My daughter Angelina is being killed by cancer 😭💔
She is only 5 years old 👧, but she does not live in childhood, but in hospitals 🏥, under IVs 💉 and with pain that a child should not know.
Since 2021, our life has become a struggle ⚔️.
A fight against a disease that does not stop and takes away my girl's strength every day 😢.
In Russia, we underwent terrible procedures 💔, but there was no result.
Only in Israel 🌍🙏 doctors managed to put Angelina into remission.
But only constant treatment with expensive targeted drugs 💊 can save her.
One day, when the drugs ran out, the cancer returned ⚡.
The Russian analogue led to severe side effects 😭.
We can no longer risk our own child's life 💔.
The cost of a new stage of treatment is 1,215,000 rubles 💰.
For our family, this is an unaffordable amount 😢, but without this money, Angelina may not survive.
I hear my daughter whispering:
"Mom, I want to live..." 🥺
And my heart is breaking into pieces, because I can lose her.
Please help us 🙏❤️.
Every penny is a day of her life.
Angelina should live, laugh, run 👧🌈, and not die in a hospital ward.

I am a mother. And next to me is my little girl, who is dying... 😢
She is only 7 years old. Her name is Zara Ozorina.
She is fragile, like a porcelain doll 👧. With long eyelashes, with a quiet voice... And with a tumor inside that is slowly killing 💔.
Undifferentiated neuroblastoma.
Retroperitoneal space... The place where fear lives. Where death has settled.
I remember how it all began...
Stomach pain... Whims... 🤕
Zara was always patient, never complained. But that day she just curled up and cried quietly... 😭
I took her to the doctor...
And a week later they were already calling us "oncological"...
I swallowed this word like poison ⚠️.
We were told: the tumor is evil, aggressive 😨. She doesn't know who she's killing - an adult or a child. She's just growing up...
And if she's not stopped, she'll take my daughter...
I hold Zara's hand every day 🤝. I watch her lose her hair... I listen to her whisper:
"Mom, are we going home today?" 🏠
And I don't know what to say... Because "home" is a hospital ward. Because "tomorrow" may never come... ⏳
We were given a referral to a Moscow clinic - Morozovskaya 🏥.
They're ready to fight for my girl there. They don't give up there 🙌.
But the cost of treatment is $8,015 💸.
For some, it's a vacation. For us, it's life...
I'm not asking for myself 🙇‍♀️.
I ask for the girl who just recently played with dolls 🧸, read fairy tales 📚 and made plans for school 🎒.
Now her life is IVs, injections, tests... 💉
Now every day of ours is a struggle ⚔️.
And I'm afraid that tomorrow she simply won't wake up... 😢
Help us not to lose her... 🙏
Help not let the disease win.
Let Zara remain a girl, and not a diagnosis 🩷.
Let her live... 🌈

MAXIM HAS A RECURRENCE... 😢
WE NEED TO START EVERYTHING FROM THE BEGINNING...
After the bone marrow transplant from his father and the long-awaited remission, we started living 🏡💫. Maxim went to a speech therapist, swam in the pool, played with the kids 👶🎨. He smiled again... 😊
But in the spring of 2025, everything collapsed... His back started hurting 😣.
We were taken by ambulance 🚑 to the Roshal Center. Suspected compression fracture, osteoporosis... And then - a bone marrow puncture... and again this diagnosis 🩸💔
RECURRENCE. CANCER HAS RETURNED.
We have already completed 2 blocks of chemotherapy. There is a temporary remission, but it is like a thread that we are holding on to with all our might 😓.
We need immunotherapy 💉 to consolidate the result and move on to BMT from an unrelated donor.
But our doctors are silent. They are waiting for the decision of others. Those who have not even seen my son 🧒😠
To refuse means to send Maxim in a circle, which he has already gone through... and where a relapse awaited him.
📞 I contacted an Israeli doctor, Irina Zaidman.
Her words: "There is a chance. But the child needs treatment: immunotherapy and a transplant from a suitable donor."
Hadassah presented a bill - 25 million rubles. This is an unaffordable amount 😭.
🙏 I BEG you, help!
My son is all I have. I will not give him up to the disease.
I won't give up ⚔️!
Every donation is a step towards my boy's life 💚
Please help us get out of this darkness 🌧️ and see the sun again 🌞!
📌 Amount to be raised is $17,665
🆘 You can donate using the link or details below
💬 Tell your friends about us, reposting is also a help!
💔👣🧬🛌🩺

Kostya is my son 👦💔 He is only 8 years old... But he is no longer a child - he is a soldier ⚔️ He has been through more than adults experience in their entire lives 😢 And he is still here... Despite the fact that his body is torn apart by cancer over and over again 🧬💥

Rhabdomyosarcoma 🧠 is a rare, aggressive tumor. The right shin is affected 🦵 PAX7-FOXO1 mutation. Like a sentence written in the cells... Doctors shrugged their shoulders 🧤 - people like him are almost never saved.

Chemotherapy 💉, surgeries 🔪, radiation therapy ☢️... Moscow. Khabarovsk. Metastases. Relapse. Dead end. Israel refused ❌ South Korea too ❌ Until one professor decided to 🧑‍⚕️🙏 And since 2021 Kostya has been receiving treatment in Seoul 🇰🇷

But this year his body began to fail... New tumors 😔 Sepsis 🦠 Cardiac edema ❤️‍🔥 9 days in intensive care 😷 Alone, without mom, without dad 😭 Among the machines, tubes and indifferent silence 🏥

Now Kostya is back in the oncology department 🛏️ The treatment continues... But the clinic issued a new bill: $126,000 💰 Almost 10 million rubles 💸 We simply don't have this money...

We sold everything 🏚️ The apartment is gone. There are no savings. All that remains is the life of my son, and it is under threat again...

Now is not about dreams, not about the future... Now is about him just living until tomorrow 🌙🙏 Until the next test 🧪 Until the next breath 💨

Please help 🙏 These are not just words... This is a request from a mother who can do nothing more 😔

Every ruble is like a breath of air for my son 🧡

Help us keep him here... among the living 🕯️

We gave birth to our daughter — and then we began to lose her.
This isn’t a story about a happy childhood.
This is a story where there are IVs instead of toys 🧪, and a diagnosis instead of bedtime stories 💔.

Veronika is our youngest 👧. She has an older sister, Alesya, who’s 8 👱‍♀️. We always believed that a real family means at least two children 👨‍👩‍👧‍👧. The pregnancy went well 🤰. Veronika was born right on time — January 6, 2021 — on the eve of Christmas 🎄. We had picked her name long before she was born.

Our baby girl started talking early, learned all her letters 🔠 and numbers 🔢 by 20 months, loved books 📚, and could count.
Always smiling 😊. Always bright 🧠.

And then came December 2024 — and everything started falling apart...
Leg pain 🦵. Sudden fevers 🌡️. Doctor after doctor told us it was just reactive arthritis. But it kept getting worse.

When a lump appeared on her head, they said it was a hematoma 🤕. Even the ultrasound didn’t find anything malignant. But we saw how fast our child was fading 😢.
Mom begged the doctors to check for cancer. They shook their heads: “No way...”

Only after we insisted, they hospitalized her 🏥. And from there — straight to the oncology center.
Diagnosis: neuroblastoma of the retroperitoneal space 🧬.
Metastases in the bone marrow. Bone lesions 🦴. It was already deep inside.

That’s when our war began ⚔️.
She’s already gone through 6 rounds of chemo 💉.
Her bone marrow responded, the tumor shrank — but that’s just the beginning.
Ahead: surgery 🔪. High-dose chemotherapy with a bone marrow transplant 🧫.
And most importantly — immunotherapy with Dinutuximab Beta (Qarziba).
This drug saves lives — but it’s not available in Belarus ❌.
The government doesn’t buy it. It’s simply not registered.

💰 Total cost of treatment: 14 645$.
Either you find this money…
Or you watch your child fade away 💔.

Veronika is braver than most adults.
She gets CT and MRI scans without anesthesia 🧠, holds test tubes during blood draws, never cries 🩸.
She fights cancer — and smiles 🌈.
Because she still doesn’t understand how expensive her life is 🧸.

But we do.
Every day is like gold ⏳. Every exam feels like stepping on a mine.
We have no other option 🚫.
Either we raise this sum — or the disease will come back.
And there won’t be a second chance 🕳️.

I am a father. And every day I watch my daughter Katya cling to life.
July 5 — 10th day after CAR-T cell injection 💉⚡️
Since the first day, I have been living in anxiety, waiting — will she hold on? Will we hold her?

July 1, on the 6th day after the injection, a cytokine storm began. 💥🔥
The temperature was jumping, the pain was wringing from the inside, we were losing her right before our eyes...
This hellish state lasted for several days. We did not sleep, did not eat — we just watched her fight.
Today the storm is over. The temperature has stabilized 🌡️, the pain has subsided. 🙏
But this is not the end. This is a respite.

Katya is currently undergoing powerful therapy:
— antibacterial 🦠
— antiviral 🧬
— antifungal ☣️
Test results are critical. 📉
Immunity is almost at zero. Any infection is mortally dangerous.
She lives under IV drips, under observation, under threat of every second. 😷💊

We pray for Katya's health 🙏
We pray for the doctors who fight this shadow, for the Benefactors who do not let us fall...
But prayers are not everything. We hold her on this side of life with our hands, day after day.

Katya's condition is stable now, but very fragile. 🩶
Next week - the decisive puncture and bone marrow examination. 🧫
They will show - is there an effect from CAR-T therapy, and whether it is possible to move on.
Will there be a next stage? Or did everything go wrong? We don't know. But we're afraid. We're waiting. We're preparing for anything. ⏳💔

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 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. 💔

💔 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! 🙌

‼️ 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!