Hi. I'm Hana. I'm two and a half years old. I want to play with my little friends, run, be a happy little girl who will one day grow up to be a beautiful, smart girl. I'll be a teacher. Or a lawyer. Or a writer. Or... Well, I'll be whatever I want. But I can't be that without you.
Parents Almir and Hasiba Ćatić, from the village of Ćatići-Pećigrad, hamlet Mehurići near Cazin, do not have money for Hana's treatment, writes the Patria News Agency.
Little Hana has a lipoma on her spinal cord, which can cause paralysis of the lower body at any moment, as well as inability to control bowel or bladder function.
The estimate for the complicated neurosurgical intervention, which must be performed at Acibadem clinic in Turkey due to the lack of modern equipment and methods, is 16,000 euros.
A council of doctors convened and recommended that the girl be operated on within the next two months, or it will be too late afterwards.
The lipoma is in an inconvenient location and grows proportionally with the child. Because of this, Hana can no longer move and play with her peers, as any fall would be fatal for her.
The diagnosis is: LIPOMYELOMENINGOCELE
A Facebook group for help, "Svi za Hanu" (Everyone for Hana), has been launched, where more information can be found.
The parents' contact number is 061 621 758.
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