The Foundation for Neuromuscular Support Nigeria (CAC/IT/ No 123373) is Nigeria’s leading Rare Diseases Awareness Foundation, recognized by RAREis. FNSN is dedicated to raising awareness about rare diseases, including muscular dystrophy and other neuromuscular disorders. Through a range of initiatives—support groups, awareness campaigns, donations, and media outreach—we provide essential support to individuals living with these conditions. Our support groups offer a safe space for people affected by rare diseases to connect, share their experiences, and learn from one another.

Additionally, thanks to public and private donations, we have been able to provide vital resources, including wheelchairs, groceries, and other essential equipment. FNSN has successfully conducted over ten awareness campaigns, both online and offline, to educate the public about rare diseases, fostering empathy and promoting inclusion within society. Under the visionary leadership of our Founder and Director, Oyindamola Aina Adeniyi, FNSN continues to champion the cause of rare disease communities across Nigeria.


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