DALLAS, Tex. (Ivanhoe Newswire) -- Each year, a thousand children are born with cystic fibrosis. Kids with it are not expected to live past their thirties, but now many could live much longer.
Rylee is a girl on the go. She won’t let her disease slow her down.
“I have cystic fibrosis,” Rylee, who has cystic fibrosis, told Ivanhoe.
Cystic fibrosis causes the body to produce a thick mucus that clog the lungs and pancreas, making it difficult to clear the lungs and break down food. A child with CF constantly fights infections and to maintain a healthy weight.
“Any kind of plan that we had for the future or dream that we had for our daughter was completely shattered,” Amy, Rylee’s mom, told Ivanhoe.
A year ago Rylee, was taking 20 pills a day. Now, she’s only taking one!
“They’re magic pills,” Rylee said.
Kalydeco is the first drug that targets the underlying cause of CF, the defective protein called CFTR. In some patients, this protein does not allow fluids to clean the surface of the lungs that can cause deadly infections.
“That infection can fester because it just doesn’t move,” Carolyn Cannon, MD, Director of the Pediatric Cystic Fibrosis Care and Teaching Center at Children’s Medical Center at Dallas, told Ivanhoe.
Kalydeco restores the function of the CFTR protein, clearing out the lungs, and relieving symptoms of the disease.
“It is absolutely a game changer. It changes their life,” Dr. Cannon said.
Giving kids like Rylee a chance for a long, healthy life.
“I can dream anything for her now,” Amy said.
Not only does Kalydeco take away the symptoms for some kids with cystic fibrosis, doctors believe it might allow them to live decades longer than expected. Kalydeco was recently FDA approved for kids over six. Rylee is using it off-label and is the first child under the age of six to start on it. The drug costs 300,000 dollars a year, but Rylee’s insurance pays all but 90 dollars a month. MORE.
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