Kefif fights for his life

I am a mother of three children. Two are healthy, but my little boy Kefif, born on February 16, 2023, in Algeria, suffers from a rare hereditary disease: congenital erythropoietic porphyria. 

Since birth, Kefif has been fighting this disease. He spent his first two months in the hospital. Light and sun are a real danger for him: his skin burns very quickly, and fluid-filled blisters appear on his body. He must be protected constantly. The disease also leads to other complications, including blood in the urine, as well as an enlarged liver and spleen. He requires regular medical monitoring. 

Unfortunately, I already know the violence of this disease. In 2016, I gave birth to a little girl who also suffered from it. I lost her. Today, my greatest fear is to lose Kefif as well. 

This is the heartbreaking message we received from this mother. Having already lost her little girl to the same disease, she is now asking us to help her save Kefif. 

Our association has already supported many families and enabled seriously ill children to access care abroad. Today, it is Kefif who needs us. 

Many of you, please help him. Every donation and every share can advance his fundraising and give him a chance to access the care he needs. 🙏 

Every gesture counts: even a small donation can advance this cause. It's fast, secure, and requires no registration. Can't donate? Share it around you. Together, we can make a difference. Thank you!