Tag Archives: Human Dignity

Science serving lives: Interview with Dr. Alice Guingané, public health researcher (Burkina Faso)

Geneva, Switzerland, 20 April 2026- /African Media Agency (AMA)/- On World Health Day 2026, under the theme “Together for health. Stand with science,” the World Health Organization (WHO) highlights individuals using science to improve lives in the African Region.

Dr Alice Guingané, a hepato-gastroenterologist and lecturer-researcher at Joseph Ki-Zerbo University in Ouagadougou, is actively engaged in clinical research and disease surveillance. She emphasises that supporting science saves lives.

What role does science play in your daily work? 
Science is at the heart of my daily work. As a physician and a lecturer-researcher at a university hospital, my role is threefold: to provide care, to teach, and to conduct research. Science guides how I think, make decisions, and act.

In clinical care, it enables me to analyse symptoms rigorously, distinguish facts from beliefs, and make evidence-based decisions. In teaching, I strive to make scientific knowledge accessible, including through awareness sessions with patients and communities.
In research, I use epidemiological data to identify public health priorities, select effective interventions, and assess their impact in the field. Science also guides my values: respect for human dignity, responsibility, and commitment to the community.

What motivated you to engage in health research? 
Above all, the desire to find solutions to patients’ problems. I will never forget a nine-year-old boy who died of liver cancer linked to hepatitis B. Like many others, he arrived at the hospital too late, even though a vaccine exists from birth.

This reality pushed me to understand why pregnant women did not access care in time, and how to improve prevention of mother-to-child transmission of hepatitis B. I oriented all my research around this issue, seeking solutions adapted to our context, training students, and conducting field projects.

Why is it essential that science be supported by society and local authorities? 
Society is at the heart of health research: without community participation, even free services may remain underused due to sociocultural barriers.

Local authorities also play a key role in guiding, regulating and financing research. Producing one’s own data means being able to define one’s health priorities. Science enables evidence-based decision-making, reduces mortality, improves quality of life, and drives innovation and national sovereignty.

How does your work contribute to strengthening disease surveillance in Burkina Faso? 
I am currently the principal investigator in Burkina Faso for a project on the triple elimination of HIV, syphilis, and mother-to-child transmission of hepatitis B. This integrated approach, supported by WHO, allows resources to be pooled and data to be generated that are directly usable by decision-makers.

I also participate in the HEPSANET network, which aims to strengthen epidemiological data on viral hepatitis in Africa. These initiatives contribute to better surveillance of diseases and their complications, particularly liver cancer.

What is needed to strengthen public trust in science? 
Science must be accessible. It is essential to communicate research findings in clear and understandable ways and to create effective channels to reach communities, health professionals, and decision-makers.

Another major challenge is tackling misinformation. In our context, some traditional beliefs may conflict with modern medicine. Encouraging dialogue and the guided integration of different care practices is essential to strengthening trust.

As a woman scientist, what message do you have for young girls? 
I would encourage them not to hesitate to pursue research it is a deeply rewarding endeavour. It requires organization and balance with family life, but it is not a sprint—it is a long-term commitment. Believe in your abilities, keep your passion alive, and you will accomplish extraordinary things.

Distributed by African Media Agency (AMA) on behalf of World Health Organisation.

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Fighting lymphatic filariasis in Madagascar: Lives transformed and hope restored

Geneva, Switzerland, 30 January 2026-/African Media Agency(AMA)/-Julien Ranjaivonirina, a 63‑year‑old farmer living in the Fitovinany region, smiles as he reflects on his journey. Standing in front of his wooden house, he recounts how the hydrocele he had for several years limited his movements and prevented him from working as he wished. Today, after receiving care, he is gradually regaining his pace and daily activities. “It feels like I’ve been given a second life; I can finally resume my days as before.”

For many people in Madagascar, lymphatic filariasis remains a difficult disease to live with on a daily basis. Transmitted by mosquitoes, it disrupts the circulation of lymph and can cause persistent swelling known as lymphedema. In severe cases, the swelling can become severe and the skin may thicken. This advanced form is commonly known as elephantiasis. In some men, as in Julien’s case, the disease leads to hydrocele—a swelling of the scrotum caused by liquid accumulation. This condition can be extremely debilitating and lead to complications, making simple daily tasks challenging.

Despite major progress, lymphatic filariasis is still present in several regions of the country. In recent years, the number of endemic districts has significantly declined, from 96 between 2018 and 2020 to 87 in 2023, four of which are now in the post‑treatment phase. The 2023 national survey recorded 15 303 cases of lymphoedema and 14 069 cases of hydrocele. In the Fitovinany region, where Julien lives, the situation remains notable: in Manakara Atsimo, 2922 cases of lymphoedema were reported, while Vohipeno and Ikongo each still count several hundred cases. These figures illustrate the ongoing burden of the disease on families and rural communities, who already face numerous challenges.

To address these persistent issues, strengthening the health system and providing technical support remain essential. Since 2023, the World Health Organization (WHO) has been working closely with the Ministry of Public Health to accelerate progress against lymphatic filariasis. This support is built on two pillars: interrupting transmission through mass drug administration and managing people already affected, particularly those living with lymphoedema and hydrocele. Thanks to this collaboration, Madagascar achieved full national coverage for the first time in 2023, followed by surveys to assess the effectiveness of interventions. In 2025, patient care was strengthened in 17 districts through additional training, supplies and follow‑up.

As part of this effort, WHO helped strengthen medical capacities by training 348 health professionals between September and December 2025, including 17 surgeons specialized in hydrocele management. These training sessions improved the quality of surgical procedures, enhanced patient safety and expanded access to specialized care in the most affected regions. In total, 61 people received surgery related to lymphatic filariasis in October 2025 in the districts of Tamatave (22 patients) and Manakara (39 patients).

Dr Yvette Ramanantsoa, head of neglected tropical diseases (NTDs) at the Regional Directorate of Public Health in Fitovinany, highlights the importance of the response. “The fight against elephantiasis is an investment in human dignity and development. Elimination is possible, but it requires collective and sustained commitment.”

On the ground, this commitment translates into concrete actions: regular campaigns, community mobilization, active screening and free surgical interventions. Community health workers walk long distances to inform, reassure and guide patients, helping reduce stigma and improving access to care.

For WHO, the vision is equally clear. “It is together, hand in hand with the ministry and communities, that we move forward so that no one has to suffer in silence,” says Dr Patricia Rasoamihanta‑Martin, NTD programme lead at the WHO office in Madagascar. She emphasizes that beyond treatment, success depends on active community participation. “Given the severe consequences of this disease, particularly in rural areas, it is essential for everyone to understand the importance of prevention, participation in treatment campaigns and access to care. Community engagement and the sustained commitment of all actors are indispensable.”

Looking ahead, the next step is to continue progressing toward the elimination of lymphatic filariasis by 2030, consolidating achievements and ensuring their sustainability within the health system.

Progress is particularly visible among surgical teams. Thanks to WHO‑supported training, surgeons are seeing immediate benefits for patients. At the Regional Hospital Centre of Mananjary, Dr Rynah Rakotomamonjy, involved in patient care since 2008, explains that these sessions have improved surgical techniques, reduced complications and ensured smoother recovery. “After the operation, many express a sense of liberation; they feel they can live a more normal life again, without shame, and it feels like a fresh start.”

In Manakara, Dr Mampionondray Razafindratovonimanana, head of the surgery department, shares similar observations. He describes sometimes complex cases but notes significant improvements: reduced swelling, restored mobility, return to work and decreased stigma.

These advances directly transform the lives of affected individuals. Behind each intervention are personal journeys marked by waiting, doubt and hope of regaining a normal life. And it is in the villages that the impact of these surgical procedures becomes most visible: where patients regain autonomy, confidence and the ability to resume activities they had long abandoned.

In a nearby village in Fitovinany, 60‑year‑old Victor Ratovonirina provides a powerful example of the long path many patients must take before receiving care. Also a farmer, he explains that he lived with the disease for nearly ten years, initially believing it was linked to an injury sustained during a football match. Gradually, he lost strength and mobility and the disease eventually affected his social life and ability to work. Informed at the health centre that treatment was available, he registered and later underwent free surgery. “This operation changed my life: I feel relieved, I’m regaining my strength and I can look forward to returning to the fields,” he says.

For Julien too, the change is profound. Before his surgery, he struggled to work and felt diminished. After finally receiving the care he needed, he enjoys a simpler, lighter daily life. Sitting on a bench surrounded by his family, his gaze fixed on his field— a symbol of his restored routine—he confides: “Now I feel reborn, and I’m confident that tomorrow will be even better.” For the communities of Fitovinany and beyond, hope is no longer a distant promise: it now takes the form of transformed lives, regained abilities and restored dignity.

Distributed by African Media Agency (AMA) on behalf of Word Health Organisation

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Thoughts on Malawi at 53: History, Education and Human Dignity

thekerani primary
thekerani primary

I would like to preface the thoughts below by offering my deepest condolences to the families of the Malawians, many of them reported to be children, who were killed in the stampede at the Bingu National Stadium today on 6th July. I convey warm thoughts to the injured and extend hope that they will get better soon.

My effort today is an attempt at crystalizing disparate thoughts that I have been pondering for many years, on human dignity. I believe this lies at the core of what we ought to be focusing on as a nation. And I believe the education system, and its origins, are a central narrative to this. In this discussion I provide an overview of what the education statistics looked like at independence, and how, 53 years later, we are yet to seal the chasms created over a hundred years ago.  Continue reading Thoughts on Malawi at 53: History, Education and Human Dignity