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5,052 result(s) for "Wilson, Janet"
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Working with bereavement : a practical guide
\"A practical guide for those who work with the bereaved in a variety of settings, from nurses and social workers to volunteers. Covering ethics, cultural issues and support networks, an essential text for those seeking to build understanding and skills in order to offer better support to the dying and the bereaved\"--Provided by publisher.
Corporeal Suffering: Performing Resistance and Resilience in Slow Man
Slow Man (2005), a novel about migration, dislocation, and belonging, marks Coetzee's withdrawal from the socio-political landscapes of South Africa coinciding with his move to Australia, and his preoccupation in writing fiction with the conflicting demands of representation, auto/biography, and realism. The leg amputation and home nursing of the protagonist, Paul Rayment, following an accident, introduce a discourse on the various meanings of care and the ethics of caring that also acknowledges Rayment's corporeal enfeeblement, aging, and mortality. An intersecting meta-commentary generated by Rayment's dialogue with the metafictional character Elizabeth Costello complicates Coetzee's \"compromised resilient narrative\" of Rayment's hesitant trajectory of resistance, adaptation, and renewal. The focus on the migrant's place in the life of the nation, represented by Rayment's French origins and his recently arrived Slovakian carer, Marijanna Jokić and her family, represents a new departure for Coetzee.
How to be cool in the third grade
When Robbie York is marked as a target by a bully at school, he decides that the only way to survive the third grade is by being cool.
Use of proton pump inhibitors to treat persistent throat symptoms: multicentre, double blind, randomised, placebo controlled trial
AbstractObjectiveTo assess the use of proton pump inhibitors (PPIs) to treat persistent throat symptoms.DesignPragmatic, double blind, placebo controlled, randomised trial.SettingEight ear, nose, and throat outpatient clinics, United Kingdom.Participants346 patients aged 18 years or older with persistent throat symptoms who were randomised according to recruiting centre and baseline severity of symptoms (mild or severe): 172 to lansoprazole and 174 to placebo.InterventionRandom blinded allocation (1:1) to either 30 mg lansoprazole twice daily or matched placebo twice daily for 16 weeks.Main outcome measuresPrimary outcome was symptomatic response at 16 weeks measured using the total reflux symptom index (RSI) score. Secondary outcomes included symptom response at 12 months, quality of life, and throat appearances.ResultsOf 1427 patients initially screened for eligibility, 346 were recruited. The mean age of the study sample was 52.2 (SD 13.7) years, 196 (57%) were women, and 162 (47%) had severe symptoms at presentation; these characteristics were balanced across treatment arms. The primary analysis was performed on 220 patients who completed the primary outcome measure within a window of 14-20 weeks. Mean RSI scores were similar between treatment arms at baseline: lansoprazole 22.0 (95% confidence interval 20.4 to 23.6) and placebo 21.7 (20.5 to 23.0). Improvements (reduction in RSI score) were observed in both groups—score at 16 weeks: lansoprazole 17.4 (15.5 to19.4) and placebo 15.6 (13.8 to 17.3). No statistically significant difference was found between the treatment arms: estimated difference 1.9 points (95% confidence interval −0.3 to 4.2 points; P=0.096) adjusted for site and baseline symptom severity. Lansoprazole showed no benefits over placebo for any secondary outcome measure, including RSI scores at 12 months: lansoprazole 16.0 (13.6 to 18.4) and placebo 13.6 (11.7 to 15.5): estimated difference 2.4 points (−0.6 to 5.4 points).ConclusionsNo evidence was found of benefit from PPI treatment in patients with persistent throat symptoms. RSI scores were similar between the lansoprazole and placebo groups after 16 weeks of treatment and at the 12 month follow-up.Trial registrationISRCTN Registry ISRCTN38578686 and EudraCT 2013-004249-17.
Corporeal Suffering: Performing Resistance and Resilience in Slow Man
Slow Man (2005), a novel about migration, dislocation, and belonging, marks Coetzee's withdrawal from the socio-political landscapes of South Africa coinciding with his move to Australia, and his preoccupation in writing fiction with the conflicting demands of representation, auto/biography, and realism. The leg amputation and home nursing of the protagonist, Paul Rayment, following an accident, introduce a discourse on the various meanings of care and the ethics of caring that also acknowledges Rayment's corporeal enfeeblement, aging, and mortality. An intersecting meta-commentary generated by Rayment's dialogue with the metafictional character Elizabeth Costello complicates Coetzee's \"compromised resilient narrative\" of Rayment's hesitant trajectory of resistance, adaptation, and renewal. The focus on the migrant's place in the life of the nation, represented by Rayment's French origins and his recently arrived Slovakian carer, Marijanna Jokic and her family, represents a new departure for Coetzee.
المنارة : قصة الذكريات
كتاب \"المنارة\" قصة الذكريات الهادئة التي تبقى بعد رحيل الجد والمعادلة الصعبة بين ما نحتفظ به من سيرة الأحباب وما يجب أن نترك خلفنا لنمضي في الطريق ويعد هذا الكتاب قصة مخصصة للأطفال تستهدف الطفولة وتعمل على استثمار الطفل في بناء المهارات المختلفة المرتبطة بالخيال والابتكار وقوة الشخصية والبحث عن حلول إبداعية وتستمد الطفل الكثير من العلم والمعرفة والمعلومات.
Evaluating a young-onset dementia service from two sides of the coin: staff and service user perspectives
Background People with young-onset dementia (YOD) can often struggle getting the right treatment. This is because of their frequently different characteristics and needs compared to people with late-onset dementia. The aim of this project was to assess a memory service for its adaptation to the needs and wishes of people with YOD and their carers. Methods This project evaluated a memory service in the North West of England by performing two focus groups with clinical staff and six semi-structured interviews with people with YOD and carers. The focus groups took place on site and lasted one hour each. People with YOD and their carers were identified via the memory clinics caseload and via the local Alzheimer’s Society charity organisation. Both focus groups and interviews were audio-recorded and transcribed, and data were analysed using thematic analysis. The public (a person living with YOD and his carer) were involved from the design stages of the project through to the analysis and dissemination. Results Eleven members of staff with different clinical backgrounds participated in the focus groups and six interviews were held with people with YOD and their carers. Both indicated that whilst the diagnostic process is relatively well conducted at the service, the post-diagnostic service has many gaps. These include limited post-diagnostic support by the service, better enabling peer support, as well as providing meaningful activities, as some activities provided might be more suitable to older adults with dementia. Conclusions Post-diagnostic services and support for people with YOD and their carers need to be improved. The next step will be to implement the findings from this service evaluation in practice and improve service satisfaction and relevance to people with YOD.