Amyotrophic Lateral Sclerosis: Lou Gehrig's Disease

I. Take a moment, and point at the computer screen. Notice that your index finger is extended and your other fingers are curled into your palm. How did your hand know to do that? It all began in your brain, the starting point for an important chain of communication. Your brain ordered nerve cells, to activate

Have you ever heard of ALS, better known as Lou Gehrig’s disease? For many people, ALS is a disorder that they may not know much about. I never heard of it either until my father was diagnosed with this disease in 2006. Because there is no known cure, it is important to detect this disease early, so that proper treatments and preparation can be done before it’s too late.

Following the diagnosis of ALS the main goal of treatment is focused at relieving the symptoms. The most important matter in managing ALS patients is that they continually sustain the highest amount of movement and activity as possible and remain comfortable while doing so. Although a cure for ALS has not yet been developed, effective treatments do exist to assist the patients in their fight with the disease. Physicians urge the patients to carry on with their everyday lives doing all the activities and physically exerting themselves as they would normally do. But, they also recommend the patients to limit their amount of physical exertion

Lou Gehrig’s Disease Thesis: Weakness in the hands, arms, legs or slurred speech. Imagine having these symptoms and not knowing what is wrong. Then the most dreaded words are uttered, “You have Lou Gehrig’s Disease”. Amyotrophic Lateral Sclerosis (ALS), or other wise known as Lou Gehrig’s Disease, is a disease that attacks muscles and brain cells. “ALS was first found in 1869 by French neurologist Jean-Martin Charcot,but it wasn’t until 1939 that Lou Gehrig brought national and international attention to the disease” (About).

The article titled “The Voices of A.L.S. by Tara Parker-Pope has given me a better insight into A.L.S. In fact, it has made me more aware of it. Amyotrophic lateral sclerosis (ALS) also known as Lou Gehrig's disease, affects parts of the nervous system that control voluntary muscle movement. Motor neurons, among the largest of all nerve cells, reach from the brain to the spinal cord and from the spinal cord to muscles throughout the body. When these motor neurons die, the brain can no longer start and control muscle movement. At this time there is no cure for the disease; however, over the past few decades, we have made amazing strides in our understanding of the brain, the nervous system, and genetics. Discoveries in each of these areas bring

Charcot begins to give lectures on the disease and he is the first to use the term Amyotrophic Lateral Sclerosis. The name of the disease can be broken down to show how Charcot came about it. The first word, Amyotrophic, can be broken down into three sections; a- meaning no, -myo- meaning muscle, and -trophic meaning nourishment. This breakdown describes what is happening to the muscles because of the disease, they are getting no nourishment. The second word, Lateral, refers to the spinal cord, which is where the motor neurons interact and redirect to the muscles. Finally, the third word in ALS, Sclerosis, is defined as the hardening of the muscles in the patient’s

Amyotrophic Lateral Sclerosis (ALS) is a terminal disease, also known as Motor Neurons Disease, Charchot Disease and Lou Gehrig disease. ALS destroys the Central Nervous System (CNS) and causes damage to the upper and lower motor neurons in the brain. Signs and symptoms are characterized as: muscles weakness, muscle atrophy, twitching and reduced muscle reflexes. Eventually the patient will become paralyzed and rely on a tracheostomy and ventilator for breathing (ALS Association [ALSA], 2010).

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease, is a terminal disease that degenerates the nerves in the brain and spinal cord. Motor neurons run from the brain, through the spinal cord, and into the muscles of person; this is what allows a person to have control over voluntary movement. When an individual is diagnosed with ALS, their motor neurons begin to degenerate, thus eradicating their ability to walk, eat, and eventually breathe.

Those who suffer from Amyotrophic Lateral Sclerosis live the rest of their lives bedridden, or are embedded to a chair. The average patient diagnosed with ALS are males between the ages of 40-70. Athletes who are diagnosed in their late 20’s due to repetitive head injuries typically live 3-5 years after the diagnosis. Those who are fortunate enough may live 10 years post

Everyday, an average of 15 people are diagnosed with Amyotrophic Lateral Sclerosis(ALS) also commonly known as Lou Gehrig's disease. Across the world there are more than 5,600 cases of ALS every year. People all around the world are open to being diagnosed with ALS, it affects people of all ages, races, and gender. Amyotrophic Lateral Sclerosis has affected millions of families and individuals since 1869. However, what is Amyotrophic Lateral Sclerosis, what does life look like for someone with ALS , and what research is being done for a cure?

ALS, better known as Amyotrophic Lateral Sclerosis, is considered as a complex genetic disorder, in which multiple hereditary and environmental factors combine to cause this disease. This is seen as an illness of parts of the nervous system that control voluntary muscle movement. In ALS, the motor neurons (nerve cells that control muscle cells) are gradually lost. When these motor neurons turn out to be lost, the muscles they control become weak and ultimately nonfunctional. We see that “amyotrophic” is rooted in Greek origin meaning without nourishment to muscles and refers to the loss of signals nerve cells normally send to muscle cells. “Lateral” simply means to the side and refers to the location of the damage in the spinal cord. “Sclerosis” means hardened and refers to the toughened nature of the spinal cord in advanced ALS. This progressive neurodegenerative disease, that was first discovered 150 years ago, is associated with a life expectancy of approximately three years after symptom onset. In the United States, ALS is also known as Lou Gherig’s Disease, named after the Yankees Baseball player who passed away because of it in 1941. In the United Kingdom and other parts of the world, it’s often referred to as motor neuron disease in reference to the cells that are lost in the disorder (ALS Association, 2015).

Amyotrophic lateral sclerosis or Lou Gehrig’s disease is a neurological disease that proves fatal for anyone diagnosed with it. Although this disease is not commonly heard of or most often diagnosed, numerous people a year (mainly those in their middle-age or older age generations) succumb to this terminal disease. This disease is progressive, meaning it continues to worsen with age, limiting one’s lifespan with only a certain number of years left to live. By definition, Lou Gehrig's disease is a rare neurological disease that attacks the motor neurons, thus affecting one’s ability to produce movements such as chewing, walking and talking (“Amyotrophic Lateral Sclerosis,” 2018). Although Lou Gehrig's disease is more prominent in the older-aged

Prior to reading Tuesdays with Morrie, my only knowledge of Amyotrophic Lateral Sclerosis (ALS) was that it is a progressive, debilitative disease with no known cure, it took the life of professional baseball player Lou Gehrig, and a video campaign called the Ice Bucket Challenge, used to promote awareness and raise money for research went viral last year. What I did not realize was just how quickly the disease can progress and how severely it physically devastates those who suffer with it. Ultimately, however, I found this book to be less about gaining a better understanding of ALS and more about learning valuable lessons on how to deal with life’s challenges, burdens, and responsibilities. Through this book, Professor Morrie Schwartz teaches

Introduction: A long-term degenerative neurological condition (LTDNC) is a term used to describe diseases that affect the nervous system leading to its degeneration. Conditions such as Parkinson’s disease, amyotrophic lateral sclerosis, multiple sclerosis etc. are all categorized by impairment in brain, nerve and spinal cord pathway cells (Canadian Institute for Health Information, 2007). Due to such disruptions, the nerve signals between the brain and the body are affected which result in problems with walking, controlling movement, balance, full or partial paralysis, breathing and talking problems, occurrence of seizures, lack of bladder and bowel control at later stages, and even problems with the heart (Canadian Institute for Health Information, 2007). In 2011, the Canadian Institute for Health Information reported that Canada has one of the highest incidences of multiple sclerosis (MS) in the world, where approximately 93,500 individuals are currently affected. Despite the prevalence of the disease, there is still much that remains unknown. According to the 2012 statistics from the ALS Society of Canada, the number of new diagnoses per year is

A distinctive characteristic of ALS is that although the motor neurons die, the brain, cognitive functions and sensory neurons stay intact (Porth & Matfin, 2009). This makes the disease especially devastating because patients become trapped inside their dying body, with a fully alert mind, but are unable to move. It is not known what causes the exact death of the motor neurons in the body, but “five percent to 10% of cases are familial; the others are believed to be sporadic” (Porth & Matfin, 2009, p.