter, which contains updates and helpful tips. Our vision is working towards a future where Alzheimer’s is nothing but a memory.

MiracleFeet increases access to proper treatment for children born with clubfoot in developing countries through our partnerships with local healthcare providers. Since we began our work, MiracleFeet has helped change the lives of more than 100,000 children in 39 different countries.

Food For Thought's mission is to foster health and healing with food and compassion.

RSRT was launched in 2008 to drive research toward a cure for Rett Syndrome and related MECP2 disorders. Our mission is urgent: 15,000 girls and women in the United States and 350,000 globally live with the agonizing symptoms of Rett Syndrome.

The National Pancreas Foundation provides hope for those suffering from pancreatitis and pancreatic cancer through funding cutting edge research, advocating for new and better therapies, and providing support and education for patients, caregivers, and health care professionals.

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.