Inhalations save lives. 4

"Where I can take more energy to get through all these things? It’s just morning.." the mothers of children with cystic fibrosis think like this when waking their children up to morning procedures and inhalations. Not one single inhalation, not two, and not even three, but at least, five or more than ten. Every day. Without any break. All their lives. Only super powerful nebulizers can withstand such load and their cost is rather expensive... That’s why our equipment waiting-line is not decreasing.

We buy the nebulizers, distribute them... and, at the same time, we receive more and more new requests. We cannot afford to waste any precious drop or milliliter of medicine which is so expensive and so hard to get…We can not afford the scariest thing to happen - to not cope with the disease, to let it win.

Do you know that cystic fibrosis is the widest spread genetic disease of the European race? It affects all systems, but especially the lungs and gastrointestinal tract. These problems and diseases seem to be far away - but they are very close, as a child with cystic fibrosis can be born practically in any family. And we can not leave those who have faced such terrible enemies cystic fibrosis - neither adults nor children.

They write to us: "We have got a prescription for Pulmozim (extremely expensive Mucolytic), and we have a low-power inhaler, please help us with professional PARI nebulizer"."We have already used our PARI for 5 years and it ceased to nebulize thoroughly, please help us with the new one”. And we know that quality of treatment of these people, their health, and their lives directly depend on the quality of the equipment.

We can help them not give up on illness. That is why we do not close our project for powerfulPARI nebulizers but proceed with collecting funds for new ones, and we believe that someday this waiting-line for free breathing will disappear... And no one will have to wait to breathe.