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The Rare Sisters Batten Foundation will help further the development of medical research for treatments and cures for CLN3 Batten Disease, and provide monetary assistance to families with children diagnosed with Batten Disease.​​

To transform the lives of disadvantaged children and young adults with physical deformities caused by birth defects, accidents, abuse or disease through the gift of free reconstructive surgery and related medical care.

The Lions Eye Foundation of California-Nevada, Inc. (LEF) preserves and restores the gift of sight by providing free ophthalmic examinations, operations, and medication to the less fortunate members of our community.

Usher 1F Collaborative is a 501c3 nonprofit foundation whose mission is to fund medical research to find an effective treatment to save or restore the vision of those with Usher Syndrome type 1F.

The mission of the Caring for Children Foundation of Texas' Care Van Program is to immunize uninsured and medically underserved children, and provide targeted preventative health services to help families throughout Texas.

The purpose of the Fund is to provide hearing devices for children with hearing losses between the ages of newborn and twenty years whose parents are unable to meet this special need financially. An estimated 100 children are provided with hearing devices each year. The Fund is the continuing philanthropic project of Job’s Daughters International. It is fully staffed by unpaid volunteers from throughout the United States and Canada. Total operating expenses are less than 5%. The HIKE Fund, Inc. is a not for profit charity incorporated under the laws of the State of Nebraska and registered with the Internal Revenue Service as a tax-exempt charity.

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.

The Propionic Acidemia Foundation is a 501(c)3 non-profit organization dedicated to finding improved treatments and a cure for Propionic Acidemia by funding research and providing information and support to families and medical professionals.

THE OBJECT OF EMPOWER IS TO ENABLE PEOPLE WITH PARKINSON'S DISEASE IN CENTRAL NEW YORK TO LIVE THE FULLEST LIFE POSSIBLE THROUGH PROGRAMS THAT INCREASE THEIR AWARENESS AND PARTICIPATION IN EXERCISE, NUTRITION, MEDICAL SUPPORT AND PSYCHOSOCIAL WELL-BEING.

MSF is the world’s leading independent humanitarian medical relief organization, providing crucial medical care to people affected by war, civil strife, epidemics, natural disasters and social marginalization. MSF strives to respond rapidly and effectively to public health emergencies with complete independence from political, economic or religious powers. In 1999, MSF was awarded the Nobel Peace Prize for its pioneering humanitarian work: rapid interventions, calling public attention to humanitarian catastrophies, respecting fellow humans’ dignity and acting as a source of hope for peace and reconciliation.

Patients with chronic or life-altering diseases (such as cancer, rheumatoid arthritis, or multiple sclerosis) must fight both their illness and the financial burden it places on their family as they struggle to pay for their medications. It is estimated that over 35% of these patients have insurance but still cannot afford the co-payments for the specialty therapeutics they need to treat or control their disease, which can range from $300 to over $3000 per month for a single dose. These underinsured patients are not eligible for most free drug or patient assistance programs, leaving them with few alternatives. They may be forced to do without their medications or go into debt to obtain them, greatly affecting their health and quality of life. Our mission is to improve the health and quality of life of underinsured patients with chronic disease, cancer, or other life-altering conditions who cannot afford the medications they so desperately need.

The National Fibromyalgia & Chronic Pain Association unites patients, policy makers, and healthcare, medical and scientific communities to transform lives through visionary support, advocacy, research and education of fibromyalgia and chronic pain illnesses.