Dear friends, respected foundation employees, 🙏💔My name is Roman Ensh. I am the father of Artem Ensh, a six-year-old boy 👦, who is currently battling a serious illness — T-cell acute lymphoblastic leukemia 🩸💥. This is one of the most aggressive forms of childhood blood cancer ⚠️. It all started with a rash on his neck... 😟 Doctors initially suspected a virus, an infection. But a routine blood test showed the terrible truth 😢. From that day on, the fight for our son's life began. We urgently flew to Turkey ✈️. At the Medipol Mega University Hospital in Istanbul, Artem underwent 10 months of excruciating treatment: multi-stage chemotherapy 💉, five severe resuscitations 🏥, one of which — with respiratory arrest and connection to a ventilator 😱. He survived. But the cancer did not give up. The latest punctures showed the growth of cancer cells ⚠️. Only a bone marrow transplant from a 100% compatible donor 🧬 can save Artem — and such a donor has been found! 🙌 This is a huge success, and the Hadassah clinic in Israel agreed to perform the operation. We are already in Israel. Artem underwent another course of chemotherapy 🧪 and is now recovering. Soon - a repeat puncture. If the indicators are good, we will immediately proceed to the transplant. 💸 The cost of the transplant is 255,000 US dollars.
✅ We have already paid 180,000.
❗ We still have 75,000 dollars to raise. This is the price of our son's life. Artem is a real light 🌟. He dreams of returning home, to his little sister 👧 and grandmother 🏡. He loves dinosaurs 🦖, making dough 🎨 and helping take care of our animals 🐶🐈. He wants to LIVE. We can't do it without your support.
Every donation, every transfer is a chance to save Artyom. 🙏❤️
Please help us complete the treatment and give our son the childhood he deserves. With hope and gratitude,
the Ensh family.

I am the mother of Alena Sergeeva. 💔
Alena is already 17 years old.
And for almost 4 years (since September 2021) she has been fighting an unequal battle with a serious illness - acute lymphoblastic leukemia (blood cancer). 😢
The disease burst into her life suddenly, when Alena was only 13. ⚠️
She went through a terrible road:
A year of basic treatment according to the protocol 🧪
Remission! ✨
Sudden relapse a few days before discharge 🩺
Six months of high-dose chemotherapy 💉
Bone marrow transplant 🧬
CAR-T therapy 🚑
During treatment, severe complications arose: gastrointestinal problems, veno-occlusive liver disease, hemorrhagic cystitis, osteoporosis... Several times, Alena found herself on the brink of life and death in intensive care. ⚰️
She endured. She gave in to the complications - and again found remission. But it turned out to be short: in the summer of 2023, the tumor appeared again - a relapse in soft tissues. 😞
In January 2024, doctors in Russia pronounced the verdict - Alena's treatment here is over. 🚫
We did not give up. A new search began: treatment abroad. Several courses in Turkey, hope...
In March 2025 — the examination showed positive dynamics 🎉.
But in May 2025, PET-CT showed that the lesions remained and even new ones appeared. 😢
We turned to independent pediatric oncologists — the only possible way out now is 4th generation CAR-T therapy.
It is only available in China, at the Boren Clinic. They are ready to accept us.
The invoice is 1,199,000 rubles, a 50% deposit must be made as soon as possible. ⏳
I ask you with all my heart to help pay for treatment at the Boren Clinic and give Alena a chance for recovery and a normal life. 🙏💔
Alena is tired of pain and endless struggle, but she lives for the sake of recovery. She is making incredible efforts to win. We beg you: help in this critical situation!
CAR-T therapy is the only way to stop the disease and give the young girl a long life. 🌟
Our family is a mother and two daughters. We are ordinary people. I was with Alena in the hospital every minute and could not work. Therefore, we are not able to pay for the treatment without your help. 💸😔
Our story is about fortitude, faith and real struggle. ❤️
But sometimes everything depends on the support of other people - from adults who are ready to lend a helping hand.
I ask you - HELP Alyonushka!!! Lend a helping hand - it is in our power!
We believe that everything will work out. 💪✨
I am ready to answer questions and provide medical documents. Thank you from the bottom of my heart.
God bless you! 🙏
Sincerely,
Alena's mother - Natalia

"I hold his hand — and pray that his heart doesn't stop…" 💔🙏 I am Tikhon's mother 👩👦 Our son has a complex heart defect 💔, he has a single ventricle, organs are mirrored 🪞, the heart is on the right, but left-formed ❤️. We have no spleen (since birth) ❌🧫 Due to its absence, there is a high risk of infection, sepsis 🦠. We also have thick blood 🩸, but according to the tests, there is no blood mutation 🔬. Now our son's saturation is 80-83% 📉. It is maintained due to the open flow in the pulmonary artery. It is difficult for our son to walk long distances 🚶♂️💨, to participate in active games 🎯 - shortness of breath appears, lips, arms, legs 💙turn blue. He gets very tired, and it is visible on him 😔. Doctor Pak Vitaly Anatolyevich is ready to take us for a Fontan operation, the cost of which we cannot afford is 14500 🏥 — this is the final and most important operation 🛑. The whole future life of our son depends on it 🙏👦. When we were 6 months old 👶, we had our first operation (called Glenn). After being transferred to intensive care, my son had an emergency second operation — they cleaned out clots 🏃♂️💉.After that, the doctor said that he left the current opened in the pulmonary artery, and it will need to be closed during Fontan operation🔒. The condition after Glenn was very serious 😓. The doctors did not give any hope 😢 — our defect has gathered in the most terrible way ... as the doctors themselves say. Now we have to undergo Fontan operation 😣. And there will be complications... But already on the lower part of the body, and this is even more dangerous ⚠️ During the first operation, my son was swollen like a balloon 🎈 - the entire upper part of the body was swollen. But these are the consequences... Now our time is like a time bomb ⏳💣. We live every day as if it were our last 🌅... because the heart may not withstand the current load 💔 Please HELP us raise the amount necessary for the surgery …

‼️ MY BABY IS DYING ‼️ HE IS ONLY 6 MONTHS OLD 💔👶 ACUTE LYMPHOBLASTIC LEUKEMIA ⚠️ BLOOD CANCER ⚠️ HE MAY NOT LIVE UNTIL TOMORROW 😭 My son's name is Salmon🧸 He was born on October 14, 2024 🎂And already in January 2025 we were told something terrible - cancer 😢 He is undergoing chemotherapy 💉, is in the Morozov hospital 🏥, his tiny body is weakening every day... Chemical therapy is destroying everything inside him. Side effects torment him every day 🤒 But without a bone marrow transplant 💔 there is no chance at all... The amount to save my child is 1.195,000 rubles 💰 For us, this is an impossible amount 😔Funds have already helped 🙏, but now we are in a hopeless situation, only you can help... 🆘🆘🆘 We are desperately asking for help! 🆘🆘🆘 Every kopeck you give is a drop of life for Salmon 🩸He's little... he shouldn't die... 💔👼 Please don't pass by... 👩👦 He's our only baby... our air, our soul... HELP SAVE HIS LIFE🙏😭💖 ❤️ SAVE HIS HEART. SAVE HIS LIFE ❤️

Vasya was born such a healthy, such a sweet baby... 🌟 Everything was fine, and we were happy, because our little miracle child grew and developed like all children. But from 8-10 months we began to notice that something was wrong... 😢 He began to lag behind in physical development: he started walking late, often fell, got tired faster than others. On playgrounds, he couldn't climb the children's slide, didn’t ride a scooter or a bike like all children... It was so painful to see that he couldn’t do what every baby does! 💔We turned to doctors, neurologists, took massage courses, drank nootropics, but all this did not bring the long-awaited improvements. And one day, when Vasya started having long-term gastroenteritis, we took tests, and the results were terrible... 😱 The ALT (alanine aminotransferase) and AST (aspartate aminotransferase) levels were abnormally high, and the doctors suspected hepatitis. But that was just the beginning. It soon turned out that we had even more terrible news: we suspected muscular dystrophy... 😢 We took a genetic test, and the results were a terrible sentence... It was the diagnosis: Duchenne muscular dystrophy. I couldn't believe it... My heart broke when I heard these words... 💔From that moment on, everything changed. Our world turned upside down. But even in this crazy and terrible world, a glimmer of hope appeared. 🌈 In 2023, the Elevidys gene therapy was developed, which can stop this terrible disease. It helps to "correct" the gene that is responsible for the production of the dystrophin protein. This treatment can save our baby's life! 💖But here's the problem... We don't fall under the age restrictions, because Vasya is already 7 years old, and the "Circle of Good" foundation purchases the gene therapy only for children aged 4 to 6. 😔 We are beyond the limit, and this opportunity is literally slipping away from us... But we found a clinic in the UAE, in Dubai, at Medcare Women & Children's Hospital, which is ready to provide treatment at our expense. At the clinic, the cost of treatment is 1,200,000 rubles. We need to raise this amount as soon as possible. Every minute counts... If Vasya ends up in a wheelchair, the medicine will no longer help. 😞💔Now Vasya can still move, but his strength is fading. He can't walk long distances, he needs help on the stairs to get dressed and undressed... When we first learned about the diagnosis, we had to take Vasya out of kindergarten because he couldn't cope with the physical activity. He often fell, and I saw how much pain and hard it was for him. 😓 But Vasya doesn’t give up! He attends pre-school classes, works with a speech therapist, goes to the pool… But every day it hurts me so much to watch him suffer, to see him say: “Mom, I’m tired…” 😢Our Vasya is the most affectionate, kind and gentle boy. 🌷 He is always ready to hug and share joy. He loves to make up fairy tales, especially about dragons, and watches cartoons about animals and space with great interest. 🌌 He adores his dog Lisa, he is always the first to grab the leash, walk her, play with her! 🐶 But the worst thing for me is that Vasya, like any other child, loves to walk. But very soon he may lose this opportunity, and I can’t imagine how it will be… 😭 I see how he suffers, climbing the stairs, and his every word “Mom, I’m tired…” pierces my heart like a knife… 💔I don’t know how to live with this pain and hopelessness, but I can’t give up. I will fight for my son until the very end! 💪 I believe that a miracle is possible! 🌟 When I learned about the possibility of saving Vasya, my heart warmed again. Maybe this world is not so cruel if we fight and don’t give up! 🌈I ask you to help us, help to save Vasya. His life depends on this treatment, and I believe that together we can work a miracle! 🙏💖

My son is only 8 years old. He is a child who should enjoy life, play, run, dream. But instead of it, every second he fights a disease that is destroying his body, his future, his life. He has Duchenne muscular dystrophy, a rare and terrible genetic disease that slowly and inexorably destroys his muscles. 😞

At first, we didn’t understand what was happening. He couldn’t get up from the floor, he couldn’t climb the stairs, he couldn’t run like other kids. We thought it was temporary, that it was just some little illness that would pass. But we were wrong. Every day his condition worsened, and the diagnosis we heard took away my last hope — Duchenne muscular dystrophy. 😔

This disease is merciless. It takes away everything from my son: strength, movement, freedom. He can’t lift his arms, he can’t run, he can’t just play with his friends. His muscles are slowly but surely deteriorating, and if we don’t start treatment immediately, he will lose everything — both the ability to walk and the opportunity to live like a normal child. We have found the only way that can give him at least a small chance for a normal life - this is the ELEVIDYS gene therapy, which can slow down the progression of the disease. It gives children with Duchenne muscular dystrophy the opportunity to move again, to live again. But this therapy costs 1,200,000 rubles. 😞

This medicine is very expensive for us. We cannot raise such a sum, and if we do not start treatment right now, it will be too late. Every day counts. Every day, if we do not get help, my life will be ruined, because I will lose my child. I will lose his chance for a normal life, for the childhood that he deserves. We cannot wait, his condition is getting worse every day. ⏳

He cannot wait any longer. He is already losing strength, and I cannot stop it. I cannot watch my son die before my eyes, because I cannot let him live. I beg you, help me! 🙏 Every donation you make is his life, it is his chance. He can't wait, he needs help right now. I don't know how much time we have. HELP before it's too late. 💔

My son, my beloved boy, is terminally ill. I can't find the words to describe the pain and despair. I feel every day, seeing him suffer. 😢 He is just a child, and he has to fight for his life, to fight a disease that no one should have to go through. 💔My son was diagnosed with acute leukemia. 😞 He is experiencing incredible pain, and I can't help him in any way. Every day, looking into his eyes, I understand that he is fighting not only for his life, but also for the opportunity to return to a normal childhood life, to games, joy and smiles. 🧸💖He needs a stem cell transplant, this is the only hope for salvation. 🌟 But this requires a huge amount of money - 1,085,000 rubles, and no matter how hard I try, I cannot raise this amount myself. 💸 We are asking you for help, because only with your support my son can survive. 🙏 I know that he needs urgent treatment, but we can’t do it without you. 🆘 He can’t wait, he can’t lose a day. Please help my boy survive this hell and start living again. 💫Each of your donations is not just money, it is a chance at life for my son. ❤️ We can’t do it without you. Please do not remain indifferent. He needs your help. 🙏

💔 Death is standing next to us... We feel her breath... 💔

😢 I am Anna, my husband is Ilya. We are the parents of Darya - our long-awaited daughter! 👧💖 But her heart... Functionally, she has the only left ventricle... 💔

When I found out the diagnosis at 21 weeks of pregnancy, the doctors said: "Think about it... Is it worth it?" 😭 But is it possible not to wait for your child? We chose to fight! ✊🔥

A birth that was like a nightmare...

😨 Darya did not scream... Her heart was barely beating... 🫀💔 Atony, brain asphyxia, convulsions...

She hasn’t opened her eyes for two weeks... 😭😢

And then the worst thing happened... Her heart stopped. 💔💔💔

⏳ Clinical death... 2 minutes between life and death... ⏳ Doctors fought with all their might, and she came back... 😭🙏

Life hanging by a thread...

👶💔 Darya underwent 5 difficult surgeries... but her heart is too weak... 😢 One blood clot - and that's it... She won't survive...

Now her life is held on by a thin 3.5 mm shunt. This is too little... 💔 At any moment, something irreparable can happen... 😭

Time is running out... But we have a chance!

🆘 The only clinic in the world ready to save Darya is in Boston (USA)! 🇺🇸🏥

Pedro del Nido, a great cardiac surgeon, works there! He can give Darya a healthy heart! ❤️🙏

But without YOUR HELP – it’s impossible… 😢💔

🙏 Please, help to save Daryushka! 🙏💖

Death is near… We saw her face… 😭 But we are fighting! ✊🔥 Give our daughter a chance to live! 👧❤️

💔 Hello! My name is Svetlana, and I am the mother of 9-year-old Alisher (born on August 05, 2014). 💔

I don't know how to start, because every word comes out of my heart with pain 😢. My son, my little angel 👼, was a healthy and active child until the very day we were given this terrible diagnosis 😞... 💔 It all started with a simple sore throat, but it quickly turned into a real fight for life 💪. The lymph nodes in his neck swelled, and my husband and I couldn't understand what was happening 😔. When the doctors said that he had nasopharyngeal cancer with metastases in the neck, I couldn't believe my ears 😱.

Every day was a fight for us ⚔️, each treatment was a new challenge 🛑. We went through 6 courses of chemotherapy 💉 and 1 course of radiation therapy 🌞, but the disease did not stop 😓. After treatment, Alisher had pneumonia 😷, and when we took a coronavirus test, it was positive 😔. We thought we had survived the worst, but then it only got worse 😢. We all went through terrible fear for his life 😞 and lost hope for treatment in Russia, since we were denied further treatment 😔, and we were forced to leave for Israel 🇮🇱.

Here, at the Ichilov clinic, Alisher receives treatment and examinations, but we do not have enough funds 💸 to continue the fight ⚔️. We have no deposit funds, and we cannot raise the necessary amount for further treatment 😔.

Alisher is my life ❤️. He fights for his future every day, and I cannot watch him suffer 😭 without being able to help him 💔. 🙏 I am asking you to help us! Without you, we have no chance, but with your help we can win! 🙌

❤️‍🩹🆘😭💔 My girl is terminally ill, and I don’t have enough words to describe how painful it is for me to watch her suffer. I pray to God every day to give her strength! 😢🙏 My heart breaks when I see my baby suffering from unbearable pain. 😓 Her eyes are inflamed, and she cries because the pain doesn’t go away. And I have to see how she fights this horror every day, and I feel powerless. 💔😿

When we found out that my daughter had retinoblastoma in both eyes, I couldn’t believe that this had happened to us. 😭 It’s a cancer that takes lives, and she suffers from pain that gets worse every day. 😢💔

The doctors offered us only one option — to remove eyesl. But we can’t accept it. We found a clinic in Switzerland where there is a chance to save my daughter, to give her a chance at life and save her from suffering. 💖 But the treatment costs a huge amount — 2,175,000 rubles, and we don’t have that kind of money. 😞

Every day I’m afraid that I might lose my girl. 😭 She suffers and worries, and I can’t stop her pain. 😥 Please help us! Only with your help, we can defeat this terrible disease and give our girl a chance to live the full life. 🌟🙏💖

‼️ Cry for help! Please help to save Efim! 💔🙏

He has been fighting for life since birth. His heart ❤️ is weakened by illness, scarred by surgeries, but it still beats. From the first days of his life, he underwent several open-heart surgeries, went through intensive care, pain and fear.

But now his heart may stop. ⏳ The disease leaves him no choice - either treatment or death. An operation is needed urgently! 🚨 Doctors are ready to help, but we can't do it without your support.

The invoice for the salvation is 1,355,000₽. This amount is too much for our family, and there is less and less time left. ⏳ We beg for help! Without urgent treatment, Efim may not survive. Please help save his heart, help him to live! 🙏💖

🆘😭💔 It's unbearably painful and scary... My little, long-awaited girl, born healthy and happy, suddenly faced the most terrible disease imaginable. Everything that I once saw as bright and joyful now seems dull and scary. My little one, who was running and laughing yesterday, today suffers from unbearable pain... 😢

In 2023, after a routine examination, we learned that my girl had retinoblastoma of the right eye, the last stage - retinal cancer. 💔 Doctors shrug their shoulders, do not believe in a chance of salvation, and offer to remove the eye, but I cannot agree with this operation. In our city, two chemotherapy cycles were completed, but they did not help. My baby continues to suffer, and I cannot leave her in this condition! 😭

I can't let this disease take her away from us. I found a clinic in Switzerland where there is a chance that Kira will keep her eye and beat cancer. The clinic has sent us an invitation and a bill for treatment, the amount of which is 2,150,000 rubles, and I cannot raise such a sum on my own. 😓

I ask all kind people to help us, support us, please! We are fighting for my girl's life, and every contribution you make is a chance for her to stay with us. ❤️🙏 We can't do it without you!

My Yanchik... My long-awaited, only son... 😢💖 His life has been full of pain and fear from the very beginning. When he was just born, we were told something terrible - his heart does not work as it should. 😭 This is a rare and terrible disease, and without urgent surgery, Yan may not survive... 💔

As a mother, I just can't believe it! 😭 Yanchik is so small, so defenseless, and he has already had to endure so much pain. He has undergone several operations, and each of them was a real nightmare for him. 😢 Every time he wakes up from anesthesia, I just beg God for him to be alive... 😔

💔🆘🙏 Our little girl is on the verge of life and death, and we cannot stand aside. CANCER is progressing every day, taking away her strength and hope. When she was born, she was a healthy, happy and beautiful girl, but everything changed when the first signs of disease appeared. She started crying often, became capricious, and we noticed changes in her eyes, which led us to consult the doctor. 😭

After the examination, we were given a terrible diagnosis: bilateral retinoblastoma - a malignant tumor of the retina in the last stage. 😢 This is a rare disease, and the chances to save her eyes would be very small if we had not found a clinic that can help. In Russia, we were offered to remove the eyes, but we are not ready to give up, even if it means fighting to the last breath. We found a clinic in Lausanne, where there is a chance to recover the eyes and save our girl. 🌟

We have already made all the medical tests and received an invitation for treatment, but the cost of treatment is 2,150,000 rubles - an amount that we cannot cover ourselves. 🥺

Please help save our girl! Every contribution you make is a chance for the future for our baby! She deserves to live a full life, play, have fun and grow like all other children. 🙏💖

Please, don't stay indifferent. Your help can save her life! 💕

🆘⚠️I am the mother of a little girl, Ekaterina Vinogradova, from Kobrin. My daughter has SMA (Spinal Muscular Atrophy Type 2), and the disease causes atrophy of the muscles of the whole body, ⚠️ swallowing and breathing. Katyusha will be 7 years old on September 1. Katyusha has already lost the ability to walk. Katyusha was diagnosed in December 2019. An expensive drug, has been developed for this, which costs more than millions of dollars 💲 US dollars. The drug is administered up to 21 kg. Katyusha already weighs 17 kg. We ask all caring people to help Katyusha collect money for an injection. We will be grateful in advance for your help. Together we can save Katyusha's life.❗