Heart 4 Susan

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The life of my 4 year old niece Susan from Poland is in jeopardy. Her aorta has narrowed down to half its previous size. Today, the vessel's lumen has a diameter of 2.5 mm - life threatening.
Every moment counts, and every euro counts and Zuzia has to get to Boston Children’s Hospital for the life-saving surgery as soon as possible. The first surgery is scheduled on 28th of Februrary 2024, followed by main surgery on 7th of March, and there is still 117,000 Euro to collect before end of January when the payment has to be transferred (full amount of EUR 311,000) . Time is running out, with just a few weeks left .
Please help this little Sparkle enjoy not only this Christmas but also many more to come. 
Susan was born in June 2019, and the moments following delivery her parents (my family) were informed that she has a congenital heart defect. Further diagnoses were even more heart-wrenching - a rare genetic disease, Williams syndrome. She has supravalvular aortic stenosis, pulmonary artery stenosis, cardiomegaly, and hypertension. The doctors did not sugarcoat the seriousness of the situation.
Doctors in Poland cannot help her anymore, and her only way-out to life is in Boston's Children Hospital in the USA.
On behalf of my cousin Natalia (Susan's mom) and her husband Maciek, I kindly ask for your help.
Thank you for your support,
Aunt of Susan - Paula Fusiara
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The life of my 4 year old niece Susan from Poland is in jeopardy. Her aorta has narrowed down to half its previous size. Today, the vessel's lumen has a diameter of 2.5 mm - life threatening.
Every moment counts, and every euro counts and Zuzia has to get to Boston Children’s Hospital for the life-saving surgery as soon as possible. The first surgery is scheduled on 28th of Februrary 2024, followed by main surgery on 7th of March, and there is still 117,000 Euro to collect before end of January when the payment has to be transferred (full amount of EUR 311,000) . Time is running out, with just a few weeks left .
Please help this little Sparkle enjoy not only this Christmas but also many more to come. 
Susan was born in June 2019, and the moments following delivery her parents (my family) were informed that she has a congenital heart defect. Further diagnoses were even more heart-wrenching - a rare genetic disease, Williams syndrome. She has supravalvular aortic stenosis, pulmonary artery stenosis, cardiomegaly, and hypertension. The doctors did not sugarcoat the seriousness of the situation.
Doctors in Poland cannot help her anymore, and her only way-out to life is in Boston's Children Hospital in the USA.
On behalf of my cousin Natalia (Susan's mom) and her husband Maciek, I kindly ask for your help.
Thank you for your support,
Aunt of Susan - Paula Fusiara