Friday, April 24, 2015

Clarification

     This week I emailed a Special Ed teacher at a high school. He had told me that I wouldn't be able to visit because I said study in my email. I wanted to clarify what I mean by study. I want to go inside the lives of special needs kids.
   

     I do not what so ever want to study special needs kids. When I think of studying people, I think of experiments with rats in a lab. Testing them trying to see if they can get the cheese in the small corner. Poking them in the brains seeing if they react the same way as human beings. I want to learn about their lives, not study them.

        Special needs children and adults are very important to me. I do not want to harm them by going to see how they live during school. I feel that if you don't have anything to hide in the Special Ed class, what's the harm of letting a high schooler see how they do things in the classroom? Nothing. Nothing is wrong with it. Unless they are hiding something. So, I hope to go to this high school and see the teenagers in their classrooms. Hopefully this clarified concerns about my subject.

Tuesday, April 14, 2015

Princess Ayleen

Today, this sweet little girl, Ayleen, passed away today. She was born with Pfeiffer Syndrome, which is a rare genetic disorder characterized by the premature fusion of bones of the skull. This prevents further growth of the skull and affects the shape of the head and face. She would've turned two years old this year and her brother is three. Three days ago, she stopped breathing, but got rest was better. She has had many surgeries with her nose, head, and heart. RIP little angel.

Emailing and Questioning

For a week I have been emailing a principle about visiting for a day to see how their special education goes through their day. I have yet received a email from them back. It has been very frustrating checking every day with nothing new. I am moving on to a different school hoping for better luck there.
 

On the brighter side, I have had asked parents of their children and have gotten responses. Both parents have a child with a rare disease. I asked them what are some struggles they face everyday with them blessing they have brought to the parents life. My mom also shared my blog page on FaceBook. Many people are interested in talking about their child or have information about someone else.
 

Hopefully this week is a better week with my project. I am going to start talking to more people about their children and hopefully get to spend a day with special education. I can't stress enough how this project is going to help not only me, but hopefully the parents too. Maybe helping them realize some things they never knew about their son,daughter, or friends.

Wednesday, April 8, 2015

What is Life Like for Special Needs and their Family?






If you think your life is hard, imagine the life of a special needs kid, teenager, or adult. They live everyday with a physical/mental illness and they can't do anything about it. I am starting Genius Hour at my school and I am tackling the tough subject of a special needs life. 

Being around and making special needs person smile is a very big part of my life. Every summer I go to a camp for a week and be with them 24/7 taking care of them and having fun with them. I want to go beyond the facts about their lives. Like down syndrome having a very low metabolism and not feeling the sensation of being full. Or autism having different ranges of the disease. 

I want to see how their everyday life is. What they do when they go to school, how they are when they get home, the activities they are invested in, etc.. I want to go to school with them and play out their day. I also want to interview parents of special needs. Asking how hard they can be at times and also what a blessing they are to their lives. Once a week, I'll post on here how the research is going.