BLANTYRE-(MaraviPost)-The Ministry of Health and Sanitation has confirmed 11 cholera cases in five districts, namely Kasungu, Neno, Lilongwe, Balaka, and Chitipa, with no reported deaths.
Minister of Health Madalitso Baloyi made the announcement during a media briefing in Lilongwe.
The government has swiftly responded to the outbreak, deploying rapid response teams to affected areas, strengthening disease surveillance, and promoting safe water and hygiene practices.
“We are working tirelessly to prevent further spread of the disease,” Baloyi assured.
The ministry is collaborating with SADC countries, the World Health Organization (WHO), and other partners to manage the situation.
WHO’s Dr Getrude Chapotera pledged the organization’s commitment to supporting the government in containing the outbreak.
The confirmed cases have triggered heightened vigilance, with health officials focusing on prevention and containment measures.
The public is urged to practice good hygiene and report any suspected cases.
Share this:
Like this:
LikeLoading…
Discover more from The Maravi Post
Subscribe to get the latest posts sent to your email.
Given the medical advancements today – in an ideal world, all children should be born free of infections like HIV, syphilis or hepatitis-B; all pregnant women should be accessing full spectrum of maternal and newborn care (including services to prevent vertical transmission of HIV, syphilis or hepatitis-B); and all people living with HIV should lead normal and healthy lives.
We have proven science- and evidence-based tools and person-centred and rights-based approaches to help us achieve these public health outcomes. But sadly, this is not an ideal world yet – and intersectional social inequities, injustices and inequalities mar lives of so many of us.
As the year 2025 draws to a close soon, we spoke to carers of a child living with HIV. Trained frontline community health workers, backed by support from their multi-tiered backbone team, is helping bridge the gap between key and other vulnerable populations and lifesaving essential public health and social welfare services.
Barriers which underserved communities face in accessing health services
We met Baba (name changed), a 4-year-old orphan boy from Uttar Pradesh. Baba was born with HIV, and his primary caregivers include his paternal aunt and his grandmother.
Before returning to their native hometown in UP, Baba’s parents were migrant workers in Mumbai who, for a brief period, also did labour work in Saudi Arabia. After returning to Mumbai, they both got diagnosed with HIV and received lifesaving antiretroviral therapy. But their treatment got disrupted (reasons not known). Unsurprisingly, their health started deteriorating.
For reasons best known to them, they did not disclose their HIV status to their family members.
By the time Baba’s mother became pregnant, the health of both parents had plummeted considerably. Baba’s mother developed TB too. People with HIV have up to 29 times more risk of developing active TB disease. When his father’s condition worsened, the couple moved from Mumbai to Delhi and eventually back to their native place in UP.
Baba was born at his grandparents’ home in UP. His mother did not undergo institutional delivery. Shortly after his birth, both parents passed away. Till this time, family members of Baba were not aware of the HIV status of Baba or his parents.
According to 5th National Family Health Survey (NFHS-5) conducted in 2019-2021, “the institutional delivery rate in UP is 83.4%, and that in public health facilities is 57.7%.”
Baba’s chronic ill-health during his first year – marked by extreme weakness and delayed physical development – were a cause of worry for his carers.
Journey from shadow to light
During routine door-to-door health awareness and screening visits, Sarojini, a frontline community health worker of Humana People to People India, learnt about the ill health of Baba.
She counselled them and accompanied them to the nearest government doctor, who recommended HIV and TB testing. This led to further referral to the nearest government-run tertiary care hospital in Lucknow (King George’s Medical University – KGMU which was around 30 kilometres away), where Baba tested negative for TB disease but tested positive for HIV.
Pre-test and post-test HIV counselling were crucial. Government counsellor and health workers like Sarojini counselled Baba’s carers to dispel fear, despair and doubts too. Soon after, Baba started receiving antiretroviral treatment.
Now Sarojini’s role became even more pronounced to help support Baba’s carers to ensure treatment adherence and attend to his other care needs on an ongoing basis.
Government of India’s National AIDS Control Organisation (NACO) has supported Humana People to People India to implement its Link Workers Scheme which is how Sarojini got trained by NACO and Humana as a Cluster Link Worker to help support people (like Baba and his family) in 9 villages. She is backed by an elaborate network of team at Humana People to People India which enables her to keep making a difference in the lives of people (and children).
Embracing HIV treatment, care and support
Administering medication posed significant challenges for Baba’s aunt. Initially his regimen of antiretroviral medicines consisted of four crushed capsules mixed with water – whose taste the child found intolerable. He frequently refused the medication or vomited after eating it, requiring his aunt to administer it forcibly at times. Sarojini’s regular follow up was important not only to ensure treatment adherence but also to help solve any other problems his carers might be encountering.
Thankfully, soon after Baba began receiving antiretroviral medicines in the form of fixed-dose combination (1 pill) to be taken once daily and at the same time. This eased the daily caregiving routine.
After 2-3 months of initiating antiretroviral therapy, Baba also received TB preventive therapy to protect him from TB disease. Sarojini’s regular follow up and support bore fruits as his health started showing substantial improvement.
Counselling remains centre-stage, and so does trust, which Sarojini and Baba’s carers share.
Sarojini guides the family on treatment adherence, precautions they need to take to stay healthy, and monitor their health and wellbeing, among addressing other issues.
Regular health screenings are vital
She also accompanies them to the antiretroviral therapy centre for periodic testing. Carers of Baba are screened for HIV once every 6 months. Baba’s CD4 test is done once every 6 months and his viral load test is done annually. As of now, his viral load has remained undetectable as shared by Pop Singh, a programme manager with Humana People to People India. This is an important indicator that Baba’s HIV treatment is working, HIV is undetectable and untransmittable, and he is healthy.
When we spoke with Baba’s aunt, she said that she clearly understands the importance of daily treatment adherence although unaware of the exact names of his medications.
Thanks to Sarojini for the facilitation, Baba currently attends an Anganwadi centre, part of India’s government-run early childhood care and development system. The Anganwadi workers provide supplementary nutrition, preschool education, health check-ups and immunisation. Staff members are aware that Baba is on medication, though his HIV status has not been disclosed.
Impacting positive change for those left behind
Baba is among over 130 people living with HIV (including children living with HIV) supported under NACO’s Link Workers Scheme implemented by Humana People to People India across 100 villages of Lucknow.
Each Cluster Link Worker, like Sarojini, is a trained local community member, who screens high-risk groups (such as, migrant workers, truckers, female sex workers, men who have sex with men, and persons who inject drugs) for HIV, syphilis and TB in approximately 5 villages. Cluster link workers are supported by their zonal supervisors (one person for every 10 cluster link workers) and overseen by a programme manager.
Those who are screened positive for presumptive TB by Cluster Link Workers, are linked to public TB services for further medical management. Those who test positive for TB disease are also helped to avail of government-run social welfare benefits.
Teams of Humana People to People India go door-to-door to raise health awareness and offer screening for HIV, sexually transmitted infections like Syphilis, and TB. Health education and dispelling myths and misconceptions also help fight stigma and discrimination. They are at times accompanied by Indian government’s National TB Elimination Programme team which performs street plays for public education and sensitisation. Humana team has also leveraged other opportunities for health awareness and screening, such as village council (Gram Panchayat) meetings.
Disease prevention is also a mainstay of key messaging
For example, promoting consistent and correct condom use to protect oneself from HIV, STIs and unplanned pregnancies, is a role donned by frontline workers like Sarojini.
Key and other vulnerable populations face a range of barriers when they try to access healthcare services. This is where frontline community health workers become so essential to link them with public health and social welfare services and support as and when needed.
Rethink, rebuild and rise
Ahead of world’s largest HIV/AIDS conference in 2026 (the 26th International AIDS Conference or AIDS 2026 in Rio de Janeiro, Brazil), we need to rethink where gaps in HIV responses are, rebuild so that we can put people first at every level of HIV response, and rise to bring the world on track to end AIDS by 2030.
While groups like Humana People to People India continue to serve the underserved, our health systems also need to ensure that all people with HIV (including key and other vulnerable populations) are able to access antiretroviral therapy and full range of HIV care services with equity and rights, all women receive institutional delivery and continuum care for maternal and newborn health, and all children are born free of preventable infections like HIV, syphilis or hepatitis-B.
Shobha Shukla – CNS (Citizen News Service)
(Shobha Shukla is a feminist, health and development justice advocate, and an award-winning founding Managing Editor and Executive Director of CNS (Citizen News Service). She was also the Lead Discussant for SDG-3 at United Nations inter-governmental High Level Political Forum (HLPF 2025). She is a former senior Physics faculty of prestigious Loreto Convent College; current President of Asia Pacific Regional Media Alliance for Health, Gender and Development Justice (APCAT Media); Chairperson of Global AMR Media Alliance (GAMA received AMR One Health Emerging Leaders and Outstanding Talents Award 2024); and Host of SHE & Rights (Sexual Health with Equity & Rights). Follow her on Twitter/X @shobha1shukla or read her writings here www.bit.ly/ShobhaShukla)
– Shared under Creative Commons (CC)
Share this:
Like this:
LikeLoading…
Discover more from The Maravi Post
Subscribe to get the latest posts sent to your email.
Luigi Mangione says he now knows the real reason why Attorney General Pam Bondi is seeking the death penalty against him … she allegedly has deep ties to the murder victim’s health care company. Mangione’s defense attorneys filed court docs…
Share this:
Like this:
LikeLoading…
Discover more from The Maravi Post
Subscribe to get the latest posts sent to your email.
p class=”MsoNormal”>The Justice Department releases a vast trove of documents relating to convicted sex offender Jeffrey Epstein. Also, Congress left Washington D.C. for its holiday break without reaching a deal on health care. Millions of Americans will face price hikes on their insurance premiums. And surviving the holiday season, we’ll have tips on what can be a stressful time of the year.
Investigation Discovery’s The Curious Case of… is coming back with a new set of episodes for season 2. While season 1 shared new insight and firsthand experiences from the people who knew most about the Natalia Grace case, the sophomore season is expected to keep viewers on the edge of their seats as the team dives into a handful of new surprising cases.
In anticipation of the show’s return, Us Weekly details what the true crime show is about, shares a glimpse into the cases that will be broken down and reveals when the new episodes will air.
Investigation Discovery Announces Season 2 of ‘The Curious Case of…’
Investigation Discovery announced that The Curious Case of … is coming back with eight new episodes in early 2026.
The new episodes promise to tackle bizarre cases filled with twists and shocking revelations as they’re told through first-hand accounts by those who know the stories best. Guided by legal analyst and expert Beth Karas, the new season will take an even deeper look into shocking crimes full of deception and obsession.
“When we launched The Curious Case of Natalia Grace, we never could have imagined how that story would take the world by storm, sparking headlines everywhere and even inspiring scripted versions on other platforms. The response was overwhelming and it quickly became ID’s highest-rated series, cementing its place as a cultural phenomenon,” said Jason Sarlanis, President of ID, said in a statement. “Knowing there were so many other ‘Curious Cases’ to tell, we expanded the franchise into an anthology that continued to captivate audiences and became our top-rated series of 2025. Now, with Season 2, we’re diving into even more stranger-than-fiction stories, each one a high-stakes puzzle full of twists, turns and unforgettable characters.”
Each episode promises to uncover deceit, greed and manipulation while proving the truth behind each mysterious case.
What Cases Will Be Discussed in ‘The Curious Case of…’ Season 2?
Following the success of season 1, the new batch of episodes will break down even more mysterious true crime cases.
The premiere episode will be called “The Curious Case Of… Death by Detox?” and will unpack the crimes of Dr. Robert O. Young after he created a platform amid the success of his pH Miracle book series.
The synopsis explained that Young’s pH Miracle book series pushed “an alkaline diet, the tentpole of which is an avocado-based green smoothie, that grows in popularity.” Young’s business quickly took off, and he found success selling books and holistic supplements. As his roster of wealthy, high-profile clients grew, his fans quickly learned that the health tips he was sharing weren’t the “miracle” cures he pitched them to be.
Other crimes that will be documented on the season will include one about a Russian woman who tried to steal the identity of a salon employee, an intense rivalry between two beauticians, a teacher who hypnotized his students that was faced with deadly consequences, a woman who committed several crimes while pretending to have cancer, a town impacted with several Tourette’s Syndrome diagnoses and a woman who took care of her late husband and sister’s corpses.
When Does ‘The Curious Case of…’ Season 2 Premiere?
Season 2 of The Curious Case of … will premiere on Monday, January 12, at 10 p.m. ET on ID, with each episode premiering weekly in the same time slot. Those who miss the live episodes will be able to stream them later on HBO Max.
Share this:
Like this:
LikeLoading…
Discover more from The Maravi Post
Subscribe to get the latest posts sent to your email.
International Day of Persons with Disabilities in 2025
To celebrate the International Day of Persons with Disabilities in 2025, the leaders of organisations of persons with disabilities and developmental organisations across Zambia, Zimbabwe, and Malawi exhibited unity of purpose speaking with one voice to affirm that now is the time to act on the African Disability Protocol (ADP).
The ADP entered into being on 7 June 2024, establishing a legally binding framework to protect and enhance the rights of over 80 million persons with disabilities across the continent.
This milestone redirected responsibility from the continental level to individual national governments. The Protocol is now legally binding, and it is up to member states to ratify, adopt, and put it into action.
In a joint statement the leaders said across the three nations, they recognise that national policies and frameworks have made progress towards promoting disability inclusion.
However, they said millions of persons with disabilities still face barriers that prevent them from fully exercising their rights.
They called for the aligning of country efforts with the ADP is necessary for a full and enforceable approach to inclusion.
For example, the Protocol requires access to quality education at all levels, with reasonable accommodations and assistive technologies.
Yet today, countless children with disabilities in our countries remain out of school, not due to inability but because systems are designed without them in mind.
Read full statement below:
To mark the International Day of Persons with Disabilities in 2025, we – leaders of organisations of persons with disabilities and development organisations across Zambia, Zimbabwe, and Malawi – spoke with one voice to affirm that now is the time to act on the African Disability Protocol (ADP).
The ADP entered into force on 7 June 2024, establishing a legally binding framework to protect and promote the rights of over 80 million persons with disabilities across our continent.
This milestone shifted responsibility from the continental level to individual national governments. The Protocol is now legally binding, and it is up to member states to ratify, adopt, and put it into action.
Across our three nations, we recognise that national policies and frameworks have made progress towards promoting disability inclusion. However, millions of persons with disabilities still face barriers that prevent them from fully exercising their rights.
Aligning country efforts with the ADP is necessary for a full and enforceable approach to inclusion. For example, the Protocol requires access to quality education at all levels, with reasonable accommodations and assistive technologies.
Yet today, countless children with disabilities in our countries remain out of school, not due to inability but because systems are designed without them in mind.
The ADP calls to eliminate discrimination in employment and promote entrepreneurship for persons with disabilities. As it stands, unemployment rates among persons with disabilities remain high in parts of our region, perpetuating cycles of poverty and dependency that the Protocol could break. The Protocol guarantees the right to vote, contest for office, and participate in public affairs on an equal basis. Too many persons with disabilities in our countries remain excluded: their voices absent from decisions that affect their lives. These are not aspirations. They represent the difference between exclusion and inclusion, between poverty and productivity, between invisibility and citizenship.
Where things stand
In Zambia, years of advocacy have built momentum. The launch of the National Policy on Persons with Disabilities and Mainstreaming Guidelines in 2025 shows the government’s commitment to inclusion. However, without ratifying the ADP and submitting the required documents to the African Union, these efforts remain disconnected from the continent’s legal framework. We call on the Government of Zambia to complete ratification of the ADP without further delay.
Malawi has ratified the ADP, but the critical next step is to make it enforceable into law. The estimated 1.7 million people aged five and above who have a disability in Malawi deserve to fully enjoy the rights enshrined in the Protocol. We urge the Government of Malawi to prioritise this process and allocate resources for implementation.
In Zimbabwe, we stand at a historic moment. With a new Disability Act enacted in the month of November 2025. We call on the government to establish strong implementation mechanisms that ensure the law translates into real change.
These are not only administrative steps; they are life-changing decisions for millions of persons with disabilities. Every day of delay means more barriers to education, jobs, healthcare, and participation in public life that could have been removed.
We also call upon the Southern African Development Community (SADC), Common Market for Eastern and Southern Africa (COMESA), Pan-African Parliament (PAP), and the African Union to exercise leadership in this critical moment. These regional bodies must:
• Actively support member states through the ratification, domestication, and implementation process
• Develop and fund disability inclusion programmes aligned with their own treaties and charters
• Lead by example by embedding disability inclusion within their own Secretariats, demonstrating commitment through accessible policies, meaningful representation of persons with disabilities in decision-making, and barrier-free operations
The human cost of delay
Behind every statistic is a person. A child denied education. A graduate unable to find work despite being qualified. A voter turned away from a polling station. A pregnant woman unable to access maternal care because the facilities are inaccessible. The ADP provides a clear roadmap to challenging these barriers. Political will must now match political rhetoric.
We represent millions of persons with disabilities whose potential remains untapped, whose voices remain largely unheard, and whose rights remain mostly unrealised. But we also represent resilience, expertise, and a vision of an inclusive Africa where no one is left behind.
Our task: To the governments of Zambia, Malawi, and Zimbabwe, to all partners, and stakeholders: ratifying and implementing the African Disability Protocol is not about doing people with disabilities a favour. It’s an investment in inclusive development that benefits everyone. It upholds constitutional promises of equality. It’s the right and smart thing to do.
Nothing About Us Without Us.
Signed by:
The RAD-P consortium
– Sightsavers – Africa Disability Alliance (ADA) – National Association of Societies for the Care of the Handicapped (NASCOH) – Federation of Organizations of Disabled People in Zimbabwe (FODPZ) – Zambia Federation of Disability Organisations (ZAFOD) – Albinism Foundation of Zambia (AFZ) – Federation of Disability Organizations in Malawi (FEDOMA) – Disability HIV & AIDS Trust (DHAT)
and
U4ADP consortium
– Leonard Cheshire Disability Zimbabwe (LCDZ) – Development Aid from People-to-People ( DAPP) Zimbabwe – Development Aid from People-to-People (DAPP) Zambia – Chesire Homes Society of Zambia – Development Aid from People-to-People (DAPP) Malawi – Human Rights of Women and Girls with Disabilities in Malawi (WAG-Disability Rights)
Share this:
Like this:
LikeLoading…
Discover more from The Maravi Post
Subscribe to get the latest posts sent to your email.