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Apr 21, 2024 · Amyotrophic lateral sclerosis (ALS) life expectancy varies, but someone diagnosed with ALS is expected to live from two to five years. Some people with ALS do live much longer, however. About 10% of those with the condition will live 10 years, and 5% will live for 20 or more years.
Apr 10, 2024 · ALS often begins with muscle twitching and weakness in an arm or leg, trouble swallowing or slurred speech. Eventually ALS affects control of the muscles needed to move, speak, eat and breathe. There is no cure for this fatal disease.
Jun 27, 2024 · ALS (amyotrophic lateral sclerosis) is a neurodegenerative condition that causes progressive muscle weakness. Treatment options can help slow progression.
Apr 10, 2024 · Treatments can't reverse the damage of ALS, but they can slow the progression of symptoms. They also can help prevent complications and make you more comfortable and independent.
Amyotrophic lateral sclerosis (ALS), formerly known as Lou Gehrig's disease, is a neurological disorder that affects motor neurons, the nerve cells in the brain and spinal cord that control voluntary muscle movement and breathing.
Feb 12, 2024 · Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is a progressive, paralytic, neurodegenerative disease affecting the upper and lower motor neurons. ALS is the most common motor neuron disease (MND) and has both sporadic and familial forms.
ALS is a fatal motor neuron disease. It causes progressive degeneration of nerve cells in the spinal cord and brain. ALS affects voluntary control of arms and legs and leads to trouble breathing. ALS doesn't affect intelligence, thinking, seeing, or hearing. There is no known cure for ALS.
