Gant Conley
1st Hour
Dr. Ward
The Battle with ALS
Amyotrophic Lateral Sclerosis is a disease that everyone should fear. Once the disease is in your body, there is no found cure but riluzole therapy is something that may extend life expectancy. Odds are for every 100,000 years, 2 people acquire the disease, with the majority being of the male sex. “Most people who develop Amyotrophic Lateral Sclerosis are between the ages of 40 and 75, with the majority after age 60, although it can occur at a younger age.” Amyotrophic Lateral Sclerosis may still be developed at a young age but it is very rare. Stephen William Hawking turns out to be a very rare man. http://www.alscenter.org/living_with_als/facts_statistics.html Stephen William
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“The famous theoretical physicist has helped to bring his ideas about black holes and quantum gravity to a broad public audience. For much of his time in the public eye, though, he has been confined to a wheelchair by a form of the motor-neuron disease amyotrophic lateral sclerosis (ALS). And since 1985 he has had to speak through his trademark computer system–which he operates with his cheek–and have around-the-clock care.” http://www.pbs.org/newshour/rundown/how-has-stephen-hawking-lived-to-70-with-als/ Stephen Hawking no doubt has had troubles with Amyotrophic Lateral Sclerosis, but those troubles have pushed him and motivated him to become better at what he enjoys doing. “However difficult life may seem, there is always something you can do and succeed at.” …show more content…
“One thing that is highlighted by this man’s course is that this is an incredibly variable disorder in many ways. On average people live two to three years after diagnosis. But that means that half the people live longer, and there are people who live for a long, long time.” - Leo McCluskey. Amyotrophic Lateral Sclerosis does not stay constant from each person that has it, this disease is different throughout each person who acquires the disease. Hawking is a man who has shown all how much Amyotrophic Lateral Sclerosis
It is truly remarkable how Randy Pausch and Morrie Schwartz stories are so similar but yet so different. They both seem to have an outlook on life in a positive way, not sad or demeaning. The only crippling difference is the fact that Morrie was at the age that wasn’t abnormal to be sick and Randy was just dealt the cards for a short life. One of Professor Randy Pausch’s many quotes during The Last Lecture makes a similar point between his experience and Morrie’s when he says, “…it’s hard to raise awareness of pancreatic cancer – people who get it don’t live long enough.” ALS is such a rehabilitating disease that scientist have issues pinpointing the causes to even get close to a cure, which didn’t hinder either of their strive to keep going as far as they could.
While reading Tuesday with Morrie by Mitch Albom, it is discovered that Professor Morrie Schwartz a genuine humble old man filled with life ends up being dignosed with a fatal disease called amyotrophic lateral sclerosis (ALS) which targets the neourological system. Slowly losing his range of motion, Morrie tries to continue his life as normal as possible, As he lost his ability to walk without tripping, he purchased a cane to help him get by. When he is unable to undress himself, he finds someone to assist him the locker room so he can change in and out of his swimwear. Morrie is a man that refuses to give, only to find different techniques to get by. Accepting death, Morrie writes aphorisms about accepting life how it is. Inspiring many people with his
In her essay “On Being a Cripple,” Mairs describes her path of acceptance of her multiple sclerosis (MS) diagnosis by declaring that she is a “cripple” in alternative to the more broadly acceptable terms: disabled or handicapped. Her essay is written with humor, satire, an open heart, and open eyes. Mair’s purpose is to describe her acceptances of her condition by using rhetorical elements and appeals, such as ethos and pathos, in order to allure her audience.
Amyotrophic Lateral Sclerosis, commonly referred to as ALS, is a disease that can alter the daily life of a human in monumental and unending ways. In one of her articles about ALS, Caroline Ingre (2015) states that the disease is a “fatal neurodegenerative disorder” and further supports this by noting how the disease is marked by the degeneration in motor neurons in the brain, brainstem, and spinal cord (p. 181). This basically means that
Amyotrophic Lateral Sclerosis is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Amyotrophic Lateral Sclerosis is better known as ALS or Lou Gehrig’s disease. Amyotrophic Lateral Sclerosis was not brought to International or national attention until Famous New York Yankees baseball player, Lou Gehrig, was diagnosed with it in 1939. Jon Stone, the writer and creator of Sesame Street, was also diagnosed with Amyotrophic Lateral Sclerosis. Amyotrophic Lateral Sclerosis is very deadly and it physically handicaps a person as it progresses. There are two types of Amyotrophic Lateral Sclerosis, Sporadic and Familial. Sporadic is the most common cause in some cases and Familial is inherited, which is rare. Amyotrophic Lateral Sclerosis is one of the most aggressive muscular atrophy disorders, it has many signs and symptoms, and it can be treated but cannot be cured.
ALS is led to mean no muscle nourishment. When a muscle has no nourishment, it atrophies or wastes away hence the name. In addition to this, lateral shows the areas in a person's spinal cord where part of the nerve cells that signal and control the muscles are located. As this area degenerates, it leads to scarring or hardening (sclerosis) in this particular region.
Dylan was born with a tumor wrapped around his spinal cord, which was successfully removed however resulted in him becoming paraplegic. The first fourteen years of his life, Dylan defined himself by his disability. He felt ‘weird and different’ because of his disability and this was why he was excluded from his peers. It was not until Grade 9 that Dylan began to see that his disability did not have the power to dictate his life or set a limit to which he could achieve. Since then, Dylan has moved on to achieve phenomenal feats, namely, winning a gold medal at the 2008 Beijing Paralympics to becoming the world’s number one paraplegic tennis player. Dylan can be found wheelchair crowd surfing at concerts, advocating for people with disabilities and training for the 2016 Rio Paralympics. Dylan is on a mission to ‘mainstream disabilities’ and shatter negative
One major reason ALS is such a frightening disease is because no cure has been established. Although no effective treatment has been developed, a number of drug trials have been conducted, and there are some devices designed to help ALS patients maintain independence as well as safety as the disease progresses.
Imagine if you loss control of your body but your mind stayed unaffected. You would be a prisoner in your own body, all leading up to your death sentence. That is the sad fate for the people diagnosed with Amyotrophic lateral sclerosis (ALS). “Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder was first described by Ran in 1850. This description was then expanded in 1873 by Charcot, who emphasized the involvement of the corticospinal tracts. In the United States, ALS is often referred to as Lou Gehrig's disease, after the famous ball player who was stricken by the disease in the midst of his career. (Yale School of Medicine, 2014)” In this paper will go through the definition, the process, the signs, the risk factors, etiology, and discus the known people that have suffered with this terminal disease.
This ironic phrase demonstrates the pride she finds in a label that others find offensive, but she finds it truthful and correct. Mairs embraces her condition because it has become part of her. Mairs continues to demonstrate her tone, now with humor when she states, “my God is not a handicapper general” (Mairs). Mairs uses this phrase to demonstrate she is different than most people including her god, but this does not stop her from being confident. She is aware of her difference but she knows she is capable of achieving all her desires. Furthermore she demonstrates that she continues to live a normal life with her family. Although individuals view Mairs differently she demonstrates her capability of achieving a regular life; for example, Stephen Hawking is a highly educated cripple who has achieved more than any other individual who does not have his condition. Hawking and Mairs prove that a disease will not stop them from living their
“Life is 10% what happens to you and 90% how you react to it,” says Charles R. Swindoll. This statement, although seemingly inaccurate, is brought to life by the testimony of Nancy Mairs. After being diagnosed with Multiple Sclerosis (MS), Mairs had every reason to give up on life, but in “On Being a Cripple” she shows her audience that pushing forward was worth the challenge. Her life as a cripple isn’t easy, but through her writing, Mairs hopes to explain and create awareness about her life living with MS. Through her personal experience and positive attitude, Mairs shows her audience that not only is she a source that others can trust but that life is exactly what you make it, no matter what cards you are dealt.
Amyotrophic lateral sclerosis (ASL), Lou Gehrig’s disease, a brutal, unforgiving illness of the neurological system with no known cure.
... adapted to his ever-changing circumstances, became a doctor, got married and, most importantly, overcame countless obstacles. He managed to do all of this in the second half of the twentieth century. Given the advancements in technology and greater acceptance of those with disabilities in today’s society it would be easier for him today. Beisser succedded and I will too. I will travel, I will find good jobs that fulfill me, I will surround myself with loving people, and, perhaps most importantly, I will be financially independent.
disease that Stephen Hawking has) 5 years ago. This is a condition that destroys motor nerves, making control of movement impossible, while the mind is virtually unaffected. People with motor neurone disease normally die within 4 years of diagnosis from suffocation due to the inability of the inspiratory muscles to contract. The woman's condition has steadily declined. She is not expected to live through the month, and is worried about the pain that she will face in her final hours. She asks her doctor to give her diamorphine for pain if she begins to suffocate or choke. This will lessen her pain, but it will also hasten her death. About a week later, she falls very ill, and is having trouble breathing.
This is a neurodegenerative disease, meaning it results in progressive loss or death of neurons. It often starts off with effecting simple motor skills like writing and holding things, after a few months usually patients start losing the ability to walk, talk, or move any of their limbs. Although the brain trauma is what causes it, ALS has little-no-effect on the brain. This fatal disease is typically diagnosed around age 60 and most patients are given about 3-5 years to live after being diagnosed. It has been found that 10% of cases are shown as genetic. It was brought to attention that athletes were beginning to get diagnosed with ALS at a younger age than most. After extensive research in the early 2000’s, Brain Analyst, Dr. Mckee ran tests and finally came to the conclusion that the toxic proteins in the brains of ALS patients were coming from repeated blows to the head. It was then made evident why so many athletes in contact sports such as football, soccer, boxing, etc… were being diagnosed at such a young age and more frequently than