Gerald Millers Processes of Persuasion as Evidenced in Real Life essays

Gerald Millers Processes of Persuasion as Evidenced in Real Life essays In Gerald Millers On Being Persuaded he talks about the definition of being persuaded. He talks about how persuasion is coercive, and how a lot of times coercive acts are usually followed after all the persuading. Coercive acts are acts that are military force, the use of guns, any economic sanctions, or any force that could be used to threatened a persons social or well being. In this paper I will be trying to compare the different techniques and assertions used in Gerald Millers On Being Persuaded to my own experience dealing with the idea of homosexuality. Out of the three techniques I will only be talking about two, and that will be response-changing. This is the process that helps reinforce convictions and the other is the changing process which is like the attitude change. In an earlier paper that I had to write I had to write about what big thing in my life that I had to change my mind or opinion about. In that paper I wrote about my views on homosexuality. I did not agree with homosexuality in any shape, size, or form. In fact I was even a little homophobic. But this all changed when I found out that one of my good friends turned out to be a homosexual. I guess in a sense I had to be persuaded into liking this fact, or actually persuade my mind into accepting the fact that one of my friends was gay. In a way I think had to deal with the whole social part of befriending someone who was a homosexual. In my head I had two sides that were forming. One was should I befriend the gay person and lose respect from those who looked down on it as something negative, or even have people think that I myself is gay just because I am friends with a gay person and hang around them. But still have a cool guy who had my back in situations or always helped me out when I needed him. Or should I ignore my friend who I knew for a good bit and try to appease those who I knew would look dow...

Brief History of the Declaration of Independence

Brief History of the Declaration of Independence Since April 1775, loosely organized groups of American colonists had been fighting British soldiers in an attempt to secure their rights as loyal British subjects. By the summer of 1776, however, a majority of Americans were pushing – and fighting for full independence from Britain. In reality, the Revolutionary War had already begun with the Battles of Lexington and Concord  and the Siege of Boston  in 1775.  The American Continental Congress turned a five-man committee including Thomas Jefferson, John Adams, and Benjamin Franklin to pen a formal statement of the colonists’ expectation and demands to be sent to King George III. In Philadelphia on July 4, 1776, Congress formally adopted the Declaration of Independence. We hold these truths to be self-evident, that all men are created equal, that they are endowed by their Creator with certain unalienable Rights, that among these are Life, Liberty and the pursuit of Happiness. The Declaration of Independence. The following is a brief chronicle of events leading up to the official adoption of the Declaration of Independence. May 1775 The Second Continental Congress convenes in Philadelphia. A petition for redress of grievances, sent to King George III of England by the First Continental Congress in 1774, remains unanswered. June - July 1775 Congress establishes the Continental Army, a first national monetary currency and a post office to serve the United Colonies. August 1775 King George declares his American subjects to be engaged in open and avowed rebellion against the Crown. The English Parliament passes the American Prohibitory Act, declaring all American sea-going vessels and their cargo the property of England. January 1776 Colonists by the thousands buy copies of Thomas Paines Common Sense, stating the cause of American independence. March 1776 Congress passes the Privateering (piracy) Resolution, allowing colonists to arm vessels in order to cruize [sic] on the enemies of these United Colonies. April 6, 1776 American seaports were opened to trade and cargo from other nations for the first time. May 1776 Germany, through a treaty negotiated with King George, agrees to hire mercenary soldiers to help put down any potential uprising by American colonists. May 10, 1776 Congress passes the Resolution for the Formation of Local Governments, allowing colonists to establish their own local governments. Eight colonies agreed to support American independence. May 15, 1776 The Virginia Convention passes a resolution that the delegates appointed to represent this colony in General Congress be instructed to propose to that respectable body to declare the United Colonies free and independent states. June 7, 1776 Richard Henry Lee, Virginias delegate to the Continental Congress, presents the Lee Resolution reading in part: Resolved: That these United Colonies are, and of right ought to be, free and independent States, that they are absolved from all allegiance to the British Crown, and that all political connection between them and the State of Great Britain is, and ought to be, totally dissolved. June 11, 1776 Congress postpones consideration of the Lee Resolution and appoints the Committee of Five to draft a final statement declaring the case for Americas independence. The Committee of Five is composed of: John Adams of Massachusetts, Roger Sherman of Connecticut, Benjamin Franklin of Pennsylvania, Robert R. Livingston of New York and Thomas Jefferson of Virginia. July 2, 1776 By the votes of 12 of the 13 colonies, with New York not voting, Congress adopts the Lee Resolutions and begins consideration of the Declaration of Independence, written by the Committee of Five. July 4, 1776 Late in the afternoon, church bells ring out over Philadelphia heralding the final adoption of the Declaration of Independence. August 2, 1776 The delegates of the Continental Congress sign the clearly printed or engrossed version of the Declaration. Today Faded but still legible, the Declaration of Independence, along with the Constitution and Bill of Rights, is enshrined for public display in the rotunda of the National Archives and Records Building in Washington, D.C. The priceless documents are stored in an underground vault at night and are constantly monitored for any degradation in their condition.

Adoption of Sarbanes-Oxley Act of 2002 as an Important Piece of Term Paper

Adoption of Sarbanes-Oxley Act of 2002 as an Important Piece of Legislation - Term Paper Example In the last section the report evaluates the costs and benefits of the changes ushered in by the Sarbanes-Oxley act of 2002. The Sarbanes-Oxley Act of 2002 was drafted by the senator Paul Sarbanes and representative Michael Oxley (SOX-online.com, 2006: Online). The primary objective of the Sarbanes-Oxley Act was to protect and safeguard the interests of the investors by assuring transparency, accuracy and reliability of the financial disclosures made by the corporations. It is a mandatory Act and all the large and small US organizations are required to abide by and follow the provisions and requirements of the Sarbanes-Oxley Act. This Act came into force in the year 2002 and brought in sweeping changes into the area of financial disclosure and corporate governance (Sarbanes-Oxley Act, 2006: Online). The Enhanced Standards Required by Sarbanes-Oxley Act The Sarbanes-Oxley Act not only established new standards of financial accounting and corporate governance but also made provisions f or the apt statutory penalties to be imposed in case of any wrongdoing not allowed for and sanctioned by this act. The Act made the corporate accounting system more transparent and responsible by formalizing and assuring the interaction between corporate auditors and corporate boards and executives . This totally obliterated the possibility of an excuse on the part of top executives in corporations regarding being unaware of the organizational accounting systems and the accompanying disclosures made by the auditors. To put it simply, the Sarbanes-Oxley Act made the top executives like CEOs and CFOs directly responsible for corporate accounting and subsequently culpable in case of any wrongdoing or misreporting in the organization’s financial reporting (US Securities and Exchange Commission 2010: Online). This act clearly specifies the responsibilities associated with the organizational financial accounting. Sarbanes-Oxley Act has also introduced a mechanism of internal contro ls and monitoring to assure the credibility of financial reporting (US Securities and Exchange Commission, 2010: Online). According to this act, the companies are required to tag an internal control report with every financial report (US Securities and Exchange Commission, 2010: Online). The yearly financial reports are also required to report on the reliability and effectiveness of the internal controls (US Securities and Exchange Commission, 2010: Online). Further, the concerned auditing firms are required to stand behind these reports (US Securities and Exchange Commission, 2010: Online). This places the onus on the auditing firms to review the associated procedures, controls and policies, besides conducting the regular financial audit (US Securities and Exchange Commission, 2010: Online). In case a company fails to abide by any requirement or section of the Sarbanes-Oxley Act, the act allows for a range of penalties for the culprit organization and executives, which include fine s amounting to

Bureaucratization of My Life Essay Example | Topics and Well Written Essays - 500 words

Bureaucratization of My Life - Essay Example Students are people too and their overwhelming academic requirements put pressure on their lives. Some deadlines cannot be met so professors must understand the situation. There are also rules that were written a long time ago which does not fit a dynamic learning environment anymore. Although is a school is a bureaucratic system, it must also be the leader in innovation and change since it leads society towards the future through the learning process.The third characteristic is Impersonality. A bureaucratic system is objective and people assigned to do their duties are impersonal in their attitude. Weber thought this was good so that people can easily perform their routine and stick to the tasks being performed. The school staff assists students regardless if they are academic performers or not. There is no discrimination as the school staff perform their duties by rendering service to all students regardless of race, creed, color or even financial status. Unfortunately, impersonali ty and objectivity have its drawbacks. What I am pointing out is that since a bureaucratic system is impersonal and objective the situation of an individual is overlooked since the rules have to be followed. Regardless if one has been sick and cannot submit on time, the student can be given a failing grade despite the circumstances. In conclusion, bureaucracy is practiced inside PGCC and it has its advantages; however, it also has its disadvantages since a school system is not a perfect organization.

Diagnosis And Treatment Of Haemoglobinopathies Biology Essay

Diagnosis And Treatment Of Haemoglobinopathies Biology Essay Haemoglobinopathy is a genetic inherited disorder. Haemoglobinopaty is associated to geographical distribution disease; it is most common in population of Africa, Middle East, Mediterranean, Asia and Southeast Asia. Haemogloninopathies are subdivided into two main significant genetic diseases thalassaemia and sickle cell disease. Transfusion treatment and bone morrow oar stem cell transplantation therapy use for treatment and management both diseases. But in sickle cell disease (SCD) there are some more treatment used as control the complication of disease such hydroxyurea, and vaccination against some pathogenic disease which are causes infection, and analgesic to relief the pain, and using prophylactic treatment against pneumococcal chest syndrome. Also the patient during the blood transfusion increased the amount of iron which is harmful for many organs in human body particularly the heart muscle tissue. In this case the patient need another therapy is iron chelation such as defer iprone with deferoxamine. The resent study declare that the most curative treatment and is bone marrow transplantation or stem cell transplantation. The most accurate test for haemoglobinopathy is including high pressure liquid chromatography (HPLC), haemoglobin electrophoresis (EP) and neonatal screening test and DNA parental test. Introduction Haemoglobinopathy is a genetic disease, associated with lack of normal haemoglobin in the red blood cells also the most common monogenic disease in the worldwide. Is inherited defect produce abnormal haemoglobin (Hb) in their structure, Hb playing an important role in red blood cells. This disorder is an autosomal recessive disorder. This disorder related to chronic haemolytic anaemia. (Marie and Fernando 2008) Haemoglobinopaty is geographical distribution disease; is most common in Africa, Middle East, Mediterranean, Asia and Southeast Asia. Also interaction between two genes among this people can causes to number types of thalassaemia disease, three aims for control are homozygous alpha-0 thallassaemia leading to Hb-Bart, homozygous beta-thalassaemia and beta-thalassaemia Hb-E. Hence that is important to detect very quick, immediate and accurate screening for prevention especially those parental are carrying the alpha-0 thalassaemia, beta-thalassaemia and Hb-E. (Fucharoen S et al 2 000) Haemoglobinopathy can spread in the many region of the world because of the mix ethnic and immigration from the countries which are prevalence the disease to non prevalence disease countries. Haemoglobinopathies occurs due to of the haemoglobins reduced their ability to carry the oxygen. This disorder associated to haemoglobin molecule disorder also that is important to understanding the structure and function of haemoglobin. There are two main types of haemoglobinopathy, SCD and thalassaemia can be passed from parental to offspring trough abnormal haemoglobin genes. Individual can be effect with these disorder while they are be inherited with two abnormal haemoglobin one from paternal and the other from maternal. But individual with only one abnormal haemoglobin gene called as carrier or trait, does not shows any clinical symptom and healthier as well. Individuals with haemoglobinopthies are either having clinical symptom of this disease, or if the individuals are carrier, unknown of their trait until screened, but If parent both carrier an abnormal hemoglobin gene there is a chance 25% of their pregnancy that offspring will affected with the clinical symptom of haemoglobinopathy If the maternal affected with haemoglobinopathy, and the paternal only carrier therefore the child 50% can be affected and 50% will carrier. The haemoglobin Hb molecule is a polymer consisting of four identical monomers. Hb molecule consist of two pairs of globins chains, each containing a haem group, every haem have an iron atom which is attached to oxygen in the lung and the haem which is responsible for transporting the oxygen from the lungs to the tissues and carrying the carbon dioxide (CO2) from the tissue to lung (Figure 1). For the period of foetus development, the foetal Hb predominate (two alpha chains and two gamma chains). Haemoglobin Hb molecule in adult composed of four globins chains two alpha subunit and two beta subunit. The structure Hb changes within embryonic, fetus and adult. Usually the main haemoglobin in normal adult is HbA, and little quantity of HbA2 and HbF. (Morven W et al 2009) Diagram showing the location of haeme in haemoglobin. Figure 1: shows the structure of haemoglobin (www.sciencelearn.org.nz) accessed 29/01/2011. Classification of heamoglobinopaties: haemoglobinopathy can divided into two main parts (figure -2) Thalassemia Sickle cell disease The name of referred object is cbr27_1p027f2.jpg Fig 2: (Ronald J 2006) Thalassemia Thalassemia is hereditary haemoglobin defect which failure the formation more than one polypeptide chain of haemoglobin protein causes mild or severe anaemia. thalassaemia classified into a few categories and each of them can causes different problems. Thalassamia is quantitative abnormality, frequently associated to chronic haemolytic anaemia, the clinical expression of disease including serious of haemolysis and some type of the disease not shows clinical symptom of the disease. Thalassaemia involved in the class of globins chain and number of defective of globins gene. The offspring with thalassamia at the birth frequently are healthy, the sign and symptom of anaemia appear in between age six month to two years old. Without detection and treatment the most of children in age one year old are death because of severe anaemia and infection. (Weatherall. D and Clegg. J 2001) Some types of thalassaemia initiate with mild condition, but some of them cases serious and life threatening and it cause death. Nearly 5% of the population in the nationwide have been affected with this disease. Foetal Haemoglobin (Hb) is predominantly alpha2 and gama2. In the normal individual the dominating haemoglobin composition is HbA i.e. alpha 2 and beta 2. This implies that the frequent forms of thalassaemia are alpha and beta, each type causes different clinical manifestation. Foetal Haemoglobin (Hb) is predominantly alpha 2 and gamma 2. In the normal individual the dominating haemoglobin composition is HbA i.e. a2b2. This implies that the frequent forms of thalassaemia are alpha and beta. (Fucharoen et al 2007) Alpha thalassemia: Individual with alpha-thalassemia characterised by lack of alpha globin chains. It is prevalence in Africa, Middle East, Asia, south east of Asia, and also Mediterranean area. The alpha-globin gene made up by four genes, found on chromosome 16p13.3 (Figure 4) and including the embryonic zeta-globins gene and two alpha globins genes, usually there are four alpha globins gene, mutation affected on one or more alpha-globins gene causes lack of formation of alpha- globin chain lead to alpha thalassaemia. (Weatherall. D and Clegg. J 2001) The patient with only one unusual alpha globin gene is called alpha thalassaemia carrier. In this case one globin genes defective or missing, and not show any clinical symptom of anaemia, and difficult to diagnosis also known as silent carrier. Normal carrier has an offspring with haemoglobin H (HbH). It is can be to detect by DNA examination. If the individual has missing two of four globin genes call as alpha thalasaemia trait, both abnormal alpha-globin genes can be found on one chromosome or one on each chromosome. The parents both have alpha thalasaemia trait therefore their offspring effective with alpha thalassaemia trait. The patient with this disease has mild anaemia and the red cells are smaller the normal size call microcytosis. And the patient does not show the clinical manifestation. (Leung. W et al 2008) Also if one of the parents has alpha thalassaemia trait and the other one has silent carrier there is 25% chance of their offspring born with HbH. But if the both parent have alpha thalassaemia trait there is 25% chance their offspring inherited with alpha-thalassaemia major. Individual with condition has no chance to live for long term and mostly die in childhood, the reason for that because of lack or defects of the alpha globin chain and causes the severe anaemia and causes health damaging such as spleenomegaly, bone malformation and tiredness. Beta-thalassemia: The beta-thalassaemia is an inherited disease associated with haemoglobin disorder, is congenital anaemia, occur because of lack or reduce formation of beta-globin chain causes reduce the number of red cells or produce unfunctional red cells, most of erythrocyte are failure to mature from the bone marrow that is cause serious anaemia. The beta- globin chain deficit causes the intracellular precipitation and increases of alpha-globin chain, leading to ineffective erythropoiesis and haemolysis anaemia. (Ronald J 2006) Beta-thalassaemia is the most common molecular deficiency as the consequence of point mutation and deletion that effect the transcription and mRNA translation. Infants with homozygous beta-thalassaemia are healthy but after birth as the haemoglobin from fetus replaced to adult haemoglobin the absent of beta-globin causes the serious anaemia. Also the level of anaemia is deference rely on the level of beta-globin deficiency and the formation of fetal haemoglobin. (Lin. Y e t al 2009) The clinical manifestations of beta-thalassaemia including of anaemia shows in the first year of life, also the spleen enlargement resulting from accumulation large amount of destruction os erythrocyte in the spleen, growth of bone marrow because the body compensated the red cells destruction which is leading to abnormal growth the long bones and deformation the skull. Beta-thalassemia is most prevalence in the Asia, and became the main health problem among people. (Weatherall. J 2001) In developing countries the patients with this disease are suffering and death within childhood. The recent study of the national thalassemia register reveals that the patients survive for longer in the UK, half population of patients with beta-thalassemia die under the age of 35 years old. Sickle cell disease (SCD) SCD is genetic defected haemoglobinopathy characterised by stiffen shaped cells which can block blood vessels and caused severe pain, organ damage and infection. Was found at the beginning the twentieth century, is an autosomal dominant genetic disorder, it is related to qualitative globin gene defect, and formation of abnormal globin chain, SCD results in morbidity and mortality. There are 500 unusual Hb found but only four of them are common such as HbS (beta 6 glu-val), HbC (beta 6 Glu-Lys), HbD (beta 87 Thr-Lys), HbE (beta 26 Glu-Lys). The disease is characterized by abnormality in shape of RBCs, the cell become sickle-shape which is rigid and stiffen and can leading to obstruction the blood vessels and tissue ischemia, which causes the organ damage. Also this abnormality can cause painful episodes, severe infection and chronic anaemia. SCD is the mutation in the haemoglobin gene and causes sickling the cells, mutation increased in different part of the Hb molecule, SCD can be de tected through infant screening haemoglobin electrophoresis. SCD occur because of mutation on short arm of chromosome 11 (figure-4), this mutation leading to replace the valine to glutamine of the amino acid at the sixth positions of beta-globin chain of HbA, resulting in the production of HbS which is biochemically unstable molecule and it can precipitate at the deoxygenated state. (Hoffbrand. A.V. 2001) chromos Figure- 4 Globin encoding genes are found on chromosome 11 and 16. Figure 3 SCD was the first disease has been described as a molecular disorder in a gene, and it is detected by infant screening program. Its causes reduce lifespan and associated to chronic disease. SCD occur in that part of the world where Plasmodium Palciparum has endemic and then spread because of migration to other part of the world for example north of Europe and United States. SCD is more common in those people are originally came from the Africa, Mediterranean, middle and south of America, Asia and middle east. (Figure 4) SCD occurs due to the newborn inherited the defect haemoglobin gene from parental mother and father HB SS causes severe anaemia, if only one sickle haemoglobin gene from one parent and one normal haemoglobin gene from other parent transfer to infant, therefore the infant become a carrier also known as sickle cell trait. (Marie. J and Ronald. L 2004) Image Reference: Marie. J and Ronald L 2004 Figure 5: Geographical distribution and representation of the sickle gene. (A) Map identifies the three distinct areas in Africa and one in the Arab-India region where the sickle gene is present (dotted lines). Numbers of individuals with sickle-cell disease (red lines) in Senegal, Benin, and Bantu are higher near the coast, and falls concentrically inland. (B) The ÃŽÂ ²-globin gene cluster haplotype is determined by DNA polymorphic sites (boxes) that are identified by endonuclease enzymes. With this information, haplotypes are constructed as shown. The pathophysiologies of CSD rely on the deoxy- HbS. That is association with two alpha globin chains with mutation of 2 beta-globin chains produce HbS. under deoxygenating circumstance, the lack of a polar amino acid at six locations of beta-globin chain lead to aggregation of Hb, which change the RBCs into sickle shape and reduced their elasticity. (Figure 5) The patients with the SCD are often visiting to hospital because of acute pain, and the patient treated by an analgesic to relief the pain, hydration and oxygen supply. The main common of clinical symptom of SCD including anaemia, episode painful, lung infection, infarctions of nervous system and strokes, spleenenlargment because of precipitation of large amount of haemoglobin in spleen, skin ulceration, organ damage, vaso-occlusive, and neurocongenitive dysfunction most common causes morbidity among the patient with this disease. Figure- 5: Normal and sickle red cell morphology SCD is known as chronic inflammatory disease, Diagnosis of haemoglobinopathies: Detection and identification of haemoglobinopathies relay on three stages: Full blood count Special haematological test DNA analysis Full blood account Full blood account is used to detection of haemoglobinopaty specially the thalasaemia, which is the earliest of haematological information. Individual with thalassaemia shows low mean corpuscular volume (MCV) or mean corpuscular haemoglobin (MCH). Also in other anaemia for example the iron deficiency the MCV is low as well, it is possible this detection will shows the thalassaemia in those region with at high risk ethnic populations. The first step after initial abnormal blood count is to elimination of iron deficiency, to cure it. The blood count test is repeated if the MCV still lower than normal value. The test show most likely is thalassemia. Also the MCV increased because of some condition especially B12 and folic deficiency causes raised the MCV. In some condition the main evidence of thalassaemis disappears due to the MCV is wrongly normal or may be increased. Measuring the MVC is used as early stage test for heamoglobinopathy. Therefore that is very important for diagnosis of thalassaemia this is the HbS carrier, the health professionals who are dealing with those people in which HbS occurs must be including the HbEPG with the demand a full blood count. Also blood film as part of full blood count can be used, it is detected the SCD (HBS) or unstable Hb. in some cases, finding the target cells and stippling in the blood film are not associated with a haemoglobinopathy but it can help as additional finding in case of thalassaemia if the MCV or MCH is lower than reference range. Special haematological test Some of test of haemoglobinopathy technically require skill the team of laboratory, must have knowledge and must be trained to use the laboratoryà ¢Ã¢â€š ¬Ã¢â€ž ¢s instrument, and obtain an experience in understand the results. More haematological test is requiring especially after detecting the more unusual HbS. Also test the oxygen affinity, stability of haemoglobin and identify the methaemoglobin. Mass spectrometry is used to characterise different mutation of HbS.( 10 )for diagnosis of individual cases is the DNA test. DNA test is the most common haematology test, due to the DNA laboratory must to understand the characterised of alpha and beta globin genes. As DNA technology in haemoglobinopathy based on PCR (polymerase chain reaction) and southern blotting, also the DNA laboratory examination deciding whether there is a point mutations or deletions. Other major source of mistake to deceive the DNA laboratory is the not a success to detection HbH. Not occasionally, a DNA detection used to diagnosis the beta globin gene due to HbH inclusion was not be found, if not mutation in DNA sequencing is detected, at this point the DNA laboratory back to the haematology test to detected the HbH inclusion. Another useful test to diagnosis a thalassaemia and it is because of an alpha and beta globin gene problem in the alpha and beta globin protein fraction. That is requiring to incubation of RBC with radioactive. The peaks indicative of alpha and beta globins are then provide an alpha and beta ratio which must equal one. If the ratio higher than one that is indicates beta thalassaemia, or if the ratio lower than one that is indicates alpha thalassaemia. The alpha and beta ratio is not longer available. That was took place due to DNA testing is became the common test and also alpha and beta ratios are now performed in those laboratory do have insufficient skill. Setting up of this assay needed fresh radioactive material. The alpha and beta ratio may be not useful while the interactions of genes are occurring. DNA testing DNA testing is requiring if the haemoglobinopathy difficult to detect by the haematological test, while it is may be suspected a haemoglobinopathy, but the haematology may not detected which gene has been involved. And the other reason to use DNA testing is the basic alteration been sought in an established haemoglobinopaty. This require as part of parental developed. (Ronald J 2006) DNA test can be used for sickle cell in neonatal by analysing of the DNA of foetal tissue Screening test for thalassaemia and haemoglobinopatphies Usually the basic screening trial all type of thalassaemia depends on the guide of haematology cut- off, which effects on the correct count using an automatic blood cell counter. The patient with MCV values lower than (80 fL), and MCH values lower than (27 pg). Therefore more tests are requiring identifying of (alpha and beta) thalassaemia. (Kanokwan, S et al 2005) But the test needs an expensive an automatic blood cell counting but that is impossible to perform in the laboratory without good facilities. Also that has been proved the osmotic fragility test tube which is containing 0.36% of saline solution could be used as like other option test to detected alpha and beta salassaemia syndrome. (Kamala. R 2008) The recent study indicated that specificity of the osmotic fragility test for detection of (beta and alpha-0) thalassaemia could be improved by reduce concentration of saline solution from 36% to 34%. But the carrier of Hb-E would not be available; in this case cichlorophenolindophenol (DCIP) test has been established for detection of Hb-E in the developing country of Southeast Asia, but this procedure is not suitable for pregnant woman because they have iron deficiency during their pregnancy. Hence the combination osmatic fragility test and DCIP test use for detection alpha,0- thalassaemia, beta thalassaemia and Hb E in pregnant woman tested and compared with other measure screening procedure linked to measure of RBCs indicator. (Kanokwan, S et al 2005) There is some more special haematology tests require to diagnosis of haemoglobinopathies: Hb EPG test can be measured by electrophoresis of globin. Different methods likely as gel and membrane based to high pressure liquid chromatography (HPLC). Unusual group separate as of normal HbA, HbF and also HbA2 can be detected.that dose mean provides some information about HbA2, and recognize some other Hb if available for example HbE and HbS. HbA2 test is detected by globin electrophoresis and quantity the HbA2. And difference methods are used as a membrane, also the more use in the world is HPLC. That does mean the increased HbA2 shows the incident of beta- thalassaemia. It dose shows that the alternative haemoglobins could be increased the HbA2. Also unusual raised the HbA2 shows the mild beta thalassaemia, the low HbA2 delta thalassaemia. HbF test detected by globin electrophoresis, and determine by deference technique. The normal value in of HbF adult is lower than 1%, if the HbF slightly increased to 2 or 3% that indicates the mild beta- thalassaemia. If HbF elevated to more than 5% are likely to be delta-beta thalassaemia in this case the level of HbA2 decreased. (Angela. H 2005) Kleihauer test is staining the red cell to diagnosis the HbF. This test uses for separate the hetrocellular from pancellular. This test is unusual for differentiation the type of hereditary persistence of Hbf because they are not often available and difficult for laboratory staff to translate the results. This test useful only in foetal blood sample to detect that the HbF passed from the fetes to the motherà ¢Ã¢â€š ¬Ã¢â€ž ¢s blood circulation. (Liu. W et al 2007) HbH inclusion test carry out by stain the red blood cells to identification of HbH inclusion, deposition of beta globin chain. This test used to detection of alpha-thalassaemia. This test causes problem due to false negative. Need a lot of knowledge and skill of laboratorian to detect HbH inclusion and with two gene deleted alpha-thalasaemia, only very HbH little inclusion can be detected. Therefore the laboratorian may miss it if do not have good experience. Must the person who is work in the laboratory must continuously look at the microscope. (Chan. A 1996) Sickle solubility and stability test, there many different type of test performed to detected the HbS or unstable variation of HbS. There are interactions between the HbS with beta thalassaemia, hence the correct test for sickling test are require for haenoglobinopathy. (Baebara J 2004) RBC count can be used for detection of thalassaimia and haemoglobinopathies while the red cells count is normal or increased. Also it is helpful if hypochromic, microcytic observed. The Red cell Distribution Width (RDW) is a numerical value that represents the coefficient of variation of the red cell volume distribution. This value indicates the variation in red cell size (anisocytosis). Anisocytosis is an abnormally of red cell size variation that is apparent on the blood smear, is the anisocytosis is increased that is indicated the beta and alpha thalassaemia as it is seen before the haemoglobin decreased and MCV and MCH reduced. Mean Cell Haemoglobin Concentration (MCHC) it is the other parameter is the concentration in g/L of haemoglobin in the RBC, But It is infrequently measured. If the MCHC reduced that is shows the hypochromic with any other causes microcytosis that is indicates the thalassaemia. Haemoglobin electrophoresis for diagnosis of CSD Diagnosis SCD can be performed by the haemoglobin electrophoresis. Simple and accurate method for diagnosis of SCD due to in can detect the Hbs, but the EP is reliable to identify the phenotype. Sickle cell test the sodium metabisulphite used for remove the agent leads to precipitate in the buffer solution to formation the cloudy suspension. This test is not useful neonatal period because of lack HbS and presence high amount of HbF which has high solubility and may generate false negative result. Sickle cell test can be used after six month of age becouse the level of HbF dropped down. For distinguish the phenotype should relying on the haemoglobin electrophoresis. Separation of molecule in this test rely on the charge at add pH. H Methods: There same key words have been used to find the journals which are related to finding the information for the topic of the project. The key words including (haemoglobinopathies, Thalassaemia (beta or alpha), Sickle cell disease, treatment of haemoglobinopathies and diagnosis of haemoglobinopathies). Treatment for thalassaemia More than 90% of the patient with thalassaemia needs to be treated by regular blood transfusion to regulate the anaemia and its side effects, transfusion therapy increase the life span of patient with quality of life. Infants who are sufficient treated by blood transfusion growth well. However the transfusion therapy causes increased the amount of iron in the organ, iron overload is fatal if untreated causes organ damage, late sexual growth, and osteoporosis. Most individuals with beta-thalassaemia major can be survive for longer with blood transfusion therapy but increasing the damaging levels of iron overload if the patient not be treated with iron chelation therapy. Increased the level of iron from blood transfusions therapy leading to destruction the macrophages and then follow that damaging the liver and later on spreads to the heart tissue, pancreas, and also the iron overload effected on the same of glands such as pituitary, thyroid and parathyroid glands, the levels of iron must be controlled by chelating treatment. Due to the blood transfusion are usually started at the beginning in life, excess of iron effects on the endocrine system can causes unusual growth and hypogonadotrophic hypogonadism. Cardiac disease is the most causes of death among the patient with beta-thalassaemia major. Iron overload causes reduce the myocardial T2 vales is detected by cardiac magnetic resonance imaging, is prevalence in the patient with beta-thal lassaemia. (Kirk P et al 2011) Iron chelating therapy supports the patient with increased the level of iron from the accumulation the toxic iron and reduce the amount of iron that harmful for tissue and many organs. Iron chelating initially used by the end of the 1970s, it is not a curative for the patient with beta-thalasaemia major but it can reduce the number of death because of this disease. The patient with this has some side effects which are related to excess iron such as diabetes, hypogonadism, and hyper thyroidism, (Rugolotto S et al 2004) The main purpose of using the iron chelation is sustain the balance of amount of iron at the safe stage in the organ tissue and stop accumulating of iron inside the organ. To reduce the level of iron in body, there are deference ways to rescue the human body from iron overload. Venesection is procedure, part of treatment. Used to withdraw large amount of blood a through the vein and discarded, use for treatment of iron overload also is known by phlebotomy used for elimination of iron in the blood circulation, removes 200-250mg iron from unit of blood. Also the iron chelating can help the patient to reduces the level of iron, iron chelation with deferoxamine causes the damaging of tissue and ultimately causes death, the resent study explore that the cardiac disease is causes death in more than 70% of patient who are treated with deferoxamine. The new oral chelater was started in 1995; oral chelater with deferiprone became very useful treatment in the clinical therapy. The prospective non randomized clinical test proved that the mortality because of the cardiac disease decreased in patient treated with deferiprone, combine and sequential the deferiprone with deferoxamine. (Aurelio. M et al 2009) The diagnosis laboratory performed the experiment on 265 patients in one of the Italia laboratory from year 2000 to 2008, 124 patients treated deferoxamine and 11 patient was death, and 55 patients treated with deferiprone none of them death, 68 patients treated with sequential deferiprone and deferoxamine only one patient death and 18 patients treated with combine deferiprone and deferoxamine none of them death. This trial give clue the best treatment for iron chelating is deferoxamine or combination between deferiprone and deferoxamine. Figure 6: trial profile 265 patient treated with iron chelater.

A Game of Thrones Chapter Two

Catelyn Catelyn had never liked this godswood. She had been born a Tully, at Riverrun far to the south, on the Red Fork of the Trident. The godswood there was a garden, bright and airy, where tall redwoods spread dappled shadows across tinkling streams, birds sang from hidden nests, and the air was spicy with the scent of flowers. The gods of Winterfell kept a different sort of wood. It was a dark, primal place, three acres of old forest untouched for ten thousand years as the gloomy castle rose around it. It smelled of moist earth and decay. No redwoods grew here. This was a wood of stubborn sentinel trees armored in grey-green needles, of mighty oaks, of ironwoods as old as the realm itself. Here thick black trunks crowded close together while twisted branches wove a dense canopy overhead and misshappen roots wrestled beneath the soil. This was a place of deep silence and brooding shadows, and the gods who lived here had no names. But she knew she would find her husband here tonight. Whenever he took a man's life, afterward he would seek the quiet of the godswood. Catelyn had been anointed with the seven oils and named in the rainbow of light that filled the sept of Riverrun. She was of the Faith, like her father and grandfather and his father before him. Her gods had names, and their faces were as familiar as the faces of her parents. Worship was a septon with a censer, the smell of incense, a seven-sided crystal alive with light, voices raised in song. The Tullys kept a godswood, as all the great houses did, but it was only a place to walk or read or lie in the sun. Worship was for the sept. For her sake, Ned had built a small sept where she might sing to the seven faces of god, but the blood of the First Men still flowed in the veins of the Starks, and his own gods were the old ones, the nameless, faceless gods of the greenwood they shared with the vanished children of the forest. At the center of the grove an ancient weirwood brooded over a small pool where the waters were black and cold. â€Å"The heart tree,† Ned called it. The weirwood's bark was white as bone, its leaves dark red, like a thousand bloodstained hands. A face had been carved in the trunk of the great tree, its features long and melancholy, the deep-cut eyes red with dried sap and strangely watchful. They were old, those eyes; older than Winterfell itself. They had seen Brandon the Builder set the first stone, if the tales were true; they had watched the castle's granite walls rise around them. It was said that the children of the forest had carved the faces in the trees during the dawn centuries before the coming of the First Men across the narrow sea. In the south the last weirwoods had been cut down or burned out a thousand years ago, except on the Isle of Faces where the green men kept their silent watch. Up here it was different. Here every castle had its godswood, and every godswood had its heart tree, and every heart tree its face. Catelyn found her husband beneath the weirwood, seated on a moss-covered stone. The greatsword Ice was across his lap, and he was cleaning the blade in those waters black as night. A thousand years of humus lay thick upon the godswood floor, swallowing the sound of her feet, but the red eyes of the weirwood seemed to follow her as she came. â€Å"Ned,† she called softly. He lifted his head to look at her. â€Å"Catelyn,† he said. His voice was distant and formal. â€Å"Where are the children?† He would always ask her that. â€Å"In the kitchen, arguing about names for the wolf pups.† She spread her cloak on the forest floor and sat beside the pool, her back to the weirwood. She could feel the eyes watching her, but she did her best to ignore them. â€Å"Arya is already in love, and Sansa is charmed and gracious, but Rickon is not quite sure.† â€Å"Is he afraid?† Ned asked. â€Å"A little,† she admitted. â€Å"He is only three.† Ned frowned. â€Å"He must learn to face his fears. He will not be three forever. And winter is coming.† â€Å"Yes,† Catelyn agreed. The words gave her a chill, as they always did. The Stark words. Every noble house had its words. Family mottoes, touchstones, prayers of sorts, they boasted of honor and glory, promised loyalty and truth, swore faith and courage. All but the Starks. Winter is coming, said the Stark words. Not for the first time, she reflected on what a strange people these northerners were. â€Å"The man died well, I'll give him that,† Ned said. He had a swatch of oiled leather in one hand. He ran it lightly up the greatsword as he spoke, polishing the metal to a dark glow. â€Å"I was glad for Bran's sake. You would have been proud of Bran.† â€Å"I am always proud of Bran,† Catelyn replied, watching the sword as he stroked it. She could see the rippling deep within the steel, where the metal had been folded back on itself a hundred times in the forging. Catelyn had no love for swords, but she could not deny that Ice had its own beauty. It had been forged in Valyria, before the Doom had come to the old Freehold, when the ironsmiths had worked their metal with spells as well as hammers. Four hundred years old it was, and as sharp as the day it was forged. The name it bore was older still, a legacy from the age of heroes, when the Starks were Kings in the North. â€Å"He was the fourth this year,† Ned said grimly. â€Å"The poor man was half-mad. Something had put a fear in him so deep that my words could not reach him.† He sighed. â€Å"Ben writes that the strength of the Night's Watch is down below a thousand. It's not only desertions. They are losing men on rangings as well.† â€Å"Is it the wildlings?† she asked. â€Å"Who else?† Ned lifted Ice, looked down the cool steel length of it. â€Å"And it will only grow worse. The day may come when I will have no choice but to call the banners and ride north to deal with this King-beyond-the-Wall for good and all.† â€Å"Beyond the Wall?† The thought made Catelyn shudder. Ned saw the dread on her face. â€Å"Mance Rayder is nothing for us to fear.† â€Å"There are darker things beyond the Wall.† She glanced behind her at the heart tree, the pale bark and red eyes, watching, listening, thinking its long slow thoughts. His smile was gentle. â€Å"You listen to too many of Old Nan's stories. The Others are as dead as the children of the forest, gone eight thousand years. Maester Luwin will tell you they never lived at all. No living man has ever seen one.† â€Å"Until this morning, no living man had ever seen a direwolf either,† Catelyn reminded him. â€Å"I ought to know better than to argue with a Tully,† he said with a rueful smile. He slid Ice back into its sheath. â€Å"You did not come here to tell me crib tales. I know how little you like this place. What is it, my lady?† Catelyn took her husband's hand. â€Å"There was grievous news today, my lord. I did not wish to trouble you until you had cleansed yourself.† There was no way to soften the blow, so she told him straight. â€Å"I am so sorry, my love. Jon Arryn is dead.† His eyes found hers, and she could see how hard it took him, as she had known it would. In his youth, Ned had fostered at the Eyrie, and the childless Lord Arryn had become a second father to him and his fellow ward, Robert Baratheon. When the Mad King Aerys II Targaryen had demanded their heads, the Lord of the Eyrie had raised his moon-and-falcon banners in revolt rather than give up those he had pledged to protect. And one day fifteen years ago, this second father had become a brother as well, as he and Ned stood together in the sept at Riverrun to wed two sisters, the daughters of Lord Hoster Tully. â€Å"Jon . . . † he said. â€Å"Is this news certain?† â€Å"It was the king's seal, and the letter is in Robert's own hand. I saved it for you. He said Lord Arryn was taken quickly. Even Maester Pycelle was helpless, but he brought the milk of the poppy, so Jon did not linger long in pain.† â€Å"That is some small mercy, I suppose,† he said. She could see the grief on his face, but even then he thought first of her. â€Å"Your sister,† he said. â€Å"And Jon's boy. What word of them?† â€Å"The message said only that they were well, and had returned to the Eyrie,† Catelyn said. â€Å"I wish they had gone to Riverrun instead. The Eyrie is high and lonely, and it was ever her husband's place, not hers. Lord Jon's memory will haunt each stone. I know my sister. She needs the comfort of family and friends around her.† â€Å"Your uncle waits in the Vale, does he not? Jon named him Knight of the Gate, I'd heard.† Catelyn nodded. â€Å"Brynden will do what he can for her, and for the boy. That is some comfort, but still . . . â€Å" â€Å"Go to her,† Ned urged. â€Å"Take the children. Fill her halls with noise and shouts and laughter. That boy of hers needs other children about him, and Lysa should not be alone in her grief.† â€Å"Would that I could,† Catelyn said. â€Å"The letter had other tidings. The king is riding to Winterfell to seek you out.† It took Ned a moment to comprehend her words, but when the understanding came, the darkness left his eyes. â€Å"Robert is coming here?† When she nodded, a smile broke across his face. Catelyn wished she could share his joy. But she had heard the talk in the yards; a direwolf dead in the snow, a broken antler in its throat. Dread coiled within her like a snake, but she forced herself to smile at this man she loved, this man who put no faith in signs. â€Å"I knew that would please you,† she said. â€Å"We should send word to your brother on the Wall.† â€Å"Yes, of course,† he agreed. â€Å"Ben will want to be here. I shall tell Maester Luwin to send his swiftest bird.† Ned rose and pulled her to her feet. â€Å"Damnation, how many years has it been? And he gives us no more notice than this? How many in his party, did the message say?† â€Å"I should think a hundred knights, at the least, with all their retainers, and half again as many freeriders. Cersei and the children travel with them.† â€Å"Robert will keep an easy pace for their sakes,† he said. â€Å"It is just as well. That will give us more time to prepare.† â€Å"The queen's brothers are also in the party,† she told him. Ned grimaced at that. There was small love between him and the queen's family, Catelyn knew. The Lannisters of Casterly Rock had come late to Robert's cause, when victory was all but certain, and he had never forgiven them. â€Å"Well, if the price for Robert's company is an infestation of Lannisters, so be it. It sounds as though Robert is bringing half his court.† â€Å"Where the king goes, the realm follows,† she said. â€Å"It will be good to see the children. The youngest was still sucking at the Lannister woman's teat the last time I saw him. He must be, what, five by now?† â€Å"Prince Tommen is seven,† she told him. â€Å"The same age as Bran. Please, Ned, guard your tongue. The Lannister woman is our queen, and her pride is said to grow with every passing year.† Ned squeezed her hand. â€Å"There must be a feast, of course, with singers, and Robert will want to hunt. I shall send Jory south with an honor guard to meet them on the kingsroad and escort them back. Gods, how are we going to feed them all? On his way already, you said? Damn the man. Damn his royal hide.†

Who Is A Peer Leader - 1362 Words

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