49 research outputs found

    Applied utility and the auto-ethnographic short story: persuasions for, and illustrations of, writing critical social science

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    In some quarters it is argued that, narrative researchers might be classified as being either storyanalysts or storytellers. They go on to suggest that one feature of storytellers is that they undertake a form of analysis as the process of writing unfolds. With these sentiments in mind, in the present paper, we consider how auto-ethnographical accounts of traumatic and challenging life events might, through the analysis contained within, demonstrate value within the realm of applied pedagogy. In making our case we embrace and adapt the literary genre of storytelling, more specifically, the short story. The story presented here, ‘Travel Writer’, offers an opaque, multicontextualised and lifelong view of career transition. The present paper, in more general terms, considers the capacity of auto-ethnography and, more specifically, the short storied version of it, to engender critical reader engagement, to encourage personal reflection in others, and to act as a point of stimulus for the enactment of applied debate through the lens of critical social science. With regards to the assumptions of critical social science, the final discussion also considers how the auto-ethnographic text, as a pedagogic tool, might help others to contest and challenge the meta-narratives that, we argue, risk stagnating established thinking

    SE 03. Financial projections for the evaluation of technological alternatives in the Mexican dual purpose production system

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    The overall objective of this work was to perform an economic analysis of technological alternatives for the dual purpose production systems under Mexico’s tropical conditions. This production unit was based on grazing 100 ha of improved species of grass and supplemented with Napier grass and corn silage during the dry season. Two alternative scenarios were analyzed: 1) the use of BST and 2) the purchase of a milk cooling tank. A farm level, income and policy simulation model (FLIPSIM), developed at Texas A&M University was used to analyze the production and financial conditions of the production unit over a six year planning horizon (1995-2000). The results indicate that to pay for the use of BST, on average, the milking herd should increase milk production by 21.38 % for the first year in the planning horizon. As inflation decreases and financial conditions improve over time, smaller increments in milk production would be necessary to pay for the hormone. The initial investment necessary for the purchase and associated facilities for a milk cooling tank and operation costs associated to cooling the milk required the net income to increase to US12,500overthebaselineduringthefirstyearforthefarmtobreakeven.Themoredramaticeffectisrealizedinthefirstyearbecauseofthe20 12,500 over the baseline during the first year for the farm to break-even. The more dramatic effect is realized in the first year because of the 20% down payment assumed for the purchase and the facilities required to install the milk tank. After the first year, the extra income required for interest payments and operation of the machinery ranges from US 4,000 to US5,700overtherestoftheplanninghorizon.TheeffectofthisontheunitaryBEmilkpriceisadifferenceofUS5,700 over the rest of the planning horizon. The effect of this on the unitary BE milk price is a difference of US 0.046 /liter of milk in the first year and a range of US$ 0.015 - 0.0213 /liter of milk over the rest of the planning horizon

    COPPADIS-2015 (COhort of Patients with PArkinson's DIsease in Spain, 2015), a global--clinical evaluations, serum biomarkers, genetic studies and neuroimaging--prospective, multicenter, non-interventional, long-term study on Parkinson's disease progressio

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    Background: Parkinson?s disease (PD) is a progressive neurodegenerative disorder causing motor and non-motor symptoms that can affect independence, social adjustment and the quality of life (QoL) of both patients and caregivers. Studies designed to find diagnostic and/or progression biomarkers of PD are needed. We describe here the study protocol of COPPADIS-2015 (COhort of Patients with PArkinson?s DIsease in Spain, 2015), an integral PD project based on four aspects/concepts: 1) PD as a global disease (motor and non-motor symptoms); 2) QoL and caregiver issues; 3) Biomarkers; 4) Disease progression.Methods/design: Observational, descriptive, non-interventional, 5-year follow-up, national (Spain), multicenter (45 centers from 15 autonomous communities), evaluation study. Specific goals: (1) detailed study (clinical evaluations, serum biomarkers, genetic studies and neuroimaging) of a population of PD patients from different areas of Spain, (2) comparison with a control group and (3) follow-up for 5 years. COPPADIS-2015 has been specifically designed to assess 17 proposed objectives. Study population: approximately 800 non-dementia PD patients, 600 principal caregivers and 400 control subjects. Study evaluations: (1) baseline includes motor assessment (e.g., Unified Parkinson?s Disease Rating Scale part III), non-motor symptoms (e.g., Non-Motor Symptoms Scale), cognition (e.g., Parkinson?s Disease Cognitive Rating Scale), mood and neuropsychiatric symptoms (e.g., Neuropsychiatric Inventory), disability, QoL (e.g., 39-item Parkinson?s disease Quality of Life Questionnaire Summary-Index) and caregiver status (e.g., Zarit Caregiver Burden Inventory); (2) follow-up includes annual (patients) or biannual (caregivers and controls) evaluations. Serum biomarkers (S-100b protein, TNF-?, IL-1, IL-2, IL-6, vitamin B12, methylmalonic acid, homocysteine, uric acid, C-reactive protein, ferritin, iron) and brain MRI (volumetry, tractography and MTAi [Medial Temporal Atrophy Index]), at baseline and at the end of follow-up, and genetic studies (DNA and RNA) at baseline will be performed in a subgroup of subjects (300 PD patients and 100 control subjects). Study periods: (1) recruitment period, from November, 2015 to February, 2017 (basal assessment); (2) follow-up period, 5 years; (3) closing date of clinical follow-up, May, 2022. Funding: Public/Private. Discussion: COPPADIS-2015 is a challenging initiative. This project will provide important information on the natural history of PD and the value of various biomarkers
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