Natalbany family, others, who rely on medicine now touted as coronavirus treament, worry about supply – The Advocate
Kaydence Lusk was just five months old when she was diagnosed with a rare lung disease. The seven-year-old is now in second grade, rarely needs to take oxygen and, earlier this year, was able to enjoy a trip to Disney World with her family, through the Make-A-Wish Foundation. Her disease, so rare that only eight… Read More »