Thank you, Mr. Chair.
I'd like to start with Cystic Fibrosis Canada because you mention some public information that I released once I had obtained it.
My experience has been that patient advocacy groups like yours and others are usually made up of teenagers who have a particular condition, and parents who are very active in it because it's very personal to them. I have three kids with a rare disease. I have a daughter who passed away just a few years ago from a different rare disease, so it's personal to me as well.
Can you tell me whether the people involved as advocates are paid lobbyists or parents?