What is Amyotrophic Lateral Sclerosis and its Symptoms – HowFlux

What is Amyotrophic Lateral Sclerosis and its Symptoms

What Is A.L.S, Amyotrophic Lateral Sclerosis


Definition of A.L.S:-

ALS OR Amyotrophic Lateral Sclerosis refers to the disease that is a specific type of disorder that includes the death of the neurons and also known as the motor neuron disease.

What is ALS Amyotrophic Lateral Sclerosis and its Symptoms

What is ALS Amyotrophic Lateral Sclerosis and its Symptoms

The disease of ALS is characterized by the stiff muscles or muscles twitching or worsening weakness because of the muscles wasting what results in having a difficulty to speak or to swallow anything or to have a difficulty in breathing. The cause of the disease is not known in most of the cases and about half of the cases include the disease to be inherited from the parents. To diagnose the disease firstly the signs and the symptoms of the disease are made to be diagnosed and then the doctors need to be consulted about the treatment strategy. The diagnosis of this disease is made on the basis of the signs and the symptoms with the testing done to rule out the other potential causes of the disease.

Cure For The Amyotrophic Lateral Sclerosis:-

There is no cure for the ALS found yet but a medication that is called as RILUZOLE may be used to extend the life of the person from a range of about two to three months and the non-invasive type of ventilation may result in providing the improved quality of life along with improved length of the life.

The disease of ALS usually starts around the age of sixty and in the cases of inheritance around the age of about fifty. The average rate of survival from the onset to death is ranging from three to four years and about ten percent of the individuals survive for longer than ten years and most of the patients that die meet their end due to the respiratory failure only.

Symptoms of ALS:-

The disorder is likely to make the muscles to be more week than before and the individuals that are affected by the disorder may ultimately lose the ability to initiate and control all of the voluntary moment although the bladder and the bowel function and the muscles responsible for movement of the eye get spared usually until the final stage of the disorder comes and the cognitive function is generally spread for most of the people although some of the individuals are also likely to develop FRONTOTEMPORAL DEMENTIA in some of the cases.

The earliest of the symptoms of the disease involve the obvious weakness or the muscle atrophy and the others might be presenting the symptoms including the trouble in swallowing or cramping or the stiffness of the affected muscles and muscles weakness might also be affecting an arm or a leg and the nasal speech.


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