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婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
婚礼摄影师Edward Olive(edwardolive)。10月10日的照片
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Dario and his family for the foundation 'Por dos pulgares de nada'

Highlighting the FOP Journey, Foundation Name, and Darío's SpiritA studio session with the courageous Darío and his loving family, captured by Edward Olive Photography, in collaboration with the foundation 'Por dos pulgares de nada'.Darío is a young boy from León who lives with Fibrodisplasia Osificante Progresiva (FOP), an extremely rare and severe disease. FOP causes the progressive osificación (turning into bone) of muscles, tendons, and ligaments, gradually limiting movement and leading to the formation of a 'second skeleton.'The name of the foundation, 'Por dos pulgares de nada' (For two thumbs of nothing), refers to a characteristic physical sign of FOP: a deformity in the big toes (which are turned inward). This deformity, initially viewed as minor, became a profound symbol of the reality of the disease.The mission of the foundation, created by Darío's parents, is twofold: to fund research to find a treatment as soon as possible, and to increase the visibility of FOP to help other families.These portraits, taken by Edward Olive, honor the family's resilience and their dedication to this vital cause. Their story is one of unwavering hope and the continuous fight for a cure.

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