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Carrier Conversation: Talking about Genotype with your Partner
By: Jagun Quareeb Alabi Talking about genotype and genetic testing…
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The Traditional Wedding Hurdle: Planning Igba Nkwu when your Sibling has MD.
By Jagun Quareeb Alabi Traditional weddings like Igba Nkwu are…
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Living with Rare Neuromuscular Diseases, Why No One Should Face It Alone
By: Olasehinde Oluwadamilola People living with these rare conditions often…
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Neuromuscular Disorders, What’s The Hardest Part?
By: Jagun Quareeb Alabi Many Nigerians suffer silently from neuromuscular…
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Inclusion and Advocacy, how Nigeria can become a safe place for people living with muscular dystrophy.
By: Jagun Quareeb Alabi Living with a disability in Nigeria…
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The Impact and Progress of the Massive Awareness on Rare Diseases (M.A.R.D) Campaign
By: Olasehinde Oluwadamilola For millions of people around the…
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Shining a light on Rare Neuromuscular Diseases
By: Olasehinde Oluwadamilola Awareness is essentially about creating opportunities for…
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Muscular Dystrophy: Causes, Challenges, and How We Can Help
Have you ever seen a child who stumbles often, or…
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Reflections on Duchenne Awareness Day 2025: The Importance of Supporting Caregivers.
On Sunday, September 7th, the Foundation for Neuromuscular Support Nigeria…
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