Skarbonka

Nowy bonus/ Pomoc dla Malgosi/ Help Malgosia

Avatar organizatora
Organizator:Ewelina

Skarbonka została założona z inicjatywy organizatora, który odpowiada za jej treść.

 

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

I jeszcze raz!!!!! 2500PLN  po raz kolejny 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!!!!

2000 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 

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

 

 

160 192 złCEL: 25 000 zł
Wsparły 7074 osoby

Wszystkie środki zebrane na skarbonce trafiają
bezpośrednio
na docelową zbiórkę:

Przekaż 1,5% podatku

Numer KRS0000396361
Cel szczegółowy 1,5%0123687 Margarita

 

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

I jeszcze raz!!!!! 2500PLN  po raz kolejny 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!!!!

2000 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 

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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