What is ALS?
Many people know ALS as Lou Gehrig’s disease, named after the famous baseball player who got the illness and had to retire in
1939 because of it. ALS is a disease that affects the nerve cells that make muscles work in both the upper and lower parts of
the body. This disease makes the nerve cells stop working and die. The nerves lose the ability to trigger specific muscles, which
causes the muscles to become weak and leads to paralysis.
How many people have ALS?
Although no one knows for sure, reports suggest 12,000 – 15,000 people in the United States have ALS; every year doctors tell about 5,000 people
that they have it. Because records on ALS have not been kept throughout the country, it is hard to estimate the number of ALS cases in the United States.
ALS is slightly more common in men than women. ALS is age related; most people find out they have it when they are between 55 and 75 years of age, and live
from 2 to 5 years after symptoms develop. How long a person lives with ALS seems to be related to age; people who are younger when the illness starts live
slightly longer. To read the latest prevalence of ALS for Oct. 2010 – December 11, 2011, click here.
About 5–10% of ALS cases occur within families. This is called familial ALS and it means that two or more people in a family have ALS.
Familial ALS is found equally among men and women. People with familial ALS usually do not fare as well as persons with ALS who are not
related, and typically live only one to two years after symptoms appear.
What causes ALS?
No one knows what causes most cases of ALS. Scientists have been studying many factors that could be linked with ALS such as heredity
and environmental exposures. Other scientists have looked at diet or injury. Although no cause has
been found for most cases of ALS, a number of inherited factors have been found to cause familial ALS. In the future, scientists may find
that many factors together cause ALS.