Resources- Specific Diagnosis Card Catalog- Esophageal Atresia and Tracheoesophageal Fistula

Who to Contact

EA/TEF Child and Family Support Connection, Inc.
111 West Jackson Boulevard
Suite 1145
Chicago IL 60604-3502
312-987-9085
312-987-9086 (fax)
E-mail: info@eatef.org
Web: www.eatef.org

The ea | tef Child and Family Support Connection was formed by and for families of children born with (Esophageal Atresia and Tracheoesophageal Fistula) ea | tef and the medical professionals who treat them. We are a 501(c)(3) nonprofit organization dedicated to providing educational resources as well as emotional and practical support to aid in the daily care of our medically fragile children.

Where to go to Chat with Others

TOFS Community Area
A list for families whose child's main issue is OA and/or TOF.

AT / TEF Web Board
Discussion Forums

Esophageal Atresia
Welcome to the International Rare Disease Support Network's (www.raredisorders.com) support group for people affected by 'Esophageal Atresia.' This support group is open to anyone interested in making friends, sharing information and support with others affected by this disorder.

Learn More About It

What Problems are TOF Children Likely to Have?

Esophageal Atresia and Tracheoesophageal Fistula
Information for families

What is Esophageal Atresia and Tracheoesophageal Fistula?

Esophageal Atresia and Tracheoesophageal Fistual (EA / TEF)

Links

TEF/Vater International

TOFS - Tracheo-Oesophageal Fistula Support Group
United Kingdom

EA/TEF Child and Family Support Connection

EA/TEF Website
From the University of Minnesota, Medical School