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Promote programs of research, advocacy, education, support and awareness in order to discover treatments and a cure for Polycystic Kidney Disease and improve the lives of all it affects... program supports PKD scientists and their research. The Foundation also provides scientific ... The Foundation raises awareness of PKD through national, regional ...

The BlinkNow Foundation’s mission is to provide an education and a loving, caring home for orphaned, impoverished and at-risk children. We also provide community outreach to reduce poverty, empower women, improve health, and encourage sustainability and social justice. The Foundation fulfills its mission by providing financial support and management oversight to the Children’s Home and Kopila Valley School in Surkhet, Nepal.

Established in the year 2000, the Preeclampsia Foundation is a 501(c)(3) non-profit organization whose mission is to reduce maternal and infant illness and death due to preeclampsia and other hypertensive disorders of pregnancy by providing patient support and education, raising public awareness, catalyzing research and improving health care practices.

The Epilepsy Foundation is the national organization that works for people affected by seizures through research, education, advocacy and service. We are an organization of volunteers committed to the prevention and cure of epilepsy and a positive quality of life for everyone who lives with seizure disorders. Our current strategic goals include broadening and strengthening of research, providing individuals and families with easy access to reliable information, and assuring access to appropriate medical care for those affected by seizures.

OUR MISSION LUNGevity Foundation is firmly committed to making an immediate impact on increasing quality of life and survivorship of people with lung cancer by accelerating research into early detection and more effective treatments, as well as providing community, support, and education for all those affected by the disease. OUR VISION A world where no one dies of lung cancer. OUR VALUES We believe it's important for our board, our staff, and our constituents to know the values that drive all our actions. We are: FOCUSED ON SURVIVORSHIP 100% dedicated to increasing and improving lung cancer survivorship RESULTS-ORIENTED Always challenging the status quo and seeking a more efficient and effective way Rigorously measuring our performance to ensure maximum impact COMPASSIONATE AND RESPECTFUL Building and sustaining a community for all those affected by lung cancer Respectful of all people with lung cancer, caregivers, loved ones, medical professionals, donors, board members, and employees COLLABORATIVE Committed to being good partners and strategic collaborators to enable us to reach our goal more quickly and efficiently, including through our scientific endeavors TRANSPARENT Fiscally responsible and holding ourselves to the highest ethical standards

Supporting patients and families while promoting research, education and awareness.

The American Foundation for the Blind removes barriers, creates solutions, and expands possibilities so people with vision loss can achieve their full potential.

The Retina Foundation of the Southwest is an independent, nonprofit research institution whose mission is to prevent vision loss and restore sight through innovative research and treatment.

The Children's Medical Research Foundation, Inc. was formed in 1995 for the purpose of raising public awareness and funds to support medical and scientific research into the causes of, and cures for Sanfilippo Syndrome and other neuro-genetic diseases afflicting children.

The Kidney Foundation of Canada is the national volutneer organization committed to reducing the burden of kidney disease through: funding and stimulating innovative research; providing education and support; promoting access to quality healthcare; and increasing public awareness and commitment to advancing kidney health and organ donation.

The Kendall Burrows Foundation was founded by the Deb and Dave Burrows to honor the memory of their daughter, Kendall, who passed away from Evan’s Syndrome in 1996. During her lifetime, Kendall was an inspiration for how she lived with grace and strength despite intermittent and sometimes lengthy hospital stays. She stands for all children who must face incredible odds and yet do so with a smile on their face.

Support everyone affected by Waldenstrom's macroglobulinemia while advancing the search for a cure.