About us

The Safiyah Sickle Cell Foundation is a non-profit organization dedicated to improving the lives of individuals affected by sickle cell disease. Named in honour of Safiyah, a remarkable individual who embodied resilience and positivity despite battling sickle cell, the foundation strives to carry forward her legacy by providing support, resources, and advocacy for those impacted by this condition. Safiya’s journey, marked by her unwavering determination and vibrant spirit, is the foundation’s guiding inspiration. Despite facing the challenges of sickle cell disease from a young age, Safiya refused to let it define her. She pursued knowledge, excelled in academics, and found innovative ways to express herself. Safiya’s resilience in the face of adversity and her commitment to living a meaningful life left an indelible mark on all who knew her. Though significant milestones marked Safiya’s life, her legacy lives on through the work of the Safiyah Sickle Cell Foundation, which is dedicated to supporting individuals and families affected by sickle cell disease and advocating for a brighter future for all.

Mission

To create a healthier future for individuals affected by sickle cell in local communities by providing free genotype testing, organizing blood drives for sickle cell patients, conducting informative sessions in secondary schools and local communities, and facilitating access to comprehensive care and support services.

Vision

To build a world where individuals affected by sickle cell can live without limitations, stigma, or barriers, and where the community is well-informed and supportive, enabling everyone to lead fulfilling and empowered lives despite the challenges of sickle cell.

Core Values

  1. Compassion: empathizing with and supporting individuals affected by sickle cell in every aspect.
  2. Integrity: upholding the highest ethical standards in all our endeavors.
  3. Collaboration: working hand in hand with local communities, medical professionals, and volunteers to combat sickle cell.
  4. Empowerment: equipping individuals with knowledge and resources to manage and live a fulfilling life with sickle cell.
  5. Advocacy: being the voice for those affected by sickle cell, advocating for better healthcare and societal support.

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