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The Foundation's vision is: "To create a community where patients, healthcare professionals and researchers come together to conquer the complexities of Sjögren's." The Foundation's mission is to: * Support Sjögren’s patients and their loved ones through education, resources and services * Provide credible resources and education for healthcare professionals * Serve as the voice for all Sjögren’s patients through advocacy and awareness initiatives * Lead, encourage and fund innovative research projects to better understand, diagnose and treat Sjögren’s

Our two major programs provide hope for the future through the support of MS research into the cause, treatment and cure of the disease and hope for today through our many services that assist people with MS and their families. Since our founding in 1948, the core support of the MS Society has been from tens of thousands of dedicated individuals, companies and foundations in communities across Canada. The Society receives almost no funding from government.

Established in 2000, SIUT North America, is a charitable organization under Section 501(c)(3), is dedicated to health-related humanitarian causes, with our major focus on helping Sindh Institute of Urology and Transplantation (SIUT) Pakistan secure necessary funds for medicines, treatments and equipment so that patients are treated free of charge and without discrimination. SIUT North America also helps organizations in the U.S.A. through voluntary services and donations.

Keep Memory Alive and Lou Ruvo Center for Brain Health at Cleveland Clinic Nevada, aims to find, fund, and facilitate the most effective and innovative research and caregiver programming for patients and their families.Cleveland Clinic Lou Ruvo Center for Brain Health offers a unique integrated care model, social services, and research. With more than 30 clinical trials in its portfolio, the center is among the country's largest Alzheimer's clinical research programs

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.

Wellspring is open to all cancer patients, their families and care givers, all of whom are known as members. Wellspring is welcoming and comfortable in nature, external to hospitals or treatment centres, and is devoid of any “institutional” feeling. Volunteers and group leaders providing programs at Wellspring deliver only cancer support services and not medical treatment or medical therapies, nor services for patients with diseases other than cancer. Wellspring receives no government funding and offers all programs and services at no charge to our members and without referral.

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.

CURED is a not for profit foundation dedicated to those suffering from Eosinophilic Gastrointestinal Diseases (EGID), including eosinophilic esophagitis (EoE), eosinophilic gastritis (EG), eosinophilic colitis (EC) and other eosinophilic disorders. CURED is committed to raising substantial funding to aid in research, advocating on behalf of EGID patients and their families, and working to educate and increase awareness about this complex group of diseases. It is our heartfelt belief that CURED can make a difference for the individuals and their families who are touched by these diseases.

We are the largest nonprofit dedicated to funding research aimed at treating and ultimately curing EB, a group of devastating and life-threatening genetic skin disorders that affect children from birth. Leading researchers say treatments and a cure for EB are within reach—for Shane, Ryan, Jackson, Michael, Jennifer and every other person suffering from this horrific condition. Though we have made significant progress, we need much greater resources in our pursuit of a cure.  

Founded in 2015 by Juliet de Baubigny, Nick Jonas, Sarah Lucas + Sam Talbot, Beyond Type 1 is leveraging the power of social media and technology, changing what it means to live with a chronic disease. By educating the global community about this autoimmune disease, as well as providing resources and supporting those living with Type 1 diabetes, Beyond Type 1 is bridging the gap from diagnosis to cure, empowering people to live well today and funding a better tomorrow.

Our mission is to provide comfort care at the end of life. We believe that a life fully lived, no matter how long, should include an end-of-life experience of comfort, dignity, and peace. Our goal is to keep each patient as comfortable and independent as possible, while supporting the emotional and spiritual needs of our patients and their loved ones. We were the first non-profit Hospice in the area and one of the first 100 Hospices in the nation. Our founders were a group of dedicated doctors, nurses and community volunteers that began providing care to the dying on their own time. Our organization began in 1979 before there was insurance reimbursement for Hospice care and this dedication to our patients remains our culture to this day. Ionia Area Hospice approached Hospice of Lansing joined forces and a formal partnership was formed in 1984. Should the time come when it is no longer possible for a patient to remain at home, Stoneleigh Residence is a unique, comfortable, peaceful, and home-like alternative. Surrounded by gardens, a cascading pond, trees and wildlife, the Residence is designed to take full advantage of the natural beauty of its wooded 20-acre site. We are a true community-based Hospice, created out of necessity and driven by our mission to serve all by bringing kindness, respect and quality to the end-of-life. Hospice of Lansing, Stoneleigh Residence and Ionia Area Hospice provide pain management and personal care, respite care, emotional and spiritual support for patients, volunteer support and grief support for family members after the loss.

Every cure has a starting point. Like Dr. Jonas Salk when he conquered polio, Salk scientists are dedicated to innovative biological research. Exploring the molecular basis of diseases makes curing them more likely. In an outstanding and unique environment we gather the foremost scientific minds in the world and give them the freedom to work collaboratively and think creatively. For over 50 years this wide-ranging scientific inquiry has yielded life-changing discoveries impacting human health. We are home to Nobel Laureates and members of the National Academy of Sciences who train and mentor the next generation of international scientists. We lead biological research. We prize discovery. Salk is where cures begin.