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1.
Indian J Lepr ; 2006 Jul-Sep; 78(3): 217-29
Article in English | IMSEAR | ID: sea-54437

ABSTRACT

To assess the level of awareness about the different provisions of the Persons with Disability Act (PWD Act) among leprosy patients and other disabled, 233 disabled persons from the self-help groups formed by Vadathorasalur Leprosy Control Unit have been interviewed using a structured interview checklist. The results show that 74.7% of the respondents were aware that identity cards are available for the disabled, 56.2% were aware of the free education benefit to the disabled, as low as 35.6% were aware of the scholarships, 33% knew about the employment reservations, 24.9% heard about the housing scheme of the government for the disabled, but 24.5% only knew about law against discrimination, 31.8% came in contact with institutions for the severely disabled and only 16% were aware of the unemployment allowance to the disabled. The level of awareness is low among women with regard to all components of the Act. It was found that students studying up to secondary level were not aware of the availability of scholarships and free education, which needs to be seriously looked into, especially by educational institutions. The level of formal education played a significant role in increasing awareness about the Act among literates. The knowledge is low among persons of all occupations. The study showed that there is a great need for an educational intervention programme to publicize the provisions of the Act among the disabled and their families.


Subject(s)
Adolescent , Adult , Aged , Disabled Persons/legislation & jurisprudence , Discrimination, Psychological , Education , Employment , Female , Housing , Humans , India , Institutionalization , Leprosy/economics , Male , Middle Aged , Mycobacterium leprae , Self-Help Groups , Unemployment
2.
Indian J Lepr ; 2005 Jul-Sep; 77(3): 247-53
Article in English | IMSEAR | ID: sea-55595

ABSTRACT

Leprosy, manifesting during adolescence when significant physical and emotional changes are taking place, poses further stress and strain both on the individual and on the family. Based on hospital records, focus group discussions and in-depth interviews, data on 258 adolescent leprosy patients seen at a leprosy referral hospital in Kolkata, India, are presented. The male-female sex ratio was 1.93:1, 56.6% were multibacillary patients and 13.2% had grade 2 disability. At the time of final follow up, 10% of PB and 33% of MB patients had already discontinued treatment. The commonest complication was reaction (14.5%). Adolescents were still dependent on their parents for health matters. Data obtained from questionnaires confirmed the role of social stigma in hiding, delay in starting of MDT and defaulting. Frequent hospital admissions resulted in loss of jobs and disruption of studies and caused psychological disturbances. It is critical to identify and treat adolescent leprosy on a priority basis. Health education and counselling programmes must be more focused and acceptable. Further research is necessary.


Subject(s)
Adolescent , Psychology, Adolescent , Attitude to Health , Family/psychology , Female , Humans , India/epidemiology , Leprosy/drug therapy , Male , Prevalence , Surveys and Questionnaires , Stereotyping
3.
Indian J Lepr ; 2003 Jul-Sep; 75(3): 243-58
Article in English | IMSEAR | ID: sea-55054

ABSTRACT

Integration of the vertical leprosy programme into the existing horizontal health programme poses various administrative and operational challenges to programmers. In order to understand the preparedness of the PHC workers for integration of leprosy into primary health care services, 71 PHC workers were interviewed using a structured interview schedule. The results showed that about 42% of the staff have heard of the concept of integration earlier and 90% of the PHC staff are willing to treat leprosy patients in the primary health care centre, but only 72% were in favour of integration. The reasons for favouring integration were (1) wider coverage with MDT, (2) frequent field visits by the worker, (3) better rapport with the community, (4) timely treatment and (5) cost-effectiveness. About 28% of the staff members did not favour integration for the reasons that the leprosy programme would suffer, targets cannot be met, supervision would be difficult, knowledge of the staff was inadequate and importance cannot be given to leprosy as family planning is always a priority in PHC centres. About 43% of the staff felt that the performance of the leprosy programme would be better after integration. With regard to workload, 60% of the sample felt that there would be increase in the workload in the field, record maintenance and supervision. The difficulties foreseen by the workers were grouped into 6 categories, viz., administrative, managerial, technical, personnel, social and miscellaneous. It is worth noting that 91% of the staff that included all categories said they were not afraid of leprosy, but needed training in leprosy work. About 50% of the staff expected increase in salaries and promotions if integration took place.


Subject(s)
Attitude of Health Personnel , Humans , India , Leprostatic Agents/therapeutic use , Leprosy/drug therapy , Primary Health Care/organization & administration
5.
Indian J Lepr ; 1995 Oct-Dec; 67(4): 389-403
Article in English | IMSEAR | ID: sea-54946

ABSTRACT

Divorcing a leprosy afflicted spouse is one of the manifestations of social stigma attached to leprosy. It mostly depends on the community's decision resulting from the physical and social threat perceived. In order to find out who were prone to divorce their leprosy afflicted spouses, 1199 community members drawn from two States, Orissa and Andhra Pradesh, were asked what their advice would be if a spouse of leprosy patient approached them for advice. The responses were cross tabulated against their demographic characteristics. While, only a small proportion of respondents advised divorce in Andhra Pradesh, they were mainly females, above SSC educated, those who did cultivation, labourers and were from poor economic group. On the other hand, in Orissa, a high proportion of the respondents suggested divorce.


Subject(s)
Adolescent , Adult , Age Factors , Attitude , Divorce , Educational Status , Female , Humans , Leprosy/psychology , Male , Middle Aged , Occupations
6.
Indian J Lepr ; 1995 Jul-Sep; 67(3): 259-72
Article in English | IMSEAR | ID: sea-54912

ABSTRACT

NLEP, through its survey-education-treatment (SET) pattern, attempts to educate the community members about the scientific facts of leprosy with the view to improve their knowledge leading to a more positive attitude towards the leprosy afflicted. This paper explores the impact of knowledge on the attitudes of 1199 community members drawn from two States, Andhra Pradesh and Orissa, towards leprosy. The results show that, overall, a high knowledge level did not necessarily generate positive attitudes. There was a general negative attitude despite 35% to 50% of the respondents having high knowledge level. There were, however, situations in which a high level of knowledge helps to have positive attitudes. These situations differ in the two states studied.


Subject(s)
Adolescent , Adult , Congenital Abnormalities , Divorce , Employment , Female , Food , Health Education , Health Knowledge, Attitudes, Practice , Humans , Leprosy , Male , Surveys and Questionnaires , Social Isolation
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