Thank you, Chair, for the opportunity to appear before you. My associate executive director is with me.
Just at the outset, I'd like to say I've appeared before a large number of standing committee meetings over the last 40 years of my activities in Ottawa, and I am so happy to see the members taking such a terrific interest in this topic. Frequently, standing committees show up with four or five members and it's rather impromptu. It's obvious you take this seriously and I'm really happy to see that.
Mood Disorders Society of Canada is a national, not-for-profit charity managed and membered by people with lived experience in their families. We are active at the national level only, and we have been around since 2011. We are active in many areas, some of which Dave will mention. We become engaged when we think there is an opportunity to do something for the people who need help. Those are the people who live with mental illnesses, whether they're on the street, whether they're veterans, whether they're first responders—whoever we can be involved with to help.
We've focused on that primarily because you can become involved in Ottawa with an awful lot of meetings and a lot of consultations, a lot of round tables, that produce not a whole lot of effective knowledge translation that will assist the people who need help. The material is important, and if you're involved in that stuff, that's fine; it's just not our bag.
One of the things we have done in the past, and we currently do, is become involved with the research community. We became involved with them initially when CIHR came into existence and with Bill C-300. We sat on their institute advisory board for many years. We're founders of the Canadian Depression Research and Intervention Network. The reason we did that is because there is a lot of research out there that I'm sure you've found is not translated into helping people who need help. We try to motivate the researchers and the community generally to pick up what we know will work and get it working, and still support research.
In 2004, we worked to help people with mental illness improve their quality of life. In 2011, we hosted a round table at the War Museum on PTSD. It was called Out of Sight, Not Out of Mind. The entire proceedings are on our website. It involved 75 people from all walks of life, including the Minister of Veterans Affairs, the military chief of staff, and a lot of people who were involved in the then-nascent discussion that PTSD is important.
Out of that came a report and many suggestions for improvement of our attention to PTSD. The recommendations presented in the report included addressing stigma; enhancing the knowledge of physicians and health care providers, which we think is number one on identification and treatment of PTSD; educating PTSD sufferers and their families on available support networks and resources; and promoting ongoing collaboration and dialogue among government and leaders in the field of mental illness specializing in PTSD.
We've looked at the presentations you've had in the last few days and they're terrific. You have a lot of really good information before you and there is no sense our repeating that information for you.
From our perspective, in order to address PTSD and prevent suicide, we would suggest you might look at early diagnosis of mental illness. Early diagnosis of mental illness will help us stop the movement into PTSD and into suicidal ideation. Early diagnosis requires the attention of the medical community to the issues of mental health, which is pathetically lacking at this time.
We would recommend that you increase mental health education among health care providers for the reason I just mentioned.
We strongly believe that peer support needs to be number one on your agenda. Whoever you talk to will tell you that it's the human touch, the human element. Research tells us that peer support needs to be there for you.
I'm going to turn it over to Dave Gallson to give you a bit of an overview of some of our programs.