I don't mean to take up all of your question time, but I have to put in a very strong word about rare diseases. For our patients, because they don't normally have a good plan of care and their specialists are oftentimes isolated far away, we have patients who say, “I can get a meeting with my family physician, but they know nothing about my disease.”
We come back to needing to have comprehensive plans of care for patients with rare diseases, plans that they can own, that they can hold. This is what many other countries do. We need to have the ability for patients to manage their care, and then they can actually have access to what we hear is happening in cardiovascular disease, in cancers and in other conditions. For us, this is something that has actually turned into a nightmare for most patients, because they can't get access to others who would actually know anything about their disease.