Journal articles on the topic 'Intellectually disabled persons'

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1

Milanović-Dobrota, Biljana, Aleksandra Đurić-Zdravković, Mirjana Japundža-Milisavljević, and Sara Vidojković. "The importance of educational interventions for the overcoming of obstacles in the employment of intellectually disabled persons." Andragoske studije, no. 1 (2021): 107–26. http://dx.doi.org/10.5937/andstud2101107m.

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In spite of the legal framework intended for the promotion and protection of rights of the disabled, such persons are still facing significant difficulties in the labour market. Intellectually disabled persons are in a particularly difficult position, primarily due to the negative perceptions held by citizenry which stem from the lack of knowledge and information about their labour potentials. We conducted research in order to determine the most prevalent obstacles in the employment of intellectually disabled persons, as perceived by employed non-disabled persons. The research comprised a sample of 269 subjects of both sexes, of differing educational levels and employed in the private and public sector in the Republic of Serbia. The analysis of the attained results points to the need for certain kinds of educational interventions, whose programmes would improve the knowledge and awareness of employed persons regarding the right to work of intellectually disabled persons, promote diversity and create an inclusive working environment. The different modes of training, reinterpretation and transformation of previous experience, informing and establishing positive contacts with intellectually disabled persons, conducted by a multidisciplinary team of experts would establish a stable base for the removal of obstacles in the employment process.
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Kaliszewska, Karolina, and Teresa Żółkowska. "The pattern of law principles’ comprehension by persons with mild intellectual disability." Men Disability Society 47, no. 1 (March 30, 2020): 37–69. http://dx.doi.org/10.5604/01.3001.0014.0695.

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This article presents the research conducted on intellectually disabled persons employed in the Professional Activation Municipality Institution in Dobra (Poland). The main aim of this analysis was to uncover how persons with mild intellectual disability understand law principles. In the conducted studies qualitative strategies, such as, imperative theoretical paradigm and phenomenological approach were used. Gathered empirical materials were used as a basis for reconstructing the experiences of researched employees, by decoding and describing the way mildly disabled persons understand law principles.
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3

Woodin, Sarah. "Issues in human rights protection of intellectually disabled persons." Disability & Society 28, no. 5 (July 2013): 735–37. http://dx.doi.org/10.1080/09687599.2013.798116.

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4

Morad, Mohammed, Mark Gringols, Isack Kandel, and Joav Merrick. "Vitamin B12 Deficiency in Persons with Intellectual Disability in a Vegetarian Residential Care Community." Scientific World JOURNAL 5 (2005): 58–61. http://dx.doi.org/10.1100/tsw.2005.11.

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The goal of this study was to determine the prevalence of vitamin B12 deficiency among intellectually disabled persons in a vegetarian remedial community in Israel. In this community, 47 individuals with intellectual disability (ID) live in 7 enlarged families in a kibbutz style agricultural setting. These 47 individuals and 17 of their caregivers were screened for vitamin B12 deficiency. There were 25.5% of the disabled vs. 11.8% of the caregivers found to have levels of vitamin B12 lower than 157 pg/ml. It is concluded that persons with ID in this vegetarian residential care community seemed to be at a higher risk for vitamin B12 deficiency.
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Kudeikina, I., and M. Losevicha. "LEGAL ASSESSMENT OF RESPONSIBILITY WHILE OUTPATIENT FORENSIC MEDICINE EXAMINATION OF INTELLECTUALLY DISABLED PEOPLE." Archives of Criminology and Forensic Sciences 2 (August 13, 2020): 45–51. http://dx.doi.org/10.32353/acfs.2.2020.03.

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While legal capacity emerges at the moment of a person birth and he as a natural person and legal entity possesses it throughout all his life, capability is an institution with much more nuanced nature. Not all natural persons are endowed with capability, what is more a person may lack or be deprived of capability. However, it should be stressed that people with limited capability continue to live in society, to participate in legal proceedings when it is possible, as well as to commit crimes, that is their legal status differs from actual. Evaluation of acts competence committed by persons with limited capability plays an important role both in civil and criminal proceedings. In civil proceedings the issue as to transaction legal effect has to be resolved, in criminal proceedings the issues as to a person’s responsibility committed a crime and, accordingly, as to his penalty have to be addressed. The article is devoted to the role of outpatient forensic medicine examination while assessing the acts committed by persons with limited capability and in a state of insanity.
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Żółkowska, Teresa. "Construction of intellectual disability: (de)construction of the social role of intellectually disabled persons." International Journal of Developmental Disabilities 62, no. 4 (June 10, 2015): 213–23. http://dx.doi.org/10.1179/2047387715y.0000000005.

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7

Son, Hyo-Jung, Dae-Sik Kim, and Sin-Ae Park. "Horticultural Therapy for Improving the Work Performance and Interpersonal Relationships of Persons with Intellectual Disabilities." International Journal of Environmental Research and Public Health 19, no. 21 (October 25, 2022): 13874. http://dx.doi.org/10.3390/ijerph192113874.

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For the occupational adaptation and social integration of the intellectually disabled, it is helpful to improve their work performance and interpersonal skills. The purpose of the study was to evaluate the effectiveness of horticultural therapy (HT) programs to improve work performance and interpersonal relationships of persons with intellectual disabilities. Based on observations and analyses of how people with intellectual disabilities work, we have developed a 12-session HT program that includes upper limb movements and physical activities to improve hand function. We recruited, with the consent of their legal guardians, 14 (6 males, 8 females) participants who had intellectual disabilities and were working at a sheltered workshop in K-gu, Seoul, South Korea. The program consisted of twelve sixty-minute sessions that were conducted twice a week at a rooftop garden. For pre- and post-evaluation of the program, the survey of functional adaptive behavior (SFAB), interpersonal negotiation strategies, a horticultural job evaluation (self), hand function tests (pegboard, pinch gauge, fingertips), and blood sample tests for physiological indicators of exercise were conducted. Interpersonal negotiation strategies, functional adaptive behaviors, and physical abilities for job behaviors, including agility and grasping of the hand, improved significantly from before to after the program (p < 0.05). A positive result of VEGF (vascular endothermic growth factor) in blood sample tests implies the need for further research on cognitive changes caused by horticultural activities. This study has limitations due to the small number of participants, but the results suggest that low- to medium-intensity horticultural treatment programs using the upper body and hands could be effective for vocational rehabilitation of the intellectually disabled.
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8

Leonard, Peter, Sean Shanahan, and John Hillery. "Recognising, assessing and managing offending behaviour in persons with intellectual disability." Irish Journal of Psychological Medicine 22, no. 3 (September 2005): 107–12. http://dx.doi.org/10.1017/s0790966700009137.

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AbstractThe association between intellectual disability and offending is complex. Recent evidence would suggest that the received wisdom of intellectually disabled persons being more prone to offending is either incorrect or only tells part of the story. Those within the ‘borderline’ intellectual disability range may be more prone to committing sexual and criminal damage offences but those with an IQ less than 50 rarely offend.The offender with intellectual disability shares characteristics with his counterpart from the general population. As with the general population as a whole, offending in this group is often unreported and its recognition is complicated by issues of competence. The lack of validated forensic assessment schedules for this population poses a further challenge. Some general approaches to assessment in this population are discussed. This case report illustrates the difficulties of assessing and managing offending behaviour in an individual with moderate intellectual disability. The challenge of treating offenders with an intellectual disability is immense and requires specialist expertise. Managing such cases in a generic setting is inappropriate and the need for a forensic learning disability service in Ireland is highlighted.
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Brookbanks, Warren. "Protecting the Interests of Vulnerable Defendants in the Criminal Justice System: The New Zealand Experience." Journal of Criminal Law 83, no. 1 (February 2019): 55–70. http://dx.doi.org/10.1177/0022018318814360.

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Approaches to the management of people with intellectual disabilities (IDs) vary across jurisdictions. However, the inconsistent development and implementation of official policy has often resulted in a significant over-representation of persons with developmental difficulties in criminal justice systems worldwide. This reality led the New Zealand government in 2003 to introduce dedicated legislation recognising the special needs of offenders with an ID. The article examines the New Zealand legislative response to the challenges presented by this cohort of offenders, in the light of emerging international data of the incidence of, and official responses to, offenders with special needs. In New Zealand, the emerging problem of how to manage intellectually disabled offenders who commit serious crimes, and the legislative response to it, was driven by changes in mental health legislation in the early 1990s that had effectively disenfranchised persons with ID with challenging behaviours from regimes of supervisory care and treatment. The Intellectual Disability (Compulsory Care and Rehabilitation) Act 2003 has provided for a separate regime of compulsory care and rehabilitation that may be accessed either directly as a criminal justice disposition, following a finding of unfitness to plead or legal insanity, or as a result of transfer from the mental health or penal systems. The compulsory care regime has proven effective in addressing the needs of intellectually disabled offenders, increasing numbers of whom are young people, who would have great difficulty coping in a prison environment. The New Zealand experience contrasts with experience in other jurisdictions where offenders with an ID are often over-represented in prison statistics and subject to victimisation and abuse. The article suggests that change is clearly required as a matter of urgency to ensure that offenders with an ID are able to benefit from the positive rights guaranteed under the UN Convention for the Rights of Persons with Disabilities and other rights instruments.
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Park, Mi Seo, Mi Whoa Kim, Jin Hee Jeong, and Nam Hyun Cha. "Effects of a Physical Activity Program on Physical Fitness of Intellectually Disabled Persons." Journal of Korean Academy of Community Health Nursing 28, no. 1 (2017): 88. http://dx.doi.org/10.12799/jkachn.2017.28.1.88.

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Tilinger, Pavel. "Comparison of Athletics Records of Intellectually Disabled Persons with Records of Intact Athletes." AUC KINANTHROPOLOGICA 49, no. 2 (July 23, 2014): 52–64. http://dx.doi.org/10.14712/23366052.2014.6.

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12

Brison, Susan J. "Valuing the Lives of People with Profound Intellectual Disabilities." Philosophical Topics 49, no. 1 (2021): 99–121. http://dx.doi.org/10.5840/philtopics20214917.

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Some prominent contemporary ethicists, including Peter Singer and Jeff McMahan, do not consider human beings with profound intellectual disabilities to have the same moral status as “normal” people. They hold that individuals who lack sufficiently sophisticated cognitive abilities have the same moral value as nonhuman animals with similar cognitive capacities, such as pigs or dogs. Their goal—to elevate the moral standing of sentient nonhuman animals—is an admirable one which I share. I argue, however, that their strategy does not, in fact, achieve this goal and that there are better ways to advance it than to attach lesser value to the lives of profoundly intellectually disabled persons.
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13

Benda, P., M. Ulman, and M. Šmejkalová. "Augmented Reality As a Working Aid for Intellectually Disabled Persons For Work in Horticulture." Agris on-line Papers in Economics and Informatics 7, no. 4 (December 30, 2015): 31–37. http://dx.doi.org/10.7160/aol.2015.070403.

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14

Innstrand, Siw Tone, Geir Arild Espnes, and Reidar Mykletun. "Burnout among people working with intellectually disabled persons: a theory update and an example." Scandinavian Journal of Caring Sciences 16, no. 3 (September 2002): 272–79. http://dx.doi.org/10.1046/j.1471-6712.2002.00084.x.

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15

Junestrand, Stefan, Göran Molin, Konrad Tollmar, and Ulf Keijer. "User Study of Video-Mediated Communication in the Domestic Environment With Intellectually Disabled Persons." International Journal of Human-Computer Interaction 15, no. 1 (February 2003): 87–103. http://dx.doi.org/10.1207/s15327590ijhc1501_07.

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16

Sapkota, N., A. K. Pandey, BK Deo, and MK Shrivastava. "Anxiety, depression and quality of life in mothers of intellectually disabled children." Journal of Psychiatrists' Association of Nepal 6, no. 2 (November 22, 2018): 28–35. http://dx.doi.org/10.3126/jpan.v6i2.21757.

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Introduction: Studies have shown that there is an association between Anxiety, Depression in mothers of children having Intellectual disability with poor quality of life (QOL) in mothers of such children. This study was carried with the objectives to describe the clinico-socio-demographic profile of mothers of intellectually disabled children and to investigate the relationship among anxiety and depression with quality of life in mothers with intellectually disabled children.Material And Method: Mothers (N=31), whose children's IQ score was below 70, were enrolled in to the study with their informed consent. Depression and Anxiety disorders were diagnosed as per ICD 10. Severity of depression was measured with BDI and Anxiety symptoms with STAI. WHOQOL-BREF was used to assess Quality of life. The relationship among anxiety, depression and QOL were analysed using diagonal matrix, ANOVA and Pearson correlation test.Results: The mean age of participants was 50.23 (S.D= 6.11), BDI score was 13.65(S.D= 11.301), STAI score was 53.90 (SD= 15.821), WHOQOL- BREF in all four domains was 290.90 (S.D=49.42). There was significant correlation between BDI and STAI (P=0.01, r:0.651 ) and the three domains of WHOQOL- BREF(P=0.01, r:0.821, 0.843, 0.635 respectively) scale except Environment domain. Among the participants, 48.4% (ICD 10) had depression of varying degree along with 54.8% depression as per BDI cut off score. Anxiety disorder was seen in 22.6% as per ICD 10 but as per STAI it was 53.90(SD=15.821) which was statistically significant (p:0.01, r: -0.507). Depression when compared with no diagnosis persons has poor quality of life in WHOQOL-BREF physical domain (p:0.002) but with compared to Anxiety or both it was not statistically significant.Conclusion: The findings of this study revealed that mothers of children having Intellectual disability have high level of Anxiety and Depression which indeed had impact in quality of life. J Psychiatrists’ Association of Nepal Vol. 6, No. 2, 2017 Page: 28-35
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17

Reichenberg, Monica. "‘I liked the text about the little bird.’ Five intellectually disabled persons talk about texts." Scandinavian Journal of Disability Research 15, no. 2 (June 2013): 108–24. http://dx.doi.org/10.1080/15017419.2012.676565.

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18

de Laat, Stijn, Ellen Freriksen, and Mathijs P. J. Vervloed. "Attitudes of children and adolescents toward persons who are deaf, blind, paralyzed or intellectually disabled." Research in Developmental Disabilities 34, no. 2 (February 2013): 855–63. http://dx.doi.org/10.1016/j.ridd.2012.11.004.

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19

von Barnekow, Ariel, Núria Bonet-Codina, and Dani Tost. "Can 3D Gamified Simulations Be Valid Vocational Training Tools for Persons with Intellectual Disability?" Methods of Information in Medicine 56, no. 02 (2017): 162–70. http://dx.doi.org/10.3414/me16-02-0014.

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SummaryObjective: To investigate if 3D gamified simulations can be valid vocational training tools for persons with intellectual disability.Methods: A 3D gamified simulation composed by a set of training tasks for cleaning in hostelry was developed in collaboration with professionals of a real hostel and pedagogues of a special needs school. The learning objectives focus on the acquisition of vocabulary skills, work procedures, social abilities and risk prevention. Several accessibility features were developed to make the tasks easy to do from a technological point-of-view. A pilot experiment was conducted to test the pedagogical efficacy of this tool on intellectually disabled workers and students.Results: User scores in the gamified simulation follow a curve of increasing progression. When confronted with reality, they recognized the scenario and tried to reproduce what they had learned in the simulation. Finally, they were interested in the tool, they showed a strong feeling of immersion and engagement, and they reported having fun.Conclusions: On the basis of this experiment we believe that 3D gamified simulations can be efficient tools to train social and professional skills of persons with intellectual disabilities contributing thus to foster their social inclusion through work.
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Pickering, G., A. Boyer, N. Danglades, S. Arondo, C. Lucchini, J. Goubayon, M. Dangin, and Y. Boirie. "Pain management in persons with intellectual disabilities living in institutions." Douleur et Analgésie 33, no. 1 (March 2020): 35–39. http://dx.doi.org/10.3166/dea-2020-0087.

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Background: Persons with severe intellectual disabilities often live in specialised care settings and suffer from comorbidities, some of them generating pain. The literature concerning pain assessment and management in this population is however limited. The main objective of this study was to determine the modalities of pain care in a sample of French institutions. Methods: This observational study focused on the modalities of pain assessment and management in six specialised care settings for persons with intellectual and/or psychomotor disabilities. Information about patients, pain evaluation, prevalence and how do healthcare professionals assess pain in noncommunicating intellectually disabled people was recorded. Results: The study included 218 residents and over the last month, 55% had pain, 87% suffered from acute pain and 16% from neuropathic pain. The use of pain scales for patients with communication impairment was unknown to the majority of healthcare professionals. Patients were prescribed 4 drugs a day, 68% had psychotropic drugs and over the last month, 98% of painful residents had received a non-opioid analgesic combined with a non-pharmacological technique in 78 % of them. Conclusion: Pain management must be carried out through accurate pain assessment and the limited knowledge of caregivers about pain assessment methods might contribute to insufficient pain care. It is necessary to train all caregivers about pain evaluation tools that must be adapted to the disability profile of the residents in order to provide the most effective assessment and treatment in these vulnerable patients.
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Savita, Km, and Sarika Sharma. "A SYSTEMATIC REVIEW OF TEACHERS PERCEPTIONS TOWARDS EFFECTIVE TEACHING-LEARNING OF STUDENTS WITH INTELLECTUAL DISABILITY." International Journal of Advanced Research 9, no. 11 (November 30, 2021): 669–74. http://dx.doi.org/10.21474/ijar01/13789.

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The phrase intellectual impairment refers to a persons level of cognitive functioning. By specific children it occurs when a childs cognitive functioning is hampered to the extent that he or she is unable to receive information from his or her environment. After that, successfully absorbing, problem-solving, and adapting to the knowledge is required. The purpose of this study is to provide an overview of children with intellectual disability and their education for conceptual knowledge, define cause, and classify. Intellectual disability is defined as significant deficits in intellectual functioning and adaptive behaviour manifested as conceptual, social, and practical adaptive skills. An intellectual disability is characterized as having an IQ of less than 70 and having problems with adaptive behaviour or daily living abilities (eating, dressing, communicating, and participating in group activities). Intellectually disabled people learn slowly and have trouble grasping abstract concepts. So there is a dire need of appropriate teaching methodologies for effective Teaching-Learning of such students. The features of people with intellectual disability according to their education are also discussed in this study.
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Gupta, Harshal, and Vishal Agrawal. "Dermatological manifestations and medico-social correlates among intellectually disabled students in Central India." Asian Journal of Medical Sciences 10, no. 5 (August 9, 2019): 27–32. http://dx.doi.org/10.3126/ajms.v10i5.24770.

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Background: People with intellectual disabilities (PwID) are particularly more vulnerable to dermatological manifestations due to their associated disabilities and hygiene negligence. Aims and Objective: To estimate the prevalence and pattern of skin diseases considering various medico-social correlates among PwID in two districts of Central India. To apply multinomial logistic regression analysis to examine the medico-social factors associated with no, one and more than one dermatological manifestations. Materials and Methods: A total of 204 PwID receiving rehabilitation services under a NGO serving two districts were examined for dermatological manifestations and various medico-social factors were studied. Descriptive analysis like chi-square and multinomial logistic regression analysis (MLR) was performed. Results: We found that 87.25% of study participants had one or more dermatological manifestations {infectious (64.7%) and non-infectious (84.3%)}. Among the various medico-social variables studied, socio-economic status, education of parents and associated co-morbidities were independently associated with increase in frequency of skin disorders. MLR analysis showed that Illiteracy of parents, lower socio-economic status and associated co-morbidities in PwID had higher odds of developing one and more than one dermatological manifestations when compared to literate and high income families and PwID with no associated co-morbidities. Conclusion: This study delineates the importance of additional attempts to be made by dermatologist while dealing with PwID while considering carefully their associated co-morbidities and various social factors. Strict hygiene measures, periodic skin examination and health education of persons caring for students with disabilities are recommended.
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Leonard, P., A. Morrison, M. Delany-Warner, and G. J. Calvert. "A national survey of offending behaviour amongst intellectually disabled users of mental health services in Ireland." Irish Journal of Psychological Medicine 33, no. 4 (August 18, 2015): 207–15. http://dx.doi.org/10.1017/ipm.2015.21.

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BackgroundOffenders with an intellectual disability pose a major challenge to Intellectual Disability Service providers in the Republic of Ireland. This is especially so as no national Forensic Intellectual Disability Service currently exists.The Forensic Intellectual Disability Working Group of the Irish College of Psychiatrists was established in order to take steps to address this issue by establishing the level of need for a Forensic Intellectual Disability Service in Ireland and developing a college position paper.No previous study has been carried out to measure offending behaviour amongst persons with an intellectual disability attending mental health services in Ireland.MethodsA postal survey was undertaken targeting the lead clinicians of all Intellectual Disability Psychiatry, General Adult Psychiatry and Forensic Psychiatry Services in the Republic of Ireland. This survey requested anonymous data regarding service users with an intellectual disability and offending behaviour in this population.ResultsData relating to 431 service users was returned. Those reported to engage in offending behaviour were predominantly young males. Assault was the most common offence type. A significant number of serious offences such as unlawful killing, sexual assault and arson were reported.ConclusionsThere is an urgent need for the development of a Forensic Intellectual Disability Service in the Republic of Ireland. The current efforts of the National Forensic Mental Health Service to establish such a service by the creation of a post of Consultant Forensic Psychiatrist (special interest in intellectual disability) are to be welcomed.
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SATAKE, Hiroyuki, and Takahiro HAYASHI. "Labor Saving and Reduction of Working Hours Enable Intellectually Disabled Persons to Engage in Cultivation of the Japanese Yam,." Japanese Journal of Farm Work Research 57, no. 2 (June 20, 2022): 73–81. http://dx.doi.org/10.4035/jsfwr.57.73.

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Barelds, A., I. Van de Goor, G. Van Heck, and J. Schols. "The development of the QUALITRA-ID: a user-orientated interview to assess the quality of care and service trajectories for intellectually disabled persons." Journal of Intellectual Disability Research 54, no. 3 (March 2010): 224–39. http://dx.doi.org/10.1111/j.1365-2788.2010.01253.x.

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26

Scuticchio, D., M. O. Bertelli, G. Chiodelli, R. Cavagnola, and F. Manna. "Prevalence of Psychopathological Features in Intellectual Diability: The Italian SPAID-G Multicentric Study." European Psychiatry 41, S1 (April 2017): S92—S93. http://dx.doi.org/10.1016/j.eurpsy.2017.01.289.

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IntroductionDespite increasing awareness of high prevalence of psychiatric disorders in people with intellectual disability (ID), diagnostic tools are few and scarcely used in daily practice. SPAID-G (psychiatric instrument for the intellectually disabled adult-general version) is the first Italian for carrying out psychiatric diagnostic orientations in adults with ID. It was designed to be easy and quick instrument for daily clinical practice.Objectives/AimsThe present study was aimed at evaluating psychometric and psychodiagnostic characteristics of the SPAID-G and at supplying new data on the prevalence rate of psychiatric disorders in a multicentric Italian sample of people with ID living in different settings.MethodsThe SPAID-G was consecutively administered to more than 800 persons with ID attending residential, rehabilitative or clinical services across Italy. A part of the sample was also assessed for psychopathology through the use of DASH-II, PDD-MRS and clinically diagnosed in accordance to DSM-IV-TR and DSM-5 criteria.ResultsSPAID internal consistency, inter-rater reliability and concordance with DASH-II and PDD-MRS resulted to be good. Around 40% of the sample was assessed to have a cluster of psychopathological symptoms that could be consistent with a psychiatric diagnosis. Autism, impulse control disorder and personality disorder resulted to be the most frequent over threshold scores.ConclusionsThe SPAID-G seems to be a valid and cost-effective screening tool for the psychiatric assessment within the Italian population with ID.Disclosure of interestThe authors have not supplied their declaration of competing interest.
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Gil-Monte, Pedro R. "The Influence of Guilt on the Relationship Between Burnout and Depression." European Psychologist 17, no. 3 (January 1, 2012): 231–36. http://dx.doi.org/10.1027/1016-9040/a000096.

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Burnout is a serious problem that can be expressed as psychological symptoms, such as depressive mood. Earlier studies have shown that feelings of guilt appear to be involved in the burnout process. However, the exact nature of the relationships among burnout, guilt, and depression is unclear. The purpose of this study was to test the mediator role of guilt in the relationship between burnout and depression. The sample of this cross-sectional study consisted of 700 employees working with intellectually disabled persons. Hypotheses were tested together in a path model. Two models were constructed to test the relationships among the variables. The difference between the models was the order of the Guilt-Depression relationship. The Hypothesized model (i.e., Indolence → Guilt → Depression) showed an adequate fit to data, and all hypothesized relationships were significant. The fit of the Alternative model (i.e., Indolence → Depression → Guilt) was worse than the fit of the Hypothesized model. The hypothesized model offers a good representation of the relationships among burnout, guilt, and depression. The results point to recommending the incorporation of the evaluation of guilt as a symptom of burnout, in order to perform a more complete diagnosis and discriminate among subjects affected by burnout.
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Burghardt, Madeline, Victoria Freeman, Marilyn Dolmage, and Colleen Orick. "Unheard Voices: Sisters Share about Institutionalization." Canadian Journal of Disability Studies 6, no. 3 (August 21, 2017): 92. http://dx.doi.org/10.15353/cjds.v6i3.367.

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The recent emergence of institutional survivors’ accounts of mistreatment and abuse in Ontario’s institutions for the “feebleminded” offers a window into Canada’s long history of segregation, mistreatment, and neglect of people labelled intellectually disabled. The breaking of this silence has also allowed the stories of others who were deeply affected by institutionalization to come forward. Narratives from siblings of institutionalized individuals, although not first-hand accounts of the life inside institutional walls, offer much needed perspective on the extensive and ongoing effect of institutionalization in the lives of thousands of families, and offer additional insight from another marginalized group that until now has not held a place in Canada’s visible and spoken history. This paper is a weaving together of three sibling narratives that were part of a panel at the Canadian Disability Studies Association (CDSA) conference in Ottawa, Ontario in June 2015. All sisters of institutionalized persons, the three contributors remark in particular on their profound experiences of loss after their brother or sister was sent away from the family home. The contributors believe that it is through the sharing of such experiences that society can better come to understand the devastation wreaked upon both individuals and families through misinformed and prejudicial policies over a period of more than 150 years.
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Abullais, Shahabe Saquib, Falah Mohammed Falah Al-Shahrani, Khalaf Mohammed Saeed Al-Gafel, Al-Harthi Abdulrahman Saeed, Shouq Abdulrahman Al-Mathami, Shaeesta Khaleelahmed Bhavikatti, and Abdul Ahad Ghaffar Khan. "The Knowledge, Attitude and Practices of the Caregivers about Oral Health Care, at Centers for Intellectually Disabled, in Southern Region of Saudi Arabia." Healthcare 8, no. 4 (October 21, 2020): 416. http://dx.doi.org/10.3390/healthcare8040416.

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Oral health is perhaps the most neglected aspect of healthcare for persons living in rehabilitation centers, compared to the general population. The caregivers play a vital role in administering daily oral care to residents in rehabilitation centers: The aim of the present questionnaire-based study was to evaluate the caregivers’ knowledge, attitude and practices towards oral healthcare at centers for the intellectually disabled in the Southern region of Saudi Arabia (SA). The present study was designed as a cross-sectional one-point time survey. The samples were selected by using a non-probability convenience sampling method. The self-administered closed-ended questionnaire comprised of 22 items divided into four sections, which was designed to elicit the demographic information, awareness of oral care, attitude towards oral health and practice of the oral healthcare regime among the participants. Of the164 participants, 53.0% and 47.0% were male and female, respectively. Most of the participants—54.9%—were between 30–39 years of age. Participants were almost equally distributed between educational groups, and about 87% had more than 2 years of experience. A brief overview showed a fair level of knowledge and attitude among 61.6% and 58.5% of respondents, respectively. Participants with an education level above that of high school showed good knowledge and attitude scores (p < 0.05), whereas females showed better attitude scores compared to the males (p < 0.05). Respondents mentioned the difficulties they faced while treating the subjects. The special healthcare workers generally had acceptable oral health knowledge and practices. Caregivers who had lower education levels should be advised for training programs that addressed the importance of oral health services.
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Barelds, Anna, Ien van de Goor, Guus van Heck, and Jos Schols. "Development and Preliminary Validation of the QUALITRA-ID-P: A User-Orientated Questionnaire for Parents and Relatives to Assess the Quality of Care and Service Trajectories for Intellectually Disabled Persons." Journal of Applied Research in Intellectual Disabilities 24, no. 5 (March 28, 2011): 468–81. http://dx.doi.org/10.1111/j.1468-3148.2011.00627.x.

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Kaffemanienė, Irena, and Margarita Jurevičienė. "Strengths perspective in assessing the expression of social skills of a person with moderate intellectual disability." Social welfare : interdisciplinary approach 2, no. 2 (December 28, 2012): 126–38. http://dx.doi.org/10.15388/sw.2012.28199.

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The article contains case study of social skills of the moderately intellectually disabled person. This study complied with the view that social skills are a complex construct, which consists of integrating and complementary structural components, such as: 1) interaction skills; 2) communication skills; 3) participation skills; 4) emotional skills; and 5) social cognition skills; and each of these social skills’ structural components is constituted of complexes of social abilities. When identifying the social skills of a person with moderate intellectual disability, the concept of strengths perspective has been observed. Strengths perspective emphasizes the child’s capabilities (strengths), rather than the child’s inability. Scientifi c research problem could be defi ned in the following questions: what kind of social skills expression do the family members and pedagogues of a moderately intellectually disabled person notice? What strengths (available social skills) and problem areas do they identify?
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Baum, Susan. "Book Review: Intellectual Giftedness in Disabled Persons." Journal for the Education of the Gifted 11, no. 1 (October 1987): 71–73. http://dx.doi.org/10.1177/016235328701100107.

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Munusamy, Rajesh, and Nithin Nagaraja. "Sexual abuse leading to secondary syphilis in an intellectually disabled person: a case report." International Journal of Research in Dermatology 7, no. 6 (October 27, 2021): 872. http://dx.doi.org/10.18203/issn.2455-4529.intjresdermatol20214217.

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<p class="abstract">Syphilis is a sexual transmitted infection (STI) caused by a spirochete, <em>Treponema pallidum</em>. Condylomata lata is a characteristic lesion seen in secondary syphilis. Here we reported a case of 24 year old unmarried male with intellectual disability who presented with condyloma lata over the scrotum, prepuce and perianal region and with moth eaten alopecia over scalp since 1 month. Here the patients mother revealed he had promiscuous relationship with multiple friends, which is a sexual abuse since the patient is intellectually disabled. Clinically diagnosed as secondary syphilis. Venereal disease research laboratory (VDRL) test titre was reactive at 1:32 and <em>Treponema pallidum </em>hemagglutination test (TPHA) was positive. Biopsy was also done, which confirmed diagnosis. Single dose of injection benzathine penicillin G, 2.4 million units was administered intramuscularly. Patient did not develop a Jarisch-herxheimer reaction. On follow up his lesions healed and VDRL titres also came down and non-reactive at 3 months. Here in this case sexual abuse lead to secondary syphilis since patient was intellectually disabled so he couldn’t address his complaints clearly. Hence counselling was done to the patient and family members by dermatologist and psychiatrist.</p><p class="abstract"> </p>
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34

Kilgannon, David. "The death of Veronica L.: intellectual disability and statutory welfare in mid twentieth-century Ireland." Irish Historical Studies 45, no. 167 (May 2021): 81–100. http://dx.doi.org/10.1017/ihs.2021.24.

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AbstractVeronica L., a woman with an intellectual disability, died of starvation in 1961 while the recipient of a Disabled Person's Maintenance Allowance (D.P.M.A.) from the Dublin Health Authority. Her death occured after a prolonged period of deficient care, a neglect that was exacerbated by flaws in statutory welfare. During the preceding decade the state intervened in disability provision to an unprecedented degree through the expansion of institutional care and social welfare reform. Yet, these services remained characterised by a chronic pressure on resources and a reluctance to intervene in potentially neglectful family situations, which allowed cases of failing care to go unaddressed. Drawing on contemporary documents, in particular the depositions collected for the coroner's court inquest into Veronica's death, this article offers an insight into the exigencies underlying the later life of one woman with an intellectual disability. In doing so, it explores the way in which this singular case provides a distinctive avenue for better understanding the experiences of the intellectually disabled more broadly, including the nature of community care and the operation of statutory welfare during the mid twentieth century.
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Moceviciene, Aldona, and Gunars Strods. "Sustainability and Empowerment in Context of Inclusion of Disabled Persons." SOCIETY, INTEGRATION, EDUCATION. Proceedings of the International Scientific Conference 3 (May 17, 2015): 173. http://dx.doi.org/10.17770/sie2015vol3.390.

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<p><em>Creation without disassembling, using wisely, responsible planing and estimation longer-term consequences giving priority to the person, respecting his/her individuality, diversity - this is a new approach and sustainable society features.</em> <em>Quality of life include all aspects of the way we live our lives. They allow us to fulfil our needs and aspiration</em>s<em>. On the basis of results of the research EU policy materials and Lithuania and Latvia ways of realization these laws in the regional policy, that all global methods and wellbeing development actions have a direct impact for people with intellectual disabilitiess and influentto expanding possibilities self-expression, activating self-action, stimulating self-conception. Creatiwity –the way and possibility in empowering these people socialization and self – realizing. The researches in this field would answer to the questons: possible to optimize the quality of life for people with intellectual deseases in their abilities limited space.</em></p>
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SUZUKI, Yoshihiro, and Masaki KATAOKA. "ANALYSIS ON THE TERRITORY IN DWELLING LIFE ON INTELLECTUAL DISABLED PERSONS." Journal of Architecture and Planning (Transactions of AIJ) 64, no. 520 (1999): 123–30. http://dx.doi.org/10.3130/aija.64.123_4.

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37

Blik, H., E. G. Harskamp, S. van Leeuwen, and R. Hoekstra. "Video instruction with explanation to another person for intellectually disabled students." Journal of Computer Assisted Learning 33, no. 6 (June 30, 2017): 606–20. http://dx.doi.org/10.1111/jcal.12204.

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38

Arimoro, Augustine Edobor. "Persons with Intellectual Disability and Access to Justice in Nigeria: Challenges and the Way Forward." Hasanuddin Law Review 5, no. 2 (August 14, 2019): 180. http://dx.doi.org/10.20956/halrev.v5i2.1561.

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Conservatively, there are approximately about two million persons in Nigeria who may be referred to as persons with intellectual disabilities. These persons suffer from several challenges ranging from economic to non-inclusion in the society. In the paper, the discussion focuses on persons with intellectual disabilities and the effective access to justice as a fundamental right. The paper finds that even though Nigeria has adopted and ratified the United Nations Convention on the Rights of Persons with Disabilities, the Federal Government of Nigeria has not been proactive in supporting the persons with disabilities in the country to enjoy these rights. Furthermore, despite the provision in the 1999 Constitution of the Federal Republic of Nigeria to ensure freedom from discrimination, there is no direct effect on procedure to ensure that the rights of the disabled persons are protected. The paper proposes for a framework for the protection of the person with intellectual disability which includes legal protection, legal awareness, legal aid, adjudication and for civil society oversight of the access of persons with intellectual disabilities to justice.
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SUZUKI, Yoshihiro, Masaki KATAOKA, Hiroshi NAKATAKE, and Mitoko YOSHIDA. "ANALYSIS OF THE FACTOR PRESCRIBED THE BEHAVIOR IN DWELLING LIFE ON INTELLECTUAL DISABLED PERSON : A basic study on the architectural planning for intellectual disabled person." Journal of Architecture and Planning (Transactions of AIJ) 63, no. 503 (1998): 77–84. http://dx.doi.org/10.3130/aija.63.77_1.

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40

Zurzycka, Patrycja, Katarzyna Wojtas, and Grażyna Puto. "Methods of communication in medical care respecting the dignity of an intellectually disabled person." Sztuka Leczenia 37, no. 1 (September 8, 2022): 43–50. http://dx.doi.org/10.4467/18982026szl.22.005.15996.

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People with intellectual disabilities experience stigma and discrimination. In caring for people with intellectual disabilities, special attention should be paid to respecting their dignity and subjectivity. The aim of this study is to emphasize the importance of respecting the dignity and subjectivity of adults with intellectual disabilities and the importance of communicating with them. The paper is based on a literature analysis of intellectual disability issues. The literature analysis indicates that the subject of intellectual disability concerns the subjectivity and the dignity of the people as well as the barriers to communication with the environment and medical personnel. It is fundamental to conduct research into care of people with intellectual disabilities. In addition, there is a need to organize training for all members of the therapeutic team, especially in the area of communication issues with people with intellectual disabilities.
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Oravec, Jo Ann. "Depraved, Distracted, Disabled, or Just “Pack Rats”? Workplace Hoarding Personas in Physical and Virtual Realms." Persona Studies 1, no. 2 (October 23, 2015): 75–87. http://dx.doi.org/10.21153/ps2015vol1no2art472.

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This article provides some potential directions in exploring the construction of the persona of the “hoarder” and addresses how such a persona can move to the foreground of an individual’s set of workplace-related personas. Hoarding throws into relief some critical concerns about the social standings of individuals in workplaces and the extent to which they have autonomous expression. The article frames hoarding in terms of its capacity to externalize particular social issues (such as environmental problems) and generate public discourse, and examines both physical hoardings (books and papers in academic and office settings, for example) and hoardings of virtual goods (such as digital music, video files, and pornographic images). Virtual hoardings have been constructed as problematic as they create barriers to the free flow of information in the workplace and can challenge organizational interests related to intellectual property concerns. Hoarding as a whole is becoming more tightly circumscribed as a workplace and community condition, in part because the ability to manage physical and virtual items in confined settings is considered central to many forms of competent societal functioning.An assortment of human resource management initiatives to mitigate hoarding concerns has developed, including the consideration of hoarding as a disability. However, hoarding behavior is increasing creating problems for those who are searching for simple definitions or straightforward diagnostic criteria. This article also provides some structures for analysis of the class-related and economic dimensions of workplace hoarding personas, and explores potential implications of lifelogging initiatives and hoarding acceptance approaches.
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42

Bogacki, David F., Kenneth J. Weiss, Joan A. Vail, and Deborah J. Armstrong. "Assessing High-Risk Behavior in the Developmentally Disabled: Measurement and Forensic Implications." Journal of Psychiatry & Law 33, no. 2 (June 2005): 207–26. http://dx.doi.org/10.1177/009318530503300203.

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In the age of postinstitutional care, less attention is paid to the residual population of developmentally disabled persons within public facilities. Many such individuals are court ordered from the criminal justice system; they require varying intensities of mental health services. Level of risk to self and others is one component assessed by service providers as they plan resource allocation to meet the residents' support needs. Although it may be presumed that lower-functioning clients need more mental health services, this has not been tested systematically. The Developmental Disability Risk Inventory (DDRI) was designed to measure high-risk behavior in adults with developmental disability. This study investigated intellectual functioning, adaptive functioning, and high-risk behavior in 92 persons with mental retardation. The results indicated that DDRI scores correlated positively with level of intellectual functioning but did not show a statistically significant relationship with level of adaptive functioning. Together, these findings suggest construct validity for the DDRI. Implications for the clinical and forensic utility of the DDRI are discussed.
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43

Sudiatmaka, Ketut, Ratna Artha Windari, Made Sugi Hartono, and I. Gusti Ayu Apsari Hadi. "LEGAL PROTECTION AND THE EMPOWERMENT OF THE DISABLED COMMUNITY IN BULELENG REGENCY." Ganesha Law Review 2, no. 1 (May 5, 2020): 1–16. http://dx.doi.org/10.23887/glr.v2i1.112.

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This study aims to find out about the protection and empowerment of people with disabilities in Buleleng Regency. In Buleleng regency, either government or private buldings including their public places are not built with fully provided accessibility for persons with disabilities. Furthermore, the persons with disabilities still having trouble to obtain their rights due to social and cultural factors, economic factors, weak policies and law enforcement in favor of disabled and also there is no legal umbrella that clearly regulates the protection and empowerment of persons with disabilities. As for this research is the normative legal study with using qualitatively analysis techniques. The fulfillment of social and economic rights is realized by the government of Buleleng Regency in the form of Social Assistance for Persons with Disabilities with giving an amount of money each month. The persons with disabilities are also trained to be given jobs according to their abilities. There are also Regional Regulations on the protection and fulfillment of the Rights of Persons with Disabilities which is soon be enacted that is include rights and legal protections for persons with disabilities, such as : the right to fullfill equality before the law until intellectual rights are protected.
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Gvozdanović Debeljak, Aleksandra, Borko Baraban, and Robert Lovrić. "Voting of people with intellectual disabilities in the context of fundamental human values." Nova prisutnost XVI, no. 2 (July 9, 2018): 246. http://dx.doi.org/10.31192/np.16.2.2.

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The aim of the paper is to show the level of awareness of people with intellectual disabilities on political elections and to describe the reasons, ways and expectations for which persons with intellectual disabilities do (not) vote. The sample is a heterogeneous group of ten persons with intellectual disabilities from the Inclusion Centre Osijek aged from 28 to 65. Interview (semi-structured interview) has been used as a research method. The interviews took place on the Centre’s premises. The participants responded to three basic questions, as well as to sub-questions asked by the interviewers. Research data have been shown at a qualitative level. The interview results point to inadequate awareness of the respondents on political elections, resulting in the lack of awareness of the respondents on the purpose of political elections and the functionality of voting participation. Also, the voter turnout is low and, consequently, there is an inadequate use of their voting rights in terms of political participation as disabled persons. Realization of rights of persons with disabilities must not depend on the (non)readiness of the system or the will of individuals but must be the primary goal of inclusive policy and society in general.
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TAMAOKI, Yusuke. "The Awareness and Social Relationship on the Body of Intellectual Disabled Person." Annual review of sociology 2007, no. 20 (2007): 84–95. http://dx.doi.org/10.5690/kantoh.2007.84.

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46

Lewis, Hope. "Marrakesh Treaty to Facilitate Access to Published Works for Persons Who are Blind, Visually Impaired, or Otherwise Print Disabled." International Legal Materials 52, no. 6 (December 2013): 1309–20. http://dx.doi.org/10.5305/intelegamate.52.6.1309.

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On June 27, 2013, delegates to a Diplomatic Conference of the World Intellectual Property Organization (WIPO) adopted the Marrakesh Treaty to Facilitate Access to Published Works for Persons Who Are Blind, Visually Impaired, or Otherwise Print Disabled (Marrakesh Treaty). Governmental delegates and international disability rights advocates hope that the new instrument will increase access to information for millions of visually impaired people around the world, especially in developing countries.
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Subramani, Vaidehi. "Day Care - As a Method of Disability Care towards the Inclusion." Global Journal of Enterprise Information System 7, no. 1 (March 1, 2015): 54. http://dx.doi.org/10.18311/gjeis/2015/3035.

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The second decade of this century has often hailed as the decade of aspirations, ambitions and development, yet relinquished the phenomenon of inclusion at the back benches of the develop - mental discourses. Disabled persons constitute fifteen percent of world population. The stigmatizing terminology 'mental retarda - tion' was in use world over till late 20th century. This term has been gradually replaced by 'intellectual disability' in most of English speaking countries very recently.
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48

Danforth, Scot. "Independence, Dependence, and Intellectual Disability: From Cultural Origins to Useful Application." Research Articles 28, no. 2 (October 25, 2021): 95–109. http://dx.doi.org/10.7202/1082918ar.

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American government educational policy and leading advocacy groups commonly espouse independence as a primary goal for young people with intellectual disabilities. An extensive philosophical literature of autonomy has focused mostly on analyses of cognition that achieve individual self-governance. But the loosely defined concept of independence used by disability policymakers and advocates provides a more malleable , social understanding that involves someone actively relying on the assistance of others. The purpose of this paper is to examine the cultural, historical origins of the notion of independence for disabled persons through an exploration of the biography of Ed Roberts, the father of the independent living movement, and the cultural context of Berkeley, California, in the 1960s and 1970s , where the movement began. The paper applies those cultural concepts to the life situations of persons with intellectual disabilities, asking how well independence serves as a useful goal for the group.
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Bryndin, Evgeniy. "Professional Training of Intellectual Disabled Person by Holographic Image of Competent Healthy Specialist." International Journal of Psychological and Brain Sciences 6, no. 3 (2021): 44. http://dx.doi.org/10.11648/j.ijpbs.20210603.12.

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50

Maebara, Kazuaki. "Case Study on the Employment of a Person with Intellectual Disability in Childcare Work in Japan." Journal of Intellectual Disability - Diagnosis and Treatment 10, no. 3 (July 15, 2022): 122–29. http://dx.doi.org/10.6000/2292-2598.2022.10.03.1.

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Background: In recent years, it has become necessary to promote the employment of persons with intellectual disabilities in new occupations. Objective: This study aimed to analyze the case of a person with an intellectual disability employed in childcare work and examine it from the perspective of issues in securing employment for the disabled. Method: As a case study, an in-depth interview was conducted to survey a director of the Center for Early Childhood Education and Care, which had been hiring persons with intellectual disabilities and organizing the employment process for about four years. Results: The person with intellectual disability was assigned to perform direct support work, mainly childcare work, and was aided by staff members responsible for guidance and the verbalization of job instructions. In addition, the staff provided specific guidance for solving problems that occurred in daily life. The work could be carried out smoothly. Conclusion: While many people with intellectual disabilities are engaged in indirect support work, participating in direct support work, mainly childcare work, may positively affect their career development. Additionally, in focusing on the workplace, it is important to reconsider daily life issues from the viewpoint of long-term stability in the workplace and improve the methods used for transition support. The data were collected from a single case, which may limit the generalisability of the findings.
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