Children with Disabilities

There is always more than meets the eye when spotlighting different realms. I wanted this paper to meet more than just the standards set by my professor. I wanted to be able to lean towards or away from a career choice. Being able to step outside of my own world into one where I would truly try to understand people with disabilities in their lives was what I had chosen. Spending a day in the Mary Cariola Children’s Center allowed me to do this by interacting with children at various different levels and learning disabilities. I have quite a bit of knowledge on children with special needs but have never truly been able to interact with them further than my cousin who has been confined to a wheelchair (for reasons unknown to any doctor). When a child has a disability it becomes their master status. A master status is one that cuts across each other statuses you hold. Throughout this day I was able to speak and interact directly with three main children.

One of my teachers from high school had a son with autism who I knew was in the Mary Cariola Center. Due to this I was able to set up a day long volunteer/observation experiment. I was explained a breakdown of their day and how these children were here because their families could no longer provide the help necessary to take care of them. I could not imagine being so excited to have a child only to learn you cannot provide for them what they need to live a fulfilling life. I can only imagine what this could possibly feel like being a parent and having to do this. Upon arriving I was taken on a tour of the facility where I was able to see many children in their own familiarity. In the beginning I was told to stay “behind the scenes” let the children slowly discover I was there for themselves. This was so I could first simply observe before interacting and allow the children discover me. For a while none of the students noticed I was there but slowly there were a couple whispers and children wondering who I was. Eventually some children were coming up to me and some still remained doing their own thing. I was able to directly interact with small groups of children by playing games with them.

The first was Sarah a nine year old child who has been with Mary Ciarola since she was 3 years old, when she was diagnosed with cerebral palsy. Cerebral refers to the brain and palsy means the weakness or lack of control in one’s muscles. Luckily Sarah’s case was not extremely severe. This was the first child I was able to come in contact with, she seemed so happy and I couldn’t figure out if it was on the basis of “ignorance is bliss” or if it was her ability to accept and live as any other human being would. It seemed she was well aware of her situation but there were only one to two times I ever witnessed her asking for any sort of help. She strived for independence as much as she could to the point where other employees would have to step in because of her lack of asking for help. Although Sarah was well past the age of needing any sort of diapers, her cerebral palsy had created bladder control problems. It was horrible to see how much one disease affects so much of what you do day to day.

The second child I was able to meet was Matthew. During his developmental period at the age of two, Matthew’s parents began to notice his problems with communication and interactions with other children. Off the bat I was able to notice Matthew did not want the same amount of affection as the other children seemed to starve for. I later learned this was simply another symptom caused by autism. It was hard to truly hold a conversation with Matt because he would constantly tune out as if he went into “his own world.” To me I believe the art of conversation is one of the most important things this life has to offer, so this was in fact enormously frustrating. My personal opinion is that expressing yourself is extremely significant and important throughout life. We must all try to understand each other and each individual situation without bias. Matthew as any other child has much to say but his ability to process these thoughts and release them are not the same as other children.

There are different levels of mental retardation varying in severity. Rebecca was considered to luckily have a mild case of mental retardation. She was 14 years old and quite honestly a joy to be around. Surprisingly her social skills as she spoke to me seemed to be right on track, one would not even be aware of her mental retardation unless they truly put her to the test. When it actually was time to do an activity that needed step by step concentration, Sarah was given what any 14 year old would consider simple, and struggled excessively. She acted out in what I later learned what embarrassment in front of someone she didn’t know (me) because she could not solve the task given to her. Occasionally, there were