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Support for National Polycystic Kidney Disease Awareness Month

Original title: Expressing support for the designation of September 2024 as "National Polycystic Kidney Disease Awareness Month", and raising awareness and understanding of polycystic kidney disease.

Record date · September 25, 2024

Introduced
Committee
Floor Vote
Passed

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What This Bill Would Do

This formally expresses congressional support for designating September 2024 as National Awareness Month to increase public understanding of the genetic disorder. It encourages nationwide activities to promote awareness and recognizes the urgent need for further research into treatments and a cure.

Why it matters

The highlights a condition affecting approximately 500,000 Americans and serves as a formal federal acknowledgment of the need for increased research funding and public education regarding , which is a leading cause of kidney failure.

Who It Would Affect

Groups the bill's text would affect if enacted, as described in the record. Being affected is not a position for or against it.

Directly affected

Individuals with polycystic kidney disease

The resolution acknowledges their health challenges and the impact of the disease on their families and finances.

Directly affected

PKD Foundation

The organization is explicitly recognized for its advocacy, research, and educational activities.

Key Facts

You don't have to trust us. Each fact below is taken straight from the official document - click any one to see the exact passage, highlighted in the original.

Frequently Asked Questions

Does this resolution provide funding for medical research?
No. This is a non-binding expressing support for awareness and research goals; it does not appropriate federal funds.
What is polycystic kidney disease?
It is a progressive, genetic disorder that causes damage to the kidneys and other organ systems, including the cardiovascular, endocrine, hepatic, and gastrointestinal systems.

What else do you want to know?

News Coverage

No news coverage found yet. Articles are indexed twice daily.

Where This Stands

Currently filed. The next step in the legislative lifecycle is Committee.

Version history

Only one version on file - nothing to compare yet. As later stages (committee substitute, engrossed, enrolled) are captured, the redline appears here.

View official text →

Full breakdown

Who this bill affects and the strongest case for and against it, written only from the bill’s own text.

Discoveries

1 pattern noticed across the record

Patterns POLISCOPE noticed across the record. These are observations to investigate, not conclusions.

policy shift100% confidence

Focus on Spontaneous Mutation

The resolution explicitly highlights that 10% of cases are spontaneous mutations, emphasizing that the disease is not exclusively hereditary.

Connected Entities

118th Congress, September 2024, Mr. Luetkemeyer and 6 more
bill number118th Congress“The congress in which this resolution was introduced.”Map →
dateSeptember 2024“The designated month for awareness.”Map →
PersonMr. Luetkemeyer“Co-sponsored by Mr. Luetkemeyer.”Map →
dollar amount35,000“Number of patient and family advocates.”Map →
OrganizationHouse of Representatives“The resolution is introduced by and sponsored by the House of Representatives.”Map →
PersonMr. Cleaver“Introduced by Mr. Cleaver.”Map →
locationUnited States“The resolution refers to the United States.”Map →
dollar amount500,000“Number of people affected by the disease.”Map →
OrganizationPKD Foundation“The resolution specifically mentions the PKD Foundation's efforts.”Map →

Sources

Open source document

www.congress.gov

Analysis Score

0–100
  • Significance20
    How much this matters to a regular citizen
  • Controversy0
    Intensity of disagreement among stakeholders
  • Entertainment5
    Compellingness for a non-policy-wonk reader
  • Buzz10
    Current news / social attention level

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