The Effects Of Polio On His Body

In this book he clearly portrayed polio from different perspective, He narrated stories of different researchers he mined their

In Nancy Mairs’ article for The New York Times, “Disability”, published in 1987, she expresses her distaste with the media's representation of handicapped people. Mairs, who struggled with multiple sclerosis herself, clearly and sharply conveys this disgust by stating, “I’m not, for instance, Ms. MS, a walking, talking embodiment of a chronic incurable degenerative disease.” (Mairs 13), and that she is actually, “the advertisers’ dream: Ms. Great American Consumer. And yet the advertisers, who determine nowadays who will get represented publicly and who will not, deny the existence of me and my kind absolutely”(Mairs 14). Mairs is greatly upset that disabled people are defined by their disabilities and, therefore, are underrepresented in public media. This might lead to one asking themselves, but why are they? And the answer, according to Mairs, is quite simple, “To depict disabled people in the ordinary activities of daily life is to admit that there is something ordinary about disability itself, that it may enter anybody’s life”(Mairs 14). Mairs concludes by pointing out how this effacement could have dangerous consequences for both disabled people and, as she called everyone else, TAPs (Temporarily Abled Persons) alike. Treating disabilities as an abnormal characteristic (as opposed to viewing them “as a normal characteristic, one that complicates but does not ruin human existence” (Mairs 15)) can cause one of these repercussions, as it makes the

Unspeakable Conversations by Harriet McBryde Johnson is an article about her experience visiting Princeton University to exchange views and challenge Peter Singer, a professor who strongly believes that all disabled people, like herself, are “better off” not been born at all. The article provides an insight into Johnson’s life as a disabled person. She takes the readers on a journey that explores both sides of her own and Singer’s contrasting beliefs. She protests the prevalent stigma and prejudice of disabled people and gives voice to this marginalized community. Johnson challenges stereotypes of disability, uses her a personal experience to better understand the world and help others, and attempts to directly address oppression by arguing against Professor Singer’s theory and assemble a group of diverse and like-minded people for social change.

Lost in a Desert World relays the story of the life of Roland Johnson, a man born with an intellectual disability and placed in an institution who eventually went on to be the president of Speaking for Ourselves, a group that encourages those with disabilities to stand up for themselves and their rights. This memoir offers a rare first-person, nonfiction account of the life and experiences of someone with an intellectual disability. Though filled with the harsh realities of the treatment of those with intellectual disabilities, the book is also one of passion, strength, and hope.

People with disabilities are not completely gone. They are still there and have a mind of their own. They feel emotions and sometimes have a more complex mind than others. Two authors help enlighten this idea that disabled people are much more than helpless bodies. Both Christy Brown and Jean-Dominique Bauby perfectly illustrate their lives and what it is like to be disabled, and they prove by their stories that they think and feel, and can even develop enough to share what they feel with the world. My Left Foot is about the journey of a boy suffering from cerebral palsy. His entire life he was labeled as a loss cause by doctor after doctor, but his mom never gave up hope. Slowly, he started showing signs of development by random movements responding to certain situations. In the end he ends up being able to communicate with his left foot. The next story, The Diving Bell and the Butterfly, is about an individual who suffered a stroke at the age of 43, leaving him paralyzed, only able to blink his left eye as communication. He develops his own alphabet inspired by the French language in order to exchange conversations with others. His thoughts in the story jump from the present, him currently disabled, and the past, when he was not. Both memoirs, with very different stories, show the lives of two individuals that are not like others. One who had their disability since birth, and the other who obtained one after a tragic event. In My Left Foot by Christy Brown and The Diving Bell and the Butterfly by Jean-Dominique Bauby, both authors use characterization to show readers the struggles of disabled people and help them understand that just because they can’t use motions such as hand gestures to express how they feel, doesn’t mean that they don’t think and feel.

Everyone has their own way of achieving victory: scoring the winning point in a sport, getting chosen for a job or acing a test in school. A writer for Sport Illustrated's, Rick Reilly, tells Ben Comen’s story, a teenager with cerebral palsy who runs for his high school’s cross-country team, in his article “Worth the Wait.” In the article, Reilly informs the audience of the previously mentioned situation that Ben is in, while also mentioning Ben’s process of overcoming all odds and managing to finish the races with the entire crowd cheering him on. Reilly establishes a triumphant tone with the aid of pathos and arduous-like diction to make light of people with cerebral palsy and to show how they can accomplish goals in life like everyone else

Heather Green Wooten’s The Polio Years in Texas: Battling a Terrifying Unknown chronicles the history of polio in Texas in a very extensive timeline. The book goes all the way back to the beginning of the polio epidemic and essentially progresses to the present. The time in this book certainly exceeds that of, The Captured and Isaac’s Storm. The Captured chronicled a long period of captivity, but did not appear to exceed a decade. Isaac’s Storm traced the initial development of Weather Bureau and covered a great period, but did not exceed that of The Polio Years. Several themes begin to emerge further into the book. Obvious themes included, the support for March of Dimes, impact on families affected by polio, the growth and development of rehabilitation facilities, and more importantly the response to the disease by Texans. Oddly, Wooten discusses the fact that other diseases such as, measles, diphtheria, and tuberculosis took more lives than Polio. However, people feared Polio more than the rest. Wooten attributes polio’s terrifying affect to the uncertainty. Several uncertainties such as, how to prevent it, why did some become crippled, why did some die, and why did it only essentially affected children made polio very terrifying in the 20th century. Texas appeared to have been hit the hardest in comparison to other states. Wooten’s research examined the time during and then after World War II. During this period, Texas saw an immense amount of polio contractions. Per

Poliomyelitis (polio) is a disease that attacks the nervous tissue in the spinal cord and the brain stem resulting in paralysis (Document One). Polio is caused by the poliovirus, but it is unknown how this virus is acquired. The virus enters the digestive tract and stays in the intestines for up to eight weeks, and then attacks the lymphatic system, the blood stream and eventually travels to the brain and spine (Document Four). Once it is infected in one’s body, the disease is highly contagious and can be spread through contact of saliva, food, germs, or feces (Document Two). “The poliovirus causes most of its infections in the summer and fall. At one time, summer epidemics of polio were common and greatly feared” (Document Four). This may

Disabilities within the characters of “The Life You Save May be Your Own” by Flanner O’Connor

David Oshinsky's 2005 Polio: An American Story, is a history of the fight to eradicate polio in the 20th century. Polio became one of the most, if not THE most, feared diseases of the century due to the influence and example of President Franklin Roosevelt, who was stricken with the disease as an adult in 1921. Owner of a Warm Springs, GA resort dedicated to polio rehabilitation(where he died in 1945), Roosevelt needed to raise funds to keep the resort operational. In 1934, he allowed planners to throw a nationwide series of birthday parties (over 6,000) for him to raise money for the care of polio survivors and for the upkeep of Warm Springs. The success of these parties and recognition that the key to raising money during the Great Depression

“The only thing to fear is fear itself,” Franklin D. Roosevelt once said (“Franklin D. Roosevelt”). Polio is a virus that is usually harmless and unnoticeable, but sometimes can be very severe and deadly. Polio was very common at one point in time but current day is becoming very rare. Franklin D. Roosevelt, otherwise known as FDR, was inspirational due to he never gave up and made himself believe that his paralysis in his legs was not permanent. Franklin D. Roosevelt had polio and was determined to get a cure to help himself and others who also had polio.

What is Polio? Poliomyelitis, commonly referred to as Polio, is an incapacitating and potentially fatal, infectious virus. Although it is rare to see someone suffering from the disease, in some countries, such as Nigeria, Pakistan, and Afghanistan, the virus still exists. (Kids Health 1) Before the first vaccine was created, Polio was a threat to all Americans across the nation. The dangerous virus attacked people from all age ranges and left permanent damage on all of its victims. Luckily, at the peak of its devastation, a man named Jonas Salk created a vaccine against this catastrophic virus. This vaccine not only marked the downfall of Polio in the United States, but in a majority of nations throughout the world as well.

“A 1916 Polio epidemic in the United States killed 6,000 people and paralyzed 27,000 more” (“Polio Vaccine”). This lead to the creation of the polio vaccine that has helped to prevent polio for a very long time. The IPV and OPV vaccines played a huge role in all of this. Jonas Salk, who created the IPV vaccine and Albert Sabin, who created the OPV vaccine saved millions of people all around the world from polio (Petersen, Jennifer B). The IPV and OPV polio vaccine helped eliminate polio from the United States and helped prevent polio in other parts of the world (“Polio Vaccine”).

Exercises are beneficial to the general well-being of patients who have post-polio. The exercises implemented should not involve the overuse of muscles and should result in the patient feeling some some of improvement. Although not every single patient will feel the benefits of the exercises as seen with one of the participants in Einarsson and Grimby's study (Agre, n.d.) it a solution to the symptoms such as muscle weakness. Until a pharmaceutical cure can be found exercises can definitely help a patient manage their symptoms. As a reader, further knowledge and information about this condition is available, and can be readily accessed due to technology. The immediate cure and different treatments for the management and prevention of this

The similarity between the poliovirus and already solved plant virus’s led to a better understanding of how the poliovirus can regenerate within a host. Although the virus was similar to other plant viruses. The poliovirus was covered with more elaborate loops that are the site of monoclonal antibody escape mutations (Hogle, Chow and 229: 1358-1365Filman, Science). Individual proteins of the virus particle are produced by proteolytic cleavages from a larger precursor, yet the amino and carboxy-termini produced by proteolysis are very distinct. By noting this, Hogle and his team were able to conclude that proteolysis was not just making a lot of proteins from one gene, it is also controlling the timing of assembly (Hogle, Chow and Filman, Science 229: 1358-1365).