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Szymon i Ignacy Kropielniccy - main photo

Our sons were diagnosed with a terminal genetic disorder❗️HELP❗️

Fundraiser goal: Five stem cell injections

Szymon i Ignacy Kropielniccy, 3 years old
Laszczki, mazowieckie
Pelizaeus-Merzbacher disease (PMD)
Starts on: 8 July 2024
Ends on: 30 September 2024
PLN 106,044(107.46%)
Donated by 1262 people

Pledge 1.5% of tax

KRS0000396361
Purpose of 1.5% of tax0605337 Kropielniccy

Fundraiser goal: Five stem cell injections

Szymon i Ignacy Kropielniccy, 3 years old
Laszczki, mazowieckie
Pelizaeus-Merzbacher disease (PMD)
Starts on: 8 July 2024
Ends on: 30 September 2024

Fundraiser result

Kochani Darczyńcy! Z głębi serca dziękujemy za Waszą nieocenioną hojność i wsparcie, które umożliwiły chłopcom dostęp do kluczowej pomocy w ich walce o lepsze życie!

Dzięki Waszym darowiznom mają już za sobą pierwszą procedurę przeszczepu komórek macierzystych. Jesteśmy ogromnie wdzięczni za Wasze zaangażowanie, czas i środki przeznaczone na ten wyjątkowy cel 💚

Ignacy Kropielnicki

Wasza pomoc napełnia nas nadzieją, a chłopcom dodaje sił do dalszych działań.  Pamiętamy o Was z wdzięcznością w naszych myślach i modlitwach. Wasze wsparcie ma dla nas nieocenioną wartość.

Zachęcamy również do odwiedzenia naszej strony na Facebooku SuperBliźniaki,  (opens a new tab)gdzie regularnie informujemy o postępach w leczeniu. Wciąż można też wspierać chłopców przekazując 1,5% podatku. Będziemy wdzięczni, jeśli zechcecie pamiętać o nas podczas rocznych rozliczeń.

Z wyrazami wdzięczności,

Rodzice Ignacego i Szymona

Fundraiser description

February 21, 2023, our dream of becoming parents again came true - our twin sons Ignaś and Szymuś were born. They were both healthy and received an Apgar score of 10. After we returned home, we thought, from now on, we would all live happily ever after. Unfortunately, cruel fate decided otherwise. 

When our boys turned three months old, they had reached the developmental milestones of a one-month-old. We started searching for the reason for this abnormality. Their symptoms, like nystagmus, club foot, and delayed psychomotor development, kept us awake at night. 

Although the doctors said that all children tend to develop at a different pace, thanks to our determination and advice given by physical therapists, we found a doctor who didn't take our concerns for granted and referred our children for detailed testing and examination. At five months old, our sons underwent MRIs that detected brain lesions. Further genetic test results showed a horrifying diagnosis - Pelizaeus-Merzbacher disease, an incurable genetic disorder that leads to death.

It tore our hearts apart! How could that have happened to our babies?! Today, we can only count on the development of medical technology, and we do our best to guarantee our boys the best quality of life and provide them with the best tools for growth, like rehabilitation, cutting-edge medical equipment, and imported dietary supplements. We pay for most of the expenses and medical bills out-of-pocket. 

Recently, Ignacy and Szymon have been qualified by the Children's Hospital in Lublin for stem cell therapy - five injections, to be exact. If the treatment goes well, it must be repeated every nine months. Unfortunately, these procedures are too expensive for us, and we cannot afford them. We must ask you for support! Please help us fight for our children! 

The parents

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