Comparing SR 95 → SR 9 — Amyotrophic Lateral Sclerosis Awareness Month

Struck = only in SR 95 · added = only in SR 9.

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SENATE RESOLUTION 26-009 BY SENATOR(S) Simpson, Amabile, Baisley, Ball, Benavidez, Bridges, Bright, Carson, Catlin, Cutter, Danielson, Daugherty, Exum, Frizell, Gonzales J., Hinrichsen, Jodeh, Kipp, Kirkmeyer, Kolker, Lindstedt, Liston, Marchman, Mullica, Pelton B., Pelton R., Rich, Roberts, Rodriguez, Snyder, Sullivan, Wallace, Weissman, Zamora Wilson, Coleman.
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CONCERNING ALS AWARENESS MONTH.
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:
WHEREAS,-Amyotrophic lateral sclerosis, also commonlyknown as Lou Gehrig's disease or ALS, 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;
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, 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;
95Introduced by Senator Niello(Coauthors:
and WHEREAS, On average, patients diagnosed with ALS survive only two to five years from the time ofdiagnosis;
Senators Becker, Caballero, Choi, Dahle, Ochoa Bogh, Richardson, Seyarto, Strickland, Valladares, and Wahab)April 06, 2026Relative to Amyotrophic Lateral Sclerosis Awareness Month.
and WHEREAS, The exact causes ofALS are unknown, although asmall percentage ofcases are hereditary, and there is no known cure for ALS;
LEGISLATIVE COUNSEL'S DIGESTSR 95, Niello.
and WHEREAS, People who have served in the military are more likely to deI.lop ALS and die from the disease than those with no history of military service;
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, Securing access to new therapies, durable medical equipment, and communication technologies is of vital importance to people living with ALS;
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, Clinical trials play a pivotal role in evaluating new treatments, enhancing quality oflife, and fostering assistive technologies for those living with ALS;
andWHEREAS, On average, patients diagnosed with ALS survive only two to five years from the time of diagnosis;
and WHEREAS, Multidisciplinary care clinics improve survival rates by providingcomprehensivecareforpatientswithALS.
andWHEREAS, The exact causes of ALS are unknown and there is no known cure for ALS;
Cliniccareincludes neurology, pulmonology, nutrition, physical therapy, occupational therapy, social work, and palliative care;
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;
and WHEREAS, TheALS Association is the largestphilanthropic funder ofALS research globally and has committed more than $154 million to support more than 550 projects across the United States and 18 other countries;
andWHEREAS, Securing access to new therapies, durable medical equipment, and communication technologies is of vital importance to people living with ALS;
and WHEREAS, TheALS UnitedRockyMountainorganizationprovides Colorado, Wyoming, andUtahsupportfor severalmultidisciplinaryALS clinics, including those throughout Colorado offered byNational Jewish Health and the University ofColorado Anschutz Medical Campus;
andWHEREAS, Clinical trials play a pivotal role in evaluating new treatments, enhancing quality of life, and fostering assistive technologies for those living with ALS;
and WHEREAS, The ALS Association and othernonprofit organizations are committed to making ALS livable and curing it for everyone, everywhere;
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;
and WHEREAS, ALS Awareness Month provides an opportunity to increasepublic awareness ofthe dire circumstances ofpeople livingwith ALS and acknowledge the terrible impact this disease has on those individuals and their families.
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;
Most importantly, it can help provide support for research to eradicate this disease and for multidisciplinary ALS clinicsto administercomprehensive care for patientswithALS;
and be it furtherResolved, That the Secretary of the Senate transmit copies of this resolution to the author for appropriate distribution.
and WHEREAS, Patients with ALS have incredible courage and inspire their families, caregivers, and the community at large;
now, therefore, Belt Resolvedby the Senate ofthe Seventy-fifth GeneralAssembly of the State ofColorado:
(1) Thatwe, themembers ofthe Colorado Senate, do herebyproclaim the month ofMay 2026 as ALS Awareness Month;
and PAGE 2-SENATE RESOLUTION 26-009 (2) That we call upon all Coloradans to join in supporting ALS research, advocatingforincreasedfunding, andstandinginsolidaritywith those affected by this relentless disease.
Be It Further Resolved,That copies ofthis resolution be sent to Dr.
Jinny Tavee, chiefofthe Division ofNeurology and Behavioral Health atNationalJewishHospital;Dr.LauraFosteratUCHealthNeurosciences Center at Anschutz Medical Campus;
the ALS Association;
the ALS United Rocky Mountain organization;
Gretchen Hammer, Executive Directorofthe ColoradoDepartmentofHealthCarePolicy &Financing;
and Paul O'Neill, an ALS caregiver.
James Rashad Coleman Sr.
Esther van Mourik PRESIDENT OF SECRETARY OF THE SENATE THE SENATE PAGE 3-SENATE RESOLUTION 26-009