Born at 532g, 24 Weeks – Please Help Save Emilia!
Born at 532g, 24 Weeks – Please Help Save Emilia!
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❣️ EMILKA – A TRUE MIRACLE OF LIFE 🕊️❣️
My Name is Emilka (Emilia) 🧡I am a tiny miracle girl who came into this world far too soon—at just 24 weeks of pregnancy. I weighed barely over 500 grams.
At just 10 days old, I underwent my first highly complex surgery leaving me with only a 20% chance of survival.
I was so small and fragile that even the slightest wrong move could have caused me immense pain—or even taken my life.
My tinny, precious heart truly believes that with your support and kindness ❤️, I will one day grow up to be a healthy, happy, and full-of-life little girl - the best example that even the tiniest hearts are filled with unbreakable willpower and endless strength.

My daily reality is filled with treatments, rehabilitation, therapies, and a constant battle for my health—but I will never give up.
From the very first seconds of my life, I spent 304 days in the hospital before I could finally see the sky, feel the warmth of the sun, and return home for the first time. Despite all the pain I have endured and the dramatic fight for my life, I am incredibly grateful to be alive.
🎗️…AND THIS IS MY STORY…🎗️
❤️ I Am Truly a Miracle, an Inspiration, and Living Proof That Even the Tiniest Heart Can Fight for Life with Incredible Determination ❤️

Just days after I was born, I underwent a life-saving surgery on my digestive system. To survive, I needed a constant supply of morphine and antibiotics. I battled pneumonia, multiple infections, and relied on oxygen tubes to keep me alive.
DOCTORS GAVE ME ONLY A 20% CHANCE OF SURVIVAL - MY WEIGHT DROPPED BELOW 500 GRAMS 😔
Almost no one believed I would make it, but the doctors did everything they could to save me❤️
❣️ WEIGHT: 505 GRAMS ❣️

From my very first moments, needles pierced my tiny hands, feet, and fragile body. The dressings meant to protect me often irritated my delicate skin, causing pain, inflammation, and infections.
The beeping of life-saving machines and the flashing lights of the operating room became my everyday reality.
Countless times, I fought for every breath, filled with pain and tears, as...
MY TINY HEART GREW WEAKER AND WEAKER 💔

In my darkest moments, I thought it was the end—that I couldn't go on, that fate had been too cruel. But when my mommy held me close and I heard her heartbeat❤️I knew I had to fight with all my strength for the most precious thing—LIFE.
MOMMY AND ME — I Was So Tiny🥹

My intestines are very weak and require additional surgeries. After my first operation—when I weighed just 500 grams—the doctors left my intestines outside my body without even stitching my tummy closed.
After the second surgery, they placed a feeding tube in my tummy. I was under IV for 13 hours a day, and after the third operation the doctors close my little tummy.
Sadly, my battle is far from over. I know that more painful procedures, unknown battles, and surgeries still await me.
MY TUMMY AFTER FIRST SURGERY 💔

Every day is a struggle. I suffer with eating—every bite is a challenge. I also have neurological disorders that affect my motor development.
My spine is not properly aligned, I have limited mobility in my left leg and right arm, and I experience painful adhesions in my abdomen from my surgeries.
To prevent further complications, I need intensive rehabilitation to maintain my mobility and prevent postural defects.
I also require constant care from specialists who oversee every aspect of my health.
Doctors cannot believe how strong I am and how fiercely I fight for my life.
My health condition is unpredictable. Some days I feel joyful, but on others, I cry from pain.
I need continuous rehabilitation, therapy, and frequent specialist visits—without them, my development could stop.
🥹BUT I CAN'T DO IT ALONE😔
❤️ WITH ALL MY HEART, I ASK FOR YOUR KINDNESS AND SUPPORT
🧡 Your support is a gift of life—please help me on this journey.
🧡 I cannot do this alone—your kindness gives me strength.
I Urgently Need Funding for.....
❣️ Physical therapy rehabilitation to strengthen my tiny legs and arms.
❣️ Neurological speech therapy to help me learn to speak and eat like other children.
❣️ Continuous neonatal and pediatric care to ensure my development and health are always monitored.
❣️ Specialized sensory therapies to help me better understand the world despite my delicate senses.
❣️ Cardiological care because my heart is very weak and needs special care.
❣️ Supplements and specialized medications to boost my immune system and protect me from infections that could be life-threatening.
❣️ Ophthalmological care to ensure my eyes develop properly so I can see the world around me.
❣️ Speech therapy—so one day, I can say "thank you," I love you "mommy," and "daddy." These simple words are my biggest dreams and challenges.
❣️ Frequent visits to specialists like a gastroenterologist, cardiologist, and ophthalmologist—their help is essential for my survival.

I am the only child of my beloved parents, who have always helped others and never asked for help themselves. But now—facing overwhelming costs—they are pleading on my behalf for your support.
WITH YOUR KINDNESS, I KNOW I CAN TURN THIS PAINFUL JOURNEY INTO A STORY OF SURVIVAL AND HOPE🕊️
❣️ Even the smallest support keeps my tiny heart beating ❣️
🤝I WILL CARRY YOUR LOVE AND GENEROSITY IN MY HEART FOREVER🤝
💞PLEASE, DON’T WALK AWAY—I CAN’T DO THIS WITHOUT YOU. YOUR SUPPORT MEANS THE WORLD TO ME💞
MY BATTLE IS NOT OVER—THERE IS STILL PAIN AND SUFFERING AHEAD, BUT ALSO HOPE, LOVE, AND DETERMINATION.
MY TUMMY AFTER SECOND SURGERY 💔

HOLE IN MY TUMMY AFTER FEEDING TUBE REMOVAL 💔

💔 I DON'T HAVE A BELLY BUTTON—ONLY SCARS FOR LIFE. 💔

❤️🩹 EMILIA - A TRUE MIRACLE OF LIFE🕊️❣️
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