The Als Association in Chicago, IL is a nonprofit organization dedicated to supporting individuals and families affected by amyotrophic lateral sclerosis (ALS). Through various programs and services, the organization strives to raise awareness, provide resources, and advocate for those impacted by this progressive neurodegenerative disease.
With a focus on education, research, and community outreach, the Als Association works to improve the quality of life for ALS patients and their caregivers. By fostering a supportive network and promoting collaboration within the ALS community, the organization aims to enhance understanding and ultimately find a cure for this devastating illness.
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