Welcome to our new site

We are glad you are here. Welcome to our new address SBKC.org, please update your bookmarks. We are excited to bring you new website features and plan on growing this site over time. Check back soon. If you have any questions, comments or suggestions about the site feel free to send them to: webmaster@sbkc.org

 

Spina Bifida is the # 1 permanently disabling congenital disabilty in the nation.
Spina Bifida Kansas City is made up of children and adults with Spina Bifida, as well as parents, guardians, family, friends, healthcare providers, and other supporters. Starting very early in life, our children spend significant amounts of time in clinics and hospitals. Frequent medical tests, surgeries, visits to therapists and specialists, and hospitalizations are common. SBKC is dedicated to helping families affected by Spina Bifida emotionally, educationally, and financially. Financial support is given to families through a number of funds. Emotionally we offer support through organized social functions, fundraising events, chapter meetings, educational programs, and our office staff.

 

Spina Bifida Kansas City (SBKC) is dedicated to:
Fostering and promoting the rights and well-being of all persons with Spina Bifida

Encouraging care, treatment, education and social interactions of all persons with Spina Bifida and their families;

Raising the level of awareness in ourselves and others as to the nature of the particular and special needs of all persons with Spina Bifida.