Search Results for keywords:"sickle cell disease"

Search Results: keywords:"sickle cell disease"

S. RES. 861 — Expressing support for the designation of September 2024 as Sickle Cell Disease Awareness Month in order to educate communities across the United States about sickle cell disease and the need for research, early detection methods, effective treatments, and preventative care programs with respect to complications from sickle cell disease and conditions related to sickle cell disease.
November 19, 2024
Status:Agreed to Senate
Congress:118
Words:337
S. RES. 861 is a resolution expressing support for designating September 2024 as "Sickle Cell Disease Awareness Month." The purpose is to educate communities in the United States about sickle cell disease, emphasizing the need for research, early detection, effective treatments, and...
Simple Explanation
In September 2024, people want to make sure everyone knows about sickle cell disease, a sickness that affects the blood, by learning more about it and finding better ways to help those with it. They want everyone to join in activities to raise awareness and support for these people.
H. RES. 1495 — Expressing support for the designation of September 2024 as Sickle Cell Disease Awareness Month in order to educate communities across the United States about sickle cell disease and the need for research, early detection methods, effective treatments, and preventative care programs with respect to complications from sickle cell disease and conditions related to sickle cell disease.
September 24, 2024
Status:Introduced in House
Congress:118
Words:714
H. RES. 1495 is a resolution from the U.S. House of Representatives that supports making September 2024 "Sickle Cell Disease Awareness Month." It aims to improve public knowledge about sickle cell disease, highlighting the need for better treatments, early detection, and care...
Simple Explanation
In September 2024, people in the United States will talk about sickle cell disease, a blood condition, to help others understand it better and try to find new cures and treatments. They want the government to work together to help people with this condition get good care.
S. RES. 861 — Expressing support for the designation of September 2024 as Sickle Cell Disease Awareness Month in order to educate communities across the United States about sickle cell disease and the need for research, early detection methods, effective treatments, and preventative care programs with respect to complications from sickle cell disease and conditions related to sickle cell disease.
September 25, 2024
Status:Introduced in Senate
Congress:118
Words:324
The resolution, S. RES. 861, expresses support for designating September 2024 as "Sickle Cell Disease Awareness Month" to inform communities in the U.S. about sickle cell disease. It highlights the need for more research, early detection, effective treatments, and preventative care programs...
Simple Explanation
In September 2024, people want everyone in the U.S. to learn more about sickle cell disease, which affects a lot of people, especially in some ethnic groups. They want more research and better ways to find and treat the disease, and they're asking folks to join in activities that help spread information about it.
H. R. 7432 — To amend title XIX of the Social Security Act to enable State Medicaid programs to provide comprehensive, coordinated care through a health home to individuals with sickle cell disease.
February 23, 2024
Status:Introduced in House
Congress:118
Words:949
H.R. 7432, also known as the “Sickle Cell Disease Comprehensive Care Act,” aims to allow State Medicaid programs to offer comprehensive and coordinated care to individuals with sickle cell disease through a health home model. The bill proposes to amend section 1945 of the...
Simple Explanation
This bill wants to help people with sickle cell disease by letting states offer special care through Medicaid, starting in 2025. It means doctors and nurses can work together more to help these patients feel better.
H. R. 3884 — An Act To amend title XI of the Public Health Service Act to reauthorize the program providing for sickle cell disease and other heritable blood disorders research, surveillance, prevention, and treatment.
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September 24, 2024
Status:Referred in Senate
Congress:118
Words:254
H. R. 3884 aims to amend the Public Health Service Act to extend the program for research, surveillance, prevention, and treatment of sickle cell disease and other heritable blood disorders. The bill proposes changes, such as adding “grant” or “cooperative agreement” to the...
Simple Explanation
H.R. 3884 is a plan to give more money each year for five years to help doctors and scientists learn more about sickle cell disease and similar blood problems. This money can be given in different ways to help them find new ways to understand and treat these diseases.
H. RES. 1304 — Expressing support for the designation of June 19, 2024, as World Sickle Cell Awareness Day in order to increase public awareness across the United States and global community about sickle cell disease and the continued need for empirical research, early detection screenings, novel effective treatments leading to a cure, and preventative care programs with respect to complications from sickle cell anemia and conditions relating to sickle cell disease.
June 18, 2024
Status:Introduced in House
Congress:118
Words:658
H. RES. 1304 expresses support for designating June 19, 2024, as World Sickle Cell Awareness Day to raise global awareness about sickle cell disease (SCD). The resolution highlights the need for ongoing research, early detection, effective treatments, and preventative care...
Simple Explanation
The bill wants to make June 19, 2024, a special day to help people learn about sickle cell disease, a sickness that affects the blood. It encourages finding new ways to help people with the disease feel better and have better access to doctors and medicine.
S. RES. 738 — Expressing support for the designation of June 19, 2024, as World Sickle Cell Awareness Day in order to increase public awareness across the United States and global community about sickle cell disease and the continued need for empirical research, early detection screenings, novel effective treatments leading to a cure, and preventative care programs with respect to complications from sickle cell anemia and conditions relating to sickle cell disease.
June 18, 2024
Status:Introduced in Senate
Congress:118
Words:587
S. RES. 738 is a resolution put forth in the United States Senate expressing support for the designation of June 19, 2024, as World Sickle Cell Awareness Day. It aims to raise public awareness about sickle cell disease (SCD), highlighting the need for empirical research,...
Simple Explanation
In 2024, a group of people in the U.S. Senate wants everyone to learn more about a sickness called sickle cell disease. They think June 19 should be a special day to talk about it and find better ways to help people who have it.
S. 5097 — To amend title XIX of the Social Security Act to establish a demonstration project to improve outpatient clinical care for individuals with sickle cell disease.
September 18, 2024
Status:Introduced in Senate
Congress:118
Words:933
The bill S. 5097, titled the "Sickle Cell Disease Comprehensive Care Act," aims to modify title XIX of the Social Security Act. It proposes the establishment of a demonstration project allowing state Medicaid programs to develop health homes specifically for individuals with...
Simple Explanation
The Sickle Cell Disease Comprehensive Care Act is a plan to help people with sickle cell disease get better care from doctors, including special health services like dental and vision checkups, through a new project that will start in 2025. This project will let Medicaid in some states make special healthcare homes for sickle cell patients and learn the best ways to take care of them.
H. R. 9872 — To establish a program to address sickle cell disease and other heritable hemoglobinopathies.
September 27, 2024
Status:Introduced in House
Congress:118
Words:3,846
H. R. 9872 proposes the creation of treatment centers for sickle cell disease and other similar blood disorders in the United States. It outlines a plan to use a "hub-and-spoke" model, where a central medical hub coordinates with local spoke centers and community organizations to provide...
Simple Explanation
H. R. 9872 is a plan to make special places for helping people who have sickle cell disease, which is a problem with their blood, by using a central team to guide smaller local centers. They want to make it easier for kids with the disease to get help when they grow up and teach people more about the illness.
S. 5226 — To establish a program to address sickle cell disease and other heritable hemoglobinopathies.
September 25, 2024
Status:Introduced in Senate
Congress:118
Words:3,847
S. 5226 aims to create a program to improve care and treatment for people with sickle cell disease and other similar blood disorders. The bill proposes to establish treatment centers using a network system called "hub-and-spoke," which connects hospitals and clinics (hubs)...
Simple Explanation
S. 5226 is a plan to help people with sickle cell disease by setting up special doctor centers and making sure patients get the care they need as they grow from kids to adults. It also wants to gather information to better understand the disease and tell more people about it.
H. R. 3884 — An Act To amend title XI of the Public Health Service Act to reauthorize the program providing for sickle cell disease and other heritable blood disorders research, surveillance, prevention, and treatment.
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September 23, 2024
Status:Engrossed in House
Congress:118
Words:270
H. R. 3884 aims to update the Public Health Service Act to continue supporting programs for research, surveillance, prevention, and treatment of sickle cell disease and other inherited blood disorders. The bill proposes changes to section 1106(b), including allowing grants...
Simple Explanation
The bill is about giving more money, almost double, to help doctors and scientists study and treat sickle cell disease and other similar blood problems, making sure they have enough support to do their important work.

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