About PGC
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Galactosemia Foundation, formally, Parents of Galactosemic Children, Inc. (PGC)
is a national, non-profit, volunteer organization whose mission is to provide information, support, and networking opportunities to families affected by galactosemia.
Galactosemia Information
What is Galactosemia
Frequently Asked Questions
Web Resources
Glactosemics Survey Results
Diet Information
Diet Resources
Unacceptable Ingredients List
Calcium Supplementation
Galactose in Foods
Recipes and Products
Potential Complications
Cataracts
Learning Disabilities
Neurological Impairments
Ovarian Failure
Speech Disorders
Fundraiser
Magazine Subscriptions
PGC Awareness Bracelet
Swarovski Crystal Bracelet
Logo Items for Sale
Conference 2006
PGC Physicians Directory
PGC Recipe Book
Archive Information
Our Kids Stories
Web Articles
Interviews with Experts
2009 Newsletter
2008 Newsletter
2007 Newsletter
2006 Newsletter
2004 Newsletter
1999 Newsletter
Conference Videos
PGC Research Committee Information
Research Committee Members
Dan Lambert, Chair
Jo Beth Southard
Christy Johnson
Alison Clark
Denise Wilburn
Kristine Saylor
Gopi Sethu Rao
Brian Mannix
John Wassenaar
PGC Research Program Guidelines for Reviewers
PGC Research Program Request for Peer Reviewers
PGC Research Program Policies and Procedures
PGC Research Proposal Application
Volunteer Peer Reviewer Application
