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Narrative essay on childbirth
Narrative essay on giving birth
Narrative essay on giving birth
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September 17, 2002, my mom gave birth to Nafia Maire Carter Colson Blackshear.My grandmother named me because my mom was going to name me Aderiyah Yashera. She was happy that I was not born with Down syndrome. But we did have to stay a week after I was born because I had I yellowish pigment to my skin known as Jaundice. Then 2 years later my mom gave birth to my little brother on September 18, 2004, almost born on my second birthday he was also born with Jaundice and has asthma. Then 8 years later my little sister was born on September 13, 2012, she was also born with Jaundice she had it the worst and she also had problems with her head that she could've had surgery on her head but thankfully she grew out of it and is doing better. The crazy
Don’t ask me how I feel, I’m not going to tell you. Talking about it makes it worse. When I explain my pain, I have to think about it. Ignore it; maybe it will go away. I dwell on my fears of what may happen. I don’t want to pass that fear on to you. You don’t see it as I do. It’s not your body; it’s not your life. I don’t tell you because I don’t want you to be afraid for me. I can deal with it. I’ll be OK. I don’t tell you because I know that my words are inadequate. I can’t express what it is, yet I do want you to know (even if you can’t exactly feel it). I want to let you in to my world. I want you to know how different my life is from yours, even though it looks much the same. I’m not scarred or crippled. You can’t pick me out in a crowd. To you, I’m just another classmate, another student, another stranger on the street.
Most of my kindergarten to fourth grade years were spent in Peoria. We were a mixed family; my mother, sister, and I, with Gary Toubeau (stepfather), Tyler (stepbrother), and Michelle (stepsister). Gary had only seen a mixed family, whenever he has to choose between his children or his step children. Tyler abused this and the fact that he was the oldest, usually resulting in Tyler’s way many times. Michelle was different from the other two. Michelle, also known as, “Showie,” would spend more time with her “mixed family members” rather than her “real family.” One day, my mom had enough of Gary’s abusive treatment, when he actually physically touched her (as if he were going to hit her). The divorce ended bitterly, as Gary had found a
The liver plays central role in each of these phases of clotting process, as it synthesizes the majority of coagulation factors and proteins involved in fibrinolysis as well as thrombopoietin., which is responsible for platelet production from megakaryocytes. In cirrhosis, liver is badly get damaged. So the production of coagulation factors and proteins is impaired. Many pathological processes associated with cirrhosis, such as portal hypertension and endothelial dysfunction as well as co-morbid conditions, may also alter the coagulation process. Consequently, patients with liver disease as in cirrhosis, have a disturbed balance of procoagulant and anti- coagulant factors which deviates from the normal coagulation cascade.
Having Down Syndrome is a Horizontal identity. Most Americans view people with Down’s to be disabled and do not thing much past that. But, many people with Down’s see this simply as a part of who they are, just as much as the color of their eyes. To them, it is not a disability, but just a fact of life. Many outsiders do not understand this, which is why the Down’s community is so important. The Down’s community provides those with Down’s acceptance to their identity. While the rest of society rejects and pities them, within their community they can relate with others and be treated equally. Unlike with vertical identities where the parents are automatically insiders, parents must choose to whether or not to support their children’s horizontal identities. Some parents choose not to accept Down’s before the child is born and terminate the pregnancy while others do their best to make sure their child is comfortable in the world. Again, in more recent years, there are movements for society to be more educated and inclusive for those with Down Syndrome, but there is still a long way to go.
Down Syndrome: Critically analyze the effects of Down syndrome on people and the support that is available
Background and objectives: Many liver diseases are accompanied by jaundice. Differentiation of cholestatic from non-cholestatic jaundice is important. Cholestatic jaundice most probably occurs due to a pathological condition and the most frequent causes in early infancy are neonatal hepatitis and biliary atresia in early life. Early diagnosis and treatment of infantile cholestasis can improve prognosis of liver diseases by prevention of the complications of these disorders.
This all happened when I was very little, as soon as I learned how to talk and understand things. At the time, all I knew was that my older brother Tyler had a very bad heart. He would come home with a stethoscope and a cool balloon device which I figured out was used to open up his heart. I remember reading stories about Curious George going to the doctor so Tyler would get used to the fact he was going to have another heart procedure. I mean, I was just five years old. How does a five year old even comprehend what the heart is let alone what’s happening to her brother? So much of this was beyond my comprehension, yet it all seemed so normal. My side of normal was doctor visits, procedures every year in Miami that I couldn’t go to, and seeing a ton of pictures of his procedures! I remember him eating a lot of food to have him gain weight so he could have the procedure. He hated it so much. Even the scar on his chest seems so normal. I don’t even look twice when I see it. Yet if I see another person with a scar, my eyes are drawn to it.
It took several minutes for the doctor to explain the lifelong effects of Down syndrome, and several more for me to translate it all to the patient. In some ways, it seems like birth defects are so common and not well understood that there isn 't much social stigma associated.
Growing up I always knew I was inferior to my older brother. I’m the second and last born and they never let me forget it. It wasn’t until this year that there was an actual name for how I felt I was treated. The second child born is usually the rebellious one and in this case; that’s me.
Sickle cell anemia affects millions of people around the world, with about 70,000 Americans inheriting the disease, and many others carrying the sickle cell trait (Genetics). This disease mostly affects people that have African and Mediterranean roots, mostly because this disease provides protection for people from malaria which kills 3,000 African children daily (Malaria). Malaria is a deadly infectious disease that is transmitted by to humans when mosquitoes sting them (Learn). Sickle cell anemia is the most common blood disorder that is a result of a mutation in the genes causing a mutated form of hemoglobin, the protein that helps red blood cells transport oxygen to the body from the lungs. The mutated form of hemoglobin, hemoglobin S, causes the red blood cells to alter their shape into a fragile crescent or sickle shape, which is the main cause for any negative effects a person with sickle cell anemia might have.
My first patient that I started as student nurse on one of the long Rehab Center was a seventy two year old man who had Clostridium difficile (C.diff), Dementia, Hip replacement, and Obesity. Due to the above sickness he had many complications. I can still remember his face suffering from pain. Because of his lack of ambulation and incontinence, he had developed a very serious pressure ulcer under his sacral area. I went through to the room with my instructor and the instructor introduces me for the patient as his student nurse from Towson University and will taking care of him. However the patient was not happy and he becomes a challenging patient in my first experience day. But I may learned more from that challenging patient for my future experience.
People with down's syndrome are looked down upon. As if they are misfits who do not deserve a second thought. People with down’s syndrome are bullied everyday and excluded just because of who they are. Down’s syndrome is a genetic chromosomal disorder that 6,000 babies are born with every year. It was proven that children with visible disabilities such as down's syndrome, are more likely to be bullied by their peers. In society, people with down's syndrome are rarely even given a chance to show what qualities they uphold as a person. A study conducted in 2012 shows that thirty percent of babies that tested positive for down’s syndrome disorder were aborted. However, people with down’s syndrome are capable of doing anything they set their mind to. They can be whomever they want to be. People with down’s syndrome can be politicians, teachers, graduates, actors, business owners, author, or even an
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
Up until March 5th of 2009, I had been an only child. Many big changes occurred in my life the year prior to the birth of my new brother. My mom became remarried, we moved to a bigger house down the same street, and there was talk of a new baby in the future. The remarriage was a small celebration held at a quaint location on a chilly fall night, a night you would rather be snuggled up on the couch with warm, fuzzy blankets drinking from a mug of hot cocoa. The move was a breeze, as I can just about see the old house through the tall maple trees from the new. I carried whatever I could back and forth, running quickly back down the street to grab more. The excitement of a new house chasing me to and from. Lastly, the talk of a sibling. I wasn’t sure what to think. The thought of a sister excited me, but a brother not so much. I wanted to share my dolls and dress up, not have to play with mud and trucks. Despite my wants, I had a feeling it was going to be a boy. The day of the ultrasound, I made a bet with my step-dad the baby would be a boy. After, I was a dollar richer and a sister of a brother to be. Having to wait a few more months to meet the little guy would be torture, as the anticipation was killing me slowly. I may not have been ready for the changes made and the ones to come, but I took them like a champ.
Heartbroken my parents set up therapy for me and broke the news to my family. My grandparents were in a state of denial and said things like “He’s a good boy!” or “he’s not retarded!” (I realize this is not politically correct but unfortunately those were the words). It was really hard for me; they said that along with my mental illness they said I was very sick with pneumonia. Along with my malfunctions I have a virus. With all this my sister was born adding more drama to the time. Luckily she was made with the correct blue prints. After the sickness was overcame my parents found a woman that would change my life forever. Her name was Monna and she was very experienced with broken machines like me. She came to my house and I feared her (like many other people even my own family). She was calm asking me questions. Most I was unwilling to answer I was too consumed by fear.