💔 My daughter is only two years old. Her medical records already contain the word that thousands of parents dread: cancer. 😭

I never thought I'd be asking for help for my child. I never thought that instead of childhood parties, first drawings, and carefree laughter, our lives would turn into endless tests, waiting for results, and fear for our daughter's future. 😢

Asima was diagnosed with bilateral retinoblastoma—a malignant tumor of the retina in both eyes. One day, our family's normal life ended. All that remained were hospitals, doctors, and the constant battle for our child's health. 💔

When I was told about my daughter's illness, I looked at my little girl and couldn't believe all this was happening to us. Asima is just beginning to explore the world. She doesn't yet understand why she's constantly being taken to clinics and why her mother cries secretly more and more often. 😭

But I understand something else. Without treatment, the disease will continue to destroy what cannot be undone. 😔💔

Today, Asima needs treatment at the Swiss clinic "Hopital Ophthalmique Jules-Gonin." The cost is $17,600.

For our family, this is a huge sum, one we cannot raise on our own. 😢

Every day of waiting is difficult. As a mother, I can't calmly look at my child and understand that the necessary treatment depends on money we don't have. 💔

That's why I'm asking for help.

🙏 Please support my daughter. Any help brings her closer to treatment. Even a small contribution makes a difference.

More than anything, I want to see Asima grow, learn, play, and simply live the life of an ordinary child.

Thank you to everyone who finds a way to help my daughter. 😭💔🙏

💔 My son is only 11 years old... 😢

Just recently, my son went to school, played with friends, and made childhood plans for the future. Today, his life is filled with hospitals, examinations, and a difficult battle for his health. 😭

Mukhammadbek was diagnosed with vermis medulloblastoma of the cerebellum with spread to the fourth ventricle. For our family, these words have divided our lives into "before" and "after"... 💔

Every day I look at my son and understand that he is forced to endure trials that not every adult can withstand. 😔

Mukhammadbek now requires treatment at the N.N. Blokhin National Medical Research Center of Oncology in Moscow. The cost of treatment is $12,500. 😢

This is a huge sum for our family. We are doing everything we can, but our strength and resources are not enough. 💔

As a mother, I cannot accept the fact that money could become an obstacle to my child's treatment. 😭

Therefore, I am asking for help from all caring people.

🙏 Please support my son. Any help makes a difference.

I thank from the bottom of my heart everyone who finds a way to help Muhammadbek during this difficult time. 💙😢

I no longer know how to find the strength to look my child in the eye and pretend everything will be okay... 😭💔

My son Savva is only 5 years old.

Five is the age when children dream of new toys, argue over cartoons, run around playgrounds, and laugh for no reason. But my boy's childhood is completely different. 😢

Instead of walks, there are hospitals.
Instead of games, there are examinations.
Instead of a carefree childhood, there is fear that lives with us every day. 💔

We live in Korolev. Until recently, Savva was an ordinary child. He loved to play, hug me before bed, and make his little childhood plans. I couldn't even imagine that one day our lives would be divided into "before" and "after." 😭

I will never forget this day.

Doctors diagnosed my son with a space-occupying lesion in the posterior fossa compressing the fourth ventricle, obstructive hydrocephalus, and a brain tumor. 💔

Since then, I've lived in constant fear.

Fear of hearing bad news.
Fear of losing precious time.
Fear for my child's future.

No mother should hear such diagnoses about her son. No child should have to go through such an ordeal. 😭🕯️

Sometimes Savva looks at me with his big eyes and asks:

"Mom, when will this all end?.."

And I don't know what to say.

Because I'm afraid myself.
Fear for every new day.
Fear for his health.
Fear for his future. 💔

Every night I go to his bed, adjust the blanket, and just watch him sleep. Perhaps only parents of seriously ill children understand this fear—the fear of losing the most precious thing in life. 😭

Today, Savva needs urgent treatment at the Hadassah Clinic in Israel. For our family, this is a chance to continue the fight and do everything possible for our son's health. 🙏

💰 The cost of treatment is $18,654.

This is an unaffordable sum for our family. 😔💔

I ask you not to ignore our plight.

Please help Savva.

Help this little boy who dreams of simply returning home, playing, laughing, and living a normal childhood life. 🥺🙏

Every donation is a step towards treatment.
Every transfer is hope.
Every kind heart is a chance for my son.

Thank you to everyone who supports Savva and our family. ❤️🙏💔

I live in fear of one day opening my eyes and realizing my son is no longer breathing... 😭💔

Lyova is only 2 years old...
He hasn't even had time to start living a normal life yet...
He hasn't even had time to know what a happy childhood is... 😢🕯️

Every night I wake up and go to his crib...
I listen to his breathing...
Because I'm terrified of losing my baby... 💔

We live in Brest. Just recently, Lyova was laughing, reaching out to me, enjoying his toys, and falling asleep in my arms... 😭

And today our life has turned into an endless nightmare...
Hospitals...
Examinations...
Tears...
And the constant fear of hearing the worst from the doctors... 😢💔

My son has a diffuse brainstem glioma with spread to the cerebellar hemispheres, the fourth ventricle, and the thalamus... 😭🕯️

When the doctors told me this, it was like I stopped breathing...
How can you accept that a life-threatening disease is destroying the brain of a two-year-old child... 💔

Now the disease continues to sap my little one's strength... 😢
He's become weak...
He tires quickly...
Sometimes he just lies there exhausted and silently looks at me... 😭

He's still so tiny...
He doesn't understand why he's so sick...
Why is Mom always He's crying...
Why are there only doctors and hospital walls around me instead of home... 💔🕯️

Sometimes Lyova just cuddles up to me, and at that moment I think of only one thing—to save my son... 😭

Doctors recommend urgent treatment at the SHEBA GLOBAL clinic in Israel 🙏
This is an opportunity to continue the fight for Lyova's life...

💰 The cost of treatment is $14,788
This is an unaffordable sum for our family... 😔💔

I ask you as a mother... 😢
Please... help my baby...
Help Lyova live...
Don't let the disease take my child... 😭🕯️💔

I'm afraid every day that my daughter might die in my arms... 😭💔

Adelina is only 4 years old...
She's still so little...
She should be living her childhood right now – laughing, running, watching cartoons, and falling asleep next to her favorite toy... 😢🕯️

But instead, my girl spends almost her entire life in hospitals... 💔

We live in Arkhangelsk. And for several years now, I've been watching a serious illness slowly take my child away... 😭

Adelina has a germ cell tumor of the sacrococcygeal region with metastases...
The tumor continues to grow...
The disease doesn't stop... 😢💔

My little girl has endured more pain than even adults can bear...
Hard chemotherapy...
Hours-long surgeries...
Tumor removal...
Spinal surgeries...
Constant examinations, pain, weakness, and endless hospital walls... 😭🕯️

We've hoped so many times that things are getting better...
But again we hear those terrible words:
"Relapse..."
"Continued growth..."
"Progression..." 💔

Now the disease continues to destroy my daughter's body... 😢

Sometimes Adelina just lies next to me, exhausted...
Hugs me and whispers:
"Mommy... it hurts..." 😭💔

And I'm ready to scream in frustration, because I can't take this pain away from my child... 🕯️

Doctors recommend urgent treatment at a clinic in Israel 🙏
This is an opportunity to continue the fight for my daughter's life...

💰 The cost of treatment is $16,850
For our family, this is an unaffordable sum... 😔💔

We are already living only in hospitals and the fear of losing our child... 😢

I ask you as a mother... 🙏
Please help my girl...
Help Adelina live...
Don't let the disease take my child... 😭🕯️💔

I don't know how to watch my child die anymore... 😭💔

My son Nazar is only 6 years old...
He should be running, laughing, watching cartoons, and living a normal childhood...
But instead, my boy spends his days in hospitals, surrounded by IVs, pain, and constant fear... 😢🕯️

Nazar has a malignant tumor of the mediastinum...
The disease is destroying my child right before my eyes... 💔

I will never forget the day the doctors said those words...
It was as if my heart stopped...
Because it's impossible to accept that such a serious illness can affect such a small child... 😭

Nazar is very weak now...
Sometimes it's hard for him to even get out of bed... 😢
He tires quickly, turns pale, endures pain, and silently looks at me with his childish eyes... 💔

And then he quietly asks:
"Mom... I won't die?" 😭🕯️

And at that moment, everything inside me just breaks apart...

I can't take this pain away from him...
I can't protect him from what he goes through every day... 😢💔

Doctors recommend urgent treatment at a clinic in Israel 🙏
They are ready to accept Nazar and continue the fight for his life...

💰 The cost of treatment is $11,550
For our family, this is an unaffordable sum... 😔💔

We've already sold everything we could...
But we can't cope without help... 😭

I ask you as a mother... 🙏
Please help me save my son...
Help Nazar live... don't let this disease take my child... 😢🕯️💔

Hello... 😔
This is Vova's parents writing.
Our son is an ordinary child who desperately needs help right now... 💔
He loves cars, draws, explores the world with interest, and, like all children, dreams of playing, learning, and simply living a life free of hospitals... 😢
When Vova was 2 years and 8 months old, after examinations, he was diagnosed with stage 4 neuroblastoma with bone and bone marrow damage... 💔
From that moment on, a long treatment began...
He has already completed courses of therapy, surgery, and a bone marrow transplant...
It was a difficult journey that required a lot of effort from him... 😔
The treatment is currently ongoing...
But for the next stage, doctors recommend contacting the specialized Sant Joan de Déu Clinic (Barcelona)... 🙏
The cost of treatment is $18,300... 💔
For our family, this is a significant amount, which we cannot raise on our own... 😢
We have already done everything possible...
And now we are asking for support so that Continue my son's treatment...
If you can help, we would be grateful for any participation... 🙏
Thank you for reading this letter... 😔

Sometimes I look at my son and try to imagine what his life must be like now...

He's 13.
An age when children live without looking back, laugh, make plans, argue, dream...

Yelisey... Nefteyugansk...

But his days are completely different.
The hospital ward has become familiar to him.
IVs, tests, procedures—all of this has replaced his normal childhood... 💔

At first, it was just fatigue...
Then a weakness that wouldn't go away...
Examinations... waiting...

And the doctors' words, after which everything inside felt empty... 😔

He has acute lymphoblastic leukemia.

Since then, he's lived, overcoming each day.
He doesn't complain... doesn't ask for more...
He tries to be strong...

But I see how hard it is for him.

Sometimes he just lies there, silent...
Staring at something...

Sometimes he quietly asks:
"Will this ever end?.."

And at those moments, it's impossible to find the right words... 😢

Now he needs to continue treatment at the Schneider Clinic in Israel.
They're ready to accept him and continue his therapy...

The cost is $14,350.
For our family, this is an unaffordable sum... 💔

We can't stop now.
Because every day is his strength... his life...

Please... help Elisha... 🙏

Help him walk this path to the end...
Help him return to a place where he can simply live again...

Where there's no constant pain...
Where there's a normal childhood... 💔🕯️

I'm Rustam's mother... and it's very difficult for me to talk about what's happening to my son. 😢💔
He's only 14 years old. He's still a teenager... a child who should be living a normal life—studying, laughing, making plans.
But instead, his life is spent in hospital wards.
Rustam has a serious illness—neuroblastoma.
When we found out, I couldn't accept this reality for a long time. I looked at my son and couldn't understand how this could happen to him...
He was always a calm, kind boy. He loved to joke, dreamed of the future.
And now he tires quickly, gets weaker...
Sometimes he just lies there and is silent.
Sometimes he takes my hand and quietly asks when it will all end...
And at those moments, I'm at a loss for words... 😭
The hardest thing is to see your child suffer and feel helpless. Rustam now needs to continue treatment at a clinic in Turkey. They are ready to accept him and care for his condition.
The cost of treatment is $16,324.
For our family, this is a huge sum, which we cannot raise on our own… 💔
I am appealing to you as a mother… 🙏
Please help my son.
I have only one fear – not being able to help him in time…
I really want him to live… 😭💔🕯️

My son is 11 years old, and every day I watch how hard his battle with his illness is... 💔

Stas was always a calm and kind boy. He loved building construction sets, dreamed of hanging out with his friends, and made plans like any other child... But today, his life is filled with hospitals, examinations, and constant treatment... 😢

My son has metastatic osteosarcoma of his right tibia. The disease turned out to be very aggressive...

The most terrifying thing for our family is that Stas has already been through a difficult fight for his life. As a child, he survived retinoblastoma and overcame the disease... We hoped we would never have to deal with this again... 😭💔

But years later, the cancer returned...

Treatment in Russia failed to stop the progression of the disease. After several courses of high-dose chemotherapy, his condition continued to worsen...

We are now in Israel, at the Schneider Clinic, where doctors are continuing to treat my son 🙏

On May 21, 2026, Stas is scheduled for leg amputation... 😢💔
This is a terrifying thing for any father to accept... But right now, the most important thing is to keep him alive...

After the surgery, my son faces a long recovery and further treatment.

💰 The total bill is $100,000. The foundation is collecting a partial amount of $15,890.

For our family, this is a huge amount, which we cannot afford on our own...

I ask you to help my son continue his treatment... 🙏
Any support is very important for our family now...

We really want Stas to be able to move on with his life... 🕯️💔

💔🆘 Our daughter may not overcome this disease... 😭

Our daughter's name is Sofia Pirova. She's only 5 years old, and we live in Aksay.
This is the age when children should be playing, laughing, running around the yard, and building their little childhood dreams... But instead, Sofia spends her days in hospitals. 💔

Our daughter was diagnosed with medulloblastoma of the fourth ventricle, the anaplastic variant—an aggressive brain tumor. 😢🧠

Sofia already knows what hospital walls, injections, examinations, and fear are. Sometimes she quietly holds my hand and asks,
"Mom, when will we be home again?" 😭

And I'm at a loss for words... because now everything depends on the treatment we must continue.

The doctors said Sofia needs treatment in a specialized clinic. ACIBADEM MASLAK HOSPITAL is ready to accept our daughter and begin the necessary therapy.

But the treatment costs $8,600. For our family, that's a huge amount... 💔

We've already done everything we could. But we can't cope without people's help.

Every evening I look at my little daughter and fear only one thing—losing her... 🕯️😭

🙏 Please help Sofia continue her treatment.
Help our little girl grow up, laugh again, and live a normal childhood.

Any help is our hope of saving our daughter's life. 💔🕊️

Hello. My name is Nadezhda Sergeevna Sidenko.
I am writing to you as a mother who lives in constant fear for her child... 😢💔

My daughter, Sofia, is only six months old. She's still tiny—just beginning to smile and recognize us... But instead of a peaceful childhood, we've already heard the doctors' terrifying words.
Sofia has retinoblastoma—a malignant tumor of the retina. 😭

To stop the disease and try to preserve our little girl's vision, she needs treatment at the specialized Hospital Ophtalmique Jules-Gonin in Switzerland.
A deposit of 55,000 Swiss francs (5,733,392.50 rubles) is required to begin treatment. For our family, this is an unaffordable sum... 💔

One charity has already supported us and covered part of the collection—$14,322—but we still need to raise the rest.

This story is especially terrifying for our family...
Three years ago, we lost a child to this disease.

Our son was misdiagnosed in Kazakhstan. Precious time was lost. By the time it became clear what was happening, the disease had already progressed too far.

Our boy was discharged home to die.
Without help, without a palliative care unit...
We held him in our arms, heard his cries of pain, and watched him slowly fade away. He fell into a coma and died five days later. 😭🕯️💔

We tried to move on... We were told there was no genetic cause, and we believed this nightmare would never return.

But now the same disease has struck our little Sofia. 😢

In Kazakhstan, doctors are simply suggesting removing the eye.
But in Switzerland, they are ready to fight for our girl's sight. Sofia is in stage two, and there is a chance to save her eye and at least part of her vision.

I'm asking you as a mother who has already lost a child... 🙏
Help us not experience this tragedy again.

I can't bear to lose another baby... 😭💔
Please help us save our Sofia. 🕯️

🆘 We could lose our daughter... 😭💔

Sofia is only a few years old. Instead of a carefree childhood, her life is spent between hospitals, examinations, and difficult treatments... 😢

She was born in August 2022, a healthy girl. We made plans, rejoiced at her every step, every word. But when Sofia turned two, everything changed dramatically... 💔

At first, her legs started hurting. We thought it was just fatigue or the aftermath of an infection. But the pain intensified. Our little girl stopped running, then began walking with difficulty and crying in pain... 😭

Then came hospital visits, tests, and endless examinations. Sofia had hip surgery and a biopsy.

Then came the words that break a parent's heart:
neuroblastoma, stage four, metastases... 💔

From that moment on, a difficult fight for life began. Sofia underwent numerous rounds of chemotherapy 💉, a complex tumor removal surgery 🔪, high-dose therapy, a cell transplant, and radiation therapy.

Her tiny body endured tremendous trials. There were days of severe pain, weakness, and a difficult recovery… 😢

We thought the disease was retreating. After treatment, the tumor shrank significantly, and we began to hope for a peaceful life.

But in October 2025, an examination revealed a return of the disease… 💔

And in February 2026, her condition worsened again—the tumor began growing even faster. 😭🕯️

Doctors say the current treatment can only temporarily control the disease. But there is another method abroad—CAR-T therapy—that could help Sofia.

The cost of treatment is $20,300 💔

This amount is unaffordable for our family…

🙏 Please help us fight for our daughter's life. Every support is an opportunity to continue treatment and not give up.

We really want Sofia to live... 😭🕯️💔

🆘 I look at my daughter again and I'm afraid I might lose her... 😭💔

When Nastya was born, we couldn't even imagine that one day we'd be living between hospitals and fearing for her life. She was a normal, healthy child, our joy.

But it all started with a small bruise under her eye. They told us it was nothing, that it would go away. We believed... until the bruise began to grow and turn into a tumor.

During surgery in Moscow, the doctors saw something terrifying—the tumor had already surrounded the eye and had grown deep into the tissue. After a biopsy, we were told what breaks any parent's heart: our daughter had cancer.

From that moment on, a life without ordinary days began. Only hospital walls, difficult treatment, endless IVs, and fear for her every breath. After the first course of treatment, Nastya stopped walking and stopped talking. We had to teach her to stand on her own two feet and smile again.

She survived 15 rounds of chemotherapy, severe complications, and broken legs. Her tiny body endured incredible things.

In the summer of 2025, for the first time in a long time, we saw her alive and happy again. She walked, played, and laughed. We thought it was all over.

But in January 2026, an examination revealed what we feared most – the tumor had returned.

Today, Nastya plays and laughs again, unaware that the disease is close at hand. And we live with the constant fear of losing her.

We decided to continue treatment in Israel because we've already done everything possible here.

🙏 Please help us fight for our daughter's life.
We just want Nastya to live... 💔😭🕯️

I'm writing this as a father... and it's hard for me to admit out loud what's happening to my daughter... 😢

My little Sasha is slowly fading away before my eyes... 💔

Sasha was born in December 2020 in Rostov-on-Don. Everything seemed normal for the first few days. But by the tenth day, her body stopped accepting nutrition. Food wasn't digested, dehydration set in... signs of intestinal obstruction appeared... Her weight stopped gaining, and then began to rapidly drop... 😭

We visited hospitals, doctors, and federal centers. We were given various explanations for what was happening, but Sasha only got worse... At some point, they started feeding her intravenously because she simply couldn't get nutrition the usual way... 💉😢

In the summer of 2024, she suffered a severe attack of colitis. Fecal impaction, severe intoxication, unbearable pain... Our little girl was literally wasting away in our arms... 💔😭

To try to save her, we sold our apartment and moved to Israel. There, doctors finally found the cause... Almost all of Sasha's colon was dysfunctional. The disease was desmosis coli... 😔

Sasha underwent surgery and received an ileostomy. This helped stabilize her condition, but there's a long road to recovery ahead...

Sasha is now five years old... but she weighs only 9.5 kilograms... That's the weight of a two-year-old... 😢💔

She faces a long rehabilitation:
learning to eat again... weaning off intravenous feeding... gaining weight... restoring bowel function...

We've been through years of pain and have already spent everything we had...

I'm appealing to you as a father who is afraid of losing his child... 😭

Please... help my daughter... 🙏💔

We just want one thing—for Sasha to live... 🕯️😢

I'm writing this with the feeling that time is flying by too quickly... 😭💔
My daughter Lana is only one year old, but her life is already spent between hospital walls, injections, and difficult procedures 😢🕯️

Lana Sherstobitova is my little girl 👶💔
She had just begun to live: reaching out to me, smiling, recognizing my voice... But instead of childhood, a disease has entered her life that doesn't wait and doesn't give her time.

Diagnosis: low-differentiated neuroblastoma of the left adrenal gland 💔
This is an aggressive tumor that develops rapidly and affects even such young children 😭
Lana doesn't yet understand why she's in pain. She just cries and cuddles up to me, and I can't explain to her what's going on... 😢

The toys next to her crib now share space with IVs, and her days are spent undergoing examinations and treatment. 💔🕯️
Doctors recommend continuing therapy at the Schneider Clinic (Israel), which has experience treating children with this condition. 🙏

The cost of treatment is $17,850. 💸
For our family, this is an amount we cannot raise ourselves.

I'm asking you as a mother who is afraid of losing her child. 😭
Help Lana grow up, take her first steps, say her first "mama," and see the world she's only just beginning to explore. 💔🕯️
Please, don't leave us alone.

I'm writing this because the disease is already looming large over my daughter... 😭💔
She's only two years old, and we live every day with the fear that we might not be able to help her in time.

My daughter's name is Liza Varygina 👧💔
She has neurofibromatosis type 1—a disease that can begin to destroy the nervous system, vision, and brain at any moment 😢🖤
We don't know what the next day will bring. We live from examination to examination, from result to result, constantly expecting a blow.

Sometimes at night I wake up and just listen to her breathing... because the fear of losing my child never leaves me for a minute 😭🕯️
She's still so little, she doesn't understand why she's being taken to the doctors again, why it hurts, why her mother is always so anxious... She just hugs me and believes I can protect her 💔

Doctors recommend treatment at a clinic in Israel, where they can stop the progression of the disease 🙏
The cost of treatment is $13,250 💸
For our family, this is an unaffordable sum, and we can't cope without help.

I ask you as a mother... 😭
Help my daughter not be left alone with this disease.
Help Liza live, grow, and see her future 💔🕯️