Honor their memory with a charitable gift.

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.

Established in 1998, The Eye Cancer Foundation is an educational and supportive resource for eye cancer patients, their families, and physicians. Our mission is two-fold: one part focused on multi-center research of new diagnostic treatments for eye cancer research, the other focused on providing much needed, world-wide patient support services. Our mission is to create a world-class resource for patients and their families diagnosed with ocular tumors, radiation macular degeneration, and related ophthalmic conditions. We want to help you, your children and families around the world. ECF Specific Goals: 1) Find cures for patients with ocular tumors and related eye diseases. 2) Provide eye cancer specialists for unserved and underserved countries. 3) Coordinate international cooperative evaluations of new methods of diagnosis and treatment. 4) Support family and patient support programs to ease emotional stress and real-life adjustment issues related to eye cancer. 5) Promote transparency related to doctors and patient outcomes. 6) Promote quality assurance and education for eye cancer specialiatly centers. 7) Empower patients to find the resources to improve their lives.

Our mission is to advocate for and enhance our Southern Colorado membership's ability to improve the quality of health, life and services for individuals, families and communities affected by sickle cell disease and related conditions, while promoting the search for a cure for all people in the world with sickle cell disease.

The specific purpose of this corporation is to provide prescription eyeglasses and to help arrange vision and eye health care appointments with community eye care professionals for individuals who are otherwise unable to obtain assistance through private insurance, welfare, or other social services agencies.

THE ORGANIZATION IS A LOVING, NURTURING AND SUPPORTIVE GROUP HOME DEDICATED TO CARING FOR AND EMPOWERING YOUTH, LGBTQ YOUTH IN PARTICULAR, RANGING FROM 12 TO 17 YEARS OLD WHO ARE IN NEED OF SUCH SERVICES.

A Natural, Risk-free, Non-medical Option since 1986 For Spasmodic Torticollis, Cervical Dystonia, Dystonia Be encouraged – there’s hope!

Hemophilia Federation of America is a national nonprofit organization that assists and advocates for the bleeding disorders community.

Our mission is to restore and empower women who have been affected by human trafficking and sexual exploitation. Our program will provide a safe, nurturing living environment in North County, San Diego that will facilitate spiritual, physical, mental and emotional healing along with an array of support services and educational opportunities for survivors of human trafficking and sexual exploitation. Fostering self-understanding through personal and spiritual growth; Providing life-skill building and maintenance education; Offering opportunities to work towards self-sufficiency in a therapeutic work environment.

Our mission is to honor and obey God by providing help and healing to troubled children and families who then may bless others.