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21 Απρ 2024 · Learn about the average and variable life expectancy of people with ALS, also known as Lou Gehrig's disease, and the factors that affect it. Find out about the treatments, complications, and quality of life for people with this neurodegenerative condition.
6 Μαΐ 2024 · ALS, or Lou Gehrig's disease, is a neurological condition that affects motor functions and life expectancy. Learn about the average and possible life spans, the stages of the disease, and how to improve your quality of life.
ALS is a fatal neurological disorder that affects nerve cells and muscles. Most patients die within three to five years, but some survive longer with supportive care and medications.
10 Απρ 2024 · ALS causes loss of muscle control. The disease gets worse over time. ALS is often called Lou Gehrig's disease after the baseball player who was diagnosed with it. The exact cause of the disease is still not known. A small number of cases are inherited.
The average survival from onset to death is two to four years, though this can vary, and about 10% of those affected survive longer than ten years. [20] Descriptions of the disease date back to at least 1824 by Charles Bell. [21] .
18 Δεκ 2023 · ALS is a degenerative disease that affects the brain and spinal cord and causes muscle weakness and paralysis. People with ALS typically live for 2 to 5 years, but some may live longer with treatments and support.
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.
