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Patient education: Amyotrophic lateral sclerosis (ALS) (The Basics)

Patient education: Amyotrophic lateral sclerosis (ALS) (The Basics)

What is amyotrophic lateral sclerosis? — Amyotrophic lateral sclerosis ("ALS") is a disease that damages the nerves that control muscles. This causes the muscles to weaken. The muscles slowly stop working, leaving the person unable to move (called "paralysis"). Over time, the disease gets worse and leads to death. ALS is also known as "Lou Gehrig's disease," after the famous baseball player who died of the disease.

Most people who get ALS live only a few years after their symptoms begin. There is no cure for ALS, but doctors can treat the symptoms.

What are the symptoms of ALS? — The main symptoms include:

Weak arm or leg muscles, usually starting in 1 arm or leg and then later spreading to other parts of the body

Trouble speaking or swallowing

Slow, stiff, or awkward movements

Muscle twitches and spasms

If a person gets weak muscles in their hands or arms, they might have problems with:

Using buttons or zippers

Handling coins or other small things

Writing

If a person gets weak muscles in their legs or feet, they might have problems with:

Walking and turning

Balance

Climbing stairs

Standing up from a chair or the floor

If these symptoms happen, the person might have other problems, such as:

Feeling like the legs are "heavy"

Dragging the front of the foot on the ground when walking

Tripping or falling

If a person gets weak muscles in their head, neck, or chest, they might:

Have a stiff jaw and a hard time opening the mouth

Have trouble swallowing

Have trouble moving the mouth and tongue to speak clearly

Drool

Not be able to fully close the eyes

Have trouble holding up the head due to weak neck muscles

Have trouble breathing

Some people with ALS have mood changes. They also might laugh, cry, or yawn at times when it doesn't make sense to do those things. In some people, ALS affects the mind and causes problems with thinking and language. (For example, a person might have trouble finding the right words for things.)

Are there tests for ALS? — Yes. Your doctor might be able to tell if you have it by learning about your symptoms and doing an exam. But they will probably do tests, such as electromyography (also called "EMG"), to check how well your nerves and muscles are working. You might also need other tests to check that a different problem isn't causing your symptoms. These might include:

MRI – This is an imaging test that takes pictures of your brain and spinal cord.

Blood and urine tests

How is ALS treated? — Treatments for ALS include these medicines:

Riluzole (brand names: Rilutek, Exservan, Tiglutik)

Edaravone (brand name: Radicava)

"PB-TURSO" (brand names: Relyvrio, Albrioza)

These medicines work by slowing down the progress of the disease a little bit. They might help people live a few months longer.

Other treatments can help people cope with the symptoms of ALS. They include:

Breathing support – For this treatment, you wear a tight-fitting mask on your face or nose. Air and oxygen flow through the mask to help you breathe.

Feeding tube – This is a small, flexible tube that goes through the skin over your belly into your stomach. You can then get special liquid food and fluids through the tube directly into your stomach.

Devices to help with walking and talking, such as:

A cane, crutches, or motorized wheelchair

A special computer that "talks" for you. You can control the computer with hand or eye movements.

Medicines to treat muscle spasms and weakness, drooling, sleep problems, pain, and depression.

More on this topic

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Patient education: Dysphagia (The Basics)

This topic retrieved from UpToDate on: Jan 01, 2023.
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