How will Ania breathe? 2

Despite a serious congenital disease, Anya is a cheerful and brave girl. But when the electricity goes out, the tension in the whole family increases, because it means that the girl will not be able to make the vitally necessary  inhalations. Cystic fibrosis is a very serious and dangerous disease, and every missed procedure means a worsening of the girl's condition. A loud cough, sputum that makes it difficult to breathe, shortness of breath, a drop in saturation... This cannot be allowed.

Treatment of cystic fibrosis is daily hard work: medication, high-calorie diet, inhalations, physiotherapy, expectoration. Only in this way there is a chance to survive and live a long, quality life. And in previous years, fighting the disease was difficult and extremely expensive (the state provides only part of the treatment), and with the outbreak of a full-scale war, it became many times more difficult. Every day brings new challenges to the families of patients. Due to frequent and long power outages, Anyuta misses inhalations. The solution to this huge problem can be a portable charging station, to which Anya will connect the inhaler. We ask you to help purchase this life-saving device, on which the girl's life and health depend.

In order for inhalations to be effective, you need to change the cups and tubes, which wear out due to frequent use. Therefore, we have included 2 such sets for Anya. In order to make it easier to clean the lungs from sputum, Anyuta needs to practice with a special breathing simulator – a flutter. The vibrations created in the simulator during exhalation have a bronchodilating effect and will help the girl cough up sputum more easily. Also, we will pay for fuel for the generator, which will insure the family during long power outages, because during exacerbations, the girl also needs to connect an oxygen device.

It all sounds and looks complicated and even scary. But when Anya receives help, she will be able to breathe freely.