Aretis Kotseli
Aretis Kotseli is a translator and mother who, alongside her husband, experienced the emotional turmoil of discovering their child had a rare genetic disorder, epidermolysis bullosa, shortly after birth. Like Maria, Aretis faced challenges in finding knowledgeable medical professionals and became involved with DEBRA Greece, where she advocates for awareness and support for families dealing with this condition.
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Greece:
Aretis Kotseli is a translator who shared her experience of dealing with her child's rare condition.
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