TABLE OF CONTENTS: EXECUTIVE SUMMARY 3 INTRODUCTION 5 PROJECT CHARTER 7 SCOPE STATEMENT 10 TIMELINE FOR THE PROJECT 11 COST/BENEFITS ANALYSIS 13 DATA COLLECTION INSTRUMENTS USED 15 STRUCTURE OF THE SYSTEM 16 PROTOTYPE WEBSITE 17 IMPLEMENTATION AND TRAINING PLAN 23 EVALUATION 24 CONCLUSION 25 LESSONS LEARNED…………………………………………………………………..26 WORKS CITED…………………………………………………………………………28 Executive Summary: The goal of this project was to identify, plan and review a project that entitles you to build a website for a profit or nonprofit organization. My project was on sickle cell anemia, a diseases that carries highly among African-Americans and Hispanic descent. Sickle cell is a condition where it has a lower level of red blood cells in a person body. Sickle cell anemia is an inherited, lifelong disease. People who have the disease are born with it. They inherit two genes for sickle hemoglobin one from each parent. We are a small nonprofit organization located in Neptune, New Jersey. We are accepting your help, donations and anything that contributes to the children and their families in need. The web development we are hoping to get a strong feedback and help from our community. Our objectives would be: 1. Help families in need of assistant 2. Give back to our community 3. Help support financially and mentally Keys to success: 1. To raise money for this organization 2. Be a positive role model/ leader 3. Always available to assists Mission: The mission of this website is to inform others the nature of Sickle Cell and the affects it has on a child and their family. I want to help others become familiar with the pain and suffering a child goes through. I want us to become leaders to create an awareness for... ... middle of paper ... .... Sickle Cell Disease Association of America. N.d. Web. . Banner Sickle Cell. N.d. Web. . Sickle Cell Bacelet. N.d. Web. . Sickle Cell Anemia Someone I Love Needs A Cure Pins. N.d. Web. . Dancing with Sickle Cell Anemia. N.d. Web. . Sickle Cell Anemia Wristbands. N.d. Web. . Sickle Cell Awareness Bracelet. N.d. Web. . N.d. Web. . What is Sickle Cell Anemia. N.p., n.d. Web. 15 Sept. 2012. .
This project has helped me in a way to make a decision on how important this upcoming election is to my heritage as a black man and to take full advantage of this opportunity.
...nt of patients with sickle cell anemia. However, the choice of interventions should be done carefully so as to realize the desired outcome otherwise it may not be successful. Key among the innervations listed here, is counseling. This may help the patients to have hope and this may aid in the quick recovery.
1. Sickle Cell Disease is life-threatening and has a risk of of causing depression. In this study I examine the experiences that Sickle Cell patients go through specifically at emergency healthcare facilities to find out if there are any negative stigmatizations surrounding this disease. There may be judgments that are made about these patients from healthcare professionals when they seek drugs for their pain relief that may cause the stigmatization to occur. I will also investigate why individuals that have Sickle Cell Disease experience longer waiting times at emergency healthcare facilities and the lack of control they may have over their care regime.
What is Sickle cell disease? Sickle cell affects a disease; that disease is called which affects the hemoglobin when the red blood cells that send oxygen through the body are killed off and weakened. Sickle cells can be found in every 1 and 1000 African Americans, it is affecting about 70,000 to 80,000 Americans in the United States. Sickle cell is a death threatening disease, and the severity of symptoms can vary from person to person (Sickle cell disease (SCD), 2015). Some people have light conditions, but others can have severe conditions, which, mean they could be hospitalized. Characteristics of this disease are caused by a minimum of low blood cells, which is called anemia.
Having an inherited disease like sickle cell anemia takes a life-long of treatments and preventions of complications that comes with being diagnosed with sickle cell anemia. Many people have lived a long time while dealing with the disease because of the on-going care being provided to keep patients as healthy as possible. Knowing that both male and female have the sickle cell trait can prevent having a child with the sickle cell disease. From the help of the parents, doctors and medicine, sickle cell patients don’t have to deal with the pressure of living with a life threatening disease.
During a short break of solitude from studying, I explored and came across that the environment in which most African Americans reside in has a high occurrence of malaria virus. The malaria virus disease is contagious and when it contaminates someone with sickle cell traits, it cannot survive on the external part of the human body so therefore the individual doesn’t develop the deadly malaria virus. While looking further into our class textbook on Human Genetics 11th Edition by Ricki Lewis, and this issue of sickle-cell among the African Americans, I
Sickle cell anemia is a hereditary disorder that mostly affects people of African ancestry, but also occurs in other ethnic groups, including people who are of Mediterranean and Middle Eastern descent. More than 70,000 Americans have sickle cell anemia. And about 2 million Americans - and one in 12 African Americans - have sickle cell trait (this means they carry one gene for the disease, but do not have the disease itself).
The first funding for sickle cell disease began thirty years ago the federal legislation dealing with sickle cell was accepted. This legislation present notab...
Sickle cell anemia is an inherited disease of red blood cells. Normally red blood cells contain a protein called hemoglobin A, which carries oxygen to all the organs in the body. With sickle cell anemia, however, the body makes a different kind of protein, called hemoglobin S.
Sickle cell anemia is a blood disorder that is inherited from both parents in which the body produces abnormally shaped red blood cells. In sickle cell anemia, the hemoglobin in red blood cells links together; resulting in the red blood cells to become rigid and a C-shaped. These deformed cells block blood and oxygen flow in blood vessels. Sickle cells deteriorate quicker than normal red blood cells, which results in anemia.
Sickle Cell Anemia seems to be one of the hardest conditions to live with due to the severity of its symptoms and it can be an encumbrance to everyday life. Although this condition is hard to live with, it is possible to live with it. Thanks to the twenty-first century advancements, there is great medical care available to patients and many other resources and support groups to help families through this harsh reality of living with sickle cell. Perhaps one day there will be a readily available cure for this horrible disease. Until then, a patient with sickle cell should have a support system and take care to live a healthy life so that they can live their life to the fullest.
"Sickle Cell Research: Symptoms, Diagnosis, Treatment and Recent Developments | NIH MedlinePlus the Magazine." U.S National Library of Medicine. U.S. National Library of Medicine, 2011. Web. 06 Mar. 2014.
Having a wish fulfilled is a desire everyone keeps, but granting one is a special characteristic of a chosen few. Such is the ideology of the Make a wish foundation. This simple, but powerful belief is what drives the Make-A-Wish foundation. For children who must face the uncertainty of a tomorrow, due to their rapidly deteriorating health, a wish is more than just a desire. It’s a hope. Hope is what carries us out of the darkest of slums, to keep going. To face a tomorrow. Make-A-Wish is committed to granting the wish of every eligible child. They do this believing that wishes can make sick children feel better, and sometimes, when they feel better, they get better. Since the spring of 1980, they have been granting the wishes of children diagnosed with a life-threatening medical conditions. The make a wish foundation has the ability to not only unite a society as whole and further the awareness of life threatening illnesses, but also gives hope to individuals and a community as a whole.
Living in poverty my whole life with a single mom and twin brother and three younger siblings, constantly having to fight off situations that were trying to distract me from obtaining an education, being born three months premature and being diagnosed with Cerebral Palsy, a physical disability which I am striving successively to overcome. This past March I had the privilege to volunteer at Children’s Hospital Cerebral Palsy Adult Transition Longitudinal Study (CPAT) and they said my results were the best they had seen so far out of all the other participants because I worked hard and took on activities that I was not supposed to be able to do and loved it. The lens with which I view the world with is very different than others. I can contribute to educating others and others can educate me. Together we’ll grow in ideas, thoughts, and practices to create a more inclusive environment for our patients to thrive. As nurses, it is critical to be diverse learners so we can help a diverse population upon
The topic I picked for our community project was traffic lights. In a community, people need stop signs and traffic lights to slow down drivers from going to fast. If there were no traffic lights or stop signs, people’s lives would be in danger from divers going too fast.