Kya’s Krusade, Inc. is a volunteer-based 501(c)(3) tax-exempt organization. Kya’s Krusade was named after and inspired by a special young lady, named Kya, who was born with a rare condition called Arthrogryposis. The organization was co-founded by Kya’s mother and godmother, after several exhaustive searches to find information, resources and support for Kya and her family. Kylie and Ashandra decided to be proactive and become a resource and source of support for other children with physical disabilities and their families. Kya’s Krusade became fully operational in July 2007.
Kya’s Krusade is a comprehensive resource center serving children with physical disabilities and their families, specializing in Arthrogryposis and other less-publicized physical disabilities. We provide support, education and assistance through our website, provision of resource information and Information Packet, Art Therapy and Financial Assistance Programs. We strive to form a diverse community network and provide opportunities to enable equal access to all available informational, emotional, medical and financial sources of support.
Vision
Kya’s Krusade aspires to be a nationally recognized organization with a reputation for its exceptional delivery of client-tailored services, innovation and commitment to increasing awareness and the range of available resources dedicated to Arthrogryposis and other less-publicized physical disabilities. Strategic growth and network building will ensure the financial stability and longevity of our Krusade of hope, care, growth and results. Kya’s Krusade strives to assist children with physical disabilities to reach their maximum potentials at every stage and support their families.
Our Open Community Philosophy
Our Values and Operating Principals:
Kya’s Krusade is a comprehensive resource center, serving children and families affected by physical disabilities, specializing in Arthrogryposis and other less publicized physical disabilities. We offer education and assistance for children from diagnosis through 18 years of age. We strive to form a diverse community network and provide opportunities to enable equal access to all available informational, emotional, medical and financial sources of support.