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The organization operates free short-term medical care clinics in developing countries where such care is often lacking. At these clinics medical and dental care is provided to individuals in need as a means of introducing them to the Gospel of Christ.

The purpose of the home is to assist families in need by providing a safe home-like setting for children until they are reunited with family or achieve independence resident children range in age from infant to 22 the average resident census is 50-65 limited housing is also available for youth over the age of 18 if they are enrolled in a school of higher education  

The Cystinosis Research Foundation is dedicated to finding better treatments to improve the quality of life for those with cystinosis and to ultimately find a cure for this devastating disease.CRF is committed to finding a cure through an aggressively funded research agenda. CRF issues research grants bi-annually to accelerate the research process and to ensure that there is never a gap in funding new cutting-edge research ideas. We are focused and determined to improve the quality of life for our patients and to find better treatments, including a cure, for our adults and children living with cystinosis

ALS Arizona is dedicated to improving the quality-of-life for persons with ALS. We provide movement to those who have lost the ability to walk; communication to those who have lost the ability to speak; support to those who have lost the ability to cope; and a voice and role in the fight against Lou Gehrig's Disease in Arizona.

smashSMARD is a non-profit 501(c)3 organization whose mission is to increase awareness of SMARD1 and the IGHMBP2 gene mutation in order to fund research that will lead to treatments and cures.

Life’s WORC offers comprehensive services and support to more than 2,000 people and families with intellectual disabilities and autism in Queens, Nassau, and Suffolk counties. Our residential locations provide supportive homes to over 250 people throughout the noted communities including East Harlem. Additional programs for both families and people with developmental disabilities and autism include at-home support, skills development and behavioral intervention, social recreational programs, and vocational training opportunities. We also offer collaborative school linkage programs with both Long Island and NYC school districts supporting people and families in need of applied behavior analysis intervention.

Leading the fight to treat and cure ALS through global research and nationwide advocacy while also empowering people with Lou Gehrig’s Disease and their families to live fuller lives by providing them with compassionate care and support.

The Mission of Chestnut Hill Benevolent Association is to provide a healing refuge and services that minister to the needs of mankind with Christian Science nursing.

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.

Our vision: No child shall be denied hope, love, or a fair chance in life. At Domus we find and love young people who are shut out, unwanted, unloved, and afraid; the young people society has failed and discarded; the young people who, without our intervention, would drop out of their schools and their communities and be incarcerated, homeless, or dead. We create the conditions necessary for them to get on a path toward health and opportunity so they can engage and succeed in school and ultimately have satisfying and productive lives.

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.

CCA's mission is empowering and giving hope to individuals and families affected by facial differences. We envision a world where all people are accepted for who they are, not how they look.