WOBBLY FEET FOUNDATION INC

WFF promotes awareness of A-T and contributes to advancement in life improving therapies & a cure.

• Medical Disciplines

• 704.

Indiana Association of Osteopathic Physicians and Surgeons

The Indiana Osteopathic Association has served osteopathic physicians (DOs) & citizens of Indiana since 1898.

• Eye Diseases, Blindness & Vision Impairment

• 705.

Cincinnati Eye Institute Foundation

The Cincinnati Eye Institute Foundation is a 503C charitable foundation established to preserve and improve eye sight by providing access to eye care for those who are under-served, furthering the education of ophthalmology, and funding research.

• Birth Defects, Genetic Diseases

• 706.

Tennessee Prader-Willi Association, Inc.

We provide support and information for people with PWS & their families.

• Developmentally Disabled Services/Centers

• 707.

United Cerebral Palsy Association of Greater Chicago

The mission of United Cerebral Palsy of Greater Chicago is to advance the independence of people with disabilities, enrich their lives, provide support to their families and advocate for their inclusion in every facet of community life.

• Cancer

• 708.

GORLIN SYNDROME ALLIANCE

Empowering those with Gorlin Syndrome to live rich, full, happy lives.

• Services to Promote the Independence of Specific Populations

• 709.

Project Strong Inc

Strong missioN Our mission at Project Strong is to empower children and young adults living with neuromuscular diseases discover and express their unique strengths by providing educational programs activities events that meet their needs.

• Film, Video

• 710.

Future Vision Foundation Inc

Support breakthroughs in vision research 2025 Future Vision Honorees Geoff Tabin MD Luminary Award Dr.

• Medical Specialty Research

• 711.

Curemapk8Ip3 Foundation

Family support network for patients and their families affected by a gene mutation in MAPK8IP3 Page for individuals and families with gene variant MAPK8IP3 Improve the lives of patients and families affected by a MAPK8IP3 gene mutation by performing the following activities: raising community awareness of MAPK8IP3-Related Neurodevelopmental Disorder; facilitating research of MAPK8IP3-Related Neurodevelopmental and related Disorders; collecting and disseminating information and resources relating to MAPK8IP3-Related Neurodevelopmental and related Disorders; supporting those affected by MAPK8IP3-Related Neurodevelopmental and related Disorders; and any other charitable educational or scientific activities that are in furtherance of the Corporation's purposes.