This strategy is already working: This week, our Communications Department worked directly with the Seattle Times to include our video in the paper’s latest story on anosognosia. Read it here.
As Executive Director Lisa Dailey is quoted as saying, "If you are building a system that is based on the idea that anyone can and eventually will recognize that they need treatment... it means the population of people who literally can’t because they have anosognosia are just invisible to the system."
With your support, our loved ones with SMI will never be invisible.
Thank you, as always, for your support of our mission.
Best,
Treatment Advocacy Center