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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.

Parent Project Muscular Dystrophy fights to end Duchenne. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.

Project Alive is a 501(c)(3) nonprofit Hunter Syndrome research & advocacy foundation. Our mission is to cure Hunter Syndrome / Mucopolysaccharidosis II. Project Alive funds research programs focused on Hunter Syndrome, and assists industry and academics with designing research and clinical programs to treat Hunter Syndrome. Project Alive also advocates with regulatory and legislative bodies, as well as industry, for policies supporting the most effective and efficient clinical research programs and compassionate use / expanded access protocols.

Project 4031's mission is to provide terminally ill children, adults, and their families facing end-of-life challenges with peace and comfort by easing financial burdens and fulfilling last dreams.

Project Inform fights the HIV and hepatitis C epidemics by assuring the development of effective treatments and a cure; supporting individuals to make informed choices about their health; advocating for quality, affordable health care; and promoting medical strategies that prevent new infections.

Project A.L.S. was founded in 1998, as a non-profit 501(c)3, when Jenifer Estess, a 35-year-old New York theater and film producer, was diagnosed with ALS. Told at the time of diagnosis to “max out her credit cards and eat junk food,” Jenifer instead committed her efforts to making a difference for people with ALS—and producing treatments and a cure. Historically, ALS research was conducted by committed ALS researchers working separately on various aspects of the disease. Project A.L.S. changed that approach dramatically by requiring that researchers and doctors from many disciplines work together, share data openly, and meet shared research milestones.

The purpose of the Spiritus Project is to provide various forms of direct, need-based financial assistance to adult cystic fibrosis patients in an effort to reduce stress and provide an improved quality of life. The initial focus of the Spiritus Project is to assist North Carolina-based cystic fibrosis patients. Through Q3, 2020, your support has allowed us to touch patient lives over 1,500 times in five years through financial assistance and/or hospital admission and refill bags. This means that roughly every day since we started, we have impacted a patient’s life in some meaningful way. Some impacts were large, some were small, but all helped us to achieve Jessica Link’s vision to improve the lives of adult cystic fibrosis patients.

To accelerate breakthroughs in research to develop treatments and a cure for CASK gene disorders.

Veerni's mission is to educate and empower girls and women of rural Rajasthan so they can lead healthy and productive lives free from poverty, coercion and disease.

To create healthier futures for women and girls in Nicaragua through a women-centered model of development and care.

The Mission of International Esperanza Project (IEP) is to inspire hope in people in developing countries through healthcare, community infrastructure and education projects, improving lives and transforming communities.

World Pediatric Project is a nonprofit humanitarian organization linking worldwide pediatric surgical, diagnostic and preventative resources to heal critically ill children in developing countries. World Pediatric Project also helps build indigenous health care capacity - saving kid's lives now and transforming pediatric health outcomes for years to come.