Win a fight for life. 2

"I wrote an application to all the institutions, went to the parliamentary sessions, and addressed everyone. "Wait, there is no money", they say or promise without result", Ania tells. Meanwhile, her disease, cystic fibrosis, does not wait: without the necessary therapy, it destroys the body depriving the ability to breathe. The families of the patients with the same diagnosis often help Ania with the medicines: each providing one bottle or one packaging. But you will not live out for a long time in this way. To live Ania needs help from all of us. 

Cystic fibrosis is a severe genetic disorder affecting the entire body. A small failure in the structure of the DNA and now all the organs are working somewhat differently, not in the way it was envisaged by nature. And gradually they fail. In order to slow down this process, to keep the body fit for life as long as possible, a person with cystic fibrosis requires constant complex therapy. Medicines are just one of its components, but it's imperative to take them in time and in full. The standard procedure for cystic fibrosis treatment is the same throughout the world, and only through its compliance, the patients in Europe and the United States live for many years.

Thanks to the help of the good people and the UBB team, we have already helped the girl with the medicines, we also bought oxygen machines and other equipment, which increases the efficiency of home treatment and facilitates Ania's life. Now we kindly ask you to help to pay for a six-month supply of medicines to support her daily therapy. Ania's life literally depends on the availability of these medicines. And we really want her life to belong.

Earlier at UBB, we have already collected funds for Ania. View previous projects you can by the link.

Name: Ostroverha Anna, 22.12.1991

City: Tabanove village, Kirovograd region

Diagnosis: cystic fibrosis (mixed form, severe)