💔 MY BABY'S HEART MAY STOP 🆘 HYPOPLASIA OF THE LEFT HEART, AORTIC AND MITRAL VALVE ATRESIA⚠️❤️URGENT SURGERY IS NEEDED! 🙏😭 🚨 EVERY PASSED MINUTE IS A THREAT TO LIFE! THE BABY MAY NOT BE ABLE TO STAND UP! 💔 HELP! 🙏😭.💔 SERCE MOJEGO DZIECKA MOŻE SIĘ ZATRZYMAĆ 🆘 ZESPÓŁ LEWOKOMOROWEJ NIEWYDOLNOŚĆI SERCA, ATREZJA ZASTAWKI MITRALNEJ I AORTALNEJ ⚠️❤️POTRZEBNA JEST PILNA OPERACJA! 🙏😭 🚨 KAŻDA MINUTA JEST ZAGROŻENIEM DLA ŻYCIA! DZIECKO MOŻE TEGO NIE ZNIEŚĆ! 💔 POMÓŻCIE!💔 СЕРДЦЕ МОЕГО МАЛЫША МОЖЕТ ОСТАНОВИТЬСЯ 🆘 СИНДРОМ ГИПОПЛАЗИИ ЛЕВЫХ ОТДЕЛОВ СЕРДЦА, АТРЕЗИЯ АОРТАЛЬНОГО И МИТРАЛЬНОГО КЛАПАНОВ⚠️❤️НУЖНА СРОЧНАЯ ОПЕРАЦИЯ! 🙏😭 🚨 КАЖДАЯ МИНУТА — УГРОЗА! МАЛЫШ МОЖЕТ НЕ ВЫДЕРЖАТЬ! 💔 ПОМОГИТЕ! 🙏😭.

Eremeyev AntonEremeyev AntonЕремеев Антон, 2 years old2 lata2 годика

Диагноз

💔 MY BABY'S HEART MAY STOP 🆘 HYPOPLASIA OF THE LEFT HEART, AORTIC AND MITRAL VALVE ATRESIA⚠️❤️URGENT SURGERY IS NEEDED! 🙏😭 🚨 EVERY PASSED MINUTE IS A THREAT TO LIFE! THE BABY MAY NOT BE ABLE TO STAND UP! 💔 HELP! 🙏😭.💔 SERCE MOJEGO DZIECKA MOŻE SIĘ ZATRZYMAĆ 🆘 ZESPÓŁ LEWOKOMOROWEJ NIEWYDOLNOŚĆI SERCA, ATREZJA ZASTAWKI MITRALNEJ I AORTALNEJ ⚠️❤️POTRZEBNA JEST PILNA OPERACJA! 🙏😭 🚨 KAŻDA MINUTA JEST ZAGROŻENIEM DLA ŻYCIA! DZIECKO MOŻE TEGO NIE ZNIEŚĆ! 💔 POMÓŻCIE!💔 СЕРДЦЕ МОЕГО МАЛЫША МОЖЕТ ОСТАНОВИТЬСЯ 🆘 СИНДРОМ ГИПОПЛАЗИИ ЛЕВЫХ ОТДЕЛОВ СЕРДЦА, АТРЕЗИЯ АОРТАЛЬНОГО И МИТРАЛЬНОГО КЛАПАНОВ⚠️❤️НУЖНА СРОЧНАЯ ОПЕРАЦИЯ! 🙏😭 🚨 КАЖДАЯ МИНУТА — УГРОЗА! МАЛЫШ МОЖЕТ НЕ ВЫДЕРЖАТЬ! 💔 ПОМОГИТЕ! 🙏😭..

Цель сбора

Требуется срочная операция на сердце в клинике в СШАPilna operacja serca wymagana w klinice w Stanach Zjednoczonych AmerykiUrgent heart surgery required in a clinic in the USA

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Собрано:

15000 $

Сумма сбора:

15000 $

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History

In 2023, the second operation was performed - a bidirectional cavopulmonary anastomosis (Glenn operation), also on an open heart using a heart-lung machine, 7 days of intensive care on artificial ventilation. The child's saturation, after this operation, is within 87-88%. Six months after the operation, during the examination, it turned out that Anton had aortic recoarctation and narrowing of the left pulmonary and subclavian arteries. The child underwent endovascular surgery, in which the narrowed areas were inflated with a balloon. Now the child will have to undergo such operations every year, at least until he is five years old. In 2024, Anton also underwent such an operation. Due to the fact that we did not have time to pay the invoice this year, a similar operation is scheduled for July 2025. Considering 2 open-heart surgeries, this will be the fifth... The child is very active and inquisitive, but shortness of breath constantly bothers him, even when he just picks up the pace. He started walking only at 1 year and 4 months, after a course of massage and light gymnastics. With active movements, cyanosis of the face and nails appears. At such moments, my heart just stops... He is only 2 years old, and what next????? Fear entered our souls back in 2022, never letting go of its shackles... We realized one thing... It is not a fear when you yourself are sick. It is a fea when your child is sick, and you are powerless. Where can we get such an amount. The famous pediatric cardiac surgeon from the USA Pedro del Nido is ready to perform the third heart surgery. Children with such defects as hypoplastic left heart syndrome and a single functional ventricle are brought to him from all over the world. This is a chance for our child. We also need to solve the problem with the aorta and pulmonary artery. The cardiac surgeon from the USA wrote that the surgery must be performed before the age of 3. The Boston Children's Hospital clinic was not chosen by chance, because cardiac surgeon Pedro del Nido works there. Since cardio moms closely follow the news about children with similar defects, we have seen what miracles he works. The cardiac surgeon at Boston Children's Hospital cannot confirm what kind of surgery my son will have until the child undergoes the necessary examinations directly in the clinic and a 3D model of the heart is made. Due to the complexity of the anatomy of the aorta and arteries. Children with hypoplastic left heart syndrome have a harder time with surgeries and the postoperative period, as this is one of the most severe heart defects. The right ventricle, unfortunately, is not systemic and as powerful as the left. Considering that the United States has accumulated vast experience in such defects, there are people with such a defect who are already over 40 years old. There is also high-tech equipment, a different level of intensive care and the world-famous pediatric cardiac surgeon Pedro del Nido, who specializes in exactly this defect, like my son's. In Russia, unfortunately, there are no people with this defect over 18 years old. Just 10 years ago, such children died en masse, because, unfortunately, they could not be helped. And now, children who survive the first two operations are considered a miracle. In clinics, neither pediatricians nor specialized doctors are simply not ready for such patients ... Seeing saturation slightly more than 80, they do not understand how to behave. Over the past 2 years, they have tried to take our son to the hospital with oxygen 4 times. But it is absolutely prohibited to do this, thanks to the cardiac surgeon who instructed me and was in touch with me during the interstage period. We could have really lost the child, immediately can begin pulmonary hypertension and damage to the right side of the heart, which is the only one in the child that participates in the heart's work. Boston Children's Hospital calculated the costs of the operation and postoperative treatment and issued an invoice for 1,183,000 rubles. The amount is simply unaffordable for our large family, we have four children. Only my husband works. I am registered as a caregiver for Anton, he is considered as disabled until 18 years. I cannot send him to kindergarten, as he has 7 medications a day, scheduled by the hour, and his activity must be constantly monitored throughout the day. Dear donators, please help our son so that he lives a long and happy life. We beg you!