I’m working on a humanities writing question and need an explanation to help me study.
I’m working on a humanities writing question and need an explanation to help me understand better.question oneExplain how the issue of gender has shaped and influenced understandings of African American religious traditions. Specifically, include in your response reflections on two of the following issues:The difference between feminist and womanist theologies.How particular readings of scripture, or the language used the idea of God in many translations, influence the necessity of womanist theology or impact understanding of the issue of gender.What is the Cult of True Womanhood or Domesticity, as used in the nineteenth century, and in what ways does are these ideas present and responded to in discussion of gender.Whether there is any differences in how issues of gender are treated within Christian traditions versus Islamic traditions. How have some traditions addressed women in leadership?question two :Please explain how the idea of manifest destiny played a role in developing religious thought in America and how it influenced particular religious understandings within African American religious traditions. Specifically, define and comment on the tradition of Jeremiad and its relationship to the idea of manifest destiny.Question three : Discuss how Islamic religious traditions in American contained and expressed its understanding of the apocalyptic. Provide specific examples.question 4 Describe Christian Nationalism and how it is manifested in African American religious traditions with specific reference to Albert Cleage.question 5 Discuss how African American religious communities have addressed the issue of economics. Specifically, comment on the approach to economics found within African-based traditions, Spiritual and Christianity churches, and Islam. Give specific examples of how churches addressed economic needs in their communityquestion 6 Explain what liberation theology means within African American religious traditions and discuss some of the concrete issues liberation theology addresses with particular attention to the Statement by the National Committee of Black Churchmen of June 13, 1969.question7 Describe the three statements produced by the Catholic Church on the issue of race. For each statement produced by the Catholic Church, address the following:Identify the drivers to the production of the statement.Discuss the specific conditions each statement sought to address.Assess the effectiveness of the statement or what the statement failed to adequately address.question 8 Discuss how racism has been understood within the Catholic tradition and how the advantages AND disadvantages to this approach in facilitating racial reconciliation.
The Difference Between Feminist and Womanist Theologies Discussion
Sickle Cell Anaemia: Causes, Symptoms and Treatments
Sickle Cell Anaemia: Causes, Symptoms and Treatments. Blood disease is a disorder or disease which will affect one or more parts of the blood, preventing our blood from performing its job in an effective rate. Sometimes, it is also known as blood disorder (Martin, E.A., ed., 2010). Nowadays, there are many types of blood diseases and they are growing public health problems affecting many countries, races and also ethnic groups. They can be classified into acute or chronic. Some of the them are inherited and can cause death. Sickle cell anemia (SCD) is a serious inherited genetic condition which affects the haemoglobin molecule within the red blood cells. It is a condition in which there are lack of healthy and normal red blood cells to carry sufficient oxygen throughout our bodies. The people with sickle cell anemia normally have deformed red blood cells which look like sickles or crescent moons (Mayo Clinic, 2011). This is because the sickle cells contain haemoglobin S or sickle haemoglobin which is an abnormal haemoglobin (MedlinePlus, 2010). The unusual C – shaped cells which look like a farm tool called sickle give the disease its name (CDC, 2011). The alternative names for sickle cell anemia are sickle cell disease or sickle cell disorder, haemoglobin SS disease and HbS disease (NHLBI.NIH, 2011) . Today, millions of people have been diagnosed with sickle cell disease. This type of blood disease is much more common in Africa and Mediterranean (PubMed Health, 2012). About one of every 12 African Americans will carry the sickle cell trait in a person’s genes (MedlinePlus, 2012). Apart from that, it is estimated that 90 000 to 100 000 people in the United States mainly Blacks or African Americans are affected by sickle cell anemia. About one of every 500 Black newborns and one out of every 36 000 Hispanic-American newborns will have this blood disease (CDC, 2011). There are two risk factors that can increase the chances of getting sickle cell anemia which are inheritance and mutation. First of all, sickle cell anemia is an autosomal recessive genetic blood disease which the sickle cell gene will pass from generation to generation. To have this disease, the defective form of the gene must be inherited to a child from both of the parent. A child will have sickle cell trait if the sickle cell gene is passed from only one parent. A person is known as the carrier of sickle cell anemia if he or she has one normal haemoglobin gene and one defective form of the gene. In addition to, the defective gene can be passed to next generation and affect them. While, if both of the parent are carrier, a 50% chance of getting a child who is carrier, 25% chance of having a child who is normal and another 25% chance of having a child with sickle cell anemia (FamilyDoctor.org, 2006). Besides, substitution is a kind of gene mutation which cause this blood disease to occur. The gene mutation is caused by the mutagens which are physical or chemical substances that can affects the genetic material of an organism. Hence, the person who always stays in environment with a lot of radiation or mutagen, he or she has higher risk of getting this disease (Gan Wan Yeat, 2010). This type of blood disease can be prevented if the married couples who both carry the sickle cell trait gene do not have any children. By doing this, the recessive gene will not passed from a generation to another generation . A normal person has haemoglobin A genes which are HbA. If the person who suffers from sickle cell disease, he or she has two haemoglobin S genes (HbS) which are inherited from both parent. These HbS genes are caused by the gene mutation. The base sequence in the DNA for the synthesis of haemoglobin is changed by a single substitution. Hence, the glutamic acid codon is now instead of valine codon (BBC, 2010). When the oxygen content of an affected person’s blood is low, the sickle cell hameoglobin will aggregate into long rods that deform red cells into a sickle or crescent shape which are abnormal haemoglobin (Reece, J.B., et. al., 2011). Besides, these sickle red blood cells are rigid and sticky. This results in less oxygen is delivered to the body’s tissues (MedlinePlus, 2012). The symptoms and signs of sickle cell anemia usually become more obvious after an infant is 4 months old and they are varying. The most common symptom of this disease is painful events. They are sudden pain that happens in different parts of the body. This pain is also known as ‘sickle cell crisis’. Usually, the sickle cell crises can cause pain in the hands, bones, legs, abdomen and so on. This is because the sickle cell get stuck in the small blood vessel as they travel, interrupting the healthy blood flow (National Marrow Donor Program, 2007). People who suffer from sickle cell anemia normally have anemia which will make them feel tired and weak. This is caused by the shortage of red blood cells. Furthermore, they will look pale (WebMD, 2010). Apart from that, the other symptoms of sickle cell anemia may include shortness of breath, blindness, delayed growth, hand-foot syndrome and so on. If it is not treated, stroke, infections, acute chest syndrome and organ damage are the effects of sickle cell anemia (genomics.energy.gov, 2005). Bone marrow transplant is the only cure for sickle cell anemia. However, it is difficult to find a donor who is matched with the recipient and the procedure has serious risks and can even cause death. There are many types of treatments for this blood disease including medication. Children with sickle cell anemia can be treated by using antibiotic penicillin in order to help prevent infections. While pain – relieving medications are responsible in relieving pain during sickle cell crisis. The frequency of painful crisis also can be reduced using hydroxyuera. Moreover, blood transfusions are another type of treatments for sickle cell anemia. The blood transfusion can help to relieve anemia by increasing the number of normal blood cells in circulation (Mayo Clinic, 2011). This is because the sickle shaped cells live only 10 to 20 days which is much shorter than the normal red blood cells. Furthermore, a balanced diet is needed. The supplements of folic acid, vitamin D and zinc should be taken in order to help make new red blood cells. Alcohols and cigarette smokes should be avoided (FamilyDoctor.org, 2006). As a conclusion, sickle cell anemia is a chronic blood disease that cannot be underestimated. This is because there is no cure for the people with this blood disease. Nevertheless, there are many types of treatments and prognosis can help to prevent further problems which are associated with this blood disease. Prevention is better than cure. Hence, people from all walk of life should working out preventive action to avoid them from getting this severe and rare disease. Sickle Cell Anaemia: Causes, Symptoms and Treatments
3 page review of Dean’s Distinguished Speaker Lecture
research paper help 3 page review of Dean’s Distinguished Speaker Lecture. I’m stuck on a Health & Medical question and need an explanation.
After listening to the lecture recording https://touro.box.com/s/8mauxl0av6zxj5m4qqpqp4y8awfpho0f (Links to an external site.) (audio only)
Write and prepare a 3 page review assignment, explaining the summary of the lecture and topics discussed. Use resources from the literature to support or counter any of the claims made in the talk.
3 page review of Dean’s Distinguished Speaker Lecture
Portfolio Project Option #1: Project Management Leadership Self-Assessment
Portfolio Project Option #1: Project Management Leadership Self-Assessment.
Prepare a single MS Word paper that includes the raw results from your Chapter 1 (1-1, 1-2), Chapter 3 (3-1), and Chapter 8 (8-1) Self-Assessments in appendices. Summarize key insights and lessons learned from the self-assessment exercises and then discuss how what you learned from each of the self-assessments is or is not applicable to each of the following major project management phases: Initiating, Planning, Executing, and Closing. Arrange your paper so that it contains the following sections:IntroductionSummary of Key Insights GainedInitiating Phase (sub-sections: Chapter 1 Self-Assessments, Chapter 3 Self-Assessments, Chapter 8 Self-Assessments)Planning Phase (sub-sections: Chapter 1 Self-Assessments, Chapter 3 Self-Assessments, Chapter 8 Self-Assessments)Executing Phase (sub-sections: Chapter 1 Self-Assessments, Chapter 3 Self-Assessments, Chapter 8 Self-Assessments)Closing Phase (sub-sections: Chapter 1 Self-Assessments, Chapter 3 Self-Assessments, Chapter 8 Self-Assessments)ConclusionReferencesAppendix for Chapter 1 Self-Assessment: Raw Results (1-1, 1-2)Appendix for Chapter 3 Self-Assessment: Raw Results (3-1, 3-2, 3-3)Appendix for Chapter 8 Self-Assessment: Raw Results (8-1, 8-2, 8-3)Your paper should be 8-10 pages in length and conform to CSU-Global Guide to Writing and APA Requirements. Include at least two scholarly references in addition to the course textbooks. The CSU-Global Library is a good place to find these references.IMPORTANT NOTE: I will provide the needed chapter 01, 03, and 08 self assessments.
Portfolio Project Option #1: Project Management Leadership Self-Assessment
Harrisburg Area Community College Harrisburg Hersheys Kisses vs Wilbur Buds Essay
Harrisburg Area Community College Harrisburg Hersheys Kisses vs Wilbur Buds Essay.
What is your favorite brand of chocolate? If you’re like a lot of other people around the world, chances are it’s Hershey’s. Hershey’s Chocolate is one of the most recognized brands in the world. They launched their iconic Hershey’s Kisses in 1907, but they were not the first chocolate drop on the market. Have you ever heard of Wilbur Buds? Wilbur Buds are chocolate drop candies that were launched in 1894 by Wilbur Chocolate company, based in Lititz, PA (near Lancaster). Wilbur Buds are still available today but only at their retail store in Lititz, on their website, and at some other small local retailers. Learn more about these brands by checking out the Hershey’s and Wilbur Chocolate websites.
First tell us if you’ve ever heard of or tried Wilbur buds, then continue with the relaunch activity below.
New product development isn’t just about launching brand new products but also includes product relaunches. If you were hired as a marketing manager at Wilbur Chocolate, what would you do to relaunch Wilbur Buds? Determine each area below:
Target market. (Remember – all of your decisions for the brand, package, price, promotion, and communications should tie back to your target market)
Would you make any changes to the brand name, packaging, and/or pricing?
What would differentiate this product in the market? (Why would consumers choose Wilbur Buds over Hershey’s Kisses?)
What types of social media, advertising, or public relations would you develop to relaunch Wilbur Buds to your selected target market?
Harrisburg Area Community College Harrisburg Hersheys Kisses vs Wilbur Buds Essay