On July 24, 2006, my twin siblings, Audrey and Austin, were born. My parents sat my sister and I down and told us the babies were fine but Austin was going to be a little bit different. They said he has Down syndrome but we will love him just the same. It’s not going change the fact that he is our brother and a very important part of our family. I was so young at the time and the weight of this information hadn’t clicked yet, all that mattered was finally being able to hold my brother and sister after nine months of waiting. Over the last 10 years I have grown to understand Down syndrome and other disabilities in a different light, seeing how many people, despite their disability live productive and successful lives. I find so much …show more content…
What I find most fascinating about occupational therapy is that therapists strive to improve the lives of individuals by working on activities and skills that will benefit the clients in their everyday lives. It is not simply the treatment of a specific injury or certain part of the body; it aims to help individuals live more independent and fulfilling lives.
Throughout my time in college I have had the opportunity to participate in things that allowed me to use my passions while simultaneously growing me as a person. In 2015, I was selected by my peers to be the Vice President of Philanthropy of my sorority, Pi Beta Phi. During my time in office, I was able to grow in my leadership, communication and delegation skills through planning our annual 5K run benefitting children’s literacy. This event raised over
$39,000 and the money came back to the Northwest Arkansas community to provide books and resources to help with literacy programs in local elementary schools. One in four children in
America grow up to be illiterate and I am honored to be a part of an organization working to change that statistic by showing these kids the importance of literacy. I also had the chance to collaborate with The Miracle League of Northwest Arkansas to provide volunteer opportunities for the members of my sorority. Miracle league is a baseball league for kids with special needs in which volunteers are paired with a child and help them play baseball. The league gives them
I am a member of my high school’s student council, Girl Scouts, and also the chaplain of my school’s drama club.
An accomplishment or event that marked my transition from childhood to adulthood was being accepted to the Alpha Kappa Alpha Debutante Cotillion. The Alpha Kappa Alpha Debutante Cotillion is a six month program for ladies that are juniors or seniors in high school in order to equip and stimulate them to pursue higher education, academic excellence, and personal development. While doing the program, thirty-four other girls and I attend educational workshops, activities, community service outings, and rehearsals. At the end of the six months, the members of the program attend an elegant ball where we are presented to the community and awarded a scholarship.
Once faced with the fact you have a Down Syndrome baby however, the baby will
Due to advances in medical technology, individuals with Down syndrome are living longer than ever before. In 1910, children with Down syndrome were expected to survive to age nine. With the discovery of antibiotics, the average survival age increased to 19 or 20. Now, with recent advancements in clinical treatment, most particularly corrective heart surgeries, as many
As a sophomore now I often look back on how I got here. Aside from the apparent support of loving family and friends, other factors aided in the progression of me becoming a growing leader and overall an adult. In middle school and high school my roles in student council, girl scouts, captain on several sports teams and even management holding a job too have shaped me. My more recent influences are linked directly to my decision to join a sorority last year at West Chester University, that sorority being Zeta Tau Alpha.
For the purpose of this assignment, this section of the paper will critically reflect and analyze the portrayal of people with Down Syndrome in mass media. I chose to specifically evaluate CBC New’s portrayal because it is one of our greatest sources of news in British Columbia. This section will look into several of CBC’s most recent news stories that are about people with down syndrome and the adversity they face. We will see that there is a common trend towards advocating for these people as well as trying to rid Down Syndrome from being seen as a disability.
what’s our goal today? To provide for more people and make sure that they do not have
The day came when I would know for sure that I was getting a baby sister. My parents
With today’s technological advances people should look up a web site, www.ndss.org, specifically for information on people with Down syndrome. In today’s societies a person with Down syndrome still fall into common misconception about who or why they were born Down syndrome. Common misconceptions for a person with Down syndrome consists of them being contagious, they have three of every chromosome, and the umbilical cord wraps around their neck while in the womb. Everyone should mark their calendars for March twenty-first, national world Down syndrome
“According to the Centers for Disease Control and Prevention, one in 700 babies within the United States is born with Down syndrome. This makes Down syndrome the most common chromosomal condition, and about 6,000 babies with Down syndrome are born in the United States each year. In 1866 down syndrome was described as a disorder but there was no evidence on what caused it. Later in 1959 it was discovered that down syndrome was a genetic disorder that it was mostly known for delays in cognitive development. Down syndrome can lead to mild or moderate learning disabilities, unique facial characteristics, and low muscle tone in infancy.” Although here is no cure for Down syndrome the way we can help is by giving them the education and proper care so that they will have endless opportunities.
Carla, my aunt, is a 40-year-old woman that at the age of 36 found out that her baby was going to be born with Down Syndrome. Taking care of my little cousin hasn’t been easy for her. She had to learn how to properly shower the baby, had to carry the stroller to every place she went, she had to get used to the idea that her baby won’t be able to walk. Carla as the grandparents in the article say that they wouldn’t change the opportunity to something that beautiful. She as them said that the experience is very enjoyable and that she loves her daughter more than anything in the whole world. We all know that living with a disable child would cause a big change in everyone’s life. My aunt has told me that this unique experience has affect her family in such a positive way just like it says in the article, “Grandparents described an overwhelming drive to play a positive role in their family's and grandchild's life, obtaining much joy and satisfaction from the grandparent.” Both the article and my aunt have shown me the importance of loving and caring for a disable
‘’Down syndrome is a type of mental retardation caused by extra genetic material in chromosome 21’’ (8), Down syndrome can cause a number of medical complications (6). Some of these complications are more serious than others, but most of them can be treated (6). Although Down Syndrome patients do not live for a long time, but their short life span is challenged with many critical problems. The life expectancy of people with Down syndrome increased dramatically between 1960 and 2007 and in 1960, on average, persons with Down syndrome lived to be about 10 years old; however, in 2007, on average, persons with Down syndrome lived to be about 47 years old (7). Furthermore, Down syndrome affects the patients life mentally, socially, and physically.
When you see a person with Down syndrome you are typically able to identify them easily by characteristics such as flat facial features, an upward slant to the eyes, or a single deep crease across the center of the palm. However, there is one thing that may be harder to guess in a person with Down syndrome, and that is their age. Individuals with this condition tend to age faster than an individual without the condition. The median age for an individual with Down syndrome is now 60 years compared to a previous 25 to 30 years; this could be from advancing health care and more community involvement (Family Caregiving of Aging Adults with Down Syndrome). With this increasing age it is important that research be done on improving lifestyle and care for the older adult with Down syndrome.
Down syndrome (DS) is relatively well known as a genetic disorder to the general public and children
People all over the world are diagnosed with a terrible disease called Down Syndrome. It was discovered by a british physician who was known as Dr. Langdon Down back in 1866 in Britain. This disease causes children to be born with physical and mental abnormalities. With so many children having this disease parents wonder what they have done to cause this curse, but it isn’t their fault. It is simply a random error in cell division which causes an extra copy of chromosome 21. It is mostly inherited at a very young age if not in the womb or after birth. There is no specific treatment for this disease. The only diagnosis for this disease is therapy and help throughout these people's’ everyday lives.