Comparing SR 95 → SR 691 — ALS AWARENESS MONTH

Struck = only in SR 95 · added = only in SR 691.

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*LRB10421245LAW35888r* SR0691 LRB104 21245 LAW 35888 r SENATE RESOLUTION WHEREAS, Amyotrophic lateral sclerosis (ALS), also commonly known as Lou Gehrig's disease, is a progressive fatal neurodegenerative disease in which a person's brain loses connection with their muscles, slowly reducing a person's ability to walk, talk, eat, and eventually breathe;
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and WHEREAS, Thousands of new ALS cases are reported every year, and estimates show that someone is diagnosed with ALS and someone passes away from ALS every 90 minutes;
05/12/26 - Enrolled 04/21/26 - Amended Senate 04/06/26 - Introduced SR-95 (2025-2026) Text >> Votes >> History >> Bill Analysis >> Today's Law As Amended >> Compare Versions >> Status >> Comments To Author >> Track Bill >> Add To My Favorites >> SHARE THIS:
and WHEREAS, On average, patients diagnosed with ALS survive only two to five years from the time of diagnosis;
SR95:v97#DOCUMENTBill Start Enrolled  May 12, 2026 Passed  IN  Senate  May 11, 2026 Amended  IN  Senate  April 21, 2026 CALIFORNIA LEGISLATURE— 2025–2026 REGULAR SESSION Senate Resolution No.
and WHEREAS, The exact causes of ALS are unknown, and there is no known cure for ALS;
95Introduced by Senator Niello(Coauthors:
and WHEREAS, People who have served in the military are more likely to develop ALS and die from the disease than those with no history of military service;
Senators Becker, Caballero, Choi, Dahle, Ochoa Bogh, Richardson, Seyarto, Strickland, Valladares, and Wahab)April 06, 2026Relative to Amyotrophic Lateral Sclerosis Awareness Month.
and WHEREAS, Securing access to new therapies, durable medical equipment, and communication technologies is of vital importance to people living with ALS;
LEGISLATIVE COUNSEL'S DIGESTSR 95, Niello.
and SR0691 -2- LRB104 21245 LAW 35888 r WHEREAS, Clinical trials play a pivotal role in evaluating new treatments, enhancing quality of life, and fostering assistive technologies for those living with ALS;
Digest KeyBill TextWHEREAS, Amyotrophic lateral sclerosis (ALS), also commonly referred to as Lou Gehrig’s disease, is a progressive fatal neurodegenerative disease in which a person’s brain loses connection with their muscles, slowly reducing a person’s ability to walk, talk, eat, and eventually breathe;
and WHEREAS, The ALS Association is the largest philanthropic funder of ALS research globally and has committed more than $154 million to support more than 550 projects across the United States and 18 other countries;
andWHEREAS, Thousands of new ALS cases are reported every year, and estimates show that every 90 minutes someone is diagnosed with ALS and someone passes away from ALS;
and WHEREAS, The ALS Association is committed to making ALS livable and curing it for everyone, everywhere;
andWHEREAS, On average, patients diagnosed with ALS survive only two to five years from the time of diagnosis;
and WHEREAS, Observing ALS Awareness Month increases public awareness of the dire circumstances of people living with ALS, acknowledges the terrible impact this disease has on those individuals and their families, and supports research being done to eradicate this disease;
andWHEREAS, The exact causes of ALS are unknown and there is no known cure for ALS;
therefore, be it RESOLVED, BY THE SENATE OF THE ONE HUNDRED FOURTH GENERAL ASSEMBLY OF THE STATE OF ILLINOIS, that we declare May 2026 as ALS Awareness Month in the State of Illinois, and we urge all Illinoisans to engage in supporting amyotrophic lateral sclerosis (ALS) research, advocating for increased funding, and standing in solidarity with those affected by this relentless disease.
andWHEREAS, People who have served in the military are more likely to develop ALS and die from the disease than those with no history of military service;
andWHEREAS, Securing access to new therapies, durable medical equipment, and communication technologies is of vital importance to people living with ALS;
andWHEREAS, Clinical trials play a pivotal role in evaluating new treatments, enhancing quality of life, and fostering assistive technologies for those living with ALS;
andWHEREAS, Amyotrophic Lateral Sclerosis Awareness Month provides an opportunity to increase public awareness of the dire circumstances of people living with ALS, acknowledge the terrible impact this disease has on those individuals and their families, and support research to eradicate this disease;
now, therefore, be itResolved by the Senate of the State of California, That the Senate hereby proclaims the month of May 2026 as Amyotrophic Lateral Sclerosis Awareness Month, and calls upon all Americans to join in supporting ALS research, advocating for increased funding, and standing in solidarity with those affected by this relentless disease;
and be it furtherResolved, That the Secretary of the Senate transmit copies of this resolution to the author for appropriate distribution.