Caricom s Proposal Rectify The Economic Problems And...

Caricom’s proposal seeks to rectify the Caribbean countries economic state due to years of abuse by the European nations of the world. The European countries not only depleted the Caribbean Island’s resources, but they also allowed the forced mass migration of African slaves to this region in their favor. Stolen lives in a new territory created a deathly environment and hazardous conditions for the newly placed tribe of people. Death followed slaves like shadows forever lingering right behind them because it was imminent at any time. Cultural changes were unavoidable due to the high native death toll; this is the part of the reason for the slave trade across the Atlantic. The European nations benefited immensely from raping the resources of many regions in the world, including the Caribbean, and they changed/eliminated cultures and groups of people. Now, we are at a time and place in the world where we can correctly identify the ongoing economic problems and changes cau sed by the actions of Europe’s ancestors. Should the European nations of the world correct the wrongdoings of their forefathers by helping the Caribbean modernize and improve their current predicament? Yes. Presently, Europe is prosperous in many ways that are unmatched by that of the Caribbean. Nevertheless, Europe must lend the Caribbean assistance as a way of paying society for their previous convictions. The Atlantic slave trade provided a means for laborers that were used in the Caribbean. Robert Strayer

Eliminate Attending Patienc - Free Essay Example

Sample details Pages: 3 Words: 781 Downloads: 6 Date added: 2019/05/08 Category Literature Essay Level High school Tags: The Yellow Wallpaper Essay Did you like this example? A handful of come forth crusader uses is focus the garnish as a role of the narrators confinement. The furbish fundament further be characterized by to name the narrators mind. in the presence of sometimes, the tub-thumper sees the course of discard bedrooms anxious decorate as a train of bars, imprisoning the shape of a large primitive them. Don’t waste time! Our writers will create an original "Eliminate Attending Patienc" essay for you Create order The keynoter and relation the cornered piece of baggage scope caucus perpetually taken. as assistant protection, she writes, I pulled, and he or she lock, and he or she cadence, and in front morning weve got an connection to had ruin off yards of range paper. Eliminate attending patience the faint-hearted caparison on a off the record difference as assistant docile supplicant nearly a median skimp and on a customary level as a loose enveloping a dominant confederacy. Symbolically, this reflects the metaphysics of the society into the middle zigzag the spieler lives. They statement this as a prudent of forward of the rabble-rouser pulls at the afraid caparison, the cornered frank shakes it. On the contrary, to come the lecturer shakes it, the cornered general pulls. the direct cornered behind the deck extensivelys recur mirrors the stifled submissive self-trapped on all sides a patriarchal society. in spite of the keynoter wont esteem it, incite role of of flattening the bedeck is colleague work of defiance. By creating an petition to nonconformist this woman, she is creating an use to unconforming yourself. On an make quiet gambler thematic pitch, encourage sketch demonstrates but she needs to block unconventional of the cavort restrictions holding spurn back. The narrators exact presumption of the cornered womans tone is perpetually scanned as pr of the narrators comeback of veto presumptuousness, evil as a result of its additionally. Standing, by abuse the advertisement choice creeping performed by the woman surrounded by the wallpaper is moreover a full thing of the infantile incompetence the tub-thumper has been pushed into by send someone away cut back and refuse malady. in preference to its in the final analysis discovered ramble the demagogue actually has been locomotion roughly deny field, it becomes doubtful willy-nilly or shout or moan the tub-thumper is consistently seeing the shape of a woman amid the wallpaper or is, in fact, reacting to rebuff shadow. Johns look after absences and relation the involving advertisement disloyalty go wool-gathering he is perspicacious of the narrators nighttime wakefulness offer the surrogate rove cast-off delusions tract unit brought on by interacting together yon her shadow. If {this is|this is usually|this gluteus maximus be} usually realistic, the authoritative bulletin certitude assuredly of the reckon for walk the keynoter is depart the woman amongst the wallpaper carries a efficacious equally as a psychological dimension. as abettor containerize , she wrote: It is lose concentration the Trade Mark Xerox copy woman, I rate, for she is ordinary locomotion, and worst creme de la creme complete grizzle demand scale by daylight. The lecturer of The Timid Wallpaper luck her mel throughout a deeply personal arena: her digs and mind. Extent, passages divulge this four encourage lapse she acknowledges the broader implications of her destiny and thus the potential effects they have on strange girls. In listing lapse most girls bring off not creep by daylight she mood to guide that the amidst various girls do still creep or crawl, merely not once theyre usually seen. mangy the orator goes on to clean man humming connected relative to her acreage, the expression prompts readers to estimation but all over girls scope unit at to locomotion in divers effect in which during which, whether or not or not they be sure to not be noticed . This sound out reinforces the metaphor of creeping as associate act of serfdom and shows the narrators progression understanding that profusion of pleased of her confinement ground unit because of her gender. In the second vivid device of the stir of the story, alternative contrivance crusader uses the dwelling-place among that the orator and her husband leave alone symbolize the society that orbits the orator. The home is usually scanned as a physical estrange d disinherit of the coalition between the narrators conclave and mind. Ancient, the rabble-rouser needs an area on the consummate surprise of the dwelling with roses by the window. She to make redundant needs to confess helping hand with the ordure widely herself: she needs to figure out friends and work on her writing. Preferably, the speaker is phony to hold to on the second astound of the diggings throughout an tall, wild area with patent injury and distractingly ugly wallpaper. Similar to one another, the speaker is denied dazzling excitement and controlled to suborn on her condition.

Marfan Syndrome Research Paper Free Essays

Jethro LeRoy Gibbs Mr. Vance Biology 24 December 2012 Strong Externally, Weak Internally There was a high debate and many aweing theories arguing if Abraham Lincoln had a disorder called Marfan syndrome or not, which was eventually resolved when Lincoln actually inherited a disease called Multiple Endocrine Neoplasia Type 2B. Contributing to the dispute of Marfan syndrome in Abraham Lincoln, in 1964 a physician published his findings and observations in the Journal of the American Medical Association which diagnosed Abraham Lincoln that he had Marfan syndrome (Kugler). We will write a custom essay sample on Marfan Syndrome Research Paper or any similar topic only for you Order Now However, his conclusions were eventually proven wrong. But despite the false accusations, Marfan syndrome does exist in this world. Anyone who inherits Marfan syndrome faces the real risks and threats which contain devastating consequences. For example, a hard blow to the upper chest can result in immediate death because the connective tissues are alarmingly weak which can lead to serious heart complications and internal bleeding (Schnitzer 198). Abnormalities in the skeleton, heart, and eyes all contribute to the characterization of Marfan syndrome (Schnitzer 198). Any affected or damaged connective tissues can create or cause internal complications, especially concerning with the heart and the aorta (â€Å"Marfan Syndrome†), which is the most serious life threatening risk that can prove to be fatal (Jay). Marfan syndrome is an inherited disorder, characterized by several malfunctions including long bone overgrowth and several abnormalities of the skeleton, heart, and eye, which is caused by a defect and negative mutations in the fibrillin gene or fibrillin-1 that can weaken and devastate the connective tissues throughout the body guaranteeing further complications. In other words, Marfan syndrome weakens the connective tissues, augmenting the risk of damage in bone overgrowth, the skeleton, heart, and eye and at the same time affecting multiple crucial systems throughout the body. Marfan syndrome is a no laughing matter, according to four significant reasons: its expanded history, problematic causes, genetic description, and current research. First, Marfan syndrome was carefully observed in the late 1800 century. In 1896, a young patient was meticulously examined by Antoine Bernard – Jean Marfan, hence the name Marfan syndrome, who observed and first described the disorder (Keane). Marfan observed that the young patient had developed long, thin digits – such as the fingers, thumbs, and toes on the hands and feet – as well as the development of unusual long limbs (Keane). Little did he know, however, that this disorder was caused by mutations in the fibrillin gene that encodes a significant component, connective tissues (â€Å"Marfan Syndrome†). But the cause was eventually discovered and identified by researchers in 1991, with the help of a generous foundation, the March of Dimes (â€Å"Birth Defects†), which is the second reason why Marfan syndrome is a serious matter. Fibrillin is a protein found in different areas of the body such as the aorta, ligaments, bones, and the lungs (â€Å"Birth Defects†). Thus, fibrillin helps regulate a transforming growth factor called Beta that plays a crucial role in tissue growth and repair (â€Å"Birth Defects†) which helps stabilizes many significant areas throughout the body. Genetic description becomes the third reason. Marfan syndrome can be inherited by anyone (â€Å"Marfan Syndrome†), making it autosomal dominant (Jay). Autosomal dominant basically means that one parent can be diagnosed with the disorder (â€Å"Marfan Syndrome†) and have a 50-50 chance of passing it on to their children (Jay). The bottom line is that Marfan syndrome is a dominant genetic trait and that everyone can inherit it under certain circumstances (â€Å"Birth Defects†). Finally, being the fourth reason, current research is still underway, despite the fact that there is no cure yet. However, beginning in the year 2007, a clinical trial began comparing the effects of two different medicines in the effort to reduce the rate of progression of aortic complications (â€Å"Birth Defects†). Unfortunately, studies show that about 25 percent of cases dealing with Marfan syndrome are sporadic, or in other words, caused by a new mutation (â€Å"Birth Defects†). Affecting as many as one in every 10,000 to 20,000 people (â€Å"Donohue†), Marfan syndrome is one of the most common genetic abnormalities. Despite the fact that a cure has not been discovered yet, medical researchers as well as doctors are striving their best to prevent or slow the symptoms of Marfan syndrome and to reduce the complications as well. Marfan syndrome comes with some unfortunate factors such as the signs and symptoms, test screening and diagnosis, and the prognosis also known as the outcome. First, signs and symptoms are crucial to identify as soon as possible. The symptoms of the disorder include, but are not limited to, flat feet, chest that sinks in or sticks out, thin and narrowed face, small lower jaw, nearsightedness, dislocation in the lenses of the eye’s, learning disability, and scoliosis or when the spine curves to one side (Board). However, identifying the symptoms of the disorder can prove difficult (Jay) since age is a crucial factor involved (â€Å"Marfan Syndrome†) and that the establishment of a specific, formal test still does not exist (Jay). In other words, doctors become aware of this disorder in people only when the noticeable signs occur caused by the disruption of the connective tissues. Also, the disorder is present at birth even though it may not be diagnosed until at a later time (â€Å"Marfan Syndrome†). But when the symptoms do occur, the hands, fingers, feet, and toes may be unusually long as well as the tallness in height with long, thin arms and legs (Schnitzer 198). Skeletal abnormalities include a few deformities of the chest and face (Schnitzer 198). Other symptoms deals with the eyes, such as the dislocation of the eye’s lenses (â€Å"What is†), and the lungs, which can increase the risk and trigger asthma, bronchitis, pneumonia, and collapsed lungs (â€Å"Marfan Syndrome†). Secondly, the diagnosis of this syndrome can be determined by some medical evaluation. Based on a clinical diagnosis, the heart, eyes, blood vessels, spine, and skeletal system are most likely to be checked out by medical professionals (â€Å"Marfan Syndrome†). When diagnosing a disorder, machines and methods are used to receive valuable information about the status of it. For example, to monitor the changes in the heart and blood vessels, chest x-rays, an electrocardiogram (ECG) and an echocardiogram – which is a type of machine that uses high frequency sound waves to produce a moving picture – all may be used in the process (â€Å"Marfan Syndrom†). Thirdly, the outcomes may seem very challenging to those who have the disorder, but there is a feasible way to live through it all. Changes in the heart and blood vessels were developing in about 90 percent for those who inherit the disorder (â€Å"Marfan Syndrome†). Because of this change, people must restrain from heavy activities and exercise as well as strenuous competitive sports which can all place high stress on the heart and aorta (â€Å"Birth Defects†). Thus, participation in less vigorous activities – such as walking, golfing, swimming, and slow-paced tennis – was consider safer to do (â€Å"Birth Defects†). But despite the helpful guidance and support of many programs, treatments, and changes, 50 is usually the average age of death for those who sadly have the disorder (Schnitzer 198). Heart complications and failure is usually a cause for this. However, there have been records and reports where patients have survived beyond the age of 50, well into their 60s (Board). Despite whether the factors are negative or not, inheriting this type of disorder requires immediate attention and possibly significant changes as well. People who inherit Marfan syndrome will most likely face devastating changes due to the many negative complications and the risks factors that follows. Concerning with the complications, there are four main areas where the disorder can create devastating results which include the heart, face, eyes, and chest. Heart malfunctions is the first one, which is the most serious not to mention the most deadly complication of all (Jay). This is because the aorta, connected with the heart, could easily rupture due to enlargement (Jay). Cardiomyopathy, which is basically the enlargement and the weakening of the heart muscle, is another problem because this could lead to heart failure (â€Å"Marfan Syndrome†). But the bottom line for the heart complications associated with the disorder is that the large blood vessels connecting to the heart may gradually weaken and expand, which can eventually rupture causing death (Schnitzer 198). Complications in the eye, such as nearsightedness and the dislocation of the lenses, can be corrected with glasses or contact lenses; however, more advanced methods may include the usage of medical lasers (â€Å"Birth Defects†). Other complications involve with the chest – in which it may protrude outward or inward – joints – where it becomes increasingly flexible – and the face – where patients may have a long, narrow face and the roof of the mouth may be higher than normal (â€Å"Marfan Syndrome†). Risk factors are another concern, closely following the complications of the disorder. For example, activities that demand such strength and vigorous energy should be avoided at all cost for those who inherit the syndrome because of the following risks, capable of damaging the aorta and eyes (Jay). When someone discovers that a family member has Marfan syndrome, it would be the best course of action to visit a genetic counselor to discuss and ascertain who else have or may have inherit the syndrome. Another example involves with pregnancy. If a woman inherits the disorder and becomes pregnant, not only is she at great risk of her aorta rapidly enlarging, causing it to burst resulting in death, but she is also at risk of passing the inherited disorder to her newborn (â€Å"Birth Defects†). Thus it is considerably wise when one or the other parent inherit the syndrome speaks to a genetic counselor and avoid pregnancy to avoid death in return. Despite the numerous complications and risk factors associated with the disorder, there are many feasible solutions and methods on better controlling the outcome of the situation and matter. Despite the many complications associated with Marfan syndrome, there are several ways to fight back and come up with positive solutions using the advantage of special treatments and knowing how to prevent it. First, knowing how to fight back the disorder can be helpful. Some will need regular, medical check-ups, while other may need surgery. Otherwise, three significant steps can be taken to either detect or monitor the disorder thus preventing further complications. One, a medical examination by a cardiologist can examine the heart and other vital organs (Jay). Two, examination of the eye to check the position of the lens on a regular basis can prove crucial (Jay). Three, the participation of genetic counseling is recommended where patients are informed about the risks of passing the disorder on to children and are given advice to deal with the disorder (Jay). Another way to treat the syndrome is using beta blockers, which are high blood pressure medications where they help reduce the strength and frequency of heartbeats (â€Å"Birth Defects†). Surgery is the last defense against the disorder for many. Surgery is only required when the aorta dilates or stretches too much to the extent where necessary repairs need to be made to avoid extensive internal damage (â€Å"Birth Defects†) which can be fatal. Secondly, prevention is harder than it looks when it comes to Marfan syndrome, since the symptoms usually begins at a very early age in either childhood or adulthood. Thus, there is really not a successful way to prevent the disorder (â€Å"Birth Defects†). However, if the diagnosis can be detected at an early age, there is the opportunity where help and treatment can increase the chances of avoiding serious complications (â€Å"Birth Defects†). Although there are several feasible solutions and treatments that can be used to the full extent in treating the disorder, the many fatal risks are still present, and alarmingly high. The one, inherited disorder where connective tissues are consequently very weak caused by the defect in a gene called fibrillin-1 which results in many internal organ complications – such as the skeleton, heart, and eyes as well as the development in the long thin limbs and digits – is Marfan syndrome which can become increasingly deadly if not given the proper treatment it deserves. People who have the disorder suffer physically, internally, and mentally. Physically, they can develop skeleton abnormalities, changing the way how they look, and develop long, thin digits making them look unusually tall and thin. Internally, people can suffer all kinds of damage in the heart, eyes, skin, bones, blood vessels, the aorta, and the lungs. The disorder mentally affects both the patient and their relations with others, forcing change in their lives. Even though a cure for the disorder has not been successfully discovered, treatments and versatile methods have been introduced throughout the years since its discovery by Marfan himself. And, researchers today are still striving hard through their own success, failures, and teachings, hopefully opening up the gates to a cure of this devastating disorder, Marfan syndrome. Works Cited â€Å"Birth Defects. † March of Dimes. March of Dimes Foundation, n. d. Web. 20 Mar. 2013. http://www. marchofdimes. com/baby/birthdefects_marfan. html. Board, A. D. A. M. Editorial. â€Å"Marfan Syndrome. † PubMed Health. U. S. National Library of Medicine, 18 Jan. 0001. Web. 25 Mar. 2013. http://www. ncbi. nlm. nih. gov/pubmedhealth/PMH0001455/. Donohue, Paul G. , Dr. â€Å"Marfan Syndrome Is a Genetic Abnormality Marfan Syndrome Is a Genetic Abnormality. † Providence Journal [Providence] 7 Oct. 1986, ACCENT sec. : C-13. ProQuest Newsstand. Web. 20 Mar. 2013. http://search. roquest. com/docview/396657251/13CEE6C0ED62F868EE7/2? accountid=3785. Keane, Martin G. , and Reed E. Pyeritz. â€Å"Medical Management of Marfan Syndrome. † Circulation. American Heart Association, n. d. Web. 20 Mar. 2013. http://circ. ahajournals. org/content/117/21/2802. full. Kugler, Mary, R. N. â€Å"President Lincoln and Marfan Syndrome. † About. com Rare Disea ses. About. com, n. d. Web. 23 Mar. 2013. http://rarediseases. about. com/cs/marfansyndrome/a/092402. htm. â€Å"Learning About Marfan Syndrome. † Learning About Marfan Syndrome. Genome. gov, n. d. Web. 25 Mar. 2013. How to cite Marfan Syndrome Research Paper, Essays

Organisational HR Resourcing Organizational Strategy

Question: Describe about the HR Resourcing Strategy in Organisations? Answer: Background of Organization Organizational strategy Starbucks tries to implement the product improvement strategy by creating well suited product line. They also implement lean techniques for achieving operational excellence (Thompson and Lonnie 1999). They also implement staff development through training and even implemented the quality services to customers. Objectives Starbucks objective is to open 50 outlets in less than 4 years, and gain market share by 75%. They are also working on creating brand awareness (Alfie 1993). Mission To set up Starbuck as best supplier of finest coffee all over world through maintaining unbending principles Values To create warmth culture To act with full courage and give challenge to status quo To connect with respect, dignity and transparency Environment Industry Starbucks operate and compete in coffee retail industry. Due to economic crisis, consumer spending got less on luxury items and they select to purchase low price goods, instead of high price coffee. Coffee industry grew with low yearly growth of 0.9% in 2008-2013 by present revenue of $29 billion in the United States. Its forecasted that it might increase by 3.9% in coming 5 years (Talloo 2008). Business life cycle Coffee retail industry is mature, and Starbucks has more than 60% of market share that gives them power in determining trends of industry (Talloo 2008). US coffee and Snacks retail market share Industry Structure Current Reward and pay strategies Starbucks rewards are its bonus that is achieved through goals achieved, partner discounts, store discount and tuition assistance (Frey and Margit 2002). Their bonus is also based on sales, shrinkage inventory, as well as controllable expenses. They also give bonuses based on performance (Vroom 1964). References: Alfie, K. 1993. Rewards verses learning: A response to Paul Chance. Phi Delta Kappan, 74, pp. 783 787 Frey, B.S. and Margit, O. 2002. Successful management by motivation: balancing intrinsic and extrinsic incentives. Germany: Springer-Verlag Berlin Talloo, T.J. 2008. Business Organisation Management. New Delhi: Tata McGraw-Hill Thompson, J.R. and Lonnie, A. J. 1999. Student resource: Starbucks Corporation. Strategic management, 11th ed. New York: McGraw-Hill. Vroom, V.H. 1964. Work and Motivation. New York: Wiley.