Power Shift, Localisation and Decolonising Aid, have become strong trends, and also buzzwords in the current debate around a more legitimate and impactful aid system.
The push for more resources and decision-making power has most prominently launched at the World Humanitarian Forum in 2016, and was linked to pledges to increase the appalling low percentages of aid funding to local actors, both by donors and international civil societies organisations (ICSOs). Breakthroughs of this ‘Grand Bargain’ are yet to be seen, despite continued commitment to strengthening local Civil Society, recently confirmed by a strong OECD policy document.
Civil Society itself is struggling with implementation. The ambition has worked itself into a number of narratives on how the ‘system’ should change, how power needs to be shifted, how International ICSOs need to be re-imagined.
Not all of these narratives are positive. Nationalistic Governments in India or parts of Africa have hijacked the ‘localisation’ ambition to keep foreign CSOs at bay and discredit them as foreign agents. Even in the US and the UK localisation has become a different meaning – using foreign aid to help disaster victims at home. The recent drastic cuts by British FCDO show the trend.
Looking at the traditional ‘Power Holders’ in the aid system, donors, bilateral agencies and ICSOs, many, if not all, will agree that ‘localisation’ is a good thing, though. It strengthens the consideration of local contexts, vulnerabilities and capacities, true partnerships, inclusive decision-making etc. Many are talking about, and implementing, changing funding patterns, with promising developments linked to the increasingly localised COVID-19 responses.
International civil society organisations have, generally, a rather positive narrative on localisation that includes many past achievements they seem to have made over the last 30 years. Many have grown into confederations, with strong local chapters, and a huge armada of local staff, increasingly in leadership positions. Many will defend their business models as inclusive, decentralised, and addressing the local contexts.
The challenge comes with scrutinising whether these models are good enough. Are power imbalances being addressed, and radically changing? The Centre works with a number of ambitious ICSOs who have started putting local actors (people we work with, partners, primary actors) into the centre of decision-making processes. These are ‘Governance’ discussions in the wider sense, i.e. putting processes and structures to the test – are they designed, capable and fit for greater inclusion?
It’s an exciting journey which has no easy answers – different ways of inclusivity are being chased, and different power dimensions are being addressed – in Big ‘G’ Governance (structures, decision-making protocols, voting rights) and small ‘g’ governance issues, like relationship building, information flow, accountability and transparency, ‘expertise talks vs. money talks’, physical points of decision-making.
Who and what helps and blocks? Facilitators and blockers of power shifts are often not the same people / entities. You need almost tactical approaches (actors mapping, power analysis, finding sponsors etc.). A very good idea is to link the governance as much as possible to the intent and mandate of the organisation.
A quick insight from an initiative many have heard about, could be helpful with focus. The West Africa Civil Society Institute WACSI has just published a survey of about 500 local CSOs about their perception on how partnerships play out. The results were almost surprisingly positive, with lots of appreciation of LCSO / ICSO partnerships, many of which do consider local contexts. But a few critical issues arose: Decision-making is uneven and not mutually beneficial, ICSOs are expected to be facilitators not implementers, more consideration of local capacities, not necessarily funders.
A recent ‘Hard Talk’ event between ICSOs, partners, donors and critical friends touched upon those dimensions and showed the potential for change, but the need for more intense dialogue between groups that have different expectations of each other. One of the biggest challenges comes from inherent ‘colonial’ structures of the aid system, which can only be addressed in an intersectional way, not overlooking discriminatory practices, and engaging in an open exchange and the willingness to learn from each other. A window seems to have opened to turn an outdated aid system onto its feet, and let power go to the people and their institutions, which have been ‘recipients’ of philanthropy, goodwill but bad practices for too long.
Executive Director
International Civil Society Centre
Dr. Wolfgang Jamann is Executive Director of the International Civil Society Centre. Until January 2018 he was Secretary General and CEO of CARE International (Geneva). Before that he led NGO Deutsche Welthungerhilfe and the Alliance 2015, a partnership of 7 European aid organisations. From 2004-2009 he was CEO & Board member of CARE Deutschland-Luxemburg and President of the CARE Foundation. Previously, he worked for World Vision International as a regional representative in East Africa (Kenya) & Head of Humanitarian Assistance at WV Germany. After his Ph.D. dissertation in 1990 he started his career in development work at the German Foundation for International Development, later for the UNDP in Zambia. As a researcher and academic, he has published books and articles on East & Southeast Asia contributing to international studies on complex humanitarian emergencies and conflict management.
This blog post is part of our LNOB Knowledge Exchange Programme (KEP). Elizabeth Lockwood, Mohammed Ali Loutfy and Sally Nduta explain why organisations of persons with disabilities must be engaged in data collection, analysis, and use of data for evidence-based advocacy to influence policy and decision-makers.
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Overwhelmingly, persons with disabilities remain invisible in statistics and as a result existing and new barriers that persons with disabilities face are, once again, not addressed. This invisibility has been particularly evident in the COVID-19 pandemic with dire consequences for many persons with disabilities around the world.
Data on persons with disabilities are needed so we understand the real situation of persons with disabilities, to identify gaps that are not addressed through policies and to provide examples of successes. This is not only beneficial for evidence-based advocacy, but also to influence decision-makers and convince them on the themes where the most urgent actions and steps must be taken at national, regional and global levels. This is the beginning and foundational to all other efforts.
Gathering qualitative data and engaging in participatory research with persons with disabilities and their representative organisations are incredibly important and can complement existing quantitative data sources. This is especially important since community-driven data with representative organisations of persons with disabilities can fill the gaps that official statistics cannot from surveys and censuses alone. In fact, community-driven data is particularly relevant for measuring the SDGs for persons with disabilities since most SDG global indicators are falling behind in measuring progress for persons with disabilities, again, leaving persons with disabilities behind.
In response, the Stakeholder Group of Persons with Disabilities, the International Disability Alliance, Disabled Peoples’ International, and CBM Global Disability Inclusion produced a comprehensive disability data advocacy toolkit to address the importance of organisations of persons with disabilities (OPDs) to be engaged in data collection, analysis, and use of data for evidenced-based advocacy to influence policy and decision-makers.
The toolkit was created after feedback and requests from persons with disabilities and their representative organisations from all over the world and building on the collaboration of the International Disability Alliance and the International Disability and Development Consortium.
The toolkit highlights two particular aspects of the data journey, starting first with the need for data to understand the situation of persons with disabilities, identify gaps that are not addressed through policies, and provide examples of successes. The second aspect is once the data exist. It is crucial to understand how to analyse, use and trust data for creating advocacy messaging. This is both to protect the integrity of advocates and to ensure that the change sought is based on an understanding of the situation and what works. The toolkit includes case studies in which organisations of persons with disabilities were involved in both aspects mentioned above, including a case study on the LNOB Partnership.
There is no excuse not to have data on persons with disabilities or to include OPDs in data collection and interpretation efforts. Persons with disabilities and their representative organisations are the experts on issues affecting them and are generating community-driven data to complement official statistics. With the toolkit’s guidance, persons with disabilities and their representative organisations can respond in a highly professional manner to data needs.
An excellent example of OPD-led data advocacy was the OPD-led advocacy that led to the Washington Group (WG) short set of questions being included in the 2019 census in Kenya.
The Kenya Population and Housing Census was carried out in August 2019. To use the WG short set of questions is something that the disability movement in Kenya had advocated for with the hope that it would ensure the availability of quality data that can inform interventions. However, it took diverse interventions for this to happen.
Firstly, there was intense training of officers from the Kenya National Bureau of Statistics (KNBS) on the importance of using the WG questions to collect disability data. Secondly, and importantly, was the involvement of OPDs in this process. Through United Disabled Persons of Kenya, persons with disabilities went through training on disability data, including the WG module. In addition, the International Disability Alliance through its Bridge CRPD-SDGs’ training continued to strengthen the capacities of leaders in the disability sector on advocacy for appropriate disability data.
By these empowerment processes, both for statistics officers as well as for OPDs, the WG questions were included in the 2019 census. From the census statistics, what has been published so far includes distribution of the population aged five years and above by disability status as well as distribution by type of disability. A disability monograph shall be published that shall look at various indicators such as access to education and employment.
Through a framework of continuous engagement of OPDs and KNBS, OPDs are now members of a Technical Working Group on Disability Data which, going forward is going to play a key role in the availability of disability data in Kenya. Currently, we are engaged in discussions around having a disability survey as guided by the disability movement, specifically to collect data on the situation of persons with disabilities.
There are various efforts from partners in Kenya on ensuring that there are good data on disability. Whereas at present there are various gaps on getting disaggregated data, we hope that the collaboration with partners, including the KNBS and OPDs, in a spirit of goodwill, will ensure that going forward there are good, quality data.
Dr. Elizabeth Lockwood works for CBM Global Disability Inclusion and is the CBM Representative at the United Nations. She focuses on developing advocacy strategies to raise awareness, build capacity, and lobby for the rights of persons with disabilities at the UN level in relation to the UN Convention on the Rights of Persons with Disabilities, the Sustainable Development Goals, and disability inclusive development.
Disabled People’s International (DPI) Executive Director.
Disabled People’s International (DPI)
Dr. Mohammed Ali Loutfy is the senior advisor on capacity building and advocacy for the Global Initiative on Inclusive ICTs (G3ICT). Dr. Loutfy is also Disabled People’s International (DPI) executive director. Since 2016, Dr. Loutfy has been the Representative of Disabled Peoples’ International (DPI) at the United Nations, where he co-chairs the Stakeholder Group of Persons with Disabilities for Sustainable Development.
Programmes Manager
United Disabled Persons of Kenya (UDPK)
Sally is a disability rights champion with over ten years of experience in the disability sector. Before joining UDPK, she previously worked at the African Union of the Blind (AFUB) as a Programme Coordinator. She is experienced in managing capacity building and advocacy programmes aimed at empowering persons with disabilities and their organisations. She has experience working with multi-stakeholders, including government departments and other non-state actors. She has actively participated in programme development and implementation using rights-based and human rights approaches. She is interested in disability-inclusive policy, planning and execution, supporting the institutional strengthening of persons with disabilities, collating feedback on advocacy activities, supporting follow-up, and facilitating learning.
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