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I still remember the day when my younger brother Anuj was born. He was such a cute, precious baby, sleeping peacefully in my mom’s arm. It was a blissful moment for my family. I was so overjoyed as I couldn’t stop talking to him. I knew I had to wait for a few months until he would talk back to me. Two years went by and I was still waiting for Anuj to talk. The fact that I couldn’t understand why he wouldn’t talk to me or talk to anyone for that matter provoked me. If he wanted food, he would hold my hand, pull me towards the kitchen, and point to the food. If he was happy, he would simply jump and run in circles. If he was sad, he would sit in a corner and cry. He couldn’t express his feelings verbally, the way the siblings of my close friends had expressed theirs. …show more content…
I share responsibility for taking care of my special needs younger brother named Anuj. Teaching Anuj how to speak, taking care of him, participating in his speech and applied behavior analysis therapies, and motivating him to attempt new tasks with his abilities reflected in my personality as a mentor. As a result of prolonged care, love, and the efforts of an army of therapists, teachers, doctors, and our family, Anuj started repeating sounds and words near his third birthday. While this experience may not seem substantial, Anuj’s progress taught me importance of being empathetic and to understand other person from their point of view. I learned to focus on ability instead of disability and how Inclusion promotes a healthy interdependence, which identifies everyone as unique pieces of a larger puzzle. Anuj’s uniqueness taught me what I could never learn at my school. I learned that each of us is unique and we are all pieces of a big puzzle. Understanding other person with their point of view not only help themselves, but also helps the society and relationships through better
I. Theory After reading the voice of Inclusion “From My Friend Ro Vargo” what an intriguing and captivating story. About a young girl who is severely impaired, name Ro Vargo who is diagnosed with (rett syndrome). Defined as “a progressive neurodevelopmental genetic disorder that affects females usually during infancy that is characterized by cognitive and psychomotor deterioration, slowed head and brain growth, stereotyped hand movements, seizures, and mental retardation”www.merriamwebster.com. Ro did not want people to talk about what she had (rett syndrome). To her she’s just an ordinary person. We see through Ro’s eyes as she takes us on her life’s journey. From the beginning of kindergarten through the end of college. Ro parents reveals
“Including Samuel” is a documentary about the complexities of inclusion. Like so many other issues in our lives, the solutions are far from clear. This film explains a kid named Samuel and the family’s efforts to provide an education that involves inclusion for him and his disability. He was diagnosed with cerebral palsy at the age of 4. The film then describes other people like Nathaniel and Emily that struggle with inclusion and the difficulties they face on a day to day basis. An analysis of this film shows the filmmakers effective and accurate complexities of inclusion to a full extent.
Lavoie’s workshop provokes an emotional response. After viewing life through the eyes of a child with special needs, I cannot help but have a more significant understanding of what people, especially children with disabilities, must deal with every day, everywhere. During the many years that I have worked with children with various disabilities, I have encountered each of the topics discussed in Lavoie’s workshop and agree with the points he makes regarding children with disabilities. Particularly impacting the way I interact with my students are the topics concerning: anxiety, reading comprehension, and fairness.
Despite the differences we share many similar diversions such as good quality time with our families. Arthur was known to spend countless hours reading and listening to music with his mom. Yet at the age of 6 Arthur had to face one of the most traumatic expierences of his life when he lost his mother, Matti Ashe, to a fatal case of toxemia while in labor. Similar to this experience I lost my grandfather at the age of five. Although I was impacted greatly it was not a loss as great as Arthurs loss of a loving mother. I Can recall the day it happened just as well as Arthur recalled the details of when he last saw his mother.
Including Samuel is a documentary of the son of Dan Habib and Betsy McNamara. Samuel has cerebral palsy, and the documentary is about his challenges and joys. This documentary addresses the concerns, problem, and feelings of his parents. Also the documentary addresses the issue of inclusion and how to teach a blended class. This documentary is about being open minded and understanding of children with disabilities. Though Including Samuel, it has force me to look back on my experience with children with disabilities in the educational system.
Another powerful video, Including Samuel, ignited my insight in this week’s class. As I heard in the video, “inclusion is an easy thing to do poorly.” The movie chronicles the life of a young boy, Samuel, and his family. With the shock of learning about their son’s disability, it caused his parents, Dan and Betsy, to experience the unexpected. Nevertheless, they did everything to include their son and help him live a normal life focused on his capabilities, rather than his incapabilities. I even admired how his friends knew so much about him, his likes and dislikes, his strengths and his weaknesses.
Including Samuel is a film about how inclusion can be difficult, but it is important for these children and their success. This is an issue that people with developmental disabilities deal with on a daily basis, but not everyone knows this until you have seen it first-hand or lived with it. In the film, photojournalist and father, Dan Habib follows his son Samuel around and others with disabilities to show their stories and to help inform the viewers about this little known topic. The film was effective in its efforts to display how inclusion has many complexities, but we need to work at it in order for these children to have a contributing and successful life.
Odom, S. L., Buysee, V., & Soukakou, E. (2011). Inclusion for young children with disability: A
My personal philosophy on special education begins with this firm conviction, I believe all children are “uniquely and wonderfully” made, and regardless of their disability, posse unique gifts and talents. My philosophy of special education has developed, not from just being a general education teacher for many years, and a graduate student in special education, but also from being blessed to be a parent of a special needs child. I believe that every child deserves to have the best possible education, regardless of their disabilities or challenges. It is our responsibility, as special education teachers, to not focus on a student’s disabilities and challenges, but rather focus and develop their personal gifts and talents, in an environment
“The 1% of US students with labels of severe disabilities including mental retardation have been historically excluded from ‘inclusive’ education” (Bentley, 2008, p. 543). Laws such as PL 94-142 and “No Child Left Behind” (as cited in Bentley), say that ‘public school students with all types of disabilities be educated in the least restrictive environment—‘to the maximum extent possible…with children who do not have disabilities’ the majority of these students with special education labels, such as, mental retardation and multiple disabilities are still isolated in special education classrooms (Bentley, 2008, p. 545). Wehmeyer (as cited in Bentley), points out that mere access does not promote authentic participation (Bentley, 2008, p. 546). Burkowski et al (as cited in Webster and Cater), “Friendship has been defined as a bond between two individuals that is stable across time and involves mutual affection, mutual preference and having fun together” (Webster and Carter, 2007, p. 201). It is up to parents, teachers and other paraprofessionals to seek ways to facilitate and encourage the types of positive interactions that will foster these types of friendships. If done successfully all students will benefit and there will be true inclusion.
Previous experience of working in the care industry, with adults with a wide range of needs and disabilities, has given me the experience of working with a diverse range of people. I am currently an administrator for a charity whose service users are adults with learning disabilities. Being caring and compassionate has helped build up a strong relationship with the service users, which in turn has helped me gain their trust. This has helped me to be able to develop a better relationship
I remember the day she born. I was nervous for the simple fact that my life would never be the same. Soon no longer would I be known as just Ayanna, I would take on a new title. A title that I would share with so many woman, and after eight long hours of labor, I would now be known to the world as mommy.
Two of the greatest days of my life were the days my daughters were born. The first time I held the both of them and gazed into their eyes I felt a sense of relief and hope. The feeling is a warm tingling sensation that engulfed my entire body. The emotions that I felt are beyond what words can explain. It’s amazing to me that in the first few minutes of their lives they completely changed my perception of the world.
I remembered one night getting on my knees and asking God to send me a child that will love me unconditionally and that I will love it and that know one could ever take the love that we both shared away. I also, remembered telling God that I would love this child forever, you know God granted me my wish it was on a Thursday evening on August 16, 1979 at 4:20 P.M. that my little angel was born she was a sweet little angel. She was very special my family, she was the first granddaughter, great-granddaughter and the first niece and her father’s first of his two children to witness coming to this world. I remember when she was just a week old I laid her down on her stomach in my bed, she tried to crawl. La Shundra, was very happy and loved baby, she was so special she touch the hearts of everyone that came to know her even when, she was at her worst until the day she died.
Living my life with a brother with disabilities has never been easy. It has been difficult throughout my life watching him grow up and encounter more and more struggles in life because of his disabilities. Our biggest question throughout the years, though, has been what our plan will be for him later in life. How will he live his life as an adult? Will he work? Where will he live? Will he have friends? How happy can he be? People with children with disabilities have to explain, “How do people with disabilities really fit into American society”? It’s not just families discussing this question; experts as well are debating this unknown by looking at the same questions I mentioned before. Looking at where disabled people are living, whether they are working, and the relationships they have with other people are ways to understand how disabled people fit into American society. This topic should not only matter to people close to disabled people, but to everyone. In some way, every one of us is affected by this topic; we want everyone in our family to lead “successful” lives (have a job/have somewhere to live). The same goes for families with people with disabilities.