The only & long-awaited child in the family. He was born healthy, but at the age of 4 month his head starts to grow unproportionally. It also causes muscle weakness and everyday headaches. He can't walk until the age of 3.

Now he is 7. Despite all the pain he suffers, Abubakar is a very friendly, cheerful, and intelligent little gentleman. With big bright eyes, open smile and the way he stretched his little hand to say hello he melted @mila’s heart.

His parents do everything they can, but there is no free medicine in Senegal. There are no doctors in the village, they live. But they cannot even afford examination and diagnosis.
Abubakar Story
There is little chance for cure, because the anomaly develops several months after birth. Chance that it’s not a genetic disease. We have to hurry up.
Next steps:
Currently we are raising funds of 700$ for diagnostics: MRI, different tests, doctor's appointments. We need to find out what is causing the abnormal growth. If his brainpain continues growing epileptic seizures may join the pain, and brain cells will begin to die.

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Cost of the treatment:
Another stories
Skin cancer
4th degree burns
Blindness
Khadime Deme, 23 y.o
Amadu, 7 y.o
Nicasio Adul Baldé, 5 y.o
Residence: Small village, near Touba, Senegal
Residence: Small village, near Touba, Senegal
Residence: Small village, near Touba, Senegal
Further treatment: face reconstruction: eye, bones, skin
Further treatment:
eye surgery
Further treatment: diagnostics & cataract surgery
Khadi is a very strong albino-guy from a small village in Senegal. It’s hard to tell how difficult the life of albino person in Africa is. It’s...
Amadu met @mila, when he was 6. When she first sees the boy she organizes his transfer to Dakar. Amady is albino. He is the tool...
Nicasio Adul Baldé was born in the village Adjanco section of Buruntuma in the Gabú region. He is living in a shelter AGRICE.
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We already have kids to save. No time to lose.