
The Sarajevo-based Association of Patients with Epidermolysis Bullosa „Debra“ warns that a girl is walking around the city collecting money in their name, but is actually taking it for herself and is not a member of their organization.
It concerns a certain Adisa Šetkić, reportedly residing in Sarajevo, who has been damaging the reputation of the Association, which gathers 22 people suffering from epidermolysis bullosa, for two years.
The Association notes that they have filed criminal complaints against Šetkić on several occasions, but the Sarajevo police have not been of much help in this case.
The President of the Association, Dr. Nevzeta Kahriman, explains to the news agency Patria that the Association does not collect money on the street, precisely to avoid abuse.
- All we can do at this moment is to inform citizens not to give money to anyone posing as the „Debra“ association. The Association has its own accounts through which we receive donations – warned Dr. Kahriman, writes NAP.
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