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Thousands of Kenya’s children battle arthritis: One doctor is leading the charge

There are about 200,000 children with arthritis in Kenya, but only two specialist doctors to help them

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by JOHN MUCHANGI

Health16 December 2024 - 11:34
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In Summary


  • There is a misconception that this disease only affects the elderly. “Yet, the reality for children living with arthritis is a daily struggle with pain, disability, and the social stigma that comes with it,” Dr Angela said.

Arthritis in children is more aggressive compared to arthritis in elderly individuals because their bones have not yet achieved full growth.

BY DENIS GATUMA AND JOHN MUCHANGI

Three months into her residency at Chogoria Mission Hospital ten years ago, Angela Migowa watched a child battle Lupus and die.

Lupus – a disease where the body's immune system attacks its own tissues and organs – is not fatal in most cases. In fact, most people live a normal life span after early diagnosis and following a proper treatment plan.

The death of the 12-year-old child sealed her decision to become a paediatrician. “That's when I said, I think I need to train to take care of children with lupus and all the associated conditions. And that's how I ended up training in paediatric rheumatology at McGill University. Out of a loss,” Angela told the Lancet two years ago.

In an interview with The Star Health &Science on Saturday, she retraced her journey to becoming Kenya's first female paediatric rheumatologist. Rheumatologists specialise in disorders that affect the joints, muscles, bones, and immune system. Dr Migowa’s current focus is arthritis in children in Kenya. Arthritis is a disease that causes damage in the joints– the places where two bones meet.

There is a misconception that this disease only affects the elderly. “Yet, the reality for children living with arthritis is a daily struggle with pain, disability, and the social stigma that comes with it,” she told The Star. “We estimate that between 200,000 and 300,000 children could be living with arthritis in Kenya.”

Dr Migowa currently works as a Paediatric Rheumatologist at Aga Khan University Hospital Nairobi. She later founded the Hope Arthritis Foundation, based in Nairobi, to promote awareness about the plight of children with this disease, properly known as juvenile idiopathic arthritis (JIA).

“When a child complains of pain in a joint, please before we label the child as pretending, let us do due diligence and have the child examined. The pain of arthritis is very interesting because the pain is worse in the morning and improves as the day goes by, and it improves with activity. As the child runs and plays, the pain gets better,” she explained.

JIA in children is more aggressive compared to arthritis in elderly individuals because their bones have not yet achieved full growth. Secondly, JIA consists of seven types of arthritis, each with unique features. A child suffering from a disease that affects growing bones runs the risk of a lifelong disability, Migowa said.

This can also impact their education, emotional well-being, and future economic prospects, creating a vicious cycle of poverty and chronic illness. Early diagnosis relies on thorough history-taking and physical exams, which are critical since testing accounts for only 20 per cent of the diagnosis. Arthritis in children can be genetic, but the impact of pollution on the environment, temperature change, diet, and infections plays a big role in triggering someone to tip over from a genetic risk to the actual disease.

“All these things come together in synergy to impact the development of the disease,” she said. Historically, healthcare priorities in Kenya focused on diseases like malaria, pneumonia, and HIV, but noncommunicable diseases are emerging as major issues. Some of the JIA symptoms parents are advised to look out for are swollen joints, reduced daily activity in the morning, children crawling using their elbows instead of wrists, and sudden refusal to put their legs down if they had already started walking.

“Most children crawl on their wrists and their knees. If you notice the child is not crawling on the elbow, you have to ask yourself, what has happened to the wrist,” she said. Anna, a mother whose name has been changed, initially thought her son had allergies or had a bad fall when he began limping and dragging his feet.

“It took us three years to receive a proper diagnosis and learn that our child had arthritis, due to the rarity of JIA and the lack of awareness about it,” Dr Migowa said. The revelation was both surprising and devastating to Anna and her husband. Managing the disease has been emotionally and financially challenging.

They had to adjust their son’s diet, avoid certain foods that he likes, and manage long-term medication and frequent tests, including liver and eye checks. Anna said theyare fortunate that her husband's insurance cover from his employer has helped lessen the burden of expenses, as the tests can cost up to Sh50,000 and must be repeated periodically. Frequent eye screening and treatment also helps children with JIA not go blind.

Dr Angela Migowa is also the president of the Paediatric Society of the African League Against Rheumatism (PAFLAR)


Their son, who is now eight years old, has to undergo physiotherapy and physical activities like swimming to help manage the condition. Other recommended activities are cycling and walking, which help alleviate the pain.

There are now two paediatric rheumatologists in Kenya and 20 in Africa, with less than half of them in Sub-Sahara Africa.

The high costs and long training period to become a specialist are some of the barriers blamed for few specialists in Africa and other continents.

Migowa went to McGill University, Canada, for a two-year fellowship in paediatric rheumatology.

She is determined to help increase the numbers of paediatric rheumatologists in Africa. “To ask people to leave their home country, and go away for 2–3 years…in the long term it is not sustainable. So I’m really passionate about creating specialty trainings for health-care workers within their own countries. Tapping into digital technology to allow people to still exchange knowledge, and also create centres of excellence across Africa, to spend six months in hands-on trainings—that's a step in the right direction. That's one way we will be able to scale up specialists, she told The Lancet in 2022.

Since then, the Hope Arthritis Foundation has launched a virtual academy to enhance learning of more healthcare, online education programmes, virtual support groups, and plans to have a multidisciplinary integrated healthcare facility.

On Saturday, the foundation launched its strategic plan for 2025–2029 to promote awareness, prevention, early detection, and management of childhood arthritis and rheumatic diseases through education, research, and collaboration with healthcare professionals and stakeholders.

The five-year strategic plan also aims to provide solutions to bridge the gap in paediatric rheumatology. This includes increasing the number of paediatric rheumatologists, considering that only Kenya and South Africa offer these courses in Africa.

“If you look at Kenya, the number is clearly not enough. That is a real challenge. When it comes to accessing quality care, there will be some gaps, and that’s why empowering all cadres of health care workers and guardians is important for them to know the early signs,” Migowa said.

The pediatrician, who is also the president of the Paediatric Society of the African League Against Rheumatism (PAFLAR), said there is an ongoing discussion with experts worldwide to ensure that some medicines not covered by our public health insurance scheme are included in the World Health Organisation’s Essential Medicines List.

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