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ALS SURVIVAL GUIDE

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STEVEN SHACKEL



LOU GEHRIG'S DISEASE

Amyotrophic Lateral Sclerosis ("ALS"), is an almost always fatal disease made famous after the New York Yankee's baseball player, Lou Gehrig, was diagnosed with the condition in 1939 at the age of 38.

It is a syndrome or motor neuron disease or disease of the motor nerves that control voluntary movement. Motor nerves attach to muscles and during ALS, when the motor nerves gradually degenerate and die, the muscles no longer receive nerve impulses. As a result of the nerve death, the muscles atrophy and waste away. The disease is marked by muscular weakness and atrophy with spasticity and hyperreflexia due to degeneration of motor neurons of the spinal cord, medulla and cortex. Symptoms include tripping, stumbling and falling, loss of muscle control and strength in the hands and arms, difficulty speaking, swallowing and breathing, chronic fatigue, and muscle twitching and cramping. When the disease involves the corticobulbar area of the brainstem, it affects speech and swallowing. In such cases, the patient eventually loses the ability to speak and must rely on augmentative communication devices in order to communicate.

There are three different types of ALS:
(1) sporadic ALS (90% of all cases);
(2) familial ALS (10% of all cases, hereditary); and
(3) Guamian (high incidence of ALS on island nation of Guam).

ALS has no known cure and its cause remains a mystery. Further, there are no known drugs or treatments to stop its progression. ALS does not affect the mind. Mental acuity remains sharp. However, depression is common among ALS patients and thus a strong network of supportive family and friends is very important.

The letters ALS come from Greek words and stand for:
A-without Myo-muscle Trophic-nourishment
L-Lateral-side (of the spinal cord)
S-Sclerosis-hardeing or scarring



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