Community Resources
Personal Stories
Patient Advocacy Partners and Resources
- Resources to manage symptoms
- Resources for families
- Peer Support
- Accommodation resources in the US
- Participate in online Misophonia Research
- Resources for clinicians and those seeking clinical help
- Resources to manage symptoms
- Participate in Misophonia Research
- Resources for clinicians and those seeking clinical help
- Resources for families
- Resources for getting involved with Misophonia Research at Duke
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- Platform connecting misophonia researchers and providing education
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On July 9th, we all join together to eliminate stigma, share facts, and work to support every person whose life is impacted by misophonia.
Online support group that facilitates the connection between people with misophonia.
The Japanese Misophonia Association is an association run by the younger generation, with the ideal of creating a society where people with misophonia and those around them can live comfortably.
AIMIF is the first Italian organization exclusively dedicated to the study, research, treatment, training and cultural dissemination relating to the condition of hypersensitivity and reduced tolerance to certain sound stimuli called Misophonia.
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Share your Misophonia Story
Your story is important, and we would love to hear it. Fill out the information below to be contacted by the Misophonia Research Fund team to share your story. Stories will not be shared publicly without permission.
Research & Impact
Explore the research and publications of MRF-funded researchers.
For Researchers
Learn more about strategic priorities and scientific funding opportunities.
Community Resources
Explore a variety of resources and impactful organizations for those seeking support for misophonia or looking to get involved.