Leonardo needs treatments for cystic fibrosis

Hello everyone,

Leonardo is 3 years old and was born with cystic fibrosis, a rare genetic disease. Cystic fibrosis is a genetic disease that primarily affects the lungs and digestive system, causing thick, sticky mucus to build up in these areas, which can lead to serious respiratory and digestive problems. He was born premature and needed resuscitation. He spent 40 days in neonatal intensive care. He always had respiratory problems and lungs colonized by bacteria. He also suffers from severe constipation and intestinal obstruction syndrome due to the disease. Pancreatic insufficiency causes chronic malnutrition. There is no cure for his illness, only expensive treatments. The prognosis is unfavorable since it is a degenerative disease with no cure, which reduces his life expectancy. For Leonardo to have a better quality and life expectancy, he needs to follow lifelong treatment. This treatment costs approximately 100,000 a month, and in relapses, the cost can increase significantly. Cystic fibrosis is a rare, expensive disease with a low life expectancy, often fatal in childhood or adolescence. His life depends on these treatments. We ask for your support to continue with little Leonardo's treatment so he can have a better quality of life since his mom suffers from lupus which affects several parts of her body and makes it difficult for her. solve both diseases. Thank you very much in advance. It would make me very happy if you used the [Help by sharing] button to share my project!