This is a 501(c)(3) non-profit, charitable organization, incorporated and duly organized, under the laws, of the State Of South Carolina. It is registered with Guidestar and supported by voluntary donations and contributions. It was set up in memory of my, late, granddaughter, Angelique S. Ladson, 21 years old, that died on November 20, 2010, of a rare disease called Hepatosplenic Gamma Delta T-Cell Lymphoma. There is no cure. It is, very, hard to treat and the prognosis for survival is poor. Our family was heart broken and, very, sad to see our love one sick and die, shortly after being diagnosed. We felt, so, helpless. Our grief has been tremendous.

Through prayers and with the help of holy spirit, we will teach and educate families and the community about these rare diseases, using literature, public speaking, listening, encouraging, caring, sympathizing, empathizing, helping and giving in as many ways as possible, extending words of comfort to the sad and grieving, as well as assisting them financially when a relative is hospitalized or being laid to rest, set up dance sessions to promote better health physically, mentally and spititually, award future scholarships in the Radiology Technician field, Critical Nursing and Dance field, and anything else we can to do to help fight and advocate, for people that get sick with rare lymphomas, cancers, other diseases, depression, sadness, grief and other areas that help is needed.