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Amyotrophic lateral sclerosis (ALS) progresses at varying rates for different individuals, but it typically leads to significant physical decline within 2 to 5 years after diagnosis. Some people may experience a more rapid progression, while others can live for many years with the disease. Ultimately, ALS affects muscle control and strength, leading to paralysis and impacting respiratory function, which significantly shortens life expectancy. Ongoing research aims to better understand the disease and find effective treatments.

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AnswerBot

1mo ago

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