Answer:
There is no cure for cystic fibrosis, but treatment can ease symptoms and reduce complications.
Explanation:
1). For those with cystic fibrosis who have certain gene mutations, doctors may recommend a newer medication called ivacaftor. This medication may improve lung function and weight, increases the activity of Cystic fibrosis transmembrane conductance regulator (CFTR)protein and reduce the amount of salt in sweat. It has been approved by the Food and Drug Administration for people with cystic fibrosis who are age 6 and older. The dose depends on your weight and age.
2). For people with a certain gene mutation who are age 12 and older, another drug is available that combines ivacaftor with a medication called lumacaftor. This drug is called orkambi.
The use of Orkambi may improve lung function and reduce the risk of exacerbations.
I hope you're clear on this Daxxy
It depends on where your going and how many people are going to the trip. But in my opinion I think about 3 times because you need to make stops when you need to use the restroom and when your hungry.
Sorry if I am not right :(
I hope I helped you have a great day :)
Liver
In pediatric patients, the liver and spleen are very large in
proportion to the size of the abdominal cavity and are more easily injured. The
soft, flexible ribs of infants and young children do not protect these two
organs very well and may allow injury to underlying organs, even without fracturing
the ribs.
Answer: The cell is eukaryotic because it contains mitochondria
Explanation: Because I said so but really this is the answer
