Days of life for Katrusia

"Mom, please buy only dresses for me'', says Katrusia, looking away from jeans. She is such a girl at her 6 already. But her mother Viktoriya has some other choices to make. Katrusya should take a lot of medicines every day and do physical exercises not to be sick and grow up. If you are born with cystic fibrosis, you will not live a day without this. And her mom should think how to pay for all this because it is just impossible for an ordinary Ukrainian family!

Our today’s task is to help Katrusia’s mother to pay for the powerful Pari nebulizer. Only such kind of nebulizer can withstand the load of some inhalations per day and provide adequate quality services for several years. This is the only model that economizer medicines because it leaves the least residue of the medicine on the nebulizer walls. When the girl’s life literally depends on every day inhalations, this is very important. Then, the medicines we are planning to buy in this project will help the girl better and be more effective.

Besides, there is a kind request to us to buy a home trampoline for a girl. It is not only fun for a kid with cystic fibrosis, but also a possibility to do physical exercises which improve the process of lungs clear out and help to breathe more freely.
First two years of her life Katrusya spent mostly in the hospital until they managed to stabilize her. But even the slightest flu is still a torture. This disease is characterized by this peculiar feature. The number of days of Katrusia’s future life directly depends on the quality of everyday treatment.

Let's do what we can for her to have as much of them as possible!

Name: Bulanenko Kateryna, 14.11.2010

City: Kropyvnytskyi

Diagnosis: cystic fibrosis with pancreatic insufficiency