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The Lymphoma Research Foundation's mission is to eradicate lymphoma and serve those touched by this disease.

The Child Cancer Fund was founded in 1994 by a group of Jacksonville, FL parents whose children were being treated for cancer; they understood the stress, anxiety and heartache of a childhood cancer diagnosis. We provide practical, emotional, financial, and educational support to children and their families every step of the way to navigate the challenges of childhood cancer.

To provide a community where people heal together.

The Huntington's Disease Society of America is the premier nonprofit organization dedicated to improving the lives of everyone affected by Huntington’s disease. From community services and education to advocacy and research, HDSA is the world’s leader in providing help for today and hope for tomorrow for people with Huntington’s disease and their families. HDSA's network of chapters, affiliates, HDSA Centers of Excellence, social workers and support groups provides a seamless connection for help, education and outreach to HD families and health care professionals across the United States.

Clearbrook is committed to being a leader in creating innovative opportunities, services and supports for people with disabilities. We serve people over a range of ages and disabilities from children diagnosed with developmental delays at birth to the unique needs of seniors with disabilities and all ages in between. Annually, we support over 8,000 individuals as well as their families in 15 counties, in over 160 communities and 50 locations throughout Chicago, the suburbs, and northern Illinois. We are proud to be the largest provider of home-based services in Illinois.

Hearts of Epilepsy Foundation® - is a registered 501(c)(3) non-profit organization. We are dedicated to providing effective tools and programs to improve the quality of life for children and families living with epilepsy. Hearts of Epilepsy Foundation participates in local and national epilepsy awareness. We provide individualize – age based support groups, individual counseling, educational and safety programs. These programs will bring great hope to those living with epilepsy. During this process - we will continue to work to reaffirm existing and develop new relationships with service providers, community organizations, and volunteers who are excited about further collaboration and committed to improving the epilepsy health in our community.

The mission of SAPA is to develop and maintain a strong and dynamic professionalsociety that:(1) Supports the advancement of its Members.(2) Responsive to the needs of its Members’ communities within the United States and Sudan.(3) Aids in fulfilling its Member’s philanthropic endeavors within the United States and Sudan.

Stand Up To Cancer’s (SU2C) mission is to raise funds to accelerate the pace of groundbreaking translational research that can get new therapies to patients quickly and save lives now. SU2C brings together the best and the brightest researchers and mandates collaboration among the cancer community. By galvanizing the entertainment industry, SU2C has set out to generate awareness, educate the public on cancer prevention and help more people diagnosed with cancer become long-term survivors. Stand Up To Cancer is an initiative of the Entertainment Industry Foundation.

Assist ME enhances the lives of people with low-to-no insurance in the Charlotte metro and surrounding communities who have lost mobility by providing them with the mobility equipment they need to regain their independence. Our goal is to help those in need get back to doing the things they love and living life to the fullest. Double your donation! Check your place of business policy for matching donations and request Assist ME be added to the deserving nonprofits that can be matched.

The Foundation Fighting Blindness, Inc. is the world’s leader in providing awareness and funding that drives the research that will provide preventions, treatments and cures for people affected by retinal degenerative diseases.

A 501(c)(3) nonprofit organization raising awareness and funds for new global, cutting-edge research to find a cure for glioblastoma. The purpose of the Glioblastoma Research Organization is to provide financial support to doctors and researchers around the world, that are working on developing cutting-edge technologies and clinical trials through research, to increase the rate of survival in patients, and find a cure for this disease.

Our mission is to advance the awareness and treatment of Angelman Syndrome through education and information, research, advocacy, and support for individuals with Angelman Syndrome, their families, and other concerned parties.