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Als disease research paper
Als disease research paper
Als disease research paper
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I just want to start off by saying the Paul was such an inspiration, and it was an honor to hear him speak about ALS. Before hearing him speak, all I really knew about ALS is that it affected the muscles. I never even knew that it was such a deadly disease. It was shocking to hear that the average life expectancy for someone with ALS is only 2-5 years. It was such great news to hear that Paul is going on to his 4th year, and was only recently in need of a wheelchair. While it is unfortunate that Paul was diagnosed with ALS, it is fortunate that his disease is slowly progressing. Some of the stories he shared about his friends made me realize that some people may take a turn for the worse, only several months after being diagnosed. It was wonderful to hear Paul say that he really thinks he will surpass the odds and make it to the 5th year. I really hope that Paul is one of the lucky ones, who are diagnosed with ALS, and live past the life expectancy. …show more content…
To my surprise, he was so excited to talk about ALS and how it has personally affected him. Some people have a very hard time talking about a disease that they may have. Since Paul was not one of these people, I believe that it makes it easier for him to cope with the disease. When he was talking to us, he told us that one of the greatest things someone could do is ask him about ALS. He views a conversation like this as a lesson for the person asking, and a therapy session for
Sadly, Jim Valvano died two months after he accepted the award. But this speech is still ingrained in our minds. Through the ethos appeal in this speech, Valvano showed the audience why he deserved the Arthur Ashe award and convinced them to donate to his cancer research foundation. Throughout the different parts of the acceptance speech, Valvano shows his courage and love that helped him to win the award in the first place.
For as sick as he was, he still gave a thumbs up when he was spoken to …I think I used the last few tissues when he gave that thumbs up! So sweet and innocent, that just shows that AIDS does not discriminate, we are all human. Until we walk in someone’s shoes that is so ill, we cannot judge. Every life matters, we all need to be aware of AIDS and help change the way the world deals with AIDS.
She gives the listeners personal advice she has learned and uses pathos in a more emotional way. Her allusion to the world trade center is a perfect example of this. She reminds us how we can easily overcome obstacles when we work together with other people. Later in the address Amy Poehler shares a few things she learned from when she studied improvisation in Chicago. She says, “Say ‘yes.’ Live in the moment. Make sure you play with people who have your back. Make big choices early and often. Don’t start a scene where two people are talking and jumping out of a plane. Start the scene having already jumped. If you are scared, look into your partner’s eyes. You’ll feel better”,. The way she relates the strategies she learned there back to life touches your heart. She closes her speech with a heartfelt message, “When you feel scared, hold someone’s hand and look into their eyes. And when you feel brave, do the same thing. You are all here because you are smart. And you are brave....As you head out into the world, I wish you love and light, joy, and much
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.
In this case however under the circumstances that it was an award for humor there is leeway on how the speech could appropriately be delivered. He did a very good job at keeping the audiences attention throughout the whole speech even using aids such as his wife and other members in the crowd.
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.
Lou Gehrig was one of the best baseball players to ever play the game. He was blessed with an amazing career playing for the New York Yankees setting many major league records such as 2,130 consecutive games from 1925 to 1939. Unfortunately all good things must come to an end and on July 4, 1939 Gehrig stood before his devoted fans at Yankee Stadium and announced that he had been diagnosed with amyotrophic lateral sclerosis. The man that was known to everyone as the “Pride of the Yankees”, on this very day, showed how courageous he was by giving a passionate speech to his fans that was filled with sarcasm, emotion, and pride.
people have been known to get it. There is no specific race or ethnic background
At first, Fox’s diagnosis was extremely difficult for him to cope with. He had just been diagnosed with a disorder that not only affects motor function and leads to neuropsychiatric problems but also progressively gets worse. If it wasn’t for the support of Fox’s family and his wife Tracy Pollan, Tra, it brings to question whether Fox could have survived the hardship the news of is disease. And Fox does a fantastic job at describing the assistance he had through stories about his journey through Hollywood.
Medical history has been filled with an array of diseases and illnesses, ranging from the common cold to deadly killers. Some are easily treatable and others can be terminal, but some of the worst are those that still remain without a cure; one such disease is amyotrophic lateral sclerosis.
Hello my name is Nick and I am giving my speech on Alzheimer’s Disease. I was thinking of what I could do for a speech. Then I thought I wanted to inform people on something that little know about. Then it hit me. Alzheimer’s Disease it has affected my life so much and I know so much about it. So I am going to tell you how it has affected my life in more ways than one. Before I start I want you to imagine something. Look around you know everyone right? All these faces you see practically see everyday take all that you know about them and forget it. Can you do it? I can’t. So try to imagine now that it could happen to you years down the road and the disease gets so bad you cant remember your kids, your mother, or even your family. You probably are thinking right now, it will not happen to me. Well that is what my grandfather said about 6 years ago and now he cant even remember my name.
People that are diagnosed with Dementia have an advanced brain disorder that can make it progressively more difficult for them to think clearly, remember things, communicate to others, or even take care of themselves on their own. I have been personally affected by this disorder through members of my family and that is why this particular lecture caught my attention the most. I didn’t realize how serious this disorder can be and how much it not only impacts a person’s memory loss, but many other aspects of their life. The topics that interested me the most and ones I wanted to learn more about were normal aging memory loss versus symptoms of Dementia, how families cope with a loved one with Dementia, and the difference between Dementia and Alzheimer’s disease.
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
I enjoyed Michael’s stories and wisdom that he shared with the readers. His advice of following your dreams and happiness, accepting your fate, and the importance of learning and being curious is described in the book. His stories are entertaining and keep the reader’s attention. I think his advice can be beneficial for anyone and especially for someone starting a new journey in life. Michael is inspiring in both in how he deals with his disease and his optimism about life. I like that Michael also encourages his readers to face their fears and to follow their dreams and passions. Michael shares this valuable message throughout the book, we all face difficulties that come up in life that are not always expected, but we can play an important role in how we react to
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