Living with ALS

347 kr

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At any one time, at least 30,000 people in the U.S. are living with amyotrophic lateral sclerosis (ALS), a rapidly progressive, fatal neurological disease affecting individuals, caregivers, at-risk genetic carriers, and others. In 2022, Congress directed the National Institutes of Health to commission a National Academies committee of experts to recommend key actions public, private, and nonprofit sectors should take to make ALS a livable disease within the next 10 years. The resulting report, Living with ALS, focuses on an integrated ALS multidisciplinary care and research system to help facilitate earlier diagnosis and connections to specialty care.

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and Medicine National Academies of Sciences, Engineering, Health and Medicine Division, Board on Health Sciences Policy, Board on Health Care Services, Committee on Amyotrophic Lateral Sclerosis: Accelerating Treatments and Improving Quality of Life, Joe Alper, Rebecca A. English, Alan I. Leshner - Living with ALS, Häftad

Living with ALS

and Medicine National Academies of Sciences, Engineering, Health and Medicine Division, Board on Health Sciences Policy, Board on Health Care Services, Committee on Amyotrophic Lateral Sclerosis: Accelerating Treatments and Improving Quality of Life, Joe Alper, Rebecca A. English, Alan I. Leshner

Häftad, 2024

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