CURED NFP

CURED is a not for profit foundation dedicated to those suffering from Eosinophilic Gastrointestinal Diseases (EGID), including eosinophilic esophagitis (EoE),.

• Hospitals and Primary Medical Care Facilities

• 479.

Texas Childrens Hospital Foundation

Official X of Texas Children’s Hospital.

• Specifically Named Diseases

• 480.

Dyslexia Foundation of Memphis

Dyslexia Foundation of Memphis Saturday School Important Upcoming Dates Check out the Calendar of Events link for more details.

Coriell Institute for Medical Research, Inc.

Nonprofit biomedical research center. Recognized as the world’s leading biobank, pioneer in genomic discovery, and expert in the field of stem cell research.

• Cancer Research

• 482.

The EHE Foundation

The leading global advocacy and research organization for epithelioid hemangioendothelioma (EHE) We envision a world where epithelioid hemangioendothelioma (EHE) is easily diagnosed and treatable.

RECURRENT RESPIRATORY PAPILLOMATOSIS FOUNDATION

The Recurrent Respiratory Foundation is on a mission to find a cure and ultimately eradicate RRP, so that it becomes a disease of the past.

• Remedial Reading, Reading Encouragement

• 484.

Achieving Your Potential Inc

Our Mission The Achieving Your Potential mission is toassist elementary schools to establish programs with fully packaged and affordable evidencedbased curriculum to address the specific needs of dyslexic children.

• Patient Services�Entertainment, Recreation

• 485.

A Rae of Joi

A RAE OF JOI Childhood Cancer Support Home About News Resources Donate Contact Us Make a Wish More Our mission is to help parents of children going through cancer treatment by providing items or services that bring them joy as they navigate through a pediatric diagnosis and treatment.

• Alliance/Advocacy Organizations

• 486.

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.