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A resolution expressing support for the designation of November 2022 as "National Alpha-1 Antitrypsin Deficiency Awareness Month".
12/29/2022, 1:18 PM
Summary of Bill SRES 792
Bill 117 S.Res. 792 is a resolution that expresses support for the designation of November 2022 as "National Alpha-1 Antitrypsin Deficiency Awareness Month." Alpha-1 Antitrypsin Deficiency is a genetic disorder that can lead to lung and liver disease. The resolution aims to raise awareness about this condition and the importance of early detection and treatment.
The resolution highlights the impact of Alpha-1 Antitrypsin Deficiency on individuals and families, as well as the need for increased research and resources to support those affected by the disorder. It also recognizes the efforts of organizations and advocates working to raise awareness and improve outcomes for individuals with Alpha-1 Antitrypsin Deficiency.
By designating November 2022 as "National Alpha-1 Antitrypsin Deficiency Awareness Month," the resolution seeks to educate the public, healthcare professionals, and policymakers about this often overlooked condition. It emphasizes the importance of early diagnosis, access to treatment, and support for individuals living with Alpha-1 Antitrypsin Deficiency. Overall, Bill 117 S.Res. 792 aims to bring attention to Alpha-1 Antitrypsin Deficiency and advocate for increased awareness, research, and support for individuals affected by this genetic disorder.
The resolution highlights the impact of Alpha-1 Antitrypsin Deficiency on individuals and families, as well as the need for increased research and resources to support those affected by the disorder. It also recognizes the efforts of organizations and advocates working to raise awareness and improve outcomes for individuals with Alpha-1 Antitrypsin Deficiency.
By designating November 2022 as "National Alpha-1 Antitrypsin Deficiency Awareness Month," the resolution seeks to educate the public, healthcare professionals, and policymakers about this often overlooked condition. It emphasizes the importance of early diagnosis, access to treatment, and support for individuals living with Alpha-1 Antitrypsin Deficiency. Overall, Bill 117 S.Res. 792 aims to bring attention to Alpha-1 Antitrypsin Deficiency and advocate for increased awareness, research, and support for individuals affected by this genetic disorder.
Congressional Summary of SRES 792
This resolution supports the designation of November 2022 as National Alpha-1 Antitrypsin Deficiency Awareness Month. Alpha-1 antitrypsin deficiency is a genetic disease that increases the risk of harm to the lungs, liver, skin, and blood vessels.
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Current Status of Bill SRES 792
Bill SRES 792 is currently in the status of Bill Introduced since September 22, 2022. Bill SRES 792 was introduced during Congress 117 and was introduced to the Senate on September 22, 2022. Bill SRES 792's most recent activity was Referred to the Committee on Health, Education, Labor, and Pensions. (text: CR S4973) as of September 22, 2022
Bipartisan Support of Bill SRES 792
Total Number of Sponsors
1Democrat Sponsors
0Republican Sponsors
1Unaffiliated Sponsors
0Total Number of Cosponsors
2Democrat Cosponsors
0Republican Cosponsors
2Unaffiliated Cosponsors
0Policy Area and Potential Impact of Bill SRES 792
Primary Policy Focus
HealthAlternate Title(s) of Bill SRES 792
A resolution expressing support for the designation of November 2022 as "National Alpha-1 Antitrypsin Deficiency Awareness Month".
A resolution expressing support for the designation of November 2022 as "National Alpha-1 Antitrypsin Deficiency Awareness Month".
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Sponsors and Cosponsors of SRES 792
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