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Newborn Screening and Support for Glutaric Acidemia Type 1 (GA-1)

Newborn Screening and Support for Glutaric Acidemia Type 1 (GA-1)

FromPatient Stories with Grey Genetics


Newborn Screening and Support for Glutaric Acidemia Type 1 (GA-1)

FromPatient Stories with Grey Genetics

ratings:
Length:
41 minutes
Released:
Jul 23, 2019
Format:
Podcast episode

Description

Five days after Allison’s son Isaac was born, she received a phone call from her physician’s office, telling her that her son had received positive test result on Newborn Screening (NBS). A long two days later, they were meeting with a geneticist at a hospital an hour and a half drive away, learning what a diagnosis of Glutaric Acidemia (GA-1), a rare metabolic disorder only part of NBS since the mid-2000s, meant for their son and their family. Allison is a passionate advocate for NBS and shares studies she has been involved with that point to ways to improve parents’ experience with receiving positive NBS results—and ideas for involving genetic counselors early in the process! Allison is also currently a second year genetic counseling student in the graduate program at Bay Path University.




Links and Resources

Baby’s First Test

Organic Acidemia Association

Medical Nutrition Equity Act

Information on Katie Beckett and similar programs: Kids’ Waivers

Genetic Alliance

Rare New England (RNE)

New England Regional Genetics Group (NERGG)

Bay Path University Genetic Counseling Program




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Released:
Jul 23, 2019
Format:
Podcast episode

Titles in the series (92)

Genetics isn’t always black and white. And the emotions and decisions surrounding genetic testing can be even more complex. Hosted by genetic counselor Eleanor Griffith, the show brings you the personal experiences of patients and genetic counselors.