Sam Berns and Elizabeth “Lizzie” Velasquez were both born with genetic diseases. Even some might see their conditions as unfortunate and pity them they were happy and found ways to live and thrive with their diseases. They both became sources of inspiration to the world. Sam Berns had a movie made about him and his family, Life According to Sam, to share his story of survival and inspiration. Lizzie Velasquez became a motivational speaker to shared stories with the world fulfill her purpose and touch others with her story of bullying and insecurity. Even though both of these figure \s have some points of agreement they also are different from each other. Sam Berns was a seventeen year old junior who was born with the illness progeria, a genetic …show more content…
Due to her disease she is small, visually impaired, and weighs less than 64 pounds. She, like Sam Berns is an optimist, and even though her life has been difficult she believed that it has been ok and that every negative had a positive. She liked to believe that her syndrome did not define who she was and unlike Sam Berns she believed her success and accomplishments defined who she was. She believed in using others negativity as a ladder to reach her dreams. Like Sam Berns she had dreams such as going to college, having a family, publishing a book, and having a career as a motivational speaker. Similarly to Sam Berns she found ways to accomplish her goals and has become a college graduate, published three books, and has a career as a motivational speaker. Similarly to Sam she wished to share her story with others and that “[t]o be able to connect with people around the world who are touched by my story and now feel confident to stand up for themselves makes me feel like I'm living out my purpose” (Zaslow). On a final note, Sam Berns and Lizzie Velasquez are truly brave for being able to embrace who they are and use it to inspire others to do the same. Sam Berns later died from complication of Progeria. His legacy will continue to live on through the people he has touched. Lizzie Velasquez continues share her story and inspire others to be themselves. Even though they have many differences the two figures are also drastically
Epigenetics is the word that is used for genes that are modified in order to assist certain genome sequences that lead to diseases and disorders. Epigenetics has come a long way since the first genome sequence had its draft breakthrough in the year 2000 (NOVA 2012). From depression to cancer, epigenetics has made its way through to provide families with the appropriate knowledge and perhaps medication in order to avoid these diseases and disorders in the future.
Her essay is arranged in such a way that her audience can understand her life - the positives and the negatives. She allows her audience to see both sides of her life, both the harsh realities that she must suffer as well as her average day-to-day life. According to Nancy, multiple sclerosis “...has opened and enriched my life enormously. This sense that my fragility and need must be mirrored in others, that in search for and shaping a stable core in a life wrenched by change and loss, change and loss, I must recognize the same process, under individual conditions, in the lives around me. I do not deprecate such knowledge” (Mairs, 37). Mairs big claim is that she has accepted herself and her condition for what is it, yet she refuses to allow her condition to define her. Through her particular diction, tone, satire, and rhetorical elements, Mairs paints a picture of her life and shows how being a cripple has not prevent her from living her life. She is not embarrassed nor ashamed of what she is, and accepts her condition by making the most of it and wearing the title with
feelings towards life. Also they were recognized as a good impact on life because of their stories
Dan and Betsy go through their emotions on hearing about Samuel condition of cerebral palsy. The roll coaster of emotion they felt. As a parent I could relate to their emotion of having a child with disabilities. I would love my child regards of condition but the emotion I would feel would be fear. Dan and Betsy both went through fear; asking themselves what about his education, and interaction with others. I would have those same question; as
Hazel Grace, is a teenage girl who unfortunately suffers several of the cruelties of life, yet she is shining symbol of hope. Even though since she got diagnosed she quit school, her friends don’t exactly treat her like the girl she used to be she is as smart as can be, and kind at the same time. She has stayed alive lo...
Before starting this research paper my only awareness of Progeria was having seen pictures of children with this disease and briefly discussing it in my Biology class. After studying Progeria in depth, I not only know more, but also have a greater admiration of the strength and optimism in the families and children with Progeria. Additionally, I have realized how much I have taken for granted such as health, a long life, and ability to participate in activities easily. After learning about Progeria and Sam’s life, I realize how important it is for us to focus on how much we have instead of what we don’t have and live our life to the fullest.
This writing piece will be explaining the differences and the similarities of Morrie Schwartz and Randy Pausch. They have a lot of differences but their are a fair number of similarities between the two and that is what I will be dissecting in this essay. The background about Morrie and Randy are in a way similar to each other. They both have a disease that gives them a time-table to live.
The struggles both characters face demonstrate character development and contribute to the themes of the stories. Both short stories prove to be literally effective in that they disclose the main themes at the outset of each story. Although the themes may alter over the course of the stories, they are clearly defined in their respective introductions.
One of the main qualities that both these heroes had was courage. The reason for this is that there were many bad things that happened in their lives, and even though it was scary they push forward. Courage is one of the main qualities that people say when asked “What is a quality that a hero should possess?” We all what to be courageous, and when we see a “hero” being that, it makes us believe that we can be too. That is another good thing heroes do; they inspire us to, be courageous, to help somebody, or to not give up. "You blaze the trail. And sometimes that involves doing something that scares the heck out of you." (http://www.theglobeandmail.com/life/liz-murray-shares-her-tale-of-life-from-homeless-to-harvard/article1314532/) That is a quote by Liz Murray that inspires us to try something new and be courageous.
Outside of literature, within the electrifying and humming buzz of a swirling society, such results of perseverance can also be viewed through the extraordinary stories of everyday people. Such examples of figures like these include Nick Vujicic. Nick Vujicic lives a life that resembles everyone else, eating, sleeping, playing and anything else in between. However he is severely limited by a severe disability, known as tetra-amelia syndrome, being born without limbs. Instead of shriveling up and lying defeated and limited by his rare condition, Nick has instead chosen a path of wondrous results and adventurous expeditions. Optimistically pursuing new and breathtaking activities, Nick has enjoyed a life bubbling with boisterous and amusing hobbies including swimming, running, and other activities enjoyed by the ordinary public. Providing inspiration and hope to others who may suffer from the condition he has, Nick has spoke up about his syndrome and gave motivation and words of perseverance to those who need it most. By exceeding and experiencing the bounties of life with an open spirit, Nick Vujicic has let his rare condition be merely a tiny obstacle in his bigger path and vision, in which he faces even more barriers and disputes, that with the mindset fueled by
Christina became disabled due to a severe attack of polio, at the young age of two years old. But in spite of this, she never let any of it block her path, and charged right at her goal like a bull. All her life Christina had only wanted to be accepted as a normal person. Now, she got what she wanted.
Ernie Feld and Werner Klemke were both part of world war II and survived the holocaust. In tough situations they never gave up and powered through it until the war was finally over. Although they were the only ones to survive in their family both men saved lives beside their own. Both inspired jewish people by showing them there is always hope and to never give up. They both used their talents to get threw the war and help other people. Now that their stories are out there they show the world what never give up hope really means.
She believes that if we lived in a society where rights were equal, disabilities and genetic defects wouldn’t be seen as a disadvantage. She however believes that is should be the choice of the couple to whether or not they believe they can parent a child with a disease. She mentions that people who ask “what about the suffering” come from positions of privilege and ignorance. She states the assumption that my life has involved suffering is prejudice. She thinks that it should be a personal choice and whatever that choice may be should be respected.
Most individuals are either related to or know someone who is effected by some type of disability. Many of these disabilities are caused by genetic disorders. Genetic disorders may alter physical appearance and cause mild to severe mental retardation. Fragile X syndrome, Down syndrome, Turners syndrome and many other syndromes result from a mutation of a chromosome, an extra chromosome, or too few chromosomes.
It was after this ceremony that a group of students got together to write articles included in this publication. There were many stories submitted of inspiration and hope. Many of them parallel what was shown at the ceremony. Yet the thing which stands out the most is the concept that these are people. They are not the disability but they are the person. It is often forgotten that there is more to see than the disability. The personal struggles and acceptances point out what is really important.