Let's save little Szymon!

The moment Szymon was born our life was about to change and grace us with tenderness, happiness and joyful laughter.
Our first son  just came into this world. What could possibly go wrong?
Yet, about a year ago stormy clouds  appeared over this peaceful life...

Little simon was diagnosed with Cavernous Transformation of the Portal Vein (CTPV) as well as pulmonary hypertension.Problems started to pile up quickly... What made matters worse, was the rare nature of Simon's condition. In order to get full diagnostics of the issue we decided to seek help in Brussels, Belgium.

Doctors both in Poland and Belgium were unanimous. The only solution would be a liver transplant from a family member.

The time is of essence and the surgery must be performed  as fast as possible. This is the only way to ease the pain and experience normal childhood outside the walls of a hospital.

Lingering with the surgery might lead to horrible implications. We cannot let this happen! However, we can't deal with this task alone and we kindly ask people of good will for any sort of financial support.

The surgery needs to take place in a clinic in Palermo, Italy, and the total cost left us speechless and almost hopeless...

The donations from our relatives and friends will not be enough to cover this pricey undergoing.

That is why we ask you for any donations to make this happen.

With kind regards,
Monika and Marcin, Simon's parents