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Helen Keller International is a global health organization dedicated to eliminating preventable vision loss, malnutrition, and diseases of poverty.Co-founded by Helen Keller—and guided by her fierce optimism and belief in human potential—the organization delivers life changing health solutions to vulnerable families in places where the need is great but access to care is limited.In the U.S., Africa, and Asia, Helen Keller’s proven, science-based programs empower people to create opportunities in their own lives and build lasting change.

Since 1946, the Guide Dog Foundation for the Blind has trained and placed guide and service dogs to provide independence, enhanced mobility, and companionship to people who are blind, have low vision, or who have other special needs. The Guide Dog Foundation serves clients from across the United States and Canada. People come to us for our trademark small classes and personalized instruction, and we have successfully worked with individuals who are deaf-blind and those with disabilities other than blindness or hearing impairment. In addition to our guide and service dog programs, the Foundation offers extensive education and outreach programs to broaden the public's understanding of vision and visual impairment, and access and disability rights.

Wayfinder’s mission is to ensure that children, youth and adults facing challenges always have a place to turn. Founded in 1953 as the Foundation for the Junior Blind, we initially enabled blind and visually impaired children to lead fuller, more independent lives. Today, Wayfinder is a human services agency with expertise in child welfare, vision impairment and multiple disabilities. Across our programs, Wayfinder strives to achieve equity for all our clients, most of whom are low-income people of color. We serve nearly 20,000 children, youth, adults and family members annually. Our name became Wayfinder Family Services in January 2018

Mission Rabies is an international NGO headquartered in the UK with offices in the USA, India and Thailand. Despite being eliminated from many countries, rabies still takes a devastating toll on the world’s most marginalized and vulnerable. Existing models of rabies prevention remain inappropriate for implementation in most countries that remain rabies endemic, because they lie at the bottom of the UN HDR rankings. Since 2013, Mission Rabies has been implementing vaccination and education programs where the need is greatest, collecting evidence and sharing lessons to make global elimination a reality. The goal of Mission Rabies is to eliminate dog-mediated human deaths caused by rabies by 2030 through mega vaccination drives and educating communities at risk on the disease.

Life Health and Wellness Center was created to serve the homeless men, women and families. Our providers also serve Veterans and victims of Human Trafficking. Our clinic does not discriminate against race, color, sex, religion, sexual orientation, or ability to pay. We are a group of health care providers that provide family medicine to our patients. Many of our patients do not have health care but they do have chronic illnesses that have not been treated in years. We have contracts with the local universities and provide clinical education to students for Primary Care clinical rotations. The student are taught use evidence based methods to assess, diagnosis and treat patients and also educate patients about their current condition. We are also developing ways to sign patients up with insurance so they can become compliant with medications and therapies ordered to maintain positive health outcomes.

The Tegan and Sara Foundation fights for health, economic justice and representation for LGBTQ girls and women. This mission is founded on a commitment to feminism and racial, social and gender justice. In partnership and solidarity with other organizations fighting for LGBTQ and women's rights, the Foundation raises awareness and funds to address the inequalities currently preventing LGBTQ girls and women from reaching their full potential. This work is critically important because… LGBTQ women have higher rates of gynecological cancer, depression, obesity, suicide and tobacco/alcohol abuse. Discriminatory laws, provider bias, insurance exclusions and inadequate reproductive health coverage leave 29% of LGBTQ women struggling to pay for health insurance. A quarter of lesbian women live in poverty. LGB women of color are three times more likely to live in poverty than their white peers. Transgender women are four times more likely to have a household income under $10,000 and twice as likely to be unemployed. One in five transgender women has reported being homeless at some point. Less than 1% of TV characters are lesbians. In 2016, 25 queer female characters were killed on-screen – continuing a decades-long trend.

Our Mission is to work so that no one is isolated because of Parkinson’s disease. Parkinson’s Resource Organization (PRO) is dedicated to improving quality of life for families and individuals affected by Parkinson’s disease through education, support, and practical resources. PRO was established in 1990 by caregivers who were overwhelmed and struggling to find the support network they needed. So they decided to create one. What started as Children of Parkinson's morphed into Parkinson's Resource Organization and today we continue to maximize quality of life for people with Parkinson's, their families, and caregivers through education, resources, and person-to-person support. PRO works to improve quality of life for everyone impacted by Parkinson’s. We do this through emotional and practical resources, support groups, educational materials, and access to a network of professionals who can provide guidance and assistance. Additionally, we advocate for the needs and rights of caregivers and patients, ensuring they receive the necessary care and resources. Caregivers play a crucial role in the management and support of Parkinson's patients. PRO acknowledges their efforts and aims to equip them with the tools and knowledge required to provide effective care. Through continuous outreach and dedicated services, we strives to create a supportive community where caregivers and patients can find the help and companionship they need.

Wigs for Kids provides hair replacement systems to children under the age of 18 who have lost their hair as a result of medical treatments, health conditions, or burn accidents. When children lose their hair, whether as a result of medical treatments, health conditions or burn accidents, they don't just suffer physically. The change in their appearance can drastically undermine their self-image and sabotage their self-esteem. To help heal the pain of these struggles, Certified Cosmetic Therapist Jeffrey Paul founded Wigs for Kids, a nonprofit organization that has been serving children suffering from hair loss since 1981. Wigs for Kids is a cooperative effort among Certified Cosmetic Therapists throughout North America who share a common goal. “Children shouldn’t have to worry about how they look, especially when they’re in the middle of a health crisis,” says Jeffrey Paul. “We want to give these kids the opportunity to feel good about themselves again.” The value of all children’s wigs Hair Replacements is $1,800. “These are custom-made Hair Replacements,” says Jeffrey Paul. “Each prosthesis is hand-tied and is made completely from human hair. We make sure they look just like a child’s own hair.” “They won’t come off on the baseball field or in the playground,” he adds. “Kids can count on them. And because kids look just the way they did before, they feel better about themselves. They look in the mirror and their eyes light up. To see that light in their eyes … that’s priceless.”

The Transgender, Gender Variant, Intersex Justice Project's (TGIJP's) works to challenge and end the human rights abuses committed against transgender, gender variant, and intersex people, particularly against Black and transgender women of color, in California prisons, jails, detention centers, and beyond.

International Deaf Partnerships (IDP) seeks to strengthen education, promote advocacy, and improve opportunities for deaf and hard-of-hearing people in developing countries within the framework of the United Nations Convention on the Rights of Persons with Disabilities (CRPD). IDP was founded for the purpose of fostering a network of partnerships that includes deaf and hard-of-hearing communities within developing countries and the United States.

Sanford Burnham Prebys Medical Discovery Institute conducts world-class collaborative research dedicated to finding cures for human disease, improving quality of life, educating and training the next-generation of scientists, and thus creating a legacy for its employees, partners, donors, and community.