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  • Five Stories. Five Different Journeys.

    Newscorner

    September 6, 2026

    Five Stories. Five Different Journeys.

    FNSN @10 | Article 2 of 6 Ten years of…

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  • I THOUGHT MY SIBLINGS WERE THE ONLY ONES.

    Newscorner

    September 3, 2026

    I THOUGHT MY SIBLINGS WERE THE ONLY ONES.

    FNSN @10 | Article 1 of 6 Written by Oyindamola…

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  • The Traditional Wedding Hurdle: Planning Igba Nkwu when your Sibling has MD.

    Newscorner

    March 3, 2026

    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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  • Neuromuscular Disorders, What’s The Hardest Part?

    Newscorner

    January 17, 2026

    Neuromuscular Disorders, What’s The Hardest Part?

    By: Jagun Quareeb Alabi Many Nigerians suffer silently from neuromuscular…

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  • Reflections on Duchenne Awareness Day 2025: The Importance of Supporting Caregivers.

    Newscorner

    October 1, 2025

    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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Latest Posts

  • The Next Ten Years: What We Are Building for You
  • Open letter to the warriors.
  • What Nigeria Still Gets Wrong About Neuromuscular Disease.
  • A Conversation With the Woman Who Started It All
  • Five Stories. Five Different Journeys.

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FNSN

FNSN is dedicated to raising awareness about rare diseases, including muscular dystrophy and other neuromuscular disorders.

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    • Our Team
  • Contact Us
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HQ, Lagos, Nigeria.

Phone:

+234 905 667 2111

Email:

info@ffns.org.ng

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