I ask this question because I am an adoptive mother whose child has a genetic disorder that we would not have known about had the state he was born in not done expanded Newborn Screening at birth. Our son was diagnosed with MCAD a fatty oxidation disorder that left undiagnosed could have been fatal. However, since we learned of the disorder at birth, we have been able to successfully manage the disorder the past 4 years. I am concerned that since not all states test for these disorders, and often times, the decision to have the test is left to the biological mother, that adoptive parents are not getting all of the medical info about their children that they should have. I am not trying to discourage anyone from adopting! Just want to make sure everyone knows about NBS in an effort to protect our children. As adoptive parents we have a responsibility to keep our children safe & healthy and NBS can help us to do that. Hugs to all!
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