Grace EdemaThe Founder of The Nerve of My Multiple Sclerosis, Nathalie Busari, has raised concerns about the lack of awareness and information on multiple sclerosis in Nigeria.She called for increased education and support for those affected during a media meeting in Lagos on Wednesday.“We recognise that there isn’t much information available about multiple sclerosis in Nigeria, so we’re here to raise awareness.
“We want people to have a place to turn to when they experience symptoms or if they already have symptoms but are unsure of what’s happening,” she said.Busari, a suvivor, explained that their initial focus was on establishing a presence, after which they hope to organise health summits and awareness days.The Nerve of My Multiple Sclerosis is a non-profit organisation dedicated to supporting and advocating for people living with MS.
Busari further described MS as a neurological condition where the immune system, which was meant to protect the body, mistakenly attacks the central nervous system, targeting the brain and spinal cord.“This leads to the formation of lesions, which damage the protective covering around nerves. Imagine an electrical cable with its outer insulation stripped away, leaving the tiny wires inside exposed and vulnerable.
That’s how MS works,” she explained.She emphasised that while MS is a progressive disease with no known cure, treatments exist to slow its progression. “Without treatment, MS will continue to worsen,” she added.
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