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Founded in 1910, the Center for Hearing and Communication is the oldest and largest nonprofit organization providing comprehensive hearing rehabilitation and social services programs for individuals who are deaf or have hearing loss. With locations in New York and Florida, we continue to expand and enhance services for the deal/hard of hearing community, while adhering to our mission by providing services regardless of age, ability to pay, or mode of communication.

Our mission is to provide sport and physical activity opportunities for individuals who are blind or visually impaired.

Food Allergy Research & Education (FARE) works on behalf of the 15 million Americans with food allergies, including all those at risk for life-threatening anaphylaxis. This potentially deadly disease affects 1 in 13 children in the United States – or roughly two in every classroom. FARE is a 501(c)(3) nonprofit organization that was formed in 2012 as the result of a merger between the Food Allergy & Anaphylaxis Network and the Food Allergy Initiative. FARE’s mission is to ensure the safety and inclusion of individuals with food allergies while relentlessly seeking a cure.

Hospice Austin is a nonprofit organization that eases the physical, emotional and spiritual pain of any person in our community facing the final months of a serious illness by providing expert and compassionate care, education and bereavement support.

Little City is dedicated to serving children and adults with intellectual and developmental disabilities by providing the best options and opportunities to live safely, learn continuously, explore creatively and work productively throughout their lifetime. By inspiring, advocating and pursuing success with passion and purpose, lives are changed through hope, happiness, and optimism.

The Orthopaedic Foundation for Active Lifestyles encourages general practitioners and other members of the professional allied health care community whose practices include the care of persons with sports-related musculoskeletal injuries to participate in educational courses and hands-on laboratory workshops concerning advances in orthopaedic surgery, physical medicine and rehabilitation.   The Foundation is dedicated to the development and presentation of unique continuing medical education and research programs for physicians, health care professionals and interested community groups. Its focus is:

From the website: "We are the only Hong Kong charity dedicated to gynaecological cancers. The Karen Leung Foundation’s mission is to save lives by reducing the impact of gynaecological cancers in Hong Kong. We envision a world where women have every opportunity to live healthy and fulfilling lives free from gynaecological cancers."

The Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)3 dedicated to finding treatments and a cure for Charcot-Marie-Tooth disease (CMT) and related hereditary neuropathies while providing support and extensive information for those living with CMT and their families. HNF promotes and supports innovative therapeutic driven research.

The Hendren Project (THP) mission is to provide sponsor-supported digital resources that enable a global pediatric surgical community to help one another better serve children with complex surgical issues throughout their lives. The digital resources are provided to THP members without charge through the THP website.

Vitamin Angels reduces child mortality worldwide by connecting essential micronutrients with infants and children under five. Essential nutrients, especially vitamin A, help young immune systems fight infectious diseases, helping children attain good health and the opportunity to lead meaningful and productive lives.

Our mission is to honor our elders, by respecting and promoting their independence, spiritual vigor, dignity, and choice, and by recognizing that they are a resource to be cherished. As part of our mission, we accept special responsibility for the frailest and neediest members of our community who are most dependent on our care.

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.