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The Alpha-1 Foundation is committed to advancing research and improving the lives of those impacted by Alpha-1 Antitrypsin Deficiency. Founded in 1995, it provides resources, advocacy, and support for patients, families, and healthcare providers.
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Funding and promoting research initiatives to understand and treat Alpha-1 Antitrypsin Deficiency.
Providing resources, genetic counseling, and peer support for individuals and families affected by Alpha-1.
Hosting educational events and providing information about Alpha-1 to raise awareness and support the community.
Engaging with government and industry to advocate for the needs of the Alpha-1 community.
Alpha-1 Antitrypsin Deficiency is a genetic condition that can lead to lung and liver disease.
You can browse our database to find a doctor specializing in Alpha-1, filtering by location or area of expertise.
We offer a support line, genetic counseling, and peer guide programs for those affected by Alpha-1.
You can contribute by donating to the Alpha-1 Foundation, which funds research initiatives and clinical trials.
We host educational events such as the A1F Education Day and National Conference to support the Alpha-1 community.