By supporting Kya’s Krusade, you are supporting children and families affected by Arthrogryposis and other less publicized physical disabilities and supporting a team with a genuine commitment to their work. In return, we promise to build a diverse network and research and provide useful resource information for a safe and healthy future for our children and families in the most effective way we can.
|
![]() Thanks to the combined efforts of doctors, therapists, loved ones and Kya’s own fierce determination, she is able to stand, play and now take steps independently |
On May 25, 2007, at the age of 3 years and 7 months, Kya took her first unassisted steps, using a push toy to maintain her balance. She has undergone 14 corrective surgeries; wears splints regularly and attends physical and occupational therapy for two hours every week. Kya is bright, persistent and enjoys reading, learning and exploring new things. Her journey is challenging and she will have additional surgeries and therapy sessions to continue to improve her range of motion and ability to perform routine tasks independently. Thanks to the combined efforts of doctors, therapists, loved ones and Kya’s own fierce determination, she is able to stand, play and now take steps independently. It is in that spirit, that we invite you to join our Krusade and help other children, like Kya, continue to take steps toward fulfilling their potentials.
Kya’s Krusade
947 East Johnstown Road, Suite 143
Gahanna, Ohio 43230
(614) 478-3223 Fax Number
To receive news and campaign updates direct to your inbox simply enter your email address below. We won’t share your email address with anyone else and you can unsubscribe at any time.
As a member, you will have access to submitting posts to the Message Board. You will be contacted by email periodically.
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.