Six-year-old Artem has suffered from frequent respiratory infections, rhinosinusitis, bronchitis, and gastrointestinal problems since birth. The causes are unclear—doctors suspect cystic fibrosis, primary ciliary dyskinesia, or an immunodeficiency—and are referring the child for various diagnostic tests. And while there is no definitive diagnosis yet, the family is forced to purchase everything needed to treat his symptoms on their own, as Artem cannot receive anything through his compulsory health insurance.
Right now, to take his medication, he needs a new inhaler with nasal and airway attachments—these ensure that the medication reaches its target safely and accurately.
Diagnosing genetic diseases can take anywhere from 6 months to a year. Artem needs help so that he doesn’t go without vital treatment during this time and doesn’t face serious complications that could further worsen the course of his illness.
