Patrick W. Corrigan[1] is a US-based author and advocate for people with a mental illness, particularly in relation to the issue of stigma. He has written more than 15 books and 400 peer reviewed articles specializing in issues related to the mental illness[2] stigmas.[3] Corrigan suffered from mental illness himself and is most likely the reason his research has this focus. Corrigan currently resides in Northern Illinois, and family life is unknown.
Since 1992, Corrigan has been on the faculty at the University of Chicago and also serves as an investigator for the Chicago Consortium for Stigma Research.[4] Corrigan is currently a distinguished professor of psychology and Associate Dean at Illinois Institute of Technology,[5] where he received his doctorate in psychology.
In 1998, Corrigan was added to the Who's Who of the World. One of his most noted books is "Don't Call Me Nuts : Coping with the Stigma of Mental Illness", which discusses many issues relating to mental illness including the issue of indiscriminate disclosure.[6] More recently, he has edited "On the Stigma of Mental Illness: Practical strategies for research and social change"[7] which illustrated perspectives from a wide variety of sources, including people with a mental illness, to look at practical affirmative action tactics that can be used to fight against stigma.
Patrick Corrigan's writing is focused around the public stigma of mental illness. His research shows ways to overcome and educate others on the effects stigmas have on the mental illness community. Majority of his work highlights the importance of community, and personal contact within the recovery stages. Corrigan allows his work to be unbiased and includes many different ways to help deter stigmas including religion and faith based practices.[8] His research allows readers to see different correlations and comparisons within the topic, such as racial and suicide attempt survivor stigmas. Corrigan notes that the idea of color blindness[9] can transfer to mental illness and has the same effect on the population. His work also references how a prognosis can be detrimental to a patient in a way were they are held to the same stigmas of their newly named illness.
Follows is a list of published books[10]
