LEAP
Introducing
Das Lived Experience Action Panel for Misophonia* Media and Research
*and misokinesia and related afflictions.
What is the Lived Experience Action Panel for Misophonia [LEAP]?
The Lived Experience Action Panel for Misophonia [LEAP] is a diverse panel of 5-8 volunteers, all of whom have lived experience with misophonia and/or misokinesia, including individuals with the disorder and their family members.
LEAP evolved as a response to growing research and awareness of misophonia and the need for inclusive representation of personal experience with misophonia in the ongoing research, media, and beyond.
Submission Process
What types of content does LEAP review?
study concepts
academic/research papers
social media posts
blog articles & essays
presentations
news publications
and more!
At this time, LEAP will also give feedback on unrelated content that the creator aims to adapt for a misophonic audience.
Inquiring researchers, clinicians, journalists, etc. should submit their work to LEAP via the form below, allowing three weeks for reviewing and processing.
Researchers seeking feedback during the development of scientific research should include the following if applicable:
Abstract: 1 page or less
Aims: 1 page or less
Impact statement: 1 page or less
Goals of the LEAP:
To review materials submitted by misophonia researchers, clinicians, and other content creators in an effort to:
Assist researchers, clinicians, and content creators in understanding the needs and viewpoints of those with lived experience of misophonia, in general.
Helfen Sie Forschern, Forschungsthemen und Hypothesen über Misophonie zu entwickeln, die von eigenen Erfahrungen geprägt sind und die Misophonie-Community repräsentieren.
Support researchers and content creators to better understand the impact of wording used in social media posts, research papers, blog articles, presentations, news publications, and more to help build a more cohesive representation of misophonia that includes accurate lived experience.
Support and uphold ethics in research as stated by the National Institutes of Health with the understanding that science and its institutions are vulnerable to disability discrimination, racism, sexism, homophobia and the like. LEAP will attend to the potential intersection of scientific research and these forces of oppression that are sometimes repeated within the practice and production of science and scientific knowledge.
Read about a study that included the LEAP here:
LEAP-Panelisten
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Jennifer Brout, PsyD
Hat Misophonie und ist Elternteil einer Person mit Misophonie.
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Cris Edwards, MFA, CPS
Hat Misophonie.
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CJ Gibson, MS
Hat Misophonie.
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Ellie Rapp, BA
Hat Misophonie.
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Samantha Zimbler, BA
Hat Misophonie.
Published Studies on Misophonia Reviewed by LEAP
Quality of life among youth with misophonia: The role of internalizing symptoms and pessimism [September 2024] by Minjee Kook, Catherine E. Rast, Matti Cervin, Jane Clinger, Eleanor Smith, Isabel Draper, Nicholas Murphy, Marijn Lijffijt, Sophie Schneider, Mered S. Parnes, Caitlin Pinciotti, Wayne K. Goodman, Eric A. Storch, and Andrew G. Guzick [Zeitschrift für Psychopathologie und Verhaltensbewertung].
Untersuchung schlafbedingter Probleme bei Jugendlichen mit Misophonie [Dez. 2025] von K. M. Wagner, M. Cervin, C. E. Rast, M. Parnes, N. Murphy, S. Spencer, E. A. Storch, A.G. Guzick

