Symptoms
The symptoms of
amyotrophic lateral sclerosis (ALS) include:
- Weakness or clumsiness in the hands and
feet.
- Gradual loss of strength of the arms and
legs.
- Inability to control the use of the arms and
legs.
- Muscle twitches (fasciculations).
- A stiff, clumsy
walking style.
- Difficulty swallowing, speaking, and
breathing. You may notice a problem with drooling.
- Fatigue.
- Trouble controlling your emotions. You may burst into tears or start laughing for no reason.
- Muscle cramps, especially at night,
which may occur late in the course of the disease.
- Pain during the
late stages of the disease.
It is important to remember that having muscle weakness, fatigue,
stiffness, and twitching doesn't necessarily mean that you have ALS.
The first sign of ALS is usually slight weakness in one leg, one
hand, the face, or the tongue. Other problems may include increasing clumsiness
and difficulty performing tasks that require precise movements of the fingers
and hands. Muscle twitching may also occur. The weakness slowly spreads to the
arms and legs over a period of months or years. As the nerves continue to waste
away and decrease in number, the muscle cells that would normally be stimulated
by those nerves also start to waste away, and the muscles weaken.
ALS is a progressive, disabling disease. Walking, speaking, eating,
swallowing, breathing, and other basic functions become more difficult with
time. These problems can lead to injury, illness, and other
complications.
Respiratory problems are the most common serious complication of
ALS. As the muscles in the throat and chest area become weak, swallowing and
coughing become more difficult, which may sometimes cause food and saliva to be
inhaled into the windpipe (aspiration). This may lead to
pneumonia. Breathing problems tend to get worse as the
disease progresses, increasing the risk of infection and respiratory
failure.
Pneumonia,
pulmonary embolism, lung failure, and
heart failure (probably due to lack of adequate
breathing as the chest muscles weaken) are the most common causes of death
among people with ALS. In most cases, death will occur within 3 to 5 years
after symptoms begin, although some people live for many years, even
decades.1