Labour rights of the rare diseases population ‒ breaking the glass ceiling
This paper aims to introduce a legal framework for exercising one of the most basic socio-economic rights of people with rare diseases: the right to decent work. Considering the specificity of the medical and, consequently, social status of the people affected, the appropriate labour-law measures ne...
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doaj-463440044498430b8ad96407f135e1c72021-02-05T08:26:21ZengInstitute of Social Science, BelgradeStanovništvo0038-982X2217-39862020-01-01582435610.2298/STNV200617005S0038-982X2000005SLabour rights of the rare diseases population ‒ breaking the glass ceilingStojković-Zlatanović Sanja0Sjeničić Marta1Sovilj Ranko2Centre for Legal Research, Institute of Social Sciences, Belgrade, SerbiaCentre for Legal Research, Institute of Social Sciences, Belgrade, SerbiaCentre for Legal Research, Institute of Social Sciences, Belgrade, SerbiaThis paper aims to introduce a legal framework for exercising one of the most basic socio-economic rights of people with rare diseases: the right to decent work. Considering the specificity of the medical and, consequently, social status of the people affected, the appropriate labour-law measures need to be determined. Applying the comparative and normative method along with the contemporary anti-discrimination principle, the labour status of the rare diseases population has been analysed based on the proposed classification in legal terms. As a precondition for labour legislation, new Serbian healthcare legislation on rare diseases should be supported through the process of implementation to reduce adverse cases as effectively as possible, advance genetic and other clinical diagnoses, and thus increase the efficiency of available medical treatment. Concerning public health policy, updated registries and better health statistics should be created. These activities require certain amendments to both general and specialist labour legislation (disability legislation), aiming to include patients with rare diseases in the working (and social) environment without discrimination.http://www.doiserbia.nb.rs/img/doi/0038-982X/2020/0038-982X2000005S.pdfrare diseases populationlabour statusanti-discrimination lawlegal classificationdignity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Stojković-Zlatanović Sanja Sjeničić Marta Sovilj Ranko |
spellingShingle |
Stojković-Zlatanović Sanja Sjeničić Marta Sovilj Ranko Labour rights of the rare diseases population ‒ breaking the glass ceiling Stanovništvo rare diseases population labour status anti-discrimination law legal classification dignity |
author_facet |
Stojković-Zlatanović Sanja Sjeničić Marta Sovilj Ranko |
author_sort |
Stojković-Zlatanović Sanja |
title |
Labour rights of the rare diseases population ‒ breaking the glass ceiling |
title_short |
Labour rights of the rare diseases population ‒ breaking the glass ceiling |
title_full |
Labour rights of the rare diseases population ‒ breaking the glass ceiling |
title_fullStr |
Labour rights of the rare diseases population ‒ breaking the glass ceiling |
title_full_unstemmed |
Labour rights of the rare diseases population ‒ breaking the glass ceiling |
title_sort |
labour rights of the rare diseases population ‒ breaking the glass ceiling |
publisher |
Institute of Social Science, Belgrade |
series |
Stanovništvo |
issn |
0038-982X 2217-3986 |
publishDate |
2020-01-01 |
description |
This paper aims to introduce a legal framework for exercising one of the most basic socio-economic rights of people with rare diseases: the right to decent work. Considering the specificity of the medical and, consequently, social status of the people affected, the appropriate labour-law measures need to be determined. Applying the comparative and normative method along with the contemporary anti-discrimination principle, the labour status of the rare diseases population has been analysed based on the proposed classification in legal terms. As a precondition for labour legislation, new Serbian healthcare legislation on rare diseases should be supported through the process of implementation to reduce adverse cases as effectively as possible, advance genetic and other clinical diagnoses, and thus increase the efficiency of available medical treatment. Concerning public health policy, updated registries and better health statistics should be created. These activities require certain amendments to both general and specialist labour legislation (disability legislation), aiming to include patients with rare diseases in the working (and social) environment without discrimination. |
topic |
rare diseases population labour status anti-discrimination law legal classification dignity |
url |
http://www.doiserbia.nb.rs/img/doi/0038-982X/2020/0038-982X2000005S.pdf |
work_keys_str_mv |
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