Caroline Ravello
“When the stakes are measured in lives, global and national health decision-making cannot be left to chance.”
The World Health Organization (WHO) made this statement as it celebrated World Health Day yesterday (April 7), the day that marks its founding.
As the organisation kicked off its campaign, the call has been made for people everywhere to support science under the theme “Together for Health. Stand with Science.” There is adequate justification too, for this bold ask, as the statistics on the WHO leadership in improving public health globally for over 75 years remain outstanding.
Since the WHO’s inception at the First Health Assembly in 1948 and taking effect in 1950, it has used its founding day as an awareness day to advocate for and highlight a priority area of concern. The 2026 advocacy urges a global commitment to not only evidence-based health policies but also One Health approaches and equitable access to care.
One Health speaks to the interconnectedness of people, plants, animals and the environment in which they all exist. It focuses on the collaboration needed in the sciences that represent each group and the need for sustainability and a whole-of-society approach to managing risks at “the animal-human-environment interface before they become pandemics.”
Together for Health. Stand with Science is a year‑long campaign spotlighting “both scientific achievements and the multilateral cooperation needed to turn evidence into action.” The theme, WHO says, celebrates “the power of scientific collaboration to protect the health of people, animals, plants and the planet.”
Yesterday’s One Health Summit in France towards this goal included the collaboration of the “One Health Quadripartite,” which comprises the World Health Organization (WHO), the Food and Agriculture Organization (FAO) of the United Nations, the United Nations Environment Programme (UNEP) and the World Organisation for Animal Health (WOAH).
As a public health master, I support science. Science supports my best argument for managing personal and community health issues and helps me make sense of navigating this world.
Where science fails me and others like me is where the “equitable access” argument collapses. My feathers were ruffled as I read “equitable access.” There are those I know who live with the disappointment and denial of equity and human rights, having been punished because of health history.
Then we get to see loud campaigns for advocacy days for issues like cancer, autism, mental health and the like by the very people who legitimately discriminate and legally practise inequity. In fact, it is one of those Autism Awareness Day (April 2) social media outputs that prompted this focus on the equity argument of the noble WHO campaign.
The goal of science should be to protect lives. If health is a human right, why do I live in a space where my right to health, including the means to protect and support my health, is limited? Why am I and those like me denied the much-bandied equity? Whither the human rights framework?
I want to reclaim my time from all the hours I have spent listening to scientists and professionals here hype me up about universal health coverage, where my government is supposed to ensure high-quality medical care is not a privilege dependent on risk profiling.
As I read all the brilliant promotional pieces for World Health Day in my miffed mood, my memory recollected how elevated I felt as an advocate, especially under the Convention on the Rights of Persons with Disabilities (CRPD, 2006), at the passing of the Affordable Care Act (ACA, 2010), aka Obamacare, into US federal law.
Health insurance companies were/are prohibited from denying coverage, charging higher premiums, or excluding treatment for pre-existing conditions. And this provision includes treatment for pre-existing mental health, developmental disability (behavioural health treatment, autism services, physical therapy, occupational therapy, etc.) and substance use disorders.
If the aim is to bridge inequities, then I look forward to the day when scientific data melded with personal health history are not weaponised against people, when actuarial sciences do not churn out “unfavourable” numbers to legitimately discriminate against us while we are being asked to support advocacy for “rights-based health” and “health as a human right” on paper.
The WHO defines equity as “the absence of unfair, avoidable or remediable differences among groups of people, whether those groups are defined socially, economically, demographically, or geographically or by other dimensions of inequality (eg, sex, gender, ethnicity, disability, or sexual orientation).”
“Health is a fundamental human right,” says the WHO.
“Health equity is achieved when everyone can attain their full potential for health and well-being (www.who.int/health-topics/health-equity).”
This instalment might be considered cyclopean because I have narrowed the big issue of supporting science to how science determines people as a risk and undeserving of protection and support. But what benefit is science to us if, instead of serving the need for protection and health security, it is turned into a dimension of inequality?
I support science. I want science to stand with me, not profile me for discrimination.
