Urgent!
Egor Yarmalovich - main photo

A therapy worth MILLIONS is the only chance❗️Save Egor❗️

Fundraiser goal: Gene therapy in Dubai

Fundraiser organizer:
Egor Yarmalovich, 9 years old
Grodno
Duchenne muscular dystrophy
Starts on: 28 April 2025
Ends on: 2 June 2026
PLN 51,120(0.42%)
Still needed: PLN 12,019,579
DonateDonated by 675 people
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Phone number
75365
Text
0806141
Cost PLN 6.15 gross (including VAT)
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KRS0000396361 The Siepomaga Foundation
Purpose of 1.5% of tax0806141 Egor

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  • VIktoryia Karalkova
    VIktoryia Karalkovahas been supporting for 2 months
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Fundraiser goal: Gene therapy in Dubai

Fundraiser organizer:
Egor Yarmalovich, 9 years old
Grodno
Duchenne muscular dystrophy
Starts on: 28 April 2025
Ends on: 2 June 2026

Fundraiser description

I noticed the first symptoms of the disease when my son started crawling. He was doing it in a very unique way, using only his arms without engaging legs. When sitting down, he often fell down. The doctors said: hypotonia. Unfortunately, rehabilitation was not helping and I was more and more worried. Today, I am fighting for my son’s life. Igor was sentenced to death...I am begging for help!

When he turned 4, we did additional tests. Then, it seemed that the doctors were wrong and that hypotonia is not the source of my son’s issues. They were looking for a correct diagnosis for a long time and when they finally found it, our world fell apart...

It turned out that my son is suffering from DMD – a serious and terminal muscular disease which left untreated, leads to a long, painful and premature death!

Currently, Egor is on steroids, exercises daily, participates in rehabilitation sessions and tries to fight for the best possible mobility. The doctors claim that at this moment, my son’s condition is good but the disease is going to progress, and he is going to feel worse each day…

My son started complaining about pain in his legs more often. When I walk him to school, we have to often make stops and sit down on a bench. Igor cannot jump, run or play like other children...

Gene therapy is the ONLY chance for my child. There is no other treatment. I have to pay over 12 MILLION PLN. Otherwise, my child will be taken away by death. Egor will pass away in great pain, suffering and not knowing why he does not deserve to have a regular childhood and life...

I cannot allow for this to happen! I have to do everything possible to save his life. I have to...

I only need your help. A regular person does not have so much money but unfortunately that is the price for my son’s life. I have to do everything to raise this huge amount. Egor has to live!

I am sincerely asking for support. Only with your support a miracle can happen...

Egor’s Mum

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