Life Expectancy of ALS Patients

ALS, also known as Amyotrophic Lateral Sclerosis, is a progressive neurological disorder characterized by the degeneration of motor neurons. The exact cause and mechanisms of the disease remain unclear, making it a challenging condition to treat effectively.

Symptoms and Progression

The disease typically begins with weakness in the small muscles of the hands, gradually spreading to the other side of the body. Over time, patients experience muscle atrophy and loss of strength in the upper limbs and eventually throughout the entire body. This deterioration is progressive and tends to worsen over time.

Treatment Options

Due to the unknown origin of ALS, there are currently no highly effective Western medical treatments specifically targeting the disease. While some medications may help slow progression or manage symptoms, they are not curative. On the other hand, traditional Chinese medicine approaches, such as treatments focused on strengthening the spleen and kidneys, have shown some promise in alleviating symptoms and improving quality of life.

Managing the Disease

Regardless of whether patients choose Western or Eastern treatment methods, managing ALS effectively often requires a combination of medical care and lifestyle adjustments. In the early stages of the disease, symptoms may progress rapidly over the first one to two years, but the rate of decline typically slows in later stages.

Prognosis and Life Expectancy

On average, patients diagnosed with ALS have a life expectancy ranging from approximately 5 to 10 years, though some individuals may live even longer. Factors such as age at diagnosis, overall health, and access to supportive care can significantly influence outcomes.

In addition to medication, proper care and support play a crucial role in managing the condition. This includes physical therapy, nutritional support, and emotional and psychological assistance for both patients and their families.