Alia was born on August 1st, 2024, a tiny baby girl with a big journey ahead of her. Weighing only 1.7 kilograms, she spent her first weeks in the intensive care unit, where doctors worked hard to care for her. Despite the challenges, she was a strong little fighter, and after three months, she finally came home to her loving family.
Alia was diagnosed with Edwards Syndrome, a rare condition that made every day a little more complicated. She couldn’t eat like most babies, so she was fed through a tube called the “raile.” Her father, Abdullah, watched over her every moment, noticing every little change. Sometimes she would throw up after eating, and she had frequent bowel movements, but he was always there to make sure she got the care she needed.
Her mother, Zahra, was just as strong. She barely slept, staying awake to make sure her baby girl was comfortable and safe. Zahra believed in her daughter’s strength and saw Alia as her little princess, always making sure she looked like the most beautiful bride in her tiny dresses.
Alia’s parents followed a strict medication schedule to keep her as healthy as possible. Every day, early in the morning, Abdullah would give her L-thyroxin, and throughout the day, the other medicines would follow. Though small in size and fragile in health, Alia was surrounded by love. Her journey may have been full of challenges, but her family’s care and dedication made every moment worthwhile.
And Alia’s journey is far from over—her story is still being written, and with each passing day, she continues to show just how strong she really is.