5-year-old Krzyś is fighting with Duchnne's muscular dystrophy. The TVN Foundation joined the help

The TVN Foundation joined in help for 5 -year -old Krzysie, who is struggling with Duchnne's muscular dystrophy – a rare disease leading to muscle atrophy. For his treatment you must collect several million zlotys. All collected funds paid to the Foundation's account with the note “For Krzysia” will be transferred to the boy's treatment. – We had a hill all the time. And now so many nice things meet us – admitted in an interview with tvn24.pl Mr. Łukasz, the boy of the boy.

5-year-old Krzyś Zawada is struggling with Duchnne's muscular dystrophy, a rare genetic disease that leads to a progressive and irreversible muscle atrophy. The boy began to observe her symptoms when he was eight months old.

The Siepomaga Foundation has created a fundraiser for special gene therapy in USAstay and flights, treatment and rehabilitation. However, you need to collect over PLN 14.5 million. Until now, half of this amount has been collected – just over 7.5 million zlotys.

Now the TVN Foundation has also joined the help for Krzysia. All collected funds paid to the Foundation's account with the note “For Krzysia” will be transferred to the boy's treatment. Payments can be made through the Foundation's website https://fundacja.tvn.pl/.

– I don't know what to say. Your foundation is now saving our lives. I am really touched and I do not know how to thank that such a thing is now. Because we really had uphill all the time. And now so many nice things meet us – said Mr. Łukasz, the boy's father in an interview with tvn24.pl.

“Krzyś, our little son, lives with a sentence that has given him a deadly illness. He suffers from Duchaenne's muscular dystrophy … His muscles disappear, and we are desperately fighting for the rescue. We found ourselves in a situation where we must once again begged for help. This time it is not about rehabilitation stays or treatment. The US doctors want to give children from 4 to 5 years old. Genary therapy is a method that can change everything. – we read in the description of the collection.

“Muscles … They allow us to move, walk, grab, but also smile, speak, eat and breathe … Everyone wants them to be functional and strong. When they weaken despite the hard work, a real drama takes place. Man loses more skills … he stops moving, swallowing, breathing – his life depends on the wheelchair, respirator and probe … Loved son ” – write the boy's parents.