Inhalations save lives. 6

Imagine that your life depends on medical devices. To be honest – this is rather nervous experience. The treatment protocol states that daily inhalation is mandatory for cystic fibrosis (in moderate or severe disease progress there may be 8 or 16 inhalations per day!). But a sick child does not even need to read the protocol, she feels: did not inhale - and you are difficult to breathe, you start to suffocate and do not have the strength to go to the next room...

Sometimes the condition of the patient may be worsened very quickly, sometimes rather slowly without being noticed, but anyway – this is a fact that without regular inhalations lungs are clogged with viscous sputum with infections, breathing becomes difficult. Our cheap inhalers, having such a load, get broken very quickly. The most part of our patients can not buy at once a professional model of the inhaler. That's why they need help from outside. They really need your help. 

Cystic fibrosis is a severe genetic disease, one of the most common among Caucasians. It affects the whole body, disrupting the internal organs. This diagnosis is characterized by a special vulnerability to pre-infectious diseases and especially severe and long-term course of disease, they often become chronic. Cystic fibrosis is characterized by increased viscosity of sputum in the lungs, thus it clogs the airways and interferes with breathing. That is why lungs cleaning becomes a daily task.

Due to the support of philanthropists, our foundation has already supplied more than 230 high-quality inhalers. However, new patients requiring the same help are constantly appeared on our radar. In this project we are raising funds for 4 new sets of Pari inhalers with extra sets of consumables for them. The effectiveness of daily treatment of our patients and sooner or later their life time will depend on the availability of high-quality device. Please, help them!