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Corazon de Vida (CDV) is a 20+ year US 501c3 non-profit organization providing life-changing support for orphaned and abandoned children in Baja, Mexico by funding local orphanages, providing quality of life improvement services and investing in the children’s future by funding higher education.

"To bring awareness and provide funding for the research of rare kidney cancers like HLRCC in children and young adults." -Driven To Cure www.driventocure.org

To eradicate cancer as a life-threatening disease in children by funding promising and innovative childhood cancer research that might otherwise go unfunded.

TO EDUCATE THE PUBLIC ON BATTEN DISEASE, PROVIDE EMOTIONAL SUPPORT TO FAMILIES OF CHILDREN WITH THE DISEASE AND PROVIDE FUNDING FOR CRITICAL RESEARCH IN THE TREATMENT AND CURE OF BATTEN DISEASE

Our main focus is Cystic Fibrosis (CF) awareness and to raise funds through the selling of our global crafts which include handmade Soy Candles, Jewelry, Crocheting, Pottery and much, much more. Our Story: Our daughter Hannah was born with Cystic Fibrosis, a genetic life-threatening disease. Our family’s and friends mission in life has been to make a difference by raising awareness through volunteering and fundraising for Cystic Fibrosis. Our lives drastically changed on July 22nd, 2012 when our only other child, our son, SPC Brenden N. Salazar-Nelson was killed in the line of duty in Afghanistan, decorated with the Bronze Star and Purple Heart. I created Angel’s Life in 2003, I chose this name because it is the symbol of peace and salvation. Now this name means that more than ever. Together with my friends and family, we create soy-based candles and sell them to help draw awareness for Cystic Fibrosis.

SLC6A1 Connect is a patient advocacy group dedicated to improving the lives of children and families affected by SLC6A1. Our focus is to raise awareness and funding to advance scientific research that will ultimately result in a cure.

Liv4TheCure’s mission is to promote awareness, help families and fund research for Rare Genetic Diseases (starting with Wolf Hirschhorn Syndrome). ​​ A rare disease is a disease that affects less than 200,000 people at any given time. Rare diseases affect 25-30 million Americans. Our goal is to bring awareness to rare diseases, specifically Wolf Hirschhorn Syndrome which is a genetic deletion on the 4th chromosome that affects children in highly varied ways. A portion of our funds will go to helping families in need. The other portion of our funds will go to research, specifically gene therapy and replacement for the missing areas of the 4th chromosome that have been deleted. ​ Liv4TheCure wants to fund the creation of a new platform technology such as CRISPR that will not only help children with WHS but any child with a genetic deletion.

The Evanosky Foundation exists for the purpose of generating funds to support two main objectives. It will support pediatric leukodystrophy research as well as assist and care for children and families affected by one of the leukodystrophies and/or other disabling conditions.