Health
MSF Closes Final Ebola Projects For Survivors

By Modupe Gbadeyanka
The Ebola outbreak that swept across West Africa infected more than 28,700 people and killed more than 11,300 men, women and children.
Whole families were ripped apart and communities were devastated by the disease, which saw schools close, economies grind to a halt and health systems collapse, leading to even greater loss of life.
The shocking human toll of the outbreak was exacerbated by the painfully slow international response.
“The suffering caused by the Ebola outbreak was immeasurable,” says Brice De La Vingne, operations director for MSF. “It has left an indelible mark on every MSF staff member who travelled to work in West Africa. For our staff from the region, the impact was even greater – they were living with the daily threat of the disease, while at work they faced the devastating reality of Ebola head on. But for those who were infected with the disease, and for their families, it was nothing short of hell.”
Those who survived Ebola often found the battle was not over – many faced significant medical and mental health problems. However, because there had never before been an outbreak of this magnitude, there was limited understanding of what assistance people would need to pick up the pieces.
“As the outbreak subsided, it became apparent that Ebola survivors and their families would need significant support,” says Petra Becker, MSF head of mission in Liberia. “The majority of survivors experienced physical disorders such as joint pain and neurological or ophthalmological problems. At the same time, many survivors, as well as their friends, family and caregivers, experienced significant mental health problems, including post-traumatic stress disorder and depression, after being confronted so closely with death.”
MSF set up dedicated survivors’ clinics in the three worst affected countries.
The first opened in Monrovia, Liberia, in January 2015 and provided more than 1,500 medical consultations before closing in August 2016.
A second clinic in Guinea, Conakry, cared for 330 survivors and more than 350 of their relatives in the Coyah and Forécariah districts of the city.
A similar clinic in Freetown, Sierra Leone, provided mental and medical healthcare to more than 400 survivors and their families, organising more than 450 individual and group sessions to provide psychological support.
“Over time and after treatment, the severity of people’s psychological and physical disorders has gradually diminished,” says Jacob Maikere, MSF head of mission in Sierra Leone. “Yet many survivors say that they are still deeply disturbed by the smell of chlorine, which immediately transports them back the horror of the Ebola management centres.”
Fight against discrimination and stigma
Ebola survivors and their families also faced stigma when they returned to their communities.
MSF, together with other organisations and alongside national initiatives, sent teams out into affected communities to spread health messages and to help reduce stigma and discrimination. In Guinea, for example, MSF reached 18,300 people through group and individual sessions.
“Stigma remains a huge issue for those who survived Ebola and for their families, despite awareness and information campaigns during and after the outbreak,” says Jacob Maikere. “The discrimination takes many forms, with people losing their jobs or their partners, or being rejected by their family or community, all of which can have a hugely destabilising impact on their lives.”
Health workers hard hit
Health workers in the three worst affected countries paid a heavy price for responding to the disease, with many losing their lives. Those who survived witnessed countless deaths, and had to live with the fear that they too would be infected in their own communities as Ebola spread.
“Health workers in Sierra Leone, Guinea and Liberia saved many of their fellow citizens from Ebola,” says Ibrahim Diallo, MSF head of mission in Guinea. “But the virus created such fear in the country that many were viewed with suspicion or even discriminated against because of the contact that they had with people who were sick.”
MSF handing over post-Ebola care
In late-September, MSF ended its medical and mental health programmes for survivors in Guinea and Sierra Leone, while in Liberia, post-Ebola activities will finish before the end of the year. Most medical conditions affecting survivors, such as eye and joint problems, have now been treated, and MSF has arranged for those who need ongoing mental health support to receive continuing care within their national health systems or from other organisations.
Continued MSF care in West Africa
MSF says it will continue its efforts to provide services focusing on the unmet health needs of vulnerable people throughout the three affected countries.
“Any strengthening of health services in the three affected countries must include improving infection control measures, surveillance systems to ensure early monitoring of potential cases, and basic contingency plans allowing for a quick response to an outbreak of Ebola or other diseases,” says Mit Philips, health policy advisor for MSF. “The countries also need catch-up plans for services that lapsed during the epidemic, such as treatment for HIV and TB, as well as preventative services for which coverage remains low.”
In Monrovia, MSF has opened a paediatric hospital, Bardnesville Junction Hospital. Between January and August 2016, the hospital provided more than 3,280 emergency consultations and admitted 880 children as inpatients, mainly for malaria. The hospital’s neonatal unit has cared for 512 newborn babies.
MSF is also continuing to provide care to HIV patients in Conakry, the capital of Guinea, and maternity care in the Tonkolili and Koinadugu districts in Sierra Leone. The organisation has also positioned emergency supplies in the region to make sure that medical teams can respond quickly to a future outbreak of Ebola or to other epidemic threats.
Health
Resident Doctors Suspend Proposed Indefinite Strike
By Adedapo Adesanya
The Nigerian Association of Resident Doctors (NARD) has suspended its planned indefinite strike following the federal government’s reversal of the implementation of the reviewed Professional Allowance Table (PAT) and renewed assurances on outstanding payments.
The decision was announced in a communiqué issued at the end of an emergency National Executive Council (NEC) meeting held virtually on Saturday.
NARD had earlier resolved to embark on a total and indefinite strike over the government’s suspension of the reviewed allowance structure and other unresolved welfare concerns affecting resident doctors nationwide.
However, the association said it reconsidered its position after reviewing the outcomes of high-level engagements with key government officials and health-sector stakeholders.
According to the communiqué signed by NARD President, Dr Mohammad Usman Suleiman; Secretary-General, Dr Shuaibu Ibrahim; and Publicity and Social Secretary, Dr Abdulmajid Yahya Ibrahim, the Federal Government has now reversed its earlier decision on the allowance table.
“The NEC observed that the earlier decision to halt the implementation of the reviewed Professional Allowance Table (PAT) has been reversed, with implementation expected to reflect in the April salary and beyond,” the statement read.
The association also noted the government’s renewed commitment to settling outstanding promotion and salary arrears owed to resident doctors in affected institutions.
In addition, NARD said initial approval had been secured for the 2026 Medical Residency Training Fund (MRTF), with assurances that the disbursement process would be concluded.
“The NEC observed that the Budget Office has indicated its readiness to commence the process for the payment of the outstanding nineteen months’ arrears of the Professional Allowance,” the communiqué added.
Despite the progress, the doctors expressed concern about the continued delay in paying house officers’ salaries and called for urgent action to address the issue.
Following its deliberations, the NEC demanded the sustained implementation of the reviewed allowance structure, the prompt payment of all outstanding arrears, and the expedited disbursement of the residency training fund.
It also called for the immediate commencement of the process to clear the 19-month arrears and the convening of an urgent stakeholders’ meeting to resolve delays affecting house officers’ salaries.
“In light of the above developments, the NEC resolves to suspend the proposed total, indefinite, and comprehensive strike action, with a review of progress to be undertaken at the May Ordinary General Meeting (OGM) in Kano,” the statement said.
NARD expressed appreciation to President Bola Tinubu, Vice President Kashim Shettima, and several ministers, government agencies, and stakeholders for their interventions in resolving the dispute.
Health
Over 1.5 million Nigerian Children Living With Sickle Cell Disease—Report
By Modupe Gbadeyanka
More than 1.5 million children under the age of 15 are living with sickle cell disease in Nigeria, a new international study published in The Lancet Child & Adolescent Health, one of the world’s leading medical journals, has revealed.
In the report made available to Business Post, it was disclosed that Nigeria carries the highest burden of disease globally, far exceeding other high-burden countries such as the Democratic Republic of the Congo and Ethiopia.
The findings highlight both the scale of the challenge in Nigeria and the opportunity for the country to lead Africa in tackling one of the most preventable causes of childhood illness and death.
The study shows that nearly nine million children across sub-Saharan Africa are living with sickle cell disease in 2023, including around 1.17 million infants and 2.75 million children under five, who face the highest risk of early death without treatment.
Sickle cell disease is an inherited blood disorder present at birth. With early diagnosis and access to simple, low-cost interventions such as newborn screening, penicillin prophylaxis, routine vaccinations, malaria prevention, and hydroxyurea, most complications and deaths can be prevented.
However, in Nigeria, access to these essential services remains limited. Many children are only diagnosed after severe and avoidable complications, while others are never diagnosed at all, contributing to high levels of preventable illness and early childhood deaths.
The researchers emphasise that strengthening Nigeria’s health system response will be critical. This includes expanding newborn screening programmes, improving access to essential medicines, and integrating sickle cell care into primary healthcare services.
They called for urgent and coordinated action across government, health institutions, and development partners, including expanding newborn screening programmes, improving access to essential medicines and vaccines, and embedding sickle cell care within primary healthcare services.
The researchers, led by Professor Davies Adeloye, Professor of Public Health at Teesside University, United Kingdom, and Director of the International Society of Global Health (ISoGH), also called for increased domestic investment, supported by international partnerships, as well as stronger data systems to improve surveillance and guide policy decisions.
They concluded that even modest improvements in early-life screening and treatment in high-burden countries like Nigeria could transform child survival and significantly reduce preventable deaths.
“Nigeria now stands at the centre of the global sickle cell crisis. With over 1.5 million children affected, the scale is enormous, but so is the opportunity to act. We already know what works. Newborn screening and early treatment are effective, affordable, and can be delivered through existing health systems.
“If Nigeria prioritises sickle cell disease within its national health agenda and integrates care into routine maternal and child health services, we could save hundreds of thousands of young lives and significantly reduce avoidable deaths.” Professor Adeloye noted.
It was learned that the study analysed data from 40 studies across 22 African countries to produce the most comprehensive country-level estimates of childhood sickle cell disease to date.
Health
Helical Secures $10m Funding Package for Expansion
By Dipo Olowookere
A $10 million capital has been raised by Helical to support expansion across more top-20 pharma programmes and growth of its deployed science engineering team.
The firm will also use the money to build the compounding evidence layer that improves performance across diseases, as its mission is to make every scientist able to test hypotheses at the speed of inference and to turn in-silico discovery into a reliable engine for R&D throughput.
The funding package was from redalpine, Gradient, BoxGroup, Frst and notable angels, including Aidan Gomez (CEO Cohere), Clement Delangue (CEO HuggingFace) and Mario Goetze (pro soccer player).
Helical has a product known as the virtual AI lab for pharma, an application layer that turns biological foundation models into decision-ready, reproducible in-silico discovery workflows.
The platform has two product surfaces — the Virtual Lab for biologists and translational scientists, and the Model Factory for ML engineers and data scientists — built on the same data, the same models, and the same results.
By putting both sides in the same system, Helical closes the gap between computational predictions and biological decision-making, so teams that traditionally worked in silos can collaborate on the same evidence.
Helical was founded in early 2024. It was created by three school friends who took different paths to the same problem.
Rick Schneider built tech at Amazon and later helped the German enterprise Celonis scale in France and Japan. Maxime Allard led data science teams at IBM before pursuing a PhD focused on reinforcement learning and robotics. Mathieu Klop became a cardiologist and genomics researcher.
When bio foundation models emerged, the trio saw the chance to build the missing application layer that would let pharma teams move from model experimentation to reproducible, production discovery.
“The models alone don’t discover drugs. The system does. Pharma teams need a system that turns foundation models into workflows scientists can run, validate, and defend.
“We built Helical to make in-silico science reproducible at pharma scale, so teams can go from hypothesis to decision in days instead of months,” the co-founder of Helical, Mr Rick Schneider, said.
“We are at a unique point in time where biological foundation models and general language reasoning models are converging.
“We backed Helical because we strongly believe they have what it takes to build the pharma AI orchestration platform that will drive this transition from siloed AI models to integrated virtual AI labs,” the General Partner at redalpine, Mr Daniel Graf, stated.
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