from Wikipedia:
This MRI (parasagittal FLAIR) demonstrates increased T2 signal within the posterior part of the internal capsule and can be tracked to the subcortical white matter of the motor cortex, outlining the corticospinal tract, consistent with the clinical diagnosis of ALS.
Amyotrophic lateral sclerosis (ALS), also referred to as Lou Gehrig's disease, is a form of motor neuron disease caused by the degeneration of neurons located in the ventral horn of the spinal cord and the cortical neurons that provide their efferent input. The condition is often called Lou Gehrig's disease in North America, after the New York Yankees baseball player who was diagnosed with the disease in 1939. The disorder is characterized by rapidly progressive weakness, muscle atrophy and fasciculations, spasticity, dysarthria,dysphagia, and respiratory compromise. Sensory function generally is spared, as is autonomic, and oculomotor activity. ALS is a progressive,[1] fatal, neurodegenerative disease with most affected patients dying of respiratory compromise and pneumonia after 2 to 3 years; although some perish within a year from the onset of symptoms, and occasional individuals have a more indolent course and survive for many years.[2]
Source: http://en.wikipedia.org/wiki/Amyotrophic_lateral_sclerosis
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Multiple sclerosis is a chronic disease that affects the nervous system. The inflammation of these nerves makes communications difficult and the system begins to fail. The pattern seems to vary from person to person and therefore the symptoms also vary. The inflammation and loss of the myeline or the outer nerve coating gets damaged and this leads to and creates a scar or sclerosis.