The ALS Association Arizona Chapter in Phoenix, AZ is dedicated to providing resources, support, and assistance to individuals and families affected by ALS, also known as Lou Gehrig's disease. They offer information and tools free of charge to help navigate the challenges of living with ALS, including newly diagnosed support, assistive technology consultation, family support programs, and referrals to appropriate resources.
Working with renowned ALS physicians and clinics, the association ensures access to specialized care through their certified treatment centers of excellence and recognized treatment centers. They also facilitate support groups for individuals and caregivers, providing a platform for sharing experiences and wisdom. Additionally, the association advocates for policy changes and fundraising efforts to support research and find a cure for ALS.
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