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EA/TEF Family Support Connection Formed by and for families of children born with EA/TEF (Esophageal Atresia and Tracheoesophageal Fistula) and the medical professionals who treat them.
http://www.eatef.org/
Tef/Vater International Support group and information source for families with children born with VATER, esophageal atresia and/or traceoesophageal fistula.
http://www.tefvater.org
The Vater Forum Support organization created by parents of children diagnosed with VATER Association. [Registration required]
http://www.thevaterconnection.org/
Tracheo-Oesophageal Fistula (TOF) Support organization for children with TOF and their families. Includes information about the condition, treatment and outcomes.
http://www.tofs.org.uk
VACTERL Association Support Group Run by families, giving information support and help on vacterl association, vater syndrome and related problems.
http://www.vacterl-association.org.uk
VACTERL Association Wiki Wiki based on VACTERL Association. This is a publicly maintained reference to this rare condition, allowing anybody to update.
http://en.wikipedia.org/wiki/VACTERL_association
VACTERL Network Network of families supporting both adults and children, sharing resources, help and information.
http://www.vacterlnetwork.org/
VACTERL or VATER Association Description of the condition, including defects commonly seen, from the Cincinnati Children's Hospital.
http://www.cincinnatichildrens.org/health/heart-encyclopedia/disease/syndrome/vacterl.htm
VATER Association Description and clinical synopsis, plus links to articles and research abstracts.
http://www3.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?192350
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