Money box

Szósty Bonus dla Malgosi/ Help Malgosia

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Organizer:Ewelina

The money box was created on the initiative of the Organizer who is responsible for its content.

 

 Razem dla Malgosi!!!!! Następny bonus czeka!!! DZIEKUJE WSZYSTKIM KTORZY WSPIERAJA MALGOSIE!!! TYLKO RAZEM NAM SIE UDA!! 

I jeszcze raz!!!!! 2500PLN  po raz szósty będzie dodane jako bonus gdy zbiórka osiagnie 100%

This little girl, Malgosia,  suffers from SMA type 1, Spinal Muscular Atrophy. 
As you might know the disease is  deadly cruel and every day  takes a  piece of this littlegirl away, her muscles deteriorate instead of developing,. She is now 7 years old and moved with her parents to Poland as it was the way to slow down the progression of the desease by getting refunded drug, otherwise surely she would not get even get to her 2nd birthday. She wanna go to school as all other kids, she is bright and full of life but....  she can't , SMA destroys her muscles every day. 

Please help  before it's too late!!!!

2500 PLN będzie dodane jako bonus gdy zbiórka osiagnie 100%

 Malgosia has been qualified for getting USA gens therapy (Zolgensma) drug but that costs 9.000000 PLN. We can still help her in getting it on time, the weight limit is 13,5Kg, she is 11kg now.

Why is the drug so expensive:

https://www.drugs.com/cdi/zolgensma.html (opens a new tab) 

Lets do it together!!

500 EUR will be added to the funds after the goal of 250000PLN has been reached 

6 PLN = 2,23 EUR

10 PLN = 4,46 EUR

 50 PLN = 11,15 EUR

 

 

PLN 185,135GOAL: PLN 250,000
Donated by 7987 people

All funds accumulated in the money box are transferred
directly
to the target fundraiser:

Pledge 1.5% of tax

KRS0000396361
Purpose of 1.5% of tax0123687 Margarita

 

 Razem dla Malgosi!!!!! Następny bonus czeka!!! DZIEKUJE WSZYSTKIM KTORZY WSPIERAJA MALGOSIE!!! TYLKO RAZEM NAM SIE UDA!! 

I jeszcze raz!!!!! 2500PLN  po raz szósty będzie dodane jako bonus gdy zbiórka osiagnie 100%

This little girl, Malgosia,  suffers from SMA type 1, Spinal Muscular Atrophy. 
As you might know the disease is  deadly cruel and every day  takes a  piece of this littlegirl away, her muscles deteriorate instead of developing,. She is now 7 years old and moved with her parents to Poland as it was the way to slow down the progression of the desease by getting refunded drug, otherwise surely she would not get even get to her 2nd birthday. She wanna go to school as all other kids, she is bright and full of life but....  she can't , SMA destroys her muscles every day. 

Please help  before it's too late!!!!

2500 PLN będzie dodane jako bonus gdy zbiórka osiagnie 100%

 Malgosia has been qualified for getting USA gens therapy (Zolgensma) drug but that costs 9.000000 PLN. We can still help her in getting it on time, the weight limit is 13,5Kg, she is 11kg now.

Why is the drug so expensive:

https://www.drugs.com/cdi/zolgensma.html (opens a new tab) 

Lets do it together!!

500 EUR will be added to the funds after the goal of 250000PLN has been reached 

6 PLN = 2,23 EUR

10 PLN = 4,46 EUR

 50 PLN = 11,15 EUR

 

 

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