David dreams, parents dream

Cystic fibrosis is a disease in which daily cycles of quality inhalation are vital. Otherwise, the lungs of the patient are clogged with viscous sputum, which is almost impossible to cough up, and pulmonary infections become chronic and gradually destroy the lung tissue. Powerful nebulizers that are able to provide the proper quality of the procedure are very expensive, so David is still doing inhalation using a simple device and this is dangerous. We ask for help to pay for the equipment that will help the guy to live.

 And David tries to live as fully as he can. Friendly, open to people, David seeks to socialize with peers, likes to skateboard, skate, bike, and ride with friends. It is difficult to communicate at times, because when all the friends go to school, David studies at home. Not always his state allows going out or inviting someone home. David is fond of mathematics, computer science, English and dreams of traveling a lot in the future. The parents’ only dream is just to have this future for their son.

Living with cystic fibrosis is difficult and… expensive. However, if help comes, it is possible.
As part of this project, we plan to pay for a high-quality, powerful Pari Turbo Boy inhaler and supplies, sterilizer for decontamination of all its parts, and a bactericidal lamp for David.

The latter will help the guy to reduce the risk of infectious diseases and to safely survive the coming winter.

Name: David Godun, January 24, 2009

City: Krivoy Rog

Diagnosis: Cystic fibrosis with pancreatic insufficiency