We have not heard back from anyone.
Just thinking and listening to everyone, I sort of want to stress something. We were called out as a patient organization for spreading disinformation and being an opponent, yet we agreed with some of the changes made by the PMPRB, so I find this very curious and wanted to make that clear.
We also were asked to be part of a consultation, and we took our time. We are very busy. We are trying to get a drug funded in Canada, which is no small feat for a rare disease, so I wanted to make that clear.
In terms of the investigation, it is outlined in the CF treatment society letter. We would be looking for the guidelines to be stayed while we look at the conduct of the PMPRB, how they are consulting with patient groups, and then how they maligned us in this, or intended to. They maligned us in the document. Whether the document was put into action, I couldn't say.
As I said earlier, the board chair doubled down on this, and so did Mr. Clark, who was asked about it in a media report. There is nothing wrong with combatting...or doing a communications plan. Calling people liars and spreading fake news about those who are trying to do the best they can as a charity and for the community, I find really concerning. I think you should be concerned. I think the Prime Minister should be concerned, and I think the health minister should be concerned.