That's a great question. Thank you.
It has been very prevalent of late. We've had workshops the last two years at our AGMs that have been standing room only. We've actually had to turn people away who wanted more information, wanted to know where they can go, whom they can see, and whether they are normal. It's important for people to know that it's okay for people to talk about it; that it's an illness, it's not your fault. I think breaking those kinds of stigma is an important step that we can take.
Funding the work that Andria Jones-Bitton is doing at the University of Guelph for perhaps setting up her network would be fantastic, because now we have a central point for people to go to and to start from. There are folks such as Heather as well.