A resolution designating May 2024 as "ALS Awareness Month".
Latest Action
Resolution agreed to in Senate without amendment and with a preamble by Unanimous Consent. (consideration: CR S4023; text: 5/23/2024 CR S3893)
Official Summary
Official summary has not been imported yet.
GovScope Watchdog™
AI Government Intelligence™Senate Resolution 713 designates May 2024 as "ALS Awareness Month." The resolution aims to raise public awareness about Amyotrophic Lateral Sclerosis (ALS), a progressive neurodegenerative disease. The resolution was agreed to in the Senate without amendment and with a preamble by unanimous consent on June 11, 2024. The resolution does not include legislative text beyond the designation and does not authorize funding or new programs.
S.Res. 713 is a non-binding resolution recognizing May 2024 as ALS Awareness Month to promote awareness of ALS, passed unanimously in the Senate but has since expired without further legislative action.
- Designates May 2024 as ALS Awareness Month to increase public knowledge about ALS.
- Passed in the Senate by unanimous consent without amendments or additional provisions.
- The resolution is symbolic and does not create binding legal obligations or allocate funding.
['Individuals living with ALS and their families', 'ALS advocacy and research organizations', 'Healthcare providers involved in ALS care', 'General public through increased awareness']
['No direct funding or programmatic support is provided, limiting practical impact.', 'As a non-binding resolution, it relies on voluntary actions for awareness efforts.', 'No enforcement or oversight mechanisms are included.']
The resolution was introduced and passed in the Senate during the 118th Congress as a symbolic gesture to promote awareness of ALS. It reflects a common legislative practice of designating awareness months for various health conditions. The resolution did not advance to the House or receive further legislative action and is currently classified as failed or expired.
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['Increased public awareness may lead to greater support for ALS research and patient services.', 'Potentially encourages community and nonprofit organizations to hold awareness events during May 2024.', 'May influence future legislative or funding initiatives related to ALS by raising visibility.']
This resolution is a non-binding, symbolic measure without appropriations or regulatory authority. Transparency considerations include the lack of detailed legislative text and absence of implementation mechanisms. The resolution's impact depends on voluntary public and private sector engagement rather than government enforcement.
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