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On July 19, 2004, my baby sister, Kadie Parks Allison, was born. She had blue eyes, like the color of the sky, and red hair, like the color of a strawberry. Her skin was like a porcelain baby doll. She was a very beautiful baby, and everyone instantly fell in love. My parents quickly realized that Kadie was not a happy baby. Kadie would cry constantly, and my parents had a hard time figuring out why. She cried even harder when she was put into a car seat like someone was stabbing her. My parents decided to take her to a children’s hospital in Memphis, TN, where she was finally diagnosed. Kadie went two years in pain before the doctors finally diagnosed her with Spina Bifida in 2006. Spina Bifida is a defect in the spine and spinal cord, where a part of the backbone is exposed. It can cause paralysis in the lower limbs and sometimes a mental handicap. This is what happened to Kadie. …show more content…
My mom was so scared and would constantly say “Back surgery at only two years old, really?”. My parents were terrified for Kadie. They arrived the day before surgery and got specific orders not to let Kadie eat at all the night before. My parents decided to let kadie have a little fun before this major surgery, and took her to a small playground in the hospital. While they were there, a little girl gave Kadie a bag full of Cheetos. My parents didn’t see the bag of Cheetos until it was too late. Kadie smiled and had a bright orange Cheetos stain around her mouth. The doctors then had to reschedule the surgery to the next day. The bag of Cheetos is now framed, and hanging in the living
boy she has given birth to. The unique little boy with blond hair and blue eyes
Her face is smooth, calculated, and precision-made, like an expensive baby doll, skin like flesh- colored enamel, blend of white and cream and baby-blue eyes, small nose, pink little nostrils-everything working together except the color on her lips and fingernails, and the size of her bosom.
I was in the fourth grade crying and waiting for her, hoping she would be okay. All I remember is being so scared for her, fearing that I might have to grow up without a mother. She came out of surgery and was perfectly fine. She was left with an ileostomy bag, which is a bag attached to the small intestine on the lower right quadrant of the abdomen. That was one of the coolest things I have ever gotten to witness. Who else can say they have seen their mom’s small intestine? She went back to the hospital six months later and had it repaired on January 26th, 2009. She is perfectly healthy now and I thank the Lord every day for
Spina bifida is caused by the failure of the back bones to form over the back of the spinal cord, leaving the nerve unprotected. (Neural
The overall objective for our proposed project is to expand the partnership between the Spina Bifida Coalition and the Spina Bifida Clinic at CCHMC in determining how best to assist our young adults affected by spina bifida (aged 17+) as they begin their transition journey to independence. While we have worked together on other projects in the past, there has been changes in personnel at both organizations and we wish to improve our partnership by collaboratively working to determine and assess the need to develop and pilot a program that will assist our young adults in transition to adult life.
I had just finished facing my fears watching the metallic needle slip so seamlessly under my skin into the veins of my nervous, clammy hand. Hugging my Mom like it could have been the last time I saw her, seeing my dad's face stern and worried. I wheeled down the hall into this operating room, white was all I saw, a bed in the middle for the surgery to go down. As I lay on the bed waiting to be put under I remember seeing the blue masks of the people to be operating on me, I had to put all my trust in them, trusting someone you seen for less than 5 seconds with your life. Absolutely terrifying. The nurse slipping the fluid into my IV as I lay on my back looking up at the white ceiling, this cold sensations rushed over me. Then suddenly, I was out.
Ashley had a normal birth, but her mental and motor faculties did not develop (“The Ashley Treatment,” 2007).
A Few months later she announced she was having a baby girl named zahna. Zahna is my niece she’s 2 years old and was born on 9-1-14 When someone first meets her she gives Them a big huG she's about 2 feet tall and weighs about 25 pounds she has eye the color of a stormy night she usually wears shorts and short sleeve tee shirts her hairs a brownish blond her favorite food is Broccoli drink is Milk color Pink and purple harry the Bunny her favorite possession is her baby doll named Bay bay.
A spinal cord injury can be serious and it can result in permanent disabilities. Immediate medical treatment is necessary to minimize the damage. If you are injured in a personal injury accident, always seek medical treatment even if you believe your injuries are not severe. Even a minor spinal cord injury can keep you from returning to work and resuming your normal daily activities.
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.
February 13th, 1979, Janae and I were born in Sunrise Hospital, four minutes apart, to two anxious, ecstatic, and not to mention exhausted parents. Immediately following the birth, the doctor glanced up at my mother and father and announced that they were the proud parents of identical twin girls. My sister Janae was born first weighing a mere four pounds 11 ounces and I swiftly followed, weighing a hefty seven pounds zero ounces (very large for the average twin). The doctor proceeded to tell my mother that identical twins automatically have a special bond that exists between them, and that she was to enjoy the many fun, challenging, yet exciting experiences to come. One of the most challenging experiences to come would be the dreadful day when the two of us would realize that we couldn't be together always. That memorable day we slept together, side by side, in our rectangular clear plastic hospital beds -- determined to be inseparable for the remainder of our lives.
cerebral palsy. Though she is not in pain, she was born, and she is loved. No matter if she wasn’t
At the time, my wife Jeanne was pregnant with our soon-to-be daughter Tahlyn. We had waited eight long months for her to arrive, and finally her due date was getting closer and closer. The excitement grew stronger as the days went by.
In 2004 McAdam et al considered pica in people with developmental disabilities , and ways to deal with this. The authors were aware that the eating of non-food items is common in those with developmental disabilities, and aware also of the dangers involved. They specifically mention damage to the gastro-intestinal tract, by blocking it, or even puncturing or tearing it. In some case the form pica takes is to eat dirt and this could result in infestation by parasites. The researchers felt that pica could interfere with a person’s quality of life, as well as their learning and ability to carry out tasks.
A family friend, Rose Widmer, came over as my mom and dad were getting ready to leave. She would be staying with us because it looked like they would not be coming home that night. As Kelly and I were eating our supper, my mom came into the kitchen and sat down beside me. She explained to us that our dad was very sick, and that he was having trouble with his brain. She used the term "brain abscess." She said that this is what the doctors speculated was wrong with him, but they needed to go to Fort Wayne to take precautions.