About ALS

The onset of ALS may be so subtle that initial symptoms are frequently overlooked. Early symptoms include twitching, cramping or stiffness of muscles, muscle weakness in the arms and legs, slurred and nasal speech or difficulty chewing or swallowing.

In some cases, early symptoms affect one leg, causing awkwardness when walking or running that results in tripping or stumbling. When ALS affects the hands or arms, simple tasks such as buttoning a shirt, writing or unlocking a door may prove difficult.

Over time, muscle weakness and loss of voluntary muscle control spread, increasing problems with moving, swallowing and speaking.

A diagnosis of ALS requires signs and symptoms of upper motor neuron damage, such as tight and stiff muscles and exaggerated reflexes, and lower motor neuron damage, such as muscle weakness, degeneration, cramping and twitching.

Source: National Institute of Neurological Disorders and Stroke

 

ALS by the numbers

  • 1869 - Year that the French neurologist Jean-Martin Charcot identified ALS
  • 1941 - Year that the famous New York Yankees baseball player Lou Gehrig died of ALS
  • 30,000 - Number of Americans who have ALS
  • 5,600 - Number of new ALS cases diagnosed annually in the United States
  • 15 - Number of new ALS cases diagnosed daily in the United States
  • 40-70 - Age range of most people who develop ALS
  • 2 to 5 - Average survival in years for those affected by ALS
  • 20 - % of ALS patients who survive 5 years or more
  • 10 - % of ALS patients who survive 10 years or more
  • 2 - Annual deaths per 10,000 Americans attributed to ALS
  • 90 to 95 - % of cases in which ALS occurs randomly
  • 5 to 10 -  % of ALS cases attributed to family genetics
  • 3 - Number of genes that have been linked to inherited ALS

 

 


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