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21 Απρ 2024 · Learn about the factors that affect the life expectancy of people with ALS, a neurodegenerative condition that affects the brain, spinal cord, and muscles. Find out about the medications and interventions that may slow the progression and improve the quality of life.
10 Απρ 2024 · Half of people with ALS die within 14 to 18 months of diagnosis. However, some people with ALS live 10 years or longer. Speaking problems. Most people with ALS develop weakness of the muscles used to form speech. This usually starts with slower speech and occasional slurring of words.
6 Μαΐ 2024 · Learn how long you can live with ALS, a neurological disease that affects motor functions and life expectancy. Find out how to improve your outlook and quality of life with ALS, and what treatments and support are available.
12 Απρ 2023 · ALS is a progressive neurodegenerative condition that affects motor neurons and causes muscle weakness and paralysis. The average life expectancy for ALS is 3 to 5 years, but it can vary depending on the subtype and treatment.
17 Μαΐ 2024 · ALS is a fatal disease that affects nerve cells in the brain and spinal cord, causing progressive muscle weakness and paralysis. The mean survival time with ALS is two to five years, but some people live longer.
10 Απρ 2024 · Taken by mouth, this medicine can increase life expectancy by about 25%. It can cause side effects such as dizziness, gastrointestinal conditions and liver problems. Your health care provider typically monitors your liver function with periodic blood draws while you're taking the medicine.
19 Ιουλ 2024 · ALS is a progressive neurological disorder that affects motor neurons and causes muscle weakness, twitching, and atrophy. Most people with ALS die from respiratory failure within three to five years, but some survive longer.
