• Birth Defects, Genetic Diseases

• 181.

Upstate Cerebral Palsy Inc

Our mission at Upstate Cerebral Palsy is to provide innovative programs and services that support people and create opportunities to fulfill life choices.

• Group Home, Residential Treatment Facility - Mental Health Related

• 182.

Northwest Youth Discovery Inc

HOUSING AND BEHAVIORAL, EMOTIONAL, SOCIAL AND PSYCHOLOGICAL SUPPORT WHILE REMEDING RISK FACTORS TO GIRLS OF AGE 12 TO 18.

CHILDREN FIRST CEO KANSAS INC

Children First: CEO Kansas Inc. is a 501(c)(3) social service non-profit organization in Wichita, Kansas, with a mission to support students to feel safe and empowered, so they can learn and thrive, by staying in school and achieving in life HOME ABOUT PROGRAMS CONTACT WAYS TO GIVE ESPAOL Ting Vit More Children First is a 501c3 social service nonprofit organization serving children throughout Wichita with multiple programs SUPPORTING STUDENTS IMPROVING NEIGHBORHOODS MISSION Children First CEO Kansas Inc.

DOWN SYNDROME-AUTISM CONNECTION

The Down Syndrome-Autism Connection is a 501(c)(3) nonprofit corporation.

KANSAS HUMANE SOCIETY OF WICHITA INC

The Kansas Humane Society is a community resource for pets and people, dedicated to enhancing the welfare of all companion animals.

• Developmentally Disabled Services/Centers

• 186.

Statewide Independent Living Council of Kansas

The SILCK is established to develop, monitor, and evaluate the state plan for independent living (SPIL) PROMOTING INTEGRATION AND FULL INCLUSION OF KANSAN'S WITH DISABILITIES INTO THE MAINSTREAM OF SOCIETY.

Kruzn for A Kure Foundation

Kruzn For A Kure Foundation is a non-profit organization funding research for an extremely rare genetic disease & fatal type of dwarfism, #SIOD.

• Birth Defects, Genetic Diseases

• 188.

CTNNB1 SYNDROME AWARENESS WORLDWIDE

CTNNB1 Syndrome refers to complications resulting from either a mutation or deletion of the CTNNB1 gene.

• Specifically Named Diseases

• 189.

YBRP Inc

YBRP is a non-profit organization whose mission is to positively impact the lives of individuals with HNRNPH2 genetic variations.