In 2008, Fauzat Olapojoye Sanusi, a vibrant educator, began to notice alarming body changes—hair loss, persistent weakness, and unexplained symptoms. For years, answers remained elusive until 2018 when a dermatologist identified the condition as an autoimmune response: Lupus.
Further tests (ANA and ENA panels) confirmed the diagnosis. However, being under-dosed with medications left her battling worsening symptoms. In 2021, she met Dr. Olaosebikan, a rheumatologist at LASUTH, who provided the right guidance. By then, her kidneys had been affected, but through treatment and strict dietary adjustments, she entered a period of reversal and healing.
Her resilience and determination inspired her to create a platform that would raise awareness, offer support, and empower others facing lupus. This journey gave birth to the Lupus Remedies Global (LUREG) Support Foundation.
To provide support for people living with lupus and other autoimmune conditions through advocacy, awareness, and empowerment.
To position LUREG Support Foundation as the leading non-profit for lupus awareness and advocacy.
We strive to raise awareness, offer support, create positive change, empower others facing lupus.
is a non-profit organization dedicated to advocacy, awareness, and empowerment for people living with lupus and other autoimmune conditions. We provide support systems for patients and their families, drive education around early diagnosis and treatment, and create platforms that amplify the voices of lupus warriors.
LUREG was founded by Fauzat Olapojoye Sanusi, an educator and lupus warrior who transformed her personal journey of resilience into a mission to inspire others. After years of misdiagnosis, health challenges, and eventual recovery with the help of dedicated specialists, she chose to use her experience to raise awareness and provide hope for others living with autoimmune conditions.
At LUREG Support Foundation, our work is centered on improving lives, spreading awareness, and building support systems for people living with lupus and other autoimmune conditions. We combine advocacy, education, and empowerment programs to create lasting impact.
We organize major events like World Lupus Day and World Scleroderma Day to educate communities, dispel myths, and shine a light on the challenges faced by lupus warriors.
Through counseling, resources, and peer networks, we provide patients and their families with the guidance and emotional support needed to navigate lupus.
Our Back 2 School Project ensures that young people living with lupus have access to the education they deserve, helping them build brighter futures despite health challenges.
With our October Awareness & Endowment Program, we empower patients through advocacy, capacity-building, and direct support interventions.
At LUREG Support Foundation, our strength lies in the passion and commitment of the people behind our work. Our team is made up of survivors, caregivers, professionals, and advocates who share one mission — to support lupus warriors and raise awareness about autoimmune conditions.
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