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The Trini Foundation is a 501c3 non-profit organization dedicated to helping people with substance use disorder find long-term recovery by building environments of physical, mental, and spiritual support through integrating recovery services with Ashtanga yoga and mindfulness practices.

Our mission is to raise money for children whose families cannot afford the necessary medication or treatment for Lyme disease. We provide grants and support the medical community until a cure is found. LivLyme Foundation will promote education and awareness about Lyme and the associated diseases.

OneBlood is a not-for-profit 501(c)(3) community asset responsible for providing safe, available and affordable blood to more than 200 hospital partners and their patients throughout most of Florida, parts of Georgia, Alabama and South Carolina. Formerly known as Florida Blood Services Foundation.

The MAGIC Foundation was established by five families October 29, 1989. After countless frustrating searches for solid information regarding their own child's growth disorder, these parents decided to join together and form an organization that would make this search easier for other parents. MAGIC's primary function is to provide families and children with services to help them better understand their diagnosis, and to give them the support needed to cope with the realities of these greatly misunderstood disorders.The mission of The MAGIC Foundation is to identify and expand treatment of physical abnormalities in children resulting from growth disorders. To remain the non-profit leader committed to excellence in developing and sustaining innovative educational, outreach and support programs.

The Lelt Foundation assists severely impoverished and malnourished families in Kara Kore, Ethiopia. Lelt has a Synergy Strategy which achieves success and sustainability through a combination of programs in education, nutrition, food security, orphan care, trauma counseling, microfinance and job creation for participating families.

Our mission at Jett Foundation is to extend and enrich the lives of individuals affected by Duchenne muscular dystrophy and other neuromuscular disorders. We fulfill this mission by partnering with individuals and families through empowering educational programming, transformational direct service experiences, and by accelerating development of life-changing treatments.

Unatti Foundation is a nonprofit organization that provides Nepali girls, in vulnerable situations, with educational programs. Through comprehensive academic, health and life skills education, Nepali girls become enlightened, empowered leaders inspired to give back, benefitting the girls’ communities and future generations locally and around the world.

TO PROMOTE, ADVANCE AND INSPIRE ORGAN, EYE AND TISSUE DONATION IN NEW YORK BY RAISING AND DEPLOYING CHARITABLE CONTRIBUTIONS FOR EDUCATION AND FOUNDATION GRANTS WHICH WILL MAKE A MEANINGFUL DIFFERENCE FOR NEW YORK'S DIVERSE TRANSPLANT COMMUNITY, INCLUDING THOSE WHO HAVE RECEIVED AND THOSE WAITING FOR PRECIOUS LIFE-SAVING ORGANS.

SARAH is a family of agencies, SARAH Inc., SARAH SENECA, and SARAH Tuxis, that provide programs and services for people with intellectual and other disabilities who live in Connecticut. The SARAH Foundation, Inc. is responsible for raising funds, managing the investments and coordinating all donations in accordance with the wishes of the Donors and the mission of the SARAH agencies.

AIP Foundation's mission is to provide life-saving traffic safety knowledge and skills to the developing world with the goal of preventing road traffic crash fatalities and injuries. We envision a world in which there are safer roads, smarter road users, and countries whose road traffic environments serve their developing economies and people.

The LGS Foundation is a nonprofit organization dedicated to improving the lives of individuals impacted by LGS through advancing research, awareness, education, and family support. Our vision is to end the suffering and devastation caused by LGS. Lennox-Gastaut Syndrome (LGS) is a severe epilepsy syndrome that develops in young children and often leads to lifelong disability.

The SIMS Foundation provides mental health and substance use recovery services and supports for musicians, music industry professionals, and their families. Through education, community partnerships, and accessible managed care, SIMS seeks to destigmatize and reduce mental health and substance use issues, while supporting and enhancing the wellbeing of the music community at large.