This is a discussion board for:
People who care for a transplanted child who was born with a urea cycle disorder (UCD).
Families of a UCD-child, who may require a future transplant, that wish to ask questions of people who take care of TRUE Kids.
Please feel free to post your questions, comments, experiences, or frustrations that you want to share with other families.
NOTE: The discussion contained herein may not apply to your child's unique medical needs. DO NOT make any changes in your child's treatment without first consulting their physician. BE AWARE: INFORMATION YOU POST HERE MIGHT BE MONITORED BY HEALTH INSURANCE COMPANIES OR UNSCRUPULOUS ENTITIES TO ADVERSELY EFFECT YOUR FAMILY OR OTHERS