JETT FOUNDATION INC

Empowering families. Fighting Duchenne muscular dystrophy.

• Christian

• 308.

Toris Angels Foundation

Raises funds to support the families of children accepted for assistance who have life-threatening medical conditions.

MT WASHINGTON PEDIATRIC HOSPITAL INC

We’re a not for profit hospital where children go to heal and grow®.

• Birth Defects, Genetic Diseases Research

• 310.

Spata Foundation Inc

Our mission is to advocate, educate, and raise funds for research towards SPATA5 & SPATA5L1 Disorders The SPATA Foundation's Mission is to advocate, educate, and drive research towards SPATA5 and SPATA5L1 Related Disorders.

• Fund Raising and/or Fund Distribution

• 311.

Hudson Foundation

Helping Understand Diseases and Supporting Ones Needs The HUDSON Advocates is an organization designed to support the Juvenile Arthritis community and support researchers, legislators, scientists, doctors, and everybody who is working to find a cure to this disease.

• Mental Health Treatment

• 312.

African American Child Wellness Institute Inc

INCREASING AVAILABILITY OF MENTAL HEALTH SERVICES FOR CHILDREN AND ADULTS FROM THE AFRICAN AMERICAN COMMUNITY Start the journey to wellness today.

• Specifically Named Diseases

• 313.

Smith-Kingsmore Syndrome Foundation

Smith-Kingsmore Syndrome is a rare genetic disease.

axeALS Foundation

On a mission to #axeALS Instagram: @teamstevensnation Facebook Group: Team Stevens Nation The mission of the axeALS Foundation is to raise awareness and funding for ALS treatments and clinical trials; to help ALS patients and their families live as full and normal lives as possible; and to encourage research for the prevention, alleviation, care, treatment, and (one day) cure of ALS.

• Alliance/Advocacy Organizations

• 315.

Ctx Alliance NFP

Providing education, support, advocacy, and promoting research for CTX patients, their families, and medical professionals who treat and study this rare disease Providing education, support, advocacy, and promoting research for CTX patients, their families, and medical professionals who treat and study this rare disease.