We know the importance of lowering drug costs. As you know, 4,300 people suffer from this rare genetic disease. Most of them are children and young adults. One young woman from Calgary is a CF champion, fighting for her passion to be a famous opera singer. She's very talented. Her reality of living with CF has meant that she has had many visits to the hospital and had many health crises that have made singing impossible for a time.
CF patients are waiting for this drug, which was fast-tracked in other countries. Now it seems that the changes to the PMPRB will cause further delays or complications. Will the minister delay the implementation and review the PMPRB?