Lou Gehrig's Disease Life Expectancy at Life

Lou Gehrig's Disease Life Expectancy. The result is the gradual loss of muscle movement, speech, swallowing, and eventually, breathing. Lou gehrig’s disease is a fatal, progressive neurodegenerative disorder that is characterized by the selective loss of motor neurons in the spinal cord, brain stem, and motor cortex.

There are several pathologies related to neurons that are connected to muscles, but the most serious is amyotrophic lateral sclerosis or lou gehrig’s disease, in which the structure of the motor neurons begins to progressively deteriorate until death, affecting the function of the muscles. The official average life expectancy from diagnosis is between 2 to 5 years. A few, such as myself, live an indeterminate length of time by use of mechanical ventilation.

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Some person (s) with als (pals) live only about 18 months and some live beyond 20 years. Most people with als (amyotrophic lateral sclerosis, lou gehrig's disease) die within three to five years of the first symptoms from respiratory failure. On average, those diagnosed with als do not survive more than a few years. Als is the most common type of motor neuron disease.