Sasha needs access to quality treatment

For almost 14 years of her life, Sasha was treated incorrectly. She tried to cope with constant bronchitis, disorders of the gastrointestinal tract, and many concomitant diseases. And only now doctors have established the correct diagnosis - the genetic disease of cystic fibrosis. Much time has been lost, so the family must quickly catch up with a treatment to save their daughter.

The mother understood something was wrong with her child but was not ready for an incurable diagnosis. So, her first reaction was despair. And then the hours of consultations and training in a new way of life began. To live and breathe, you must take medication daily and perform inhalations and physical therapy. This is the only way to keep the disease under control. Sasha looks like an ordinary teenager with dreams and hobbies, but she is very thin – only 34 kg. People with cystic fibrosis don't digest food in a necessary way. Every 100 grams is essential for resistance to the disease. Therefore, the girl needs a special high-calorie diet. 

When you see an extensive list of equipment (inhaler, sterilizer, germicidal lamp, breathing simulator) and medicines that can help your child, but not even half of the necessary funds, there is only hope for people of goodwill. Please help Sasha overcome the disease.