Moira Vilsoni’s inspiring journey serves as a testament to the strength of the human spirit in the face of adversity. Ten months after battling necrotising fasciitis, a rare and life-threatening “flesh-eating” infection, the 42-year-old mother of three commemorates a significant milestone: 200 days since her diagnosis and the life-saving surgery that followed.
The ordeal was marked by a challenging month that included numerous operations, a stint in intensive care, hyperbaric therapy, and a determination to survive. Throughout this painful experience, Moira drew strength from her faith, family, and humor, helping her navigate the emotional and physical struggles of recovery.
Through her recent article in The Sunday Times, Moira aims to raise awareness about this rare disease that nearly claimed her leg—and her life. Her brave decision to share her story encourages others to openly discuss rare illnesses, urging Fijians to overcome any stigma associated with such conditions.
As she prepares to return to work, finish her MBA, and advocate for fellow survivors, Moira’s story is a beacon of hope for anyone facing similar challenges. It not only highlights the realities of such diseases but also emphasizes the importance of support and open conversation in fostering understanding and healing.
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