• Professional Societies & Associations

• 208.

Suneel Research Foundation

Our mission is to spread awareness about Duchenne Muscular Dystrophy (DMD), raise funds to support treatments and find a cure for DMD.

Community Guidance Clinic for Central CT

Youre facing a challenging time. We Can Help.

MY EPILEPSY STORY INC

My Epilepsy Story (MES) ,a nonprofit that is “Bridging the Gap” for women & girls with epilepsy.

Zttk Son-Shine Foundation Inc

Welcome to the Official Website of the ZTTK SONShine Foundation.

• Birth Defects, Genetic Diseases

• 212.

Shwachman-Diamond Syndrome Alliance Inc

Shwachman-Diamond Syndrome Alliance is a nonprofit aimed at accelerating research and therapy development for this rare disease.

• Fund Raising and/or Fund Distribution

• 213.

Chloe Strong Foundation

The Chloe Strong Foundation The Chloe Strong Foundation is a 501c3 nonprofit organization that exists to improve the quality of life for those that struggle with the rare neurological disorder Rett Syndrome by providing financial assistance support and prayers.

CHILD PROTECTION CENTER INC

The Child Protection Center is a nonprofit and nationally accredited Child Advocacy Center dedicated to the prevention, intervention, & treatment of child abuse.

• Services to Promote the Independence of Specific Populations

• 215.

1P36 DELETION SUPPORT & AWARENESS

1p36 Deletion Support & Awareness Support, Awareness & Education to improve the lives of individuals affected by 1p36 Deletion Syndrome Support Awareness and Education to improve the lives of individuals affected by 1p36 deletion syndrome If you have a loved one affected by 1p36 deletion syndrome were here to help 1p36 deletion syndrome occurs in approximately 1 in 5000 to 10000 live births and 1p36 Deletion Support Awareness is honored to currently serve hundreds of families affected by this rare genetic disorder.

NATIONAL ASSOCIATION OF CHILDREN'S

We are the voice of over 200 children's hospitals.