ALS (Lou Gehrig's Disease) information
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What is amyotrophic lateral sclerosis (ALS)?
Amyotrophic lateral sclerosis (ALS) is a neurological disorder characterized by progressive degeneration of nerve cells in the spinal cord and brain. Often referred to as "Lou Gehrig's disease" (a famous baseball player who died from the disease), it is one of the most devastating of the disorders that affects the function of nerves and muscles.
ALS does not affect senses such as seeing or hearing and it is not contagious. Currently, there is no cure for amyotrophic lateral sclerosis.
Statistics of ALS:
Consider the following statistics regarding ALS:
• Most people who develop ALS are between the ages of 45 and 80, although the disease can occur at a younger age.
• ALS occurs throughout the world with no racial, ethnic, or socioeconomic boundaries.
• ALS affects as many as 30,000 Americans, with 5,600 new cases diagnosed in the US each year.
What are the different types of ALS?
There are three known classifications of ALS, including the following:
• Sporadic - the most common form of ALS in the US, involving 90 percent to 95 percent of all cases. These cases occur randomly, without any known cause, and there is no association with persons in the family with the disease.
• Familial - suggests that the disease is inherited and accounts for a very small number of cases in the United States, about 5 percent to 10 percent.
• Guamanian - an extremely high incidence of ALS was observed in Guam and the Trust Territories of the Pacific in the 1950s.
What are the symptoms of ALS?
The following are the most common symptoms of ALS. These symptoms are usually progressive with time. However, each individual may experience symptoms differently.
Symptoms may include:
• Twitching and cramping of muscles, especially those in the hands and feet
• Loss of motor strength in the hands and arms
• Impairment in the use of the arms and legs
• Tripping and falling
• Dropping things
• Persistent fatigue
• Slurred or thick speech and difficulty in projecting the voice
• Uncontrollable periods of laughing or crying
As the disease progresses, symptoms may include:
• Difficulty swallowing
• Difficulty breathing
The symptoms of ALS may resemble other conditions or medical problems. Always consult your physician for a diagnosis.
How is ALS diagnosed?
In addition to a complete medical history and physical examination, diagnostic procedures for ALS may include the following:
• Electrodiagnostic tests (i.e., electromyography (EMG) and nerve conduction velocity, or NCV) - studies that evaluate and diagnose disorders of the muscles and motor neurons. Electrodes are inserted into the muscle, or placed on the skin overlying a muscle or muscle group, and electrical activity and muscle response are recorded.
• Magnetic resonance imaging (MRI) - a diagnostic procedure that uses a combination of large magnets, radiofrequencies, and a computer to produce detailed images of organs and structures within the body.
• Laboratory tests (including blood and urine studies and thyroid functioning tests)
• Muscle and/or nerve biopsy - a procedure performed to remove tissue or cells from the body for examination under a microscope.
• Spinal tap (also called a lumbar puncture) - a special needle is placed into the lower back, into the spinal canal. This is the area around the spinal cord. The pressure in the spinal canal and brain can then be measured. A small amount of cerebral spinal fluid (CSF) can be removed and sent for testing to determine if there is an infection or other problems. CSF is the fluid that bathes the brain and spinal cord.
Treatment for ALS:
Specific treatment for ALS will be determined by your physician based on:
• Your age, overall health, and medical history
• Extent of the disease
• Your tolerance for specific medications, procedures, or therapies
• Expectations for the course of the disease
• Your opinion or preference
There is no proven treatment to stop ALS. However, the US Food and Drug Administration (FDA) approved Rilutek®, the first drug that has prolonged the survival of persons with ALS.
For most people with ALS, primary treatment may involve the management of symptoms, and may include physical, occupational, speech, respiratory, and nutritional therapies. Some medications and/or heat or whirlpool therapy may help to relieve muscle cramping. Exercise, although recommended in moderation, may help to maintain muscle strength and function.
Managing the symptoms of ALS is a process that may be challenging for people with the condition, their caregivers, and the medical team. However, it is important to know that there are many community resources available for support and assistance.
Researchers are conducting studies to increase their understanding of the causes of the disease, mechanisms that can trigger motor neurons to degenerate, and approaches to stop the progression of weakness.
View additional health information for Nervous System Disorders
Note: the health information provided online represents common treatments and procedures, but DOES NOT indicate specific instructions for UK HealthCare patients. You should NOT utilize the information as a substitute for medical advice. Always follow your doctor's advice and ask about what to expect from treatment at UK HealthCare.