[et_pb_section fb_built=”1″ fullwidth=”on” _builder_version=”4.10.6″ _module_preset=”default” bottom_divider_style=”ramp2″ bottom_divider_color=”#FFFFFF” bottom_divider_flip=”horizontal” global_colors_info=”{}”][et_pb_fullwidth_image title_text=”RKP_0231″ _builder_version=”4.10.6″ _module_preset=”default” background_image=”http:\/\/cyprusconferences.org\/sssp2022\/wp-content\/uploads\/2021\/10\/RKP_0231.jpg” min_height=”273px” custom_margin=”||-1px|||” custom_padding=”293px||0px|||” global_colors_info=”{}”][\/et_pb_fullwidth_image][\/et_pb_section][et_pb_section fb_built=”1″ _builder_version=”3.26.2″ custom_padding=”0px|||||” global_colors_info=”{}”][et_pb_row _builder_version=”3.26.2″ global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”3.26.2″ global_colors_info=”{}”][dsm_text_divider header=”Lived experiences workshop” _builder_version=”4.10.6″ _module_preset=”default” header_level=”h1″ global_colors_info=”{}”][\/dsm_text_divider][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=”4.10.6″ _module_preset=”default” custom_padding=”||2px|||” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.10.6″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.10.6″ _module_preset=”default” custom_margin=”||-4px|||” global_colors_info=”{}”]<\/p>\n
Wednesday May 18th 3-4pm PDT (UTC-7) \u2013 please register for this event in the process of registering for the conference.<\/p>\n
<\/p>\n
[\/et_pb_text][et_pb_text _builder_version=”4.10.6″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n
A person-centered approach to psychopathy research: Considering the experiences, needs, and concerns of affected individuals and families<\/strong><\/p>\n Panelists:<\/p>\n Abigail Marsh, a psychopathy researcher and co-founder of PsychopathyIs<\/p>\n Lisa Michael, the parent of an adult child with psychopathy and co-founder of PsychopathyIs<\/p>\n Patric Gagne, writer and advocate for individuals struggling with psychopathy<\/p>\n Jen Griffis, mental health advocate and parent of a child with CU traits<\/p>\n <\/p>\n [\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=”4.10.6″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.10.6″ _module_preset=”default” global_colors_info=”{}”][et_pb_text module_id=”1″ _builder_version=”4.10.6″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n [\/et_pb_text][et_pb_text module_id=”4″ _builder_version=”4.10.6″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n A person-centered approach to psychopathy research: Considering the experiences, needs, and concerns of affected individuals and families<\/strong><\/p>\n Panelists:<\/p>\n Abigail Marsh, a psychopathy researcher and co-founder of PsychopathyIs<\/p>\n Lisa Michael, the parent of an adult child with psychopathy and co-founder of PsychopathyIs<\/p>\n Patric Gagne, writer and advocate for individuals struggling with psychopathy<\/p>\n Jen Griffis, mental health advocate and parent of a child with CU traits<\/p>\n Increasingly, psychopathology-focused organizations are moving toward considering the experiences and needs of people affected by a given disorder when creating research priorities and protocols. Until now, psychopathy has been notably distinct in this way. Unlike those with other clinical conditions, people with psychopathy are often referred to as their disorder (“psychopaths”) by clinicians and researchers. And individuals and families affected by psychopathy are not typically consulted when researchers design studies and interventions. One of the aims of the newly formed organization\u00a0Psychopathy Is<\/em>\u00a0is to bring research on psychopathy into closer alignment with research on other common and serious forms of psychopathology. This approach means, among other things, taking seriously the concerns, needs, and goals of individuals who are personally affected by psychopathy. Such individuals remain–relative to those affected by other common, serious developmental disorders–underserved by the research, clinical, and public health communities. This workshop will feature 4 individuals discussing their personal experiences with psychopathy and how research can be strengthened and enriched by taking the experiences and viewpoints of affected\u00a0individuals and families into consideration.\u00a0<\/p>\n [\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"Description<\/span><\/h3>\n
Lived experiences workshop<\/span><\/h1>\n\t\t\t\t