Drama - Writing In Role

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Drama Unit 1 Task - Writing In Role

The door loomed up in front of me, an endless plank, taunting me to open it, to reach up and face Alice up. I envisioned her, the pain, the tears, the confusion, the expression of disgust on her face. As I thought of this, though, it suddenly hit me - I didnt actually care. All I thought about these days was Anna, and being with her again. It was becoming obsessive. But that wasnt the problem right now. The problem was telling Alice I was ending it with her. I think Ill do it quickly. You know, the old; 'Im leaving you, youve got a week to get your stuff out, no, you cant have the vase your Mum gave us, oh dear, dont cry, please, I wish I hadnt hurt you so much. Boo-hoo. In and out, 15 minutes. Whats the time? 10. Ill be at Annas again by one.

Well, that didnt quite go as planned. I kept it down to an hour, at least. She wanted to go, straight away, and while I couldnt give a stuff with her wandering off, itd give me time to pack her stuff at least, I didnt want her being hit by a car. The policed investigate me, because wed had a row. And I might get in trouble for negligence, letting her go in that state.

I got her calmed down after a while, though, and she hopped in her car to go and stay at her mums. I said if she wanted a taxi Id lend her some cash, but she said she wouldnt have anything to pay me back with. Oh well. I separated out all our stuff before heading off to Annas, I dumped her crap at the bottom of the stairs. She can box it up tomorrow or whenever, but I told her to come when Ill be there, 'cause she doesnt have a key.

Once I got to Annas, I told her what had happened. She wasnt best pleased, I think she thought more of Alice than I did. Cant see what she thinks of her really. I mean, theres a time when I used to go for all that huggy, wimpy stuff. But it got tiring very quickly, she wont stop simpering up to me, its like Im the only thing in her life. Maybe thats why she was so devastated, but thats not my problem. Shes the one with boundary issues. I made it up to Anna, anyway, gave her that ugly old vase Alice was so keen to have, told her I bought it at an antiques auction, worth a mint. Alices mum probably bought it from a charity shop for 50p, silly old cow. Anna was chuffed, though, she doesnt know what shes on about with that sort of stuff.

Shes finally cleared out her stuff. Started crying again when I said Id given the old vase to Anna. Said it was an heirloom. Not my problem, didnt know, did I? Probably wasnt, anyway.

Probably just wanted to have it, she doesnt respect other peoples feelings like that, only cares about herself. Im not falling for it. Shes had a couple of weeks to stew over this, and I reckon shes feeling a bit angry, angry or clingy. She either wants me back so badly shes not going to leave, or once Im out of sight shell start smashing up everything she can find. So Im playing it safe. Ive said, shes got an hour to get it all done, (no I cant lend a hand, new suit) and Im watching her do it all, just in case. She wants a cup of tea now. Scab. I reckon therell be no end of her trying to pilfer money and stuff off me. I dont care if youve been laid off, because your Mum doesnt live locally and your cars broken down, it isnt my problem. Find a new job up there. Nothing around? You telling me there isnt a Somerfields in Milton Keynes? Im sure theyve got a shelf stacker opening somewhere. Its not my problem anymore.

This is taken from the first scene of a play by Patrick Marber, so if you use this, youll need to get that too, so the examiner knows where you are (supposedly) writing from.

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ALS - Amnyotrophic Lateral Schlerosis

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ALS is actually Amnyotrophic Lateral Sclerosis, but it is commonly known as Lou Gehrigs Disease. It comes from greek words meaning A-without; Myo-muscle; Trophic-nourishment; Lateral-side (of the spinal cord); and Sclerosis-hardening or scarring. This disease is a rare ailment where the bodys neurons die, causing the muscles in your body to waste away and become paralyzed. ALS is not contagious, however at least 10% of ALS cases are hereditary. 0,000 Americans face the grim prospect of spending their final days feeling virtually buried alive as they go through the terrible effects of ALS. This disease was named after a Yankee slugger who died at age 6 in 141 from this disease. Lou Gehrig was a famous baseball player in the US during the 10s. He became afflicted with ALS at age 6, just years after being diagnosed. Tony Cortinas is an ALS patient. He was diagnosed with ALS in 17 and since then has lost the use of his arms and hands and, at 54, is showing signs of advanced ALS respiratory problems, frequent choking, nearly unintelligible speech. This disease does not just affect a single person, it affects everybody in that persons life.

ALS attacks nerve cells in the brain as well as the spinal cord, which controls muscle movement. The motor neurons shut down and die; victims lose more and more of their ability to move. It affects speech and swallowing when the disease involves the corticobulbar area of the brainstem. Death of this disease comes when the chest muscles can no longer force air in and out of the respiratory tract or when food becomes stuck in the lungs, causing aspiration pneumonia, which usually comes -5 years after the disease is diagnosed.

Some of the first signs of ALS are in the inability to do simple tasks, such as turn a door knob or button a shirt. Other early symptoms including tripping, dropping things, abnormal fatigue of the arms and/or legs, slurred speech, muscle cramps and twitches and uncontrollable periods of laughing or crying. The hands and feet may be affected first, causing difficulty in walking or using the hands for the activities of daily living such as dressing, washing and buttoning clothes. The condition starts on one side of the body, then moves to the other side. Your muscles begin to degenerate, and the person loses weight. Soon they lose their ability to swallow or sometimes even to breath. Because the disease frequently takes it toll before being positively diagnosed, many patients are debilitated before learning that they have ALS. ALS does not affect the mind. Mental acuity remains sharp. In most cases, even when the patient is totally paralyzed, the mind functions normally. The mind remains alert, but they are trapped in a withering body.

There is no cure for ALS, but there are treatments for controlling symptoms. One drug is rilazole, which has been shown to prolong survival of ALS patients. Antipasmodic drugs, such as diazepam, are available as are drugs to help patients that have problems with swallowing. When your muscles fail to receive messages, they weaken, atrophy, and die. It affects about 7 to 8 people out of every 100,000. According to the United States National Institute of Health, some 5,000 people in the US are newly diagnosed with ALS each year (thats 1 a day!). Anyone at any age can get ALS; however most who develop ALS are somewhere between the ages of 40 and 70. There are though; however, cases of the disease attacking persons in their twenties and thirties. It was once believed men developed ALS more frequently than women. 0% of ALS cases are people with no family history of this disease. ALS is almost always fatal. There are rare cases where the disease progression plateaus or stops. There are few cases of people reporting a reversal of symptoms. Write my Essay on ALS - Amnyotrophic Lateral Schlerosis cheap

ALS was first discovered in scientific literature in 186 by the French Neurologist, Jean-Martin Charcot. ALS and Lou Gehrigs Disease are not the only names for this disease. Some other names are MND, Motor Neuron Disease known by the England. The French refer to ALS as Maladie de Charcot. People with ALS usually die within 18 months after diagnosis. Only about 0% survive 5 years, and 10% live longer than 10 years.The cause of ALS is unknown. Researchers know that an excess of a neurotransmitter called glutamate clogs the synapse of the nerve cell preventing transmission of neural impulses. Some of the effects of ALS may be painful. Common pains include pressure sores, muscle cramps, joint contractures, constipation, burning eyes, swelling feet, and muscle aches. ALS is diagnosed through a process of elimination and may take weeks or months to diagnose. Diagnostic tests include MRI, EMG, muscle biopsy and blood tests. There are three different types of ALS. The most common type is called sporadic ALS. This one accounts for 0% of ALS cases. Familial ALS is hereditary, which is passed on by a dominant gene. In familial ALS the disease is autonomic dominant, meaning that if a parent has ALS, their children have a 50% chance of inheriting the defective gene. The third type of ALS is called Guamian and is related to the high incidence of ALS on the island of Guam. ALS does affect your speech when the disease involves the corticabulbar area of the brainstem.

ALS is a very expensive disease. Medication, such as Rilutek can cost as much as $700.00 per month. Also, adaptive equipment is usually necessary, such as a power wheelchair, costing as much as $17,000. When a patient goes on a ventilator, skilled nursing care can cost in excess of $50,000 a year. Insurance companies, Medicaid and Medicare may pay some of the expenses for the patient.

REFERENCE PAGE

ALS (Lou Gehrigs Disease) Information Page

http//www.mindspring.com/~jmcmullin/als.html

The Eshlem Family. ALS Survival Guide. 00.

http//www.lougehrigsdisease.net/asl_what_is_als.htm

Wagman, Richard J. "Amyotrophic Lateral Sclerosis" The New Complete Medical and Health Encyclopedia. 00. -.

Please note that this sample paper on ALS - Amnyotrophic Lateral Schlerosis is for your review only. In order to eliminate any of the plagiarism issues, it is highly recommended that you do not use it for you own writing purposes. In case you experience difficulties with writing a well structured and accurately composed paper on ALS - Amnyotrophic Lateral Schlerosis, we are here to assist you. Your cheap research papers on ALS - Amnyotrophic Lateral Schlerosis will be written from scratch, so you do not have to worry about its originality.

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Free Essay's Rule

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Free Essays are extremely helpful whether it be with homework or long term projects. The Red River Settlement is a dreadful place to live. The land is terrible, as well as there being bug and bird infestations. Selkirk could not be anymore wrong about the area. The weather is harsh with the long cold winters. The land is right in the middle of native and company rivalries. Also the voyage is a long and treacherous one.

The long cold winters provide only a short and unfulfilling harvest season. The soil is just as bad and will not profit a good crop. If you do manage to have a profitable crop you will not be able to grow it for an extensive amount of time since the land is not even surveyed yet. There is an infestation of grasshoppers and birds, which will also affect the outcome of your crops.

The land is nestled in among native rivalries. Therefore it could be considered a target of or a threat to the natives. If that isnt enough you have to take into consideration the ongoing competitions between the Northwest Co. and the Hudson Bay Co. the area could be in constant change of possession or in the midst of battle, putting your family at unnecessary risk.

Last and not least in order to reach the Red River Settlement you must endure the perfidious journey. It can last for weeks. It can make you more susceptible to diseases like scurvy or scarlet fever, once again an easily avoidable risk. The ships to take you to the settlement are crowded and most defiantly could not be considered as luxurious. To put yourself trough all of this to reach a land that is just as bad, if not worse you would have to be delirious.

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As stated, the red river settlement is barbaric and unfit for a family or human being. It is desolate, forlorn and disconsolate. The facts are plain to see. You are better off to stay were you are, to avoid risk, and to keep a sustainable living. In conclusion it is obviously a indigent choice to move to the red river settlement.

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