Sharda Ganga, directeur van Projekta, hield een inleiding, waarbij zij de nadruk legde op het universele recht op gezondheidszorg, voor iedereen, overal. Gelijke toegang is gebaseerd op het principe van solidariteit en het uitbannen van ongelijke toegang moet onze prioriteit hebben.
De problemen met het gebrek aan transparantie en accountability zijn ook in de gezondheidszorg groot. Ganga vroeg aandacht vroeg voor de driedubbele rol van civil society: zij zijn zowel dienstverleners, als pleitbezorgers (advocates) voor rechtvaardig beleid en wetgeving, als een watch dog. In deze laatste rol ligt voor civil society organisaties de taak om de regering, maar ook bijvoorbeeld ziekenhuizen en verzekeringsmaatschappijen te controlen op de uitvoering van hun taken en verantwoordelijkheden.
Kort samengevat is een participatieve benadering is hetgeen we dringend nodig hebben, waarbij structurele dialoog en investeringen in civil society om haar driedubbele rol te kunnen uitvoeren van essentieel belang zijn.
Lees de gehele inleiding (in het Engels) hieronder.
Universal
Health Coverage, everyone, everywhere
World health
day dialogue- PAHO-Suriname, 6 april 2018, Ballroom Torarica
Here is an almost universal truth: when you are
healthy, you don’t think about health care. It is when you loose the battle
against a tiny mosquito and suddenly find yourself fighting for your life in a
broken down hospital bed, and have to deal with toilets with no running water,
that you realize: thank god I just started a job that covers my insurance. That
was almost 20 years ago, and the first time I realized not just the importance
of health coverage, but also how health care is the most important indicator of
inequality.
Because after 3 days of utter misery in the third
class ward, I was moved, by the grace of friends, to the second class- which
was pure heaven in comparison. I felt a bit guilty that I was so happy to leave
my fellow 3rd class patients behind, and embarrassed at how easily I
forgot that one aspect that underlies the idea and the practice of universal
health care: solidarity.
Last year I was again confronted with how unjust
access to health care is- when a close relative was able to receive world class
treatment outside of Suriname, simply because of the generosity of employers.
Isn’t that the most offensive idea: that your right to live and the quality of
care you can access, depends on your choice of job, and your socio economic
circumstances.
Health care must be framed as a universal right, it’s
access based on the principle of solidarity, and eradicating inequal access
must be our priority.
It does come at a steep price, but are we sure that
the price we are paying is the real price or are we paying way too much, and what
are we actually paying for? Access to health care has been used as a political
tool for too many years, for example- and we are still paying the price for the
culture of garnering votes through distribution of ‘datra karta’, in the worst
case using public service jobs as a gateway to the ‘datra karta’.
Non transparency, a lack of accountability, horrendous
management and business practices, lack of checks and balances- the whole
plethora of bad governance practices: they come at a steep price.
So this is one of the roles that civil society must
take up, and wants to take up: holding duty bearers accountable. But civil
society has more roles to play- what we call the triple role:
The first role is as Service providers- as through the
Medical Mission, Stichting Lobi, the Diabetes Education One Stop Shops, and
countless others, delivering essential services and creating public awareness. That
is the role that governments and international organisations are comfortable
with us playing, and would like to see us performing- how do I know that?
Because that is usually the only type of program that they are willing to fund.
And even then, they have us jump through hoops.
But civil society also has a role as Advocates-for
citizens, healthy or not. We see a greater understanding of this role emerging-
through for example, the Alzheimers Foundation,
and Stichting Wiesje, who are now starting to understand that they need to move
beyond service provision and need to advocate for legislation and policy change
in order to have sustainable results that will truly benefit their constituents.
We do need to hear more from the citizens, the rights
holders. For example, in the health care debate we witnessed the past months,
we only heard governments and service providers- doctors, hospitals etc-,
fighting over money. What we missed is that third voice- of citizens advocating
for and demanding affordable, effective and efficient services, and having a
say in how to achieve that.
The third role of civil society I already mentioned-
the watch dog role, to hold all duty bearers accountable, not just the
government, but also the insurance companies, the international organisations,
the hospitals, the Vereniging van Medici, all health professionals, and service
providers.
The other side of accountability is voice- you can
only demand accountability if your voice is strong enough to be heard. Civil
society must empower citizens to use their voice to claim their rights to
access, and quality of care. But empowerment only makes sense if there are
mechanisms in place for protection, so that you can dare claim your right and
hold duty bearers accountable, without the fear that it would anger your
doctor, or your insurance company to the point that your claim for your rights
puts your health in jeopardy.
So ultimately, civil society must hold governments and
partners, all duty bearers accountable, and empower citizens to claim their
rights. But duty bearers need to ensure that citizens’ voices are heard, so
that health systems are responsive to people’s needs.
In short: we need a more participatory approach, with
structured dialogue, and investment in civil society’s capacity to undertake
that triple role, not just as service providers.
Sharda Ganga
PROJEKTA &
Burgerinitiatief voor
Participatie en Goed Bestuur (BINI)
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