Resources- Specific Diagnosis Card Catalog- Galactosemia


  • Who to Contact
  • Where to Go to Chat with Others?
  • Learn More About it
  • Links
  • Who to Contact

    Parents of Galactosemic Children
    885 Del Sol Street
    Sparks, NV 89436
    775-626-0885
    E-mail: mesameadow@aol.com
    Web: www.galactosemia.org

    Parents of Galactosemic Children, Inc is a non-profit, national organization. Founded in February 1975 by a small group of mothers in New York, PGC realizes the need for further information and networking between affected families and professionals. Metabolic Clinics across the nation continue to assist PGC in researching families and information. Today our mailing list includes over 1000 families and extended families, professionals and clinics, media groups, donors, and Canadian and overseas contacts. Objectives and functions are achieved on an all-volunteer basis.

    Where to go to Chat with Others

    Galactosemia Web Board

    Liver Children
    Children's Liver Alliance List FOR FAMILIES Dedicated to empowering the hearts and minds of children with liver disease, their families and the medical professionals who care for them. Open to all families, friends and medical professionals who have an interest in pediatric liver disease and transplantation. Diseases include Alagille's Syndrome, Alpha-1 Antitrypsin Deficiency, Biliary Atresia, Crigler-Najjar, Cystic Fibrosis (liver affected), Galactosemia, Glycogen Storage Diseases, Hepatitis, Tyrosinemia, Wilson's Disease, Primary Sclerosing Cholangitis, and any other PEDIATRIC liver disease.

    Learn More About It

    Galactosemia Handbook: A Parents Guide

    What is Galactosemia?

    Galactosemia Frequently Asked Questions

    Galactosemia: An Overview

    Galactosemia (GALT)

    Links

    Parents of Galactosemic Children

    Galactosemia Resources and Information

    European Galactosaemia Society

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