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Amyotrophic lateral sclerosis (ALS)

Medical condition/treatment

Amyotrophic lateral sclerosis (ALS)

disc prolapse

Muscles and nervous system

disc prolapse

Amyotrophic lateral sclerosis, or ALS for short, is a rare neurodegenerative disease that affects the nerve cells in the brain and spinal cord. ALS causes progressive muscle loss and weakness, leading to difficulty speaking, swallowing, and moving. There is no cure for ALS, and life expectancy after diagnosis is limited. Treatment focuses on relieving symptoms and improving the patient's quality of life. This may include physical therapy, medications, and supportive measures.

Causes/Description:

Genetic predisposition, unknown causes, environmental factors

Amyotrophic lateral sclerosis (ALS)

disc prolapse

Physiotherapie, Medikamente, Muskelschwäche, Genetik, unbekannt, Keine bekannte Prävention

disc prolapse

ALS is a neurodegenerative disease in which nerve cells in the brain and spinal cord die. The exact cause is unknown, but genetic factors may play a role.

disc prolapse

ALS is a serious neurological disease for which there is currently no cure. Treatment aims to improve your quality of life and slow the progression of the disease. Multidisciplinary care is crucial. This includes collaboration between neurologists, physiotherapists, occupational therapists, speech therapists and palliative medicine specialists. Physiotherapy focuses on maintaining your muscle strength and improving your mobility. Occupational therapy helps you cope with everyday activities. Speech therapy is important to support your communication because ALS can affect the ability to produce speech. Palliative care offers support for pain control and your mental health. It is important to have an open and honest dialogue with your medical team to receive the best possible care and support.

disc prolapse

ALS was first described by Jean-Martin Charcot in the 19th century. It is a neurodegenerative disease. Fact: Most patients have a life expectancy of 2-5 years after diagnosis.

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