Surname Meaning and Family History Soto

Soto is a surname of Spanish origins commonly thought to refer to one who lived near or in a forest or grove of trees, or possibly a swamp. From the Spanish soto meaning grove or small wood. Soto (also spelled Desoto, Delsoto, de Soto, or del Soto) can also be a  habitational name from any of several places called Soto or El Soto. Soto is the 34th most common Hispanic surname. Common Locations The surname distribution data at  Forebears  ranks Soto as the 472nd most common surname in the world, identifying it as most prevalent in Mexico and with the highest density in Chile. The Soto surname is the 6th most common last name found in Chile; the next closest are Puerto Rico, where it ranks 24th, Costa Rica (40th) and Mexico (50th). The Desoto surname variant is most common in the United States, while de Soto is most prevalent in the Dominican Republic and Guam. Within Europe, people named Soto are most frequently found in Spain, especially in the regions of Murcia, Galicia, and La Rioja. The surname is also very common in Argentina, especially the Patagonia region. Famous Sotos Jesà ºs-Rafael Soto: Venezuelan kinetic painter and sculptorHernando De Soto: Spanish conquistador and explorerGary Soto: American author and poet Sources ï » ¿Cottle, Basil.  Penguin Dictionary of Surnames. Baltimore, MD: Penguin Books, 1967.Hanks, Patrick and Flavia Hodges.  A Dictionary of Surnames. Oxford University Press, 1989.

Hiding Salem The Other Witch Hunt Of 1692 By Richard...

Book Analysis: Escaping Salem: The Other Witch Hunt of 1692 by Richard Godbeer In Escaping Salem: The Other Witch Hunt of 1692 by Richard Godbeer examined the witchcraft hysteria which happened in Stamford, Connecticut as the hysteria escaped from Salem, Massachusetts and how the panic of witchcraft caused by Katherine Branch in June of 1692, intensified beliefs and readjustments in the legal system in the Puritans society in Stamford, Connecticut. Consequently, Katherine Branch’s accusations in the summer months of 1692, propelled the Puritan community of Stamford into the witchcraft hysteria, as she claimed to have been bewitched and through spectral visions blamed those of who bewitched her; be they human or animal. As such, Puritans†¦show more content†¦However, when the husband comes home and seen Branch â€Å"still lying on the for, her eyes red from crying and her hands clasped as if held in place by an invisible force.† (p.15). when the husband, Daniel, seen Branch in such a state he recalls when his daughter his eldest, Joanna, similar torment and had yet to get over the event. Nevertheless, Branch continued to stay stiff and crying on the floor even after a midwife, Sara Bates, seen to her. When relief came to her in short bursts she stated, â€Å"†¦whilst out in the field gathering herbs she had been seized with a pinching and pricking at her breast† (p. 16). During Katherine’s fits, she would fall into trances, became stiff, cried and shook, as such she began to see spectral visions of the witches who had bewitched her in both human and animal forms. Thus, these bouts of fits Katherine Branch had after picking herbs caused the witch scare to settle in Stamford, Connecticut because in her spectral visions she will go on to accuse five women, who will be tried in the Court of Oyer and Terminer. Puritan society had class system much like every colony now which started with the elite or gantry, middle class, in denture servants and lastly the slaves. The Puritans community was on based off strict religious customs. However, the people do have a voice in this society called Public Opinion which is like a jury. Moreover, Godbeer portrayed the Puritans as abrasive towards

Competitive Strategy for Alibaba and Tesco - myassignmenthelp.com

Question: Discuss about theCompetitive Strategy for Alibaba and Tesco. Answer: Alibaba Group Alibaba Group is a Chinese company established in 1999 in China. The companys headquarters are located in Hangzhou, Zhejiang, China. The company was founded by Jack Ma. The company is an e-commerce website that provides customer to customer, business to customer and business to business services to its customers. It has operations across 200 countries. In 2016 the company defeated worlds largest retailer Wallmart and secured the topmost position. The company began as a website that was designed to help small Chinese manufacturers and retailers to sell their products in global markets. Now the company is a world leader in online and mobile e-commerce. Today the company has expanded its portfolio to digital media, cloud computing and entertainment (Alibaba group 2017). Today Alibaba is more successful than eBay and Amazon together. The credit for Alibabas success could be credited to unique business model and sustaining the competitive advantage through innovation and development. The company had a unique business model that was designed only for small enterprises. This model provided value to small enterprises that were not possible individually (Pavie 2016).Alibabas business model is different from that of competitors rather than normal e-commerce company, Alibaba makes efforts to provide best service quality to sellers and buyers. The company works on the principle of collectivism and trust. People look up to Alibaba as a platform where they can build up trade connections with people internationally. It is easy to gain competitive advantage but difficult to sustain it. Every company needs to do something innovative in order to remain in the competition. The company sustained its competitive advantage through time to time innovations. The major s uccessful innovations that helped the company secure current market standing are discussed below (Success story 2017): In 2003 Alibaba founded Taobao. Taobao is a customer to customer retail sales website of Alibaba group. In 2004 the company offered Alipay. It is an app which holds payment and releases it to the seller only when the product is received. In 2005 the company entered into a partnership with Yahoo and acquired Yahoo China. In 2008 the company launched a web portal known as Tmall. In 2010 company introduced a search engine for shopping named eTao. In 2011 the cloud computing team of the company launched mobile operating system. The above examples show that company did not stop at one place it continuously evolved to sustain the competitive advantage. The other reasons for Alibabas success are consistently creating value to the firm. The company always keeps its customers at first priority. Alibaba does constant efforts to increase customer satisfaction. The company reduces cost for customers by innovation in the traditional supply chain. The company also reduces the product turnover time by application of latest technology in the business. It has also launched a venture named Alipay which allows the customer to release payment after the product is received. To analyze the needs of its customers Alibaba takes help from its huge customer behavior data. The company offers various other support services to its customers (Redaction, R. 2016). Tesco Tesco is a British multinational company. Tesco is a well-known grocery and general merchandize retailer. It was founded by Jack Cohen. The company is having in the United Kingdom but it operates in various countries around the globe. Tesco began as a small market stall in 1919 and today it is a leading market player in the industry. It has around 460,000 colleagues. It has about 6,809 across the world. Tescos vision is to serve customers little better every day. Today the company has expanded so much and emerged as a leading retailer because of its continuous innovative offers. Tesco is worlds third largest super market group (Tescoplc 2017). From a small grocery shop, Tesco became a leading retailer in the industry. The reasons for the success of the company can be credited to customer intelligence, innovation and a strong presence on social media. Tesco is the company that works to gain profound knowledge of its customers so that it could analyze customers needs ahead of the competitors. This knowledge gave Tesco an opportunity to sell more goods and services than its competitors. The company works not only to attract new customers but also takes initiatives to sustain old customers. Tesco provides club cards to its customers that provoke its customers coming back to the company. It has also offered price benefits to its customers. The company launched a scheme in 2015 that guaranteed that if the sum total of 10 or more products will be more than any of its rival, then the company will refund the amount to the customers. The company used price as a weapon to gain competitive advantage (Lee 2016). The next thing that is the essence of companys success is innovation. The company implements innovative ideas to take the first mover advantage and lie ahead of competitors. Innovation ideas at Tesco are based on two factors that are customers needs and future forces (Destination innovation 2017). One of the most successful innovations of the company is virtual stores. The company analyzed that South Korean customers are very busy and work for longer hours. They do not have time and energy to visit the stores for grocery shopping. The company came with an idea of virtual stores; these stores reduced the need for going to the stores to shop for the grocery. These stores provided product catalog at places such as bus stops and railway stations. The customers can scan the QR code of desired product through a mobile app and utilize their waiting time by shopping for groceries (Creevy 2011). This venture of the company gained immense success and a major contributor of todays market standing of the firm. Anothe r reason for the firms leading position is its effective promotional strategies. The firm is continuously engaged in social media marketing. Tescos face book and pages are constantly upgraded with the latest offers and schemes. Tesco also gives various advertizements on YouTube according to the occasion. The company keeps constantly turned up with various other digital marketing platforms. The promotional strategies of the company are aimed at creating an emotional touch with the customer. References Alibaba Group, 2017. History and milestones, viewed on 18 August 2017 from https://www.alibabagroup.com/en/about/history Creevy, J. 2011. Tesco opens virtual store in South Korea, viewed on 18 August 2017 from https://www.retail-week.com/topics/technology/tesco-opens-virtual-store-in-south-korea/5028571.article Destination innovation, 2017. The innovation process at TESCO, viewed on 18 August 2017 from https://www.destination-innovation.com/the-innovation-process-at-tesco/ Lee, A. 2016. How Tesco Became the UKs Biggest Retailer via Word-of-Mouth, viewed on 18 August 2017 from https://www.referralcandy.com/blog/tesco-marketing-strategy/ Pavie, X. 2016. Seven reasons for Alibabas success, viewed on 18 August 2017 from https://www.digitalcommerce360.com/2016/07/27/seven-reasons-alibabas-success/ Redaction, R. 2016. The seven reasons for Alibabas success ; Alibabas development and framework, viewed on 18 August 2017 from https://www.retailnews.asia/seven-reasons-alibabas-success-alibabas-development-framework/ Success story, 2017. Alibaba Group Success Story, viewed on 18 August 2017 from https://successstory.com/companies/alibaba-group Tescoplc, 2017. Our businesses, viewed on 18 August 2017 from https://www.tescoplc.com/about-us/our-businesses/

Physiotherapy management of newly diagnosed Cystic fibrosis (CF)

Introduction The diagnosis of cystic fibrosis has been enhanced in recent times. Hunt Geddes (1985) noted that, in the past, many children succumbed to the condition in less than a year after birth. In addition, very few victims lived for over a decade after diagnosis.Advertising We will write a custom essay sample on Physiotherapy management of newly diagnosed Cystic fibrosis (CF) specifically for you for only $16.05 $11/page Learn More However, great strides have been achieved in the management of the condition and over three quarters of the affected victims can now live up to adulthood with the condition. In recent times, treatment of cystic fibrosis has been advanced where both antibiotics and physiotherapy treatment are used to manage the condition. Maffessanti, Candusso, Brizzi, Piovesana (1996) noted that the diagnosis of cystic fibrosis is common among children with very few cases reported among those in middle and late adulthood. This paper di scusses the issues that one would need to consider in the physiotherapy management of the patient newly diagnosed with cystic fibrosis (CF). According to Di Sant’Agnese Davis (1976), individuals diagnosed with Cystic fibrosis (CF) should have physiotherapy procedures as part of their treatment regimen. The procedures used, and the treatment program should be specific to each person. Stern (1997) noted that the procedures should encompass the airway clearance techniques, exercise, and sustenance of the thoracic and general mobility. Airway clearance techniques focus on reducing the blockage of the airway and enhancing ventilation. This is meant to postpone the progression of the disease. Exercise strives to increase cardiovascular and respiratory capability and strength within the lower and upper muscle areas. This improves endurance, functioning of the lungs, and general health.Advertising Looking for essay on health medicine? Let's see if we can help you! Get your fir st paper with 15% OFF Learn More The maintenance of the general and thoracic mobility and body posture use certain stretching and strengthening routines that maintain or re-establish healthy body posture. They avert or treat an inflexible thoracic spine, as well as the costovertebral joints. Thus, the exercise facilitates efficient, painless rib excursion. The implications of cystic fibrosis (CF) for patients and their careers Cystic fibrosis (CF) is a complex condition that is challenging to manage. The therapeutic schedule is tedious and delicate for most patients. In addition, the therapeutic program is quite expensive and may strain the patient’s and/or family resources. Baumann, et al (2003) noted that the cost of the management rises with the age of the patient. In some countries, segregation is taken as a measure of preventing infection. This has a devastating impact on the social welfare of the patients. The segregation measures are most common among CF cente rs in some European countries. Though studies have revealed comparable educational levels between those suffering from CF and the general population, it has to be noted that CF patients experience delay in their education. Studies have also indicated that CF patients can be employed. However, according to Burker, Sedway Carone (2004), the patients’ condition seems to play a great part in influencing their careers. Another effect of CF is on the fertility of the adult patients. Male patients are normally infertile.Advertising We will write a custom essay sample on Physiotherapy management of newly diagnosed Cystic fibrosis (CF) specifically for you for only $16.05 $11/page Learn More This is due to the lack of vas deference in their genitalia. On the other hand, female patients may be fertile. However, they can expose themselves to great risks if they get pregnant. The age of the patient at diagnosis Diagnosis of CF has been advanced in modern da ys. According to Lannefors, Button McIlwaine (2004), most countries have embraced the screening of newborn infants. This has made it possible to diagnose CF in children within the first two months of birth. Initially, it was difficult to diagnose CF among the children. In this case, the diagnosis was based on symptoms that appeared when the victim was much older. During the initial stages, CF is asymptomatic and thus there are no signs of this condition. Symptoms begin to show after several months or year of birth. Tepper (1998) observed that CF is commonly diagnosed among infants and toddlers than in adults. However, this does not indicate that CF is unheard of in adults. As denoted by Hunt Geddes (1985), there are isolated cases in which adults have been diagnosed with the condition. In addition, Gershman, Mehta, Infeld Budev (2006) noted that CF cannot be considered solely as a pediatric disease. The Cystic Fibrosis Foundation (2003) noted that close to 80 percent of the CF pa tients are able to attain adult age when the condition is properly managed. Indeed, Yankaskas, Marshall, Sufian, Simon Rodman (2004) observed that those patients who were born with the condition starting from the 1990s are set to live for an average of forty years. This has been attributed to the enhanced management regimens in the modern world.Advertising Looking for essay on health medicine? Let's see if we can help you! Get your first paper with 15% OFF Learn More The role of the respiratory physiotherapist as part of a holistic, MDT approach to treatment management People should seek the services of a physiotherapist immediately after having been diagnosed with cystic fibrosis. The patients should start training in the anatomy and physiological treatment techniques, as well as the relevant regime. Stern (1997) observed that patients should be taught how to detect an increase in respiratory symptoms, when to increase the incidence, and duration of treatment and the appropriate time to seek further medical advice. According to Kulich, Rosenfeld, Goss Wilmott (2003), education and training in cystic fibrosis and its treatment should be a continuous process of care. In addition, it should form a section of each review. The quantity of information communicated at this stage is determined by each family’s needs. Written information should be cross checked accordingly. It is essential to introduce early dialogue about the exercise being an integral part of the patient’s lifestyle. Peebles (2005) observed that, the family should be encouraged to think and develop activities that allow all members to participate. Children from highly active families have a likelihood of participating in sports more than any other activity. As denoted by Bush (2006), it is essential for parents and the entire family of the patient to be actively involved in the management program of the patient at an early stage to integrate physiotherapy into their daily routine. During the initial period, it is essential for the physiotherapist to build a strong rapport with the family. This will enable the physiotherapist to reassure, encourage, and obtain a clear understanding of how each family member copes with information about the diagnosis and the potential burden of caring for the patient. Substantial levels of rapport are fundamental in achieving an acceptable and efficient treatment strategy. According to Davis (2006) and Doull (2001), all patients should be evaluated and treated by a qualified physiotherapist within the first 24 hours after admission. This treatment regime should be sustained at an appropriate level with constant reassessment of the patient’s progress. Whenever feasible, the patient’s family should not be left to conduct treatment on their own. When a patient is hospitalized, it should serve as an opportunity to relieve the family from the burden of care. Horsley, Cunningham, Innes (2010) observed that, clearing of lung fields is the cornerstone of physiotherapy management procedures for a patient diagnosed with cystic fibrosis. The main causes of mortality and morbidity are known to be bronchiectasis and obstructive pulmonary illness. However, the latter accounts for a considerable share of all known deaths. The interrelationships between those involved According to Henley Hill (1990) cystic fibrosis is a condition that requires team management. In this case, the physiotherapist , the patient, and the family members have to participate in the management program. Essentially, the disease management team may include a dietician, a physician, a physiotherapist, a CF coordinator, a community nurse, a genetic counselor, and a CF pharmacist. Members of the disease management team are critical as each has a vital role to play. This enables the patient to live as comfortable as possible. According to Jaffà © Bush (2001), the family members of the patient should be summoned to the hospital immediately after the patient has been diagnosed with the condition. Hough (2001) and West (2011) acknowledged that, this is done to ensure the physiotherapist discusses the implications of the condition with the relevant stakeholders. In most cases, such discussions are overseen by the respiratory physicians who will manage the patient’s condition. The physician may be assisted by a cystic fibrosis coordinator and a counselor. A respiratory fellow of registrar might also be present. Notably, Horsley, Cunningham Innes (2010) noted that cystic fibrosis is a complicated disorder and its diagnosis can be a big blow to the families of the newly diagnosed patients. Therefore, it is important for a thorough education program to be initiated immediately a patient is diagnosed with this condition. Given that the diagnosis may have a strong emotional effect on the family members, they may not be able to comprehend the new information on how to manage the disease. According to Ranganathan (2006), the delivery of information should be a repetitive and continuous process to enhance comprehension. In addition, the aspect of staying positive and acknowledging the gravity of the condition should be emphasized. Conclusion It can be acknowledged that cystic fibrosis is an extremely complex disease. The condition is common among children. However, isolated incidences of adult being diagnosed with the disease have been noted. Nonetheless, with the enhanced technologi es in the modern world coupled with the adoption of the policy requiring the screening of the newborns, CF is diagnosed early among children. In fact, it has been noted that the condition can be diagnosed within the first two months of birth. The management of the condition can be tedious and time consuming. However, with determination and commitment from the patient and team members, the condition can be managed successfully. Individuals who have been diagnosed with the disease can live up to an average of forty years. It is extremely essential for the physiotherapist to establish a strong rapport with the patient and the patient’s family. This enhances effective communication about the diagnosis and the subsequent treatment regimen. All members of a family should help the patient recover by providing all the necessary support. In essence, the therapy management team is critical to effective disease management. Reference List Baumann, U, et al. 2003, â€Å"Cost of care and clinical condition in pediatric cystic fibrosis patients,† Journal of Cystic Fibrosis, vol. 2, no. 2, pp. 84-90. http://www.ncbi.nlm.nih.gov/pubmed/15463855 Burker, EJ, Sedway, J Carone, S 2004, â€Å"Psychological and educational factors: Better predictors of work status than FEV1 in adults with cystic fibrosis,† Pediatric Pulmonology, vol. 38, no. 5, pp. 413-418. http://www.ncbi.nlm.nih.gov/pubmed/15470683 Bush, A 2006, Cystic fibrosis in the 21st century: 47 tables, Karger, Basel. https://books.google.com/books?id=PvPrwfv2l5ECpg=PR3lpg=PR3dq=Cystic+fibrosis+in+the+21st+century:+47+tablessource=blots=NAosVTVAVZsig=FdFlPoqRE7hjcnQB7BnhvmoCPdohl=ensa=Xei=7dZ5UNi7PMGt0QXqnICABQved=0CDkQ6AEwAw#v=onepageq=Cystic%20fibrosis%20in%20the%2021st%20century%3A%2047%20tablesf=false Cystic Fibrosis Foundation 2003, Cystic Fibrosis Foundation Patient Registry Annual Data Report 2002, Cystic Fibrosis Foundation, Bethesda, MD. http://www.cfgr.gr/cfgr/files/2002_Patient_Registry_Repor t.pdf Davis, PB 2006,†Cystic Fibrosis Since 1938†³, Am. J. Respir. Crit. Care Med., vol. 173, no. 5, pp. 475-482. http://www.nejm.org/doi/pdf/10.1056/NEJM197609022951005 Doull, IJ 2001, â€Å"Recent advances in cystic fibrosis,† Arch Dis Child, vol. 85, no. 1, pp. 62–66. http://www.ncbi.nlm.nih.gov/pubmed/11420207 Di Sant’Agnese, PA Davis, PB 1976, â€Å"Research in Cystic Fibrosis†, N Engl J Med., vol. 295, pp. 534-541, DOI: 10.1056/NEJM197609022951005. http://www.nejm.org/doi/pdf/10.1056/NEJM197609022951005 Gershman, AJ, Mehta, AC, Infeld, M Budev, MM 2006, â€Å"Cystic fibrosis in adults: An overview for the internist,† Cleveland Clinic Journal of Medicine, vol. 73, no. 12, pp. 1065-1074. http://ccjm.org/content/73/12/1065.full.pdf Henley, LD Hill, ID 1990, â€Å"Global and specific disease-related information needs of cystic fibrosis patients and their families,† Pediatrics, vol. 85, no. 6, pp. 1015-21. http://pediatrics.aa ppublications.org/content/85/6/1015.full.pdf Horsley, A, Cunningham, S, Innes, A 2010, Cystic fibrosis, Oxford University Press, Oxford. https://books.google.com/books?id=hUDeXpYPhCsCprintsec=frontcoverdq=Horsley,+A,+Cunningham,+S,+%26+Innes,+A+2010,+Cystic+fibrosissource=blots=9p4Tqk7jF4sig=Ctz27XLeU27BEn5N8CScRFtVRKQhl=ensa=Xei=itt5UMXcOc_Eswa-_4HYBAved=0CCwQ6AEwAA Hough, A 2001, Physiotherapy in respiratory care: An evidence-based approach to respiratory and cardiac management 3rd edn, Nelson Thornes Ltd, Cheltenham. https://books.google.com/books?id=Uk1NfFGMrJoCpg=PA481lpg=PA481dq=Hough,+A+2001,+Physiotherapy+in+respiratory+care:+An+evidence-based+approach+to+respiratory+and+cardiac+managementsource=blots=-MCrRKcCdvsig=1XnGKqc2LXCMsVekmc92Y-pXRDghl=ensa=Xei=xtt5UImlI8fRsgbEyoDQAQved=0CB0Q6AEwAA Hunt, B Geddes, DM 1985, â€Å"Newly diagnosed cystic fibrosis in middle and later life,† Thorax, vol. 40, no. 1, pp. 23-26. http://thorax.bmj.com/content/40/1/23.full.pdf Jaffà ©, A Bush, A 2001, â€Å"Cystic fibrosis: review of the decade,† Monaldi Arch Chest Dis., vol. 56, no. 3, pp. 240–247. http://www.ncbi.nlm.nih.gov/pubmed/11665504 Kulich, M, Rosenfeld, M, Goss, CH Wilmott, R 2003, â€Å"Improved survival among young patients with cystic fibrosis,† J Pediatr, vol. 142, no. 6, pp. 631–636. http://www.ncbi.nlm.nih.gov/pubmed/12838190 Lannefors, L, Button, MB McIlwaine, M 2004, â€Å"Physiotherapy in infants and young children with cystic fibrosis: current practice and future developments,† Journal of the Royal Society of Medicine, vol. 97, Suppl. 44, pp. 8–25. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1308795/pdf/15239290.pdf Maffessanti, M, Candusso, M, Brizzi, F Piovesana, F 1996, â€Å"Cystic fibrosis in children: HRCT findings and distribution of disease,† J Thorac Imaging, vol. 11, no. 1, pp. 27–38. http://www.ncbi.nlm.nih.gov/pubmed/8770824 Peebles, A 2005, Cystic fibrosis care: A pra ctical guide, Elsevier Churchill Livingstone, Edinburgh. https://books.google.com/books/about/Cystic_Fibrosis_Care.html?id=UStgTw9zdK8Credir_esc=y Ranganathan, S 2006, MELBOURNE Handbook for the Management of Children with Cystic Fibrosis. http://ww2.rch.org.au/emplibrary/RESPMED/handbook.pdf Stern, RC 1997, â€Å"The diagnosis of cystic fibrosis,† N Engl J Med, vol. 336, no. 7, pp. 487–491. http://www.nejm.org/doi/full/10.1056/NEJM199702133360707 Tepper, RS 1998, â€Å"Assessment of the respiratory status of infants and toddlers with cystic fibrosis,† J Pediatr., vol. 132, no. 3, pp. 380–381. http://www.jpeds.com/article/S0022-3476%2898%2970002-2/fulltext West, JB 2011, Respiratory Physiology: The Essentials, 9th edn, Waltors Kluwer/Lippincott Williams Wilkins, London. https://books.google.com/books?id=eLRjk-VDF3cCprintsec=frontcoverdq=West,+JB+2011,+Respiratory+Physiology:+The+Essentials,source=blots=RlUJ6xHwz_sig=67j0hLehNuP-i31QyAYiGCCbN1Qhl=ensa=Xei =5eF5UK34F4aFhQekqoHgCwved=0CCwQ6AEwAA#v=onepageqf=false Yankaskas, JR, Marshall, BC, Sufian, B, Simon, RH, Rodman, D 2004, â€Å"Cystic fibrosis adult care: consensus conference report,† Chest, 125, Suppl, pp. 1S–39S. https://docs.google.com/viewer?a=vq=cache:YY6yk8IAQuMJ:www.cff.org/UploadedFiles/treatments/CFCareGuidelines/AgeSpecificCare/CF-Adult-Care-Chest-2004.pdf+hl=engl=kepid=blsrcid=ADGEESgQIIcG-OVz4z7h_6VB0qbk1eZh_swPb_snp6iybtCPLyFEs9y6dy0s4ztAPu2lfi7etuspMFWqGK72PdNZuzzpyA-SUPygFITl0-Zsiy3RAlXvXfnc6irmmYm5QAALLO0hHVfdsig=AHIEtbRzx8LGw_aoxO7QM8k84OoqfYfmEw This essay on Physiotherapy management of newly diagnosed Cystic fibrosis (CF) was written and submitted by user Ka-Zar to help you with your own studies. You are free to use it for research and reference purposes in order to write your own paper; however, you must cite it accordingly. You can donate your paper here.