What are the symptoms of AXE ALS?

What are the symptoms of AXE ALS?

Signs and symptoms might include:

• Difficulty walking or doing normal daily activities.
• Tripping and falling.
• Weakness in your leg, feet or ankles.
• Hand weakness or clumsiness.
• Slurred speech or trouble swallowing.
• Muscle cramps and twitching in your arms, shoulders and tongue.
• Inappropriate crying, laughing or yawning.

How long can you live with AXE ALS?

The average life expectancy is two to five years post diagnosis.

How did Stephen Hawking live so long?

Amyotrophic lateral sclerosis or ALS is one of several types of motor neurone diseases. It gradually and inexorably paralyzes patients, usually killing within about four years. Hawking was diagnosed in 1963, when he was just 21 years old. He survived for 55 years with the incurable condition.

What are the first warning signs of ALS?

Early symptoms include:

• Muscle twitches in the arm, leg, shoulder, or tongue.
• Muscle cramps.
• Tight and stiff muscles (spasticity)
• Muscle weakness affecting an arm, a leg, the neck, or diaphragm.
• Slurred and nasal speech.
• Difficulty chewing or swallowing.

What is the longest living person with ALS?

Eighty per cent of ALS victims live only two to five years after a diagnosis, and since the passing of fellow ALS sufferer Stephen Hawking, Wells is the longest living survivor of the disease in the world. He lives at Toronto East General Hospital now.

Who is the longest living person with ALS?

Do ALS patients feel pain?

Does ALS cause pain? The answer is yes, although in most cases it does so indirectly. From what we know at this time, the disease process in ALS only affects the nerve cells controlling strength (motor neurons) in the brain, spinal cord, and peripheral nerves.

How does amyotrophic lateral sclerosis ( ALS ) affect people?

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease, is a progressive and fatal disease, attacking neurons that control voluntary movement. These neurons die over time. The result is the gradual loss of muscle movement, speech, swallowing, and eventually breathing. The exact causes of ALS remain unknown.

Is there a cure for amyotrophic lateral sclerosis?

Some cases are inherited. ALS often begins with muscle twitching and weakness in a limb, or slurred speech. Eventually, ALS affects control of the muscles needed to move, speak, eat and breathe. There is no cure for ALS, and eventually the disease is fatal.

How does a clinic help people with ALS?

Attending ALS clinics may improve the quality and length of life of people living with ALS. Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease, is a progressive and fatal disease, attacking neurons that control voluntary movement. These neurons die over time.

What are the symptoms of the early stages of ALS?

Stages of ALS. Early Stages. Muscles. Muscles may be weak and soft or stiff, tight and spastic. Muscle cramping and twitching (fasciculations) occurs, as does loss of muscle bulk (atrophy). Symptoms may be limited to a single body region or mild symptoms may affect more than one region.