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Pages:
1 page/≈550 words
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1 Source
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Other
Subject:
Health, Medicine, Nursing
Type:
Case Study
Language:
English (U.S.)
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MS Word
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Topic:

Amyotrophic Lateral Sclerosis (ALS) (Case Study Sample)

Instructions:
In this task, I was tasked with providing a comprehensive overview of Amyotrophic Lateral Sclerosis (ALS), covering its definition, risk factors, signs and symptoms, as well as treatment and management options. ALS, also known as Lou Gehrig's disease, is a progressive neurological disorder that affects nerve cells in the brain and spinal cord, leading to muscle weakness and eventually paralysis. I began by defining ALS as a combination of progressive diseases targeting nerve cells responsible for muscle movement. This definition was followed by an explanation of its impact, highlighting the continuous degeneration of nerve cells and the eventual loss of muscle function in affected individuals. Next, I discussed the risk factors associated with ALS, including gender, age, race, and genetic inheritance. Males are more likely to develop ALS than females, particularly before the age of 65, with Caucasians and non-Hispanic individuals having a higher risk. Additionally, genetics play a significant role, as children born to parents with ALS have an increased likelihood of inheriting the disease. Moving on to signs and symptoms, I outlined the common manifestations of ALS, such as muscle weakness, clumsiness, difficulty maintaining posture, and problems with breathing and swallowing. I also mentioned the potential development of frontotemporal dementia in some individuals, which can affect decision-making and memory. In terms of treatment and management, I highlighted the primary goal of alleviating symptoms and preventing complications. Riluzole and Edaravone are two drugs approved by the FDA for slowing the progression of ALS. Other medications may be prescribed to manage specific symptoms, while occupational and physical therapy can help improve quality of life and manage pain for affected individuals. Overall, this task provided a comprehensive overview of ALS, covering its definition, risk factors, signs and symptoms, and treatment options. By addressing each aspect of the disease, the sample aimed to enhance understanding and awareness of ALS and its management strategies. source..
Content:
Amyotrophic Lateral Sclerosis (ALS) Definition * Amyotrophic Lateral Sclerosis (ALS) is a combination of progressive diseases that attack the brain and spinal cord's nerve cells that control muscle movement. * The disease leads to the continuous degeneration of nerve cells in the areas. * Gradually, people affected by the disease become unable to use their muscles. * It is commonly termed Lou Gehrig's disease, taking after a popular baseball player who died from the disease. Risk Factors * The risk factors for ALS include gender, age, and race. * The disease is more common in males than women (Masrori & Van Damme, 2020). * However, the difference is realized before the age of 65 and disappears after reaching 70. * However, the disease can be developed at all ages, and there is a high chance of developing it in people in their late 50s or early 60s. * There is a high likelihood of developing the disease in Caucasian and non-Hispanic people. * The disease can also be genetically inherited, especially for children born of people with ALS.  Signs and Symptoms * People with the condition have continuous muscle weakness.  * Some of the common symptoms include: * High levels of clumsiness * Weak arms, legs, and ankles * Problems in maintaining good posture * Breathing Swallowing difficulties. * For some people, the progression of the disease can lead to issues in decision-making and memory. * As a result, frontotemporal dementia develops. Treatment and Management * Treating ALS is aimed at alleviating the symptoms and preventing complicati...
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