Legislation Details

File #: 26-1510    Version: 1 Name: ACKNOWLEDGING MAY AS AMYOTROPHIC LATERAL SCLEROSIS (ALS) AWARENESS MONTH IN COOK COUNTY
Type: Consent Calendar Resolution Status: Agenda Ready
File created: 5/11/2026 In control: Board of Commissioners
On agenda: 5/14/2026 Final action:
Title: PROPOSED RESOLUTION ACKNOWLEDGING MAY AS AMYOTROPHIC LATERAL SCLEROSIS (ALS) AWARENESS MONTH IN COOK COUNTY WHEREAS, Amyotrophic lateral sclerosis (ALS), commonly referred to as Lou Gehrig's disease, is a progressive and fatal neurodegenerative disease affecting nerve cells in the brain and spinal cord, resulting in loss of muscle control; and WHEREAS, ALS often begins with muscle weakness or stiffness and progresses to difficulty speaking, swallowing, and breathing, ultimately leading to paralysis; and WHEREAS, ALS impacts individuals, families, caregivers, and communities, often requiring continuous care in later stages; and WHEREAS, ALS affects individuals across all racial, ethnic, gender, and socioeconomic groups and can impact adults of any age; and WHEREAS, the cause of ALS is unknown in approximately 90 percent of cases, while about 10 percent are inherited and linked to genetic factors; and WHEREAS, individuals diagnosed with ALS typically survive two to five years from...
Sponsors: FRANK J. AGUILAR, ALMA E. ANAYA, SCOTT R. BRITTON, JOHN P. DALEY, BRIDGET DEGNEN, BRIDGET GAINER, BILL LOWRY, DR. KISHA E. McCASKILL, DONNA MILLER, STANLEY MOORE, JOSINA MORITA, KEVIN B. MORRISON, SEAN M. MORRISON, TONI PRECKWINKLE (President), MICHAEL SCOTT JR., TARA S. STAMPS, MAGGIE TREVOR, JESSICA VÁSQUEZ
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title
PROPOSED RESOLUTION

ACKNOWLEDGING MAY AS AMYOTROPHIC LATERAL SCLEROSIS (ALS) AWARENESS MONTH IN COOK COUNTY

WHEREAS, Amyotrophic lateral sclerosis (ALS), commonly referred to as Lou Gehrig's disease, is a progressive and fatal neurodegenerative disease affecting nerve cells in the brain and spinal cord, resulting in loss of muscle control; and

WHEREAS, ALS often begins with muscle weakness or stiffness and progresses to difficulty speaking, swallowing, and breathing, ultimately leading to paralysis; and

WHEREAS, ALS impacts individuals, families, caregivers, and communities, often requiring continuous care in later stages; and

WHEREAS, ALS affects individuals across all racial, ethnic, gender, and socioeconomic groups and can impact adults of any age; and

WHEREAS, the cause of ALS is unknown in approximately 90 percent of cases, while about 10 percent are inherited and linked to genetic factors; and

WHEREAS, individuals diagnosed with ALS typically survive two to five years from diagnosis, and most die from respiratory failure; and

WHEREAS, the period between onset of symptoms and diagnosis often exceeds one year, underscoring the need for increased awareness and earlier detection; and

WHEREAS, tens of thousands of individuals in the United States are living with ALS, with more than 5,000 new cases diagnosed each year, or approximately 15 cases per day; and

WHEREAS, on average, every 90 minutes an individual is diagnosed with ALS and another dies from the disease; and

WHEREAS, individuals who have served in the military are approximately twice as likely to develop ALS compared to those who have not served; and

WHEREAS, ALS has no known cure, and access to therapies, clinical trials, medical equipment, and communication technologies is essential to improving quality of life; and

WHEREAS, ALS Association provides care services, equipment, advocacy, and research support for individuals living with ALS and their families; and

WHEREAS, Amyotrophic L...

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