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“Genetic testing for Alpha-1 liver disease patients is important, not just for them, [but] for their families, and to open the gates for research for future generations.”
Alpha-1 antitrypsin deficiency (AATD) is an inherited, often underrecognized condition that can progress silently for years. Early detection of AATD is important to support family screening and timely intervention, such as lifestyle changes, to slow its advancement. Genotyping not only provides a definitive diagnosis, but also sheds light on a patient’s potential risk for lung and/or liver-related complications.
In this video, patient advocates highlight the power of community, the urgent need for genetic testing and the hope that comes from awareness. Their voices underscore a simple truth: understanding Alpha-1 can change lives—not just today, but for generations to come.
Everyone’s experience with AATD is different, and the experiences of those featured may not be representative of your own. The information in this video is for disease awareness only and is not medical advice. Always consult a health care professional for medical advice, diagnosis or treatment.
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