1 May 2002

 
United Nations
Economic and Social Council
Permanent Forum on Indigenous Issues
First Session, 13-24 May 2002, New York
Item 6 of the provisional agenda

 

INDIGENOUS PEOPLES AND HEALTH

 

A Briefing Paper For The Permanent Forum On Indigenous Issues
 

Prepared by the Committee on Indigenous Health

  

Annex 2

 

Summary Recommendations of the International Consultation on the Health of Indigenous Peoples, Geneva, 23-26 November 1999 (WHO/HSD/00.1)

 

 

a) Recommendations relating to major health challenges

 

WHO should:

 

1.        Recognize the value and validity of indigenous health systems and should support the maintenance and development of those systems.

2.        Explicitly take into account the health of indigenous peoples in formulating its budget and overall programme of work.

3.        Accept indigenous peoples’ concepts of health as valid and these concepts should form the basis of work to promote indigenous peoples’ health development.

4.        Promote indigenous peoples’ health within the context of their broader development.  To this end, WHO should formulate, promote, and implement indigenous peoples' health strategies that are consistent with the overall positive development of indigenous peoples.

5.        Note that the rights pertaining to health in the Draft UN Declaration on the Rights of Indigenous Peoples are compatible with the values of its own Health for All policy for the 21st Century.

 

Member States should:

 

1.        Promote the preservation and respect of the cultural heritage and practices of indigenous peoples, and the integrity of their territories and natural resources.  Traditional lifestyles should be seen as protective of indigenous peoples’ health.

2.        Consider the health impact of large-scale development projects (e.g. extractive industries and power schemes), and only approve those projects that are not detrimental to the health of indigenous peoples.

3.       Promote public education, which fosters a greater degree of tolerance and respect for the distinct cultures and special rights of indigenous peoples.

4.        Accept indigenous peoples’ concepts of health as valid and these concepts should form the basis of work to promote indigenous peoples’ health development.

5.        Promote indigenous peoples' health within the context of their broader development.

 

 

b) Recommendations relating to strategies and approaches

 

WHO should:

 

1.        Act as an advocate to ensure that equity-oriented policies on indigenous peoples’ health are promoted and developed and serve as a catalyst in promoting initiatives relating to the health of indigenous peoples.

2.        Continue the review of existing policies and strategies specific to indigenous peoples at the regional level, and may recommend to Member States policies and strategies to be implemented based on the findings of the review.

3.        Promote the right to quality information on health, which would enable indigenous peoples to have a greater degree of control over their own health.

4.        Promote the systematic collection and reporting of statistics disaggregated by ethnicity by Member States.  This will require the development of working criteria or definitions of ethnicity and the development of indicators that are able to measure what constitutes a positive health outcome in indigenous peoples’ terms.

5.        Develop, in close consultation with the Informal Indigenous Peoples Health Advisory Group, a comprehensive research agenda which places an emphasis on the broad determinants of health.

6.        Conduct a review of traditional health practices in close consultation with indigenous peoples to determine the overall acceptability in terms of traditional and accepted international standards.

7.        Develop a database primarily of government institutions with responsibilities for indigenous peoples’ health.  Relevant research institutions working with indigenous peoples’ health issues should also be incorporated.

8.        Establish a series of collaborating centres within Member States to facilitate research and development on indigenous peoples' health.

9.        Encourage universities to create departments or chairs to promote knowledge and research in traditional medicine and healing.

10.     Create a web site on indigenous peoples’ health. 

11.     Ensure the dissemination of information on upcoming meetings, activities and events which concern the health of indigenous peoples, allowing for timely input and participation.

12.     Review the impact of large-scale development interventions on indigenous peoples’ health.  If necessary, WHO should further develop existing standards and methods, so that they are more sensitive to the situations of indigenous peoples.

13.     Ensure that indigenous peoples are appropriately represented on the staff of WHO at all levels.

14.     Ensure (through designated positions) that indigenous peoples have the opportunity to participate in existing fellowship and other professional programmes at the national, regional and HQ levels.  Further, specific fellowship programmes should be established to address the unique health development needs of indigenous peoples.

15.     Develop other capacity-building mechanisms such as technical assistance to indigenous peoples’ health programmes, training of indigenous health workers and information sharing between indigenous communities.

16.     Support the development of competence in indigenous peoples’ health issues within Member States, particularly in relation to the capacity of health professionals to work with indigenous peoples.

 

Member States should:

 

1.        Ensure that the indigenous peoples' right to the highest attainable standard of health and well-being is reflected in their constitutions, national legislation, and government policies and strategies.

2.        Disseminate health information to indigenous peoples living in remote areas and find ways to communicate this information to illiterate communities. Recognize the right of indigenous peoples to determine their own health development and facilitate the control of health services for indigenous peoples, by indigenous communities.  This does not, however, replace government obligations in relation to indigenous peoples health.

3.        Formulate, in consultation with indigenous peoples, a capacity-building plan which may include:

a) exchange of knowledge between indigenous and non-indigenous health experts on indigenous and mainstream systems of health;

b) increasing the competence of health professionals so that they have the necessary skills to work with indigenous peoples; and

c) incorporating a consideration of indigenous health systems in relevant university curricula.

1.       Adopt legislation that protects indigenous peoples’ intellectual property rights in relation to health.

2.        Undertake the systematic collection and reporting of statistics disaggregated by ethnicity.  Rapid assessments of the state of indigenous peoples’ health should be carried out in all regions.

3.        Report to WHRO on the health development of indigenous peoples in countries, in terms of access and coverage of health care.

 

c) Recommendations relating to partnership mechanisms 

 

WHO should:

 

1.        In recognition of the need for partnership based upon equity, trust, and mutual respect, provide support as required to establish an informal Indigenous Peoples Health Advisory Group (IPHAG) as the counterpart to work with WHO.  The IPHAG would consist of at least 13 members (1 North America, 1 Central America, 1 South America, 1 East Africa, 1 Southern Africa, 1 Sahel, 1 South Asia, South-East Asia, Far Eastern Asia, 1 Pacific, 1 Australia/ New Zealand, and 1 Arctic and 1 Russian), representing indigenous peoples from the different regions of the world.

2.        In accordance with WHO resolution WHA 48.24 (1995), remind Member States of their commitment to the establishment of focal points on indigenous peoples’ health at the national level.  The focal points in collaboration with indigenous peoples and other relevant stakeholders (e.g. UNDP, ILO, UNFPA and UNEP) should elaborate regional health plans and establish, develop, and implement specific health strategies.

3.        Have annual meetings with the IPHAG.  WHO should make financial provisions for these meetings.

4.        Ensure that indigenous peoples’ health issues are presented to the WHA by an indigenous peoples’ spokesperson (supported by WHO) as was the case in 1993.

5.        Ensure that Regional Offices hold regular consultations with indigenous peoples to ensure that they have an input in all issues relevant to the health of indigenous peoples.

6.        Seek to work together with WIPO, WTO, and other key agencies in ensuring the protection of indigenous peoples’ intellectual property as it relates to health (e.g. traditional medicine), and identify best practises at the country level to protect indigenous peoples’ intellectual property as it relates to health.

7.        Include, at all levels (headquarters, regional offices, and country offices) in relevant programmes components specifically addressing indigenous peoples’ health issues.  These programmes should be reviewed and the impact on indigenous peoples evaluated.  The review process should include input from indigenous peoples health experts.

8.        Work with key international, regional, and national organisations (e.g. WTO, MERCOSUR, ASEAN, UN agencies and programmes) to promote policies and strategies that are compatible with indigenous peoples’ health development.

9.        Develop, with the IPHAG, a global plan of action for indigenous peoples’ health following regional consultations with indigenous peoples.  An International Conference on Indigenous Peoples’ Health should be held by the end of 2001 to endorse this plan and to provide a forum for developing new strategies and engaging in constructive dialogue aimed at improving indigenous peoples’ health globally.

10.     Following the International Conference, hold International Consultations on the health of indigenous peoples every two years to assess the health situation of indigenous peoples and then seek support from Member States and other stakeholders.

 

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