"Cystic fibrosis is a struggle for every new breath."
"Get stronger, your daughter has cystic fibrosis," said the doctors, which meant fighting, fighting for every new day, every new breath!
Since then, the parents of seven-year-old Nicole have been doing everything to make their daughter feel good. Today, Nicole's life is about frequent visits to doctors (the girl has difficulty breathing, barely breathing, sleeping with her mouth open), daily treatment with enzymes, courses of antibiotics, inhalation procedures, special meals. However, it all costs money and a lot!
Cystic fibrosis (CF) or Cystic fibrosis is the most common hereditary genetic disease, affecting mainly the lungs and digestive system. Necessary treatment due to constancy and high cost is not available to 90% of patients and therefore few people live to 50 years, and others die in 5 years.
We can influence the fate of a beautiful, large family of Abkhazians! Nicole is ready to accept for diagnostics and treatment in the Medical Center "Shaarei Tzedek" (Jerusalem), where she will have the opportunity to continue treatment started by leading specialists using the latest medical technologies.
The cost of one course of treatment is 170 000 rubles. To date, this is an unaffordable amount for a large family of Nicole.
Let's help little Nicole, for whom life is a constant struggle for every new day, every new breath.
For us it is a small sum, and for Nicole - the price of life!
