Polina had a successful operation!

AiF. Dobroe Serdce

Fundación Moscow

The first step in restoring facial expression to 9-year-old Pauline Ergardt has been taken. The other day, surgeons performed the first of two operations on the child's face, and they will do another one in three months. All this is possible thanks to your support. Polina since birth has no facial expression, it is a sign of rare Mebius syndrome. Her facial nerves are paralyzed and this prevents her from laughing and crying, she has difficulty swallowing. And her face always stays motionless like a mask, no matter what emotions overwhelm her from within. But very soon things will be different. Doctors transplanted pieces of muscle tissue from Polina's thigh into her left cheek, tying together all the nerve fibers and triggering a signal from her brain to the new muscles. And in three months, the same thing would be done on her right side. Now Polina is in the hospital, her face in bandages. Ahead of her long road to recovery. Pauline's mother Catherine says that the real miracle has already happened when strangers responded and supported her daughter, collecting a huge amount for the surgery, which, unfortunately, the MHI is not done. - I am immensely grateful to people who helped us," says Ekaterina. - Polina will be able to smile, use facial expressions, and communicate fully with her peers. I would like to thank everyone who responded and didn't pass by. After the muscles have taken root, Polina will have to undergo a rehabilitation process. She will learn how to use them: to lift the corners of her lips and stretch them into a smile. The moment the girl's lifeless mask falls from her face is very near. Thank you for giving Paula a chance for a happy and emotional life!

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Información de la colecta

Pauline dreams of smiling

Polina Ergardt, 9, has a strange illness in which nothing hurts or bothers her. It's hard to explain why her parents need to raise more than a million rubles for treatment. Only those who have seen their own child's smile will understand. Polina's dad and mom haven't. No smile, no tears, no sadness - nothing. Because of a rare Moebius syndrome (absence of facial nerves and muscles) Polina just can't smile, blink, or cry. Her face, like a stone mask, is always motionless. It doesn't hurt, but it is unbearable. Strangers her peers think her appearance is frighteningly strange, but once they get to know her better, they want to be friends. Pauline is great: she is involved in lego-construction, rock-climbing, roller-skating, and plays computer games on a par with the boys. And Polina hasn't had any problems with her friends for a long time. But she is growing up. And sooner or later the disease will hurt her in another way - emotionally. This can be avoided even without leaving Russia. A unique surgeon has long been working in Yaroslavl, who is ready to transplant pieces of muscle tissue from the girl's hip to her cheeks, connecting the nerve fibers and triggering the signal from the brain to the new muscles. And when everything has taken root, Polina will finally learn to smile. And it's no longer just family and friends who will see how cute she is. Just imagine that no one else will ever be able to understand how you feel and what you're going through inside. No one will be able to respond to your smile or ask why you are upset. Yes, with Moebius syndrome you can live to a ripe old age, travel, have a career and start a family. But it is very difficult to be happy with this disease. Without our support, it's just not possible!

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Филиппинская гимнура

Филиппинская гимнура

100 344 ₽ • hace 4 años

Merjen Artykowa

Merjen Artykowa

100 ₽ • hace 4 años

Geocapromys brownii

Geocapromys brownii

500 ₽ • hace 4 años

Горный кенгуру Дориа

Горный кенгуру Дориа

50 ₽ • hace 4 años

Агамов агамовНосибейский лемурФатима РашидовнаБухарская бурозубка
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