Health
Breast Cancer Survivor Preaches Routine Screening
Gloria Orji was 35 years old when she was diagnosed with stage 2 breast cancer in June 2010.
As an unmarried young woman in her prime, she was devastated because she thought she had her life planned out but finding out she had breast cancer was certainly not a part of her plans.
“I felt shattered and asked the doctor how long I had to live, and he answered who said you will die?” she says, recalling the day she received her result.
Today, she has every reason to be grateful as she is still alive, living healthy, and got married in 2021.
She recounted detecting a lump in her breast during self-examination and informed a friend, who advised her to visit the hospital for a medical check.
“I underwent a biopsy, and cancerous cells were found in the breast tissue sample. I was then referred to National Hospital, Abuja, for treatment,” she says.
Treatment plan
Her breast cancer is at Stage 2 and required six courses of chemotherapy, surgery, and 25 sessions of radiotherapy which lasted five weeks.
On completion of the treatment plan, she was placed on five-year-long hormonal treatment and periodic consultations with the doctor.
Believing she had scaled through, Ms Orji, unfortunately, had a reoccurrence eight years later (2018).
“In 2018, I felt another lump in the same breast during self-examination and underwent another round of surgery and treatment.”
“Treatment has been financially draining, and I soon became a charity case. Battling cancer, you have no savings as everything goes into treatment to stay alive. My family, friends and doctor have been very supportive,” she says.
A new life
During the course of her treatment in 2017, Ms Orji realized she had a big decision to make as she noticed patients like her depended on their families and themselves for information about their cancers.
Putting her ordeal to good use, Ms Orji supported by friends working as cancer advocates, created a support group for cancer patients known as the Network of People Impacted by Cancer.
“Having no reliable source for credible cancer information has been making misinformation about the disease thrive. We (patients) depended on each other for information forgetting that people had different forms of cancers and at different stages. We needed a community where we could get the correct medical knowledge to make informed decisions and advocate for government to support cancer treatment in the country.
Through the group, we have been able to use our voice to advocate for government support for cancer treatment in the country, and a notable success is that the National Health Insurance Act (NHIS) now covers some percentage of cancer treatment. It was not previously so.
Also, through a unified voice with the Health Federation of Nigeria to the legislatures, a cancer health fund (CHF) is now available to provide funding and healthcare services to indigent cancer patients in the country, she added.
The CHF program is an initiative of the Federal Ministry of Health that commenced in 2021 with six pilot hospitals.
A plea
“Going through cancer and its treatment has changed me forever. This disease gave me a better perspective on what matters and a renewed appreciation for the people in my life”.
Ms Orji, lamented that many cancer patients in the country could have survived but often present late to the hospital for treatment.
Cancer doesn’t discriminate. It can affect anyone at any age, ethnicity, educational level, and economic status, so we all need to be proactive about our health, eliminate unhealthy habits and listen to our bodies.
People should seek accurate information from reliable sources and support and not discriminate against or stigmatize people with cancer, she added.
Raising awareness about cancer
Cancer is a public health issue of concern, and on 4 February every year, the World Health Organization (WHO) joins the international community to mark World Cancer Day.
In her message to commemorate the 2023 event, WHO Regional Director for Africa, Dr Matshidiso Moeti, says approximately 1.1 million new cancer cases occur each year in Africa, with about 700,000 deaths.
According to her, data estimates show a considerable increase in cancer mortality to nearly one million deaths per year by 2030 without urgent and bold interventions.
She called on Governments to develop/update national cancer control plans, provide sustainable financing, incorporate cancer care into essential benefits packages and national health insurance systems and invest in cancer registration.
Meanwhile, in Nigeria, WHO, with funding from the Susan Thompson Buffet Foundation, provides catalytic support to five states (Anambra, Ondo, Kebbi, Niger and Ekiti) to enable routine cervical cancer secondary prevention services across primary healthcare facilities, to reach up to 5,000 women per state.
The theme of this year is “Close the care Gap: Uniting our voices and taking action.” This year’s campaign summons the government and like-minded people to be united as we build stronger alliances and new innovative collaborations in the fight against cancer. The day reminds us that millions of deaths can be prevented by raising awareness and educating people about cancer.
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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