Understanding Australian Aboriginal Experiences of Giftedness through the Lens of a Case Study

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Little research has been undertaken into high achieving (school-based) gifted Aboriginal students. This is particularly true for those gifted students that reside in remote Aboriginal communities, where there is often a need for the young person to navigate the demands of their educational aspirations with their desire to remain culturally connected. This article will present a case study that aimed to shed light on the experience of being a gifted Yolŋu (a remote Aboriginal group in East Arnhem Land) young person. This case study includes the perspective of a gifted Yolŋu student, a member of their family, as well as one of their teachers. Findings emphasised the student’s love of learning, and tensions between their educational aspirations and cultural life.

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Australian Veterinary JournalVolume 84, Issue 9 p. 317-320 Dog health program in Numbulwar, a remote Aboriginal community in east Arnhem Land L BRADBURY, L BRADBURY University of Melbourne, Veterinary School, Werribee VIC 3030. Currently at Palm City Vet Clinic, Boulter Road, Berrimah NT 0828. Email: le_bradbury@hotmail.comSearch for more papers by this authorS CORLETTE, S CORLETTE Environmental Health, Numbulwar Numburindi Community Council, Numbulwar NT 0852. Email: bae@corlette.netSearch for more papers by this author L BRADBURY, L BRADBURY University of Melbourne, Veterinary School, Werribee VIC 3030. Currently at Palm City Vet Clinic, Boulter Road, Berrimah NT 0828. Email: le_bradbury@hotmail.comSearch for more papers by this authorS CORLETTE, S CORLETTE Environmental Health, Numbulwar Numburindi Community Council, Numbulwar NT 0852. Email: bae@corlette.netSearch for more papers by this author First published: 06 September 2006 https://doi.org/10.1111/j.1751-0813.2006.00028.xCitations: 16Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume84, Issue9September 2006Pages 317-320 RelatedInformation

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"What is going on here?" Challenges experienced by white teachers in a government school in a remote Aboriginal community
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  • 10.1111/j.1444-0903.2005.00824.x
Homocysteine, renal disease and cardiovascular disease in a remote Australian Aboriginal community.
  • Apr 21, 2005
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Rates of renal and cardiovascular disease are high among Aboriginal Australians living in remote communities. Nutritional problems, in particular low folate levels, are also common. This suggests that increased homocysteine concentrations might be widespread, and a possible contributor to the high rates of cardiovascular disease. To examine homocysteine concentrations, and their relationships to folate levels, and to markers of renal disease and cardiovascular disease in a remote Aboriginal Australian community As part of a cross-sectional survey among adults in one community, homocysteine concentrations, concentrations of the crucial determinants (red blood cell (RBC) folate, vitamin B(12) and the C677T methylene tetrahydrofolate reductase polymorphism) and cardiovascular risk factors were examined. Among 221 people, geometric mean homocysteine concentration was 11.8 micromol/L (range: 11.1-12.5 micromol/L), with 57/221 (26%) values > or =15.0 micromol/L. Higher concentrations were associated with older age, male gender, lower RBC folate and lower vitamin B(12) concentrations and homozygosity for C677T. Homocysteine concentrations were not related to the presence of albuminuria, other than over the overt albuminuria range. Homocysteine concentrations were inversely correlated with calculated glomerular filtration rate (GFR). Carotid intima-media thickness, however, was not related to homocysteine concentration. In multivariate analyses, age, male gender, lower RBC folate concentrations, lower vitamin B(12) concentrations, lower calculated GFR and the C677T polymorphism were all associated with homocysteine concentrations. Homocysteine concentrations were consistent with previous limited reports in Aboriginal communities. Although superficially they are similar to reports from non-Aboriginal settings, the younger age of this cohort and the association of homocysteine concentrations with age suggest that age-specific concentrations are higher among Aboriginal Australians. In addition to dietary determinants, the high prevalence of apparently reduced renal function renal disease appears to be an important determinant of homocysteine concentrations in remote Aboriginal communities. The role of homocysteine concentrations as a potential mediator of the high rates of cardiovascular disease remains to be determined.

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The most common skin infections affecting children in remote Aboriginal communities are scabies and impetigo. Group A streptococcal skin infections are linked to the high rates of heart and renal disease occurring in Aboriginal Australians. A retrospective review of medical records was conducted in a primary health care centre in the East Arnhem region of the Northern Territory. Data was collected from all presentations to the clinic in the first 2 years of life for 99 children born between 2001 and 2005 as a component of the East Arnhem Regional Healthy Skin Project. The median number of presentations to the clinic in the first 2 years of life was 32. Skin disease was recorded in 22% of all presentations. By 1 year of age 82% of children had presented to the clinic with their first episode of impetigo and 68% with their first episode of scabies. Antibiotics were administered to 49% of children with impetigo. Skin infections are a major reason for presentation to primary health clinics and contribute to the high disease burden experienced by children in the first 2 years of life. This high frequency of presentation provides multiple opportunities for intervention and monitoring.

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