Mr. Ed
Be what you is not what you what you ain’t
- Location
- Central NY
In the ’70s, deinstitutionalization swept the nation, sparking a massive shift in mental health care that still impacts us today. This movement aimed to transition patients from long-term institutional care to community-based care, believing that mentally ill individuals would have a better quality of life and more freedom outside restrictive institutions.
However, this transition was not controversial: some critics argued that community-based care was underfunded and ill-equipped to handle the needs of those discharged from psychiatric hospitals. Additionally, concerns arose about whether or not patients’ rights were genuinely being protected and if they were receiving adequate treatment in their new settings.
Despite these controversies, deinstitutionalization persisted as a driving force behind changes in mental health policy throughout the 1970s.
Advocates for community-based care emphasized the potential for increased personal autonomy and improved social integration for people with mental illnesses. The focus shifted towards providing outpatient services, group homes, day treatment programs, and other supportive resources in local communities rather than relying solely on large-scale institutions.
I recall recieving SSDI payments and Medicare insurance shortly after being diagnosed with Borderline Schizophrenia and being forced to work by my dad. I tried a number of unskilled labor employment but no matter how much I tried to work I did not last two weeks until symptoms forced me to quit. Not only could I not keep a job I lost my Social Security for being deemed employable.
By this time my symptoms took over every aspect of being, I couldn’t work and needed medical care and hospitalization my only choice was Georgia State Mental Hospital where I stayed until given permission by the doctor to go with parents and their friends by Winnebago camper to Los Vegas Nevada.
I learned a valuable lesson back then not trust parents because they don’t always know what’s good for you and one way or another the government knows everything and does not make the right decision for individuals or society.
However, this transition was not controversial: some critics argued that community-based care was underfunded and ill-equipped to handle the needs of those discharged from psychiatric hospitals. Additionally, concerns arose about whether or not patients’ rights were genuinely being protected and if they were receiving adequate treatment in their new settings.
Despite these controversies, deinstitutionalization persisted as a driving force behind changes in mental health policy throughout the 1970s.
Advocates for community-based care emphasized the potential for increased personal autonomy and improved social integration for people with mental illnesses. The focus shifted towards providing outpatient services, group homes, day treatment programs, and other supportive resources in local communities rather than relying solely on large-scale institutions.
I recall recieving SSDI payments and Medicare insurance shortly after being diagnosed with Borderline Schizophrenia and being forced to work by my dad. I tried a number of unskilled labor employment but no matter how much I tried to work I did not last two weeks until symptoms forced me to quit. Not only could I not keep a job I lost my Social Security for being deemed employable.
By this time my symptoms took over every aspect of being, I couldn’t work and needed medical care and hospitalization my only choice was Georgia State Mental Hospital where I stayed until given permission by the doctor to go with parents and their friends by Winnebago camper to Los Vegas Nevada.
I learned a valuable lesson back then not trust parents because they don’t always know what’s good for you and one way or another the government knows everything and does not make the right decision for individuals or society.