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Sickle Cell Disease and Other Heritable Blood Disorders Research, Surveillance, Prevention, and Treatment Act of 2023
3/12/2024, 7:30 AM
Summary of Bill S 1852
Bill 118 s 1852, also known as the Sickle Cell Disease and Other Heritable Blood Disorders Research, Surveillance, Prevention, and Treatment Act of 2023, is a piece of legislation introduced in the US Congress with the aim of addressing issues related to sickle cell disease and other heritable blood disorders.
The bill focuses on four key areas: research, surveillance, prevention, and treatment. In terms of research, the bill calls for increased funding for research into sickle cell disease and other heritable blood disorders. This includes funding for studies on the causes of these diseases, potential treatments, and ways to improve the quality of life for those affected.
In terms of surveillance, the bill calls for the establishment of a national surveillance system to track the prevalence of sickle cell disease and other heritable blood disorders. This system would help to identify trends in the prevalence of these diseases and inform public health efforts to prevent and treat them. In terms of prevention, the bill calls for the development of strategies to prevent sickle cell disease and other heritable blood disorders. This includes promoting genetic counseling and testing, as well as implementing programs to educate the public about the risks and symptoms of these diseases. In terms of treatment, the bill calls for increased access to care for individuals with sickle cell disease and other heritable blood disorders. This includes funding for treatment centers, training for healthcare providers, and support for individuals and families affected by these diseases. Overall, Bill 118 s 1852 aims to improve the lives of individuals affected by sickle cell disease and other heritable blood disorders through increased research, surveillance, prevention, and treatment efforts. It represents a bipartisan effort to address a pressing public health issue and improve outcomes for those affected by these diseases.
The bill focuses on four key areas: research, surveillance, prevention, and treatment. In terms of research, the bill calls for increased funding for research into sickle cell disease and other heritable blood disorders. This includes funding for studies on the causes of these diseases, potential treatments, and ways to improve the quality of life for those affected.
In terms of surveillance, the bill calls for the establishment of a national surveillance system to track the prevalence of sickle cell disease and other heritable blood disorders. This system would help to identify trends in the prevalence of these diseases and inform public health efforts to prevent and treat them. In terms of prevention, the bill calls for the development of strategies to prevent sickle cell disease and other heritable blood disorders. This includes promoting genetic counseling and testing, as well as implementing programs to educate the public about the risks and symptoms of these diseases. In terms of treatment, the bill calls for increased access to care for individuals with sickle cell disease and other heritable blood disorders. This includes funding for treatment centers, training for healthcare providers, and support for individuals and families affected by these diseases. Overall, Bill 118 s 1852 aims to improve the lives of individuals affected by sickle cell disease and other heritable blood disorders through increased research, surveillance, prevention, and treatment efforts. It represents a bipartisan effort to address a pressing public health issue and improve outcomes for those affected by these diseases.
Congressional Summary of S 1852
Sickle Cell Disease and Other Heritable Blood Disorders Research, Surveillance, Prevention, and Treatment Act of 2023
This bill reauthorizes through FY2028 the Sickle Cell Disease Treatment Demonstration Program, which supports efforts to improve treatment and prevention of sickle cell disease and complications from that disease. (Sickle cell disease is an inherited blood disorder that can lead to pain, anemia, infections, and stroke.)
Read the Full Bill
Current Status of Bill S 1852
Bill S 1852 is currently in the status of Bill Introduced since June 7, 2023. Bill S 1852 was introduced during Congress 118 and was introduced to the Senate on June 7, 2023. Bill S 1852's most recent activity was Placed on Senate Legislative Calendar under General Orders. Calendar No. 201. as of September 6, 2023
Bipartisan Support of Bill S 1852
Total Number of Sponsors
1Democrat Sponsors
0Republican Sponsors
1Unaffiliated Sponsors
0Total Number of Cosponsors
4Democrat Cosponsors
4Republican Cosponsors
0Unaffiliated Cosponsors
0Policy Area and Potential Impact of Bill S 1852
Primary Policy Focus
HealthPotential Impact Areas
- Blood and blood diseases
- Genetics
- Health promotion and preventive care
- Hereditary and development disorders
- Medical research
- Research administration and funding
Alternate Title(s) of Bill S 1852
Sickle Cell Disease and Other Heritable Blood Disorders Research, Surveillance, Prevention, and Treatment Act of 2023
Sickle Cell Disease and Other Heritable Blood Disorders Research, Surveillance, Prevention, and Treatment Act of 2023
Sickle Cell Disease and Other Heritable Blood Disorders Research, Surveillance, Prevention, and Treatment Act of 2023
A bill to amend the Public Health Service Act to reauthorize a sickle cell disease prevention and treatment demonstration program.
Comments
Sponsors and Cosponsors of S 1852
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