Amyotrophic Lateral Sclerosis Symptoms-4u

scle·ro·sis: a pathological condition where the tissue has become hard and which is produced by overgrowth of fibrous tissue
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Amyotrophic Lateral Sclerosis

Amyotrophic

Amyotrophic Lateral Sclerosis Symptoms

Amyotrophic lateral sclerosis symptoms are frequently overlooked because of their subtle nature.  The parts of the body affected by early amyotrophic lateral sclerosis symptoms depend on which muscles in the body are damaged first. In some cases, symptoms initially affect one of the legs, and patients experience awkwardness when walking or running or they notice that they are tripping or stumbling more often. Some patients first see the effects of the amyotrophic lateral sclerosis on a hand or arm as they experience difficulty with simple tasks requiring manual dexterity. To be diagnosed with amyotrophic lateral sclerosis, patients must experience symptoms of both upper and lower motor neuron damage that cannot be attributed to other causes.

Early Amyotrophic Lateral Sclerosis Symptoms may include:

  • speech problems, slurred and nasal speech
  • muscle twitching, cramping, or stiffness
  • weakness affecting an arm or a leg muscles
  • difficulty chewing or swallowing

Regardless of the part of the body first affected by the disease, muscle weakness and atrophy spread to other parts of the body as the disease progresses. Patients have increasing problems with moving, swallowing, and speaking or forming words. Amyotrophic Lateral Sclerosis symptoms of upper motor neuron involvement include tight and stiff muscles, spasticity and exaggerated reflexes, hyperreflexia, including an overactive gag reflex. An abnormal reflex commonly called Babinski's sign where the large toe extends upward as the sole of the foot is stimulated in a certain way, also indicates upper motor neuron damage. Symptoms of lower motor neuron degeneration include muscle weakness and atrophy, muscle cramps, and fleeting twitches of muscles that can be seen under the skin.

Amyotrophic lateral sclerosis symptoms and the rate of the disease progression vary from person to person, eventually patients will not be able to stand or walk, get in or out of bed on their own, or use their hands and arms. Difficulty swallowing and chewing impair the patient's ability to eat normally and increase the risk of choking. Maintaining weight will then become a problem. Because the disease usually does not affect cognitive abilities, patients are aware of their progressive loss of function and may become anxious and depressed. A small percentage of patients may experience problems with memory or decision-making, and there is growing evidence that some may even develop a form of dementia. Health care professionals need to explain the course of the disease and describe available treatment options so that patients can make informed decisions in advance. In later stages of the amyotrophic lateral sclerosis, patients have difficulty breathing as the muscles of the respiratory system weaken. Patients eventually lose the ability to breathe on their own and must depend on ventilator support for survival. Patients also face an increased risk of pneumonia during later stages of amyotrophic lateral sclerosis symptoms.

See your doctor if you've noticed amyotrophic lateral sclerosis symptoms such as weakness in one of your limbs or twitching and cramping in your muscles. The sooner a diagnosis and treatment can be made the better.

 

 

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