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Silent Struggle: Hundreds of Ugandan Children Suffer in Secret from Rare ‘Muscle-Stealing’ Disease

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Silent Struggle: Hundreds of Ugandan Children Suffer in Secret from Rare ‘Muscle-Stealing’ Disease

by Mulengera
6 months ago
in NEWS
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By Mulengera Reporters

Ugandan children battling a rare genetic disease remain largely invisible as the country celebrated Duchenne Muscular Dystrophy (DMD) Awareness Day on 7th September.

Duchenne, a condition that progressively weakens muscles and robs children of their independence, affects an estimated 250 boys in Uganda, though many more likely remain undiagnosed due to lack of awareness, limited diagnostic services, and widespread misconceptions.

Sapphire Africa Foundation, one of Uganda’s leading humanitarian organizations addressing DMD, has been at the forefront of advocacy and care since its founding in 2014.

Operating across more than six districts, including Kampala, Wakiso, Gulu, Fort Portal, Nakaseke, and Kamwenge, the Foundation provides medical support, mobility aids, and psychosocial assistance to children and families affected by the condition.

Executive Director Collin Paul Rubaihayo emphasized that early detection is vital to slowing the disease’s progression, but many children go undiagnosed or are misdiagnosed, often with their symptoms attributed to witchcraft or curses.

“Duchenne is not an abstract medical condition; it is a daily reality of physical challenges, social stigma, and emotional strain,” Rubaihayo said. “Families often face discrimination and isolation, and children are left without the interventions they need to maintain mobility and independence.”

The disease typically appears in early childhood, between ages two and six.

Children may show delayed motor milestones, difficulty running or jumping, frequent falls, enlarged calf muscles, or struggle to rise from the floor, a sign known as Gower’s sign.

As the disease progresses, affected children face scoliosis, respiratory difficulties, and heart complications, which severely impact their quality of life.

Without timely intervention, such as physiotherapy, mobility aids, and specialized medical care, the condition can rapidly deteriorate, leaving families with few options.

Sapphire Africa Foundation has spent the past five years organizing free medical camps across the country, reaching thousands of vulnerable children and families.

Their work combines medical care with psychosocial support, adaptive devices, and educational programs to empower affected families.

Mobility aids, orthoses, swimming therapy, and assistive devices for daily living are provided to help children maintain independence and engage in social activities.

Despite these efforts, the challenges are immense. Diagnostic services for Duchenne are scarce, unevenly distributed, and often concentrated in urban centers, forcing families to travel long distances for assessments, sometimes only to be misdiagnosed or referred repeatedly.

The absence of national awareness campaigns perpetuates misconceptions, leaving children untreated until irreversible complications develop.

Policy attention remains minimal, and Duchenne is largely invisible in national healthcare and disability strategies.

Rubaihayo and the Foundation are calling for urgent policy interventions.

They advocate for official recognition of World Duchenne Awareness Day in Uganda, establishment of specialized hospital wards for neuromuscular disorders, and the creation of regional care centers to bring services closer to affected communities.

Such measures would improve access to diagnosis, therapy, and support, while also raising public awareness and reducing stigma.

“Recognition by the government, improved healthcare infrastructure, and targeted interventions are critical if we are to give these children a fighting chance,” Rubaihayo said. “With early diagnosis, proper care, and community support, children with Duchenne can live fuller, more dignified lives.”

As Uganda joins the global community in observing Duchenne Awareness Day, Sapphire Africa Foundation continues its mission to shine a light on this devastating disease.

Through advocacy, specialized care, and community education, they aim to break the cycle of invisibility, ensuring that no child with Duchenne suffers in silence. (For comments on this story, get back to us on 0705579994 [WhatsApp line], 0779411734 & 041 4674611 or email us at mulengeranews@gmail.com).

  

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