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difficulties in raising a disabled child
difficulties in raising a disabled child
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When Andy was born I was the happiest woman on Earth. When I saw his beautiful face and his tiny body I cried, I will never forget that moment. We stayed in the hospital for three days. That first night back from the hospital Andy didn’t do anything but cry all night long. I did not know what to do, this was my first child, and I didn’t know how to calm him down. I called the Doctor and he explained to me that this was the normal behavior for a first born child, and he just needed to adjust to the new environment. I would give Andy his milk, change his diaper, hold him, sing to him, but nothing would stop Andy’s crying. We didn’t much sleep. That week my husband had to work so I had to deal with Andy by myself, which was frustrating. Finally after about a week Andy gave up some. His dad couldn’t even get close to him because he would start crying again, because Andy couldn’t be held or fed by anyone but me. I had to spend every minute of the day with him to the point that I had to put a mattress in his room so I could get some sleep. I slept in his room for a whole year. There weren’t a lot of changes in Andy’s behavior during that year. The Doctor didn’t know what was wrong with him, and I didn’t know what I was going to do.
Taking care of Andy was a full time job for me. Ever since Andy was born my whole life style changed. My husband, Jack, started working long hours because he didn’t want to stay at home and deal with Andy. I couldn’t go out by myself or with my friends anymore. I had to take Andy with me everywhere I went. Basically, I didn’t have a social life anymore. My relationship with my husband was also going down the drain because we never spent any quality time together. My whole life was a big mess at that
Cabarcas 2 point, but whenever I saw Andy’s face he made my heart smile.
Andy was a year old and he didn’t talk much I got worried, but the Doctor told me to wait a few more months because boy’s take a little bit longer than girls to start talking, so I did. In despite of all the frustration and despair I always showed Andy a lot of love. My husband also realized that he was being selfish by leaving all the responsibility to me. He took some responsibility upon himself to take care of Andy so he could get closer to him. Andy was very aggressive sometimes and whenever his dad tried to touch him, he would get away from his dad and start run...
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...ee and a half years. In the near future I want Andy to go to a specialized school for where he could learned more that what he already now until now.
THE END
I chose this disability because I have a friend who has an autistic child and I babysit for her sometimes. This child is a wonderful child I baby-sit him and his sister and the are so cute together I really love these kids. I don’t charge their mom any money to take care of them; I just like to spend time with them. Al l this kid likes is to go outside and play, and when he’s tired he just comes to me, takes my hand and shows me what he wants. He is talking a lot more now that what he did a year ago. He is a child that I admire because he has come such a long way and has overcome many obstacles. I really liked writing this
Cabarcas 5 paper because I never put my self in that situation and it isn’t easy at all to deal with a disable child everyday of your life. That is a challenge that I don’t know if I’m ready to take. I was afraid to write this paper at the beginning because I was afraid that this could happen to me, but I leave everything in the hands of God. I say this because I’m pregnant now and anything could happen.
The experience changed her life, she learned to rethink her own attitude and self determination. I learned that people with mental retardation are not to be separated from society or even treated with less respect because of their disability. “Riding the Bus with My Sister” taught me to never neglect people with mental disabilities. Readers learned that people with mental retardation, just like everyone else, have families, desires, and determination. They cry, they laugh, they have emotions just like the rest of us. We can learn new things from those suffering from mental retardation. ‘Riding the Bus with My Sister” taught me that civil rights apply to
had turned 8 months. My father’s words and the experience of having a child has made my life better than I ever thought it would be. Before, I was working every day; passing off time with family just to get a paycheck. Now, I just want to be there. I want to experience everything with my son. Not like my father who only seen his children an hour a night, and regretted the time he missed out in his family . I resigned from my job and enrolled in school. I was bound and determined to get a job where I can be a part of my child’s life rather than just be the provider and miss out on what life really is. Time feels like it’s passing at breakneck speeds, and if you blink it’ll pass by without a second thought. I live life day by day and make sure to be happy and full of love. Life is too short to waste it . I’ve learned a powerful lesson from my father: Work to live the way you want, but do not live to work. Family all ways comes
I have experienced firsthand the trials of a teenager living with a disability. Life is difficult, but I’ve learned if you stay positive and make good choices, things will invariably get better. I also plan to be a counselor each summer at the Youth Rally camp for those with bowel and/or bladder disorders, teaching them the importance of doing what they love and not letting their disability hold them
I have accomplished many things that people would always doubt of especially attending college which requires a higher academic standard. But, I’m here to inspire others with autism that God is in control and our faith is what unites us.” He has dedicated his life to spreading his message through churches and on social media informing others that there is hope. Everyone can relate to the question since we all face challenges throughout life that others wouldn’t understand. In the eyes of God, Rudy is an average person who is a disable person, but it didn’t stop him from attending college. Also, Rudy explains that “Autism defines me and he understands others who have experience and related to them.” On numerous occasions, I asked my brother if he would wish wasn’t born with a disability but always replied with no. Personally, I would have never wanted my brother to be born with autism since he has experienced many difficulties in
What comes into one’s mind when they are asked to consider physical disabilities? Pity and embarrassment, or hope and encouragement? Perhaps a mix between the two contrasting emotions? The average, able-bodied person must have a different perspective than a handicapped person, on the quality of life of a physically disabled person. Nancy Mairs, Andre Dubus, and Harriet McBryde Johnson are three authors who shared their experiences as physically handicapped adults. Although the three authors wrote different pieces, all three essays demonstrate the frustrations, struggles, contemplations, and triumphs from a disabled person’s point of view and are aimed at a reader with no physical disability.
The number of children with special educational needs and disability (SEND) in England is over 1.2 million with over 230,000 having statements or education, health and care plans, a number which has continued to rise over the years (Department for education, 2016). Described by the department for education (2014, p.7) as “Children and young people with SEN all have learning difficulties or disabilities that make it harder for them to learn…”. Within this assignment I intend to outline the provision made for a SEN child in my attachment, which will be referred to as Child A.
It was August 25, 2006 and I just received the news that I was going to have a baby. At that moment so many thoughts ran through my mind. I was extremely nervous and terr...
Disability is an topic that has produced conflict, and is viewed very differently from either side. For able-bodied people to truly understand what disabled people go through they need to see disabled people more; see their lives. If seeing disabled people more often became reality, they would be viewed as normal more, and it would make interacting easier for both sides. Disabled people have a hard life, but it does not mean it is not worth living. Nancy Mairs, Andre Dubus, and Harriet McBryde Johnson all have physical disabilities, and have written about their experiences and views. In their writings, they touch upon both similar and different points. A very present similarity between the authors is they all play to the same audience. In their messages, both Mairs and Johnson agree that able-bodied people automatically assume that disabled people have a lower quality of life or are unhappy. The strategies used by each author plays to their message, and aids them in getting across their position. Disability isn’t always easy to understand, and these authors help illustrate that.
When I found out I was pregnant I could never have imagined how hard my life was going to be as a teen mom. I remember my dad sitting me down and telling me he respected my decision to keep my daughter, but that I had no idea how hard I just made my life, I don’t think that in that moment I really realized what he meant, but I would soon find out. I was just starting my 11th grade year when my daughter was born so I still had two years of school left. I also had to work so I could take care of my daughter, so trying to do both seemed impossible, at one point my school wanted me to go to school during the day and at night so I could graduate. There was no way I could work and go to school during the day and at night. I had to think long and hard about what I needed to do, my daughter and I needed to be able to survive so I definitely needed my job, so I did
In middle school I was diagnosed with a disability with the way I expressed myself through writing. Ever since, I have gained multiple values and learned several lessons about self confidence. I was taught to push past my limits, in order to be successful in reaching my goals along with my dreams. Today I am a senior in high school who was once thought to struggle, but was able to succeed beyond expectations. To some, a disability may seem like a setback from achieving goals, but to me I used it as a challenge for myself. I accepted myself for who I was and looked at my disability as a unique trait of mine. I was able to provide a message to others that anything you set your mind to is possible with dedication and hard work. It might take
A child with a disability is having someone that has been diagnosed whether at birth, from an illness, or an accident that can leave a person with a disability. Sometime a person may not be diagnosed until years later. This disability which will not allow a person to function on a regular day to day basis. Therefore, someone has to take on that responsibility to assist that child to make sure they are taken care of. A child can be born with multiple disabilities and this is only to name a few: Down’s Syndrome, Autism, Attention Deficit/Hyperactivity Disorder(ADHD), Mental Retardation. Each disability can be different. Some can be more severe than others. they can come from different cultures and financial status. Even as a person grows older a disability can occur.
On many occasions teachers have asked, "Is the volume high enough for you?" while my class watches a television documentary. Many teachers in middle school imposed strict rules about where in the classroom I could sit. I've had coaches ask if I know sign language. And during my elementary years, the school insisted I meet with a learning specialist once a week to discuss my "feelings" about being hearing-impaired. All these restrictions were placed on me despite the fact that I was an above-average student and an aggressive athlete.
I was born with a disability. Although I have done intensive physical therapy since I was small and have made significant improvements over the years, I find it difficult to do some things which most people take for granted. Until I was eleven, I needed a aide at school. I could not go shopping by myself, or stay at home alone for more than a few minutes.
Clearly, my brother claims a huge portion of my heart. His importance in my life began even before he was born,though. After more than thirteen years of living with just my mom, dad, and cat, I felt more than ready for this exciting addition to my life. Because I anticipated my brother's birth so much, it was very important to me to be involved. From the time I learned my mother was pregnant, I immersed myself in Baby World. I soaked up information from a myriad of baby books, countless websites, Parent magazine, and the like. I knew what items we would need and accompanied my mother on every shopping trip to get everything from the perfect bib to crib liners and safety locks. We visited at least 15 day-care facilities around our home in anticipation of his fi...
I have always grown up in a more ‘normal’ setting and seeing people with disabilities was something that was rare to me. When I was younger, my thoughts on people with disabilities were that they could only be physically seen, nothing else (mentally, intellectually, etc.). As I reached middle school, I realized how broad the world is and how many ways people were affected by disabilities. Some of them led a more normal life and some have a harder time adjusting. Just seeing and reading how so many are affected and how harder it is for them really opened up my mind and allowed me to have a wider perception of how broad things are in the world.