Save a child

Every day 1000 children die from a disease that no one talks about

Sickle cell disease is the world's most common genetic disorder, affecting over 12 million people, the disease kills half of children with the severe form before age five, predominantly impacting black populations.

Despite its high mortality, sickle cell remains largely underfunded and overlooked globally, with limited access to life-saving treatments.

This silent epidemic claims more lives than HIV/AIDS in Africa...

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Next event
May 9–10, 2025
Fast Lane Drive Auction for Sickle Cell Disease
Fast Lane Drive
Cathy Guetta

Auction & Lottery Catalog

The International Sickle Cell Fund extends its heartfelt thanks to Cathy Guetta whose unwavering dedication as a Global Ambassador for Sickle Cell Disease has made this partnership with Fast Lane Drive possible

Cathy Guetta
ISC Fund

Sickle cell is #1 genetic disease in the World

Sickle cell disease is a genetic disorder affecting hemoglobin, the substance in red blood cells that carries oxygen. In affected individuals, red blood cells are fragile, destroyed quickly, and deformed into a sickle shape, obstructing blood flow and causing oxygen deprivation to organs.

This results in anemia, pain crises, and a higher risk of infections. Vaso-occlusive crises, marked by severe and unpredictable pain, can affect bones and organs.

In Africa, high infant mortality rates are due to limited access to treatment, exacerbating the disease's devastating impact. Despite its scale and devastating consequences, this disease remains largely overlooked.

Sickle Cell Disease
  • Sickle Cell Disease Africa
    80% of patients are in Africa.
  • Sickle Cell Disease child
    50% of affected children die before the age of 5.
  • Sickle Cell Disease child
    < 20% of patients have access to hydroxyurea treatment

The first treatment for Sickle Cell disease produced in Africa at cost

Drepaf treatment

The International Sickle Cell Fund financially supports the NGO Drep Afrique, particularly the DREPAF® project.

The association has signed a unique humanitarian agreement with the laboratory Teranga Pharma to produce and distribute the only treatment that significantly reduces infant mortality among patients with Sickle Cell Disease using the hydroxyurea molecule.

DREPAF® is produced in Senegal by Teranga Pharma. The first treatment sold at cost, available in 2025 in all pharmacies from $60 per year.

The program will soon be available in four other African countries.

Drep Afrique

We invite you to visit Drep Africa for detailed information about the NGO and its missions supported by the ISC Fund.

For any inquiries, please feel free to contact Emmanuel Jayr, Co-founder and Treasurer of the ISC Fund, at manujayr@gmail.com.

© 2025 ISC Fund. All rights reserved