Misophonia Association

07/15/2025

Dr. Jaffe forwarded this nice piece of information about a student that has brought forward Misophonia into the national platform exciting times

WASHINGTON, D.C. — Today, U.S. Reps. Young Kim (CA-40) and Valerie Foushee (NC-04) introduced a bipartisan resolution to recognize World Misophonia Awareness Day, which is held annually on July 9, and increase understanding of this complex neurological condition. Misophonia is a condition characte...

07/14/2025

My revision/proposal:

The Misophonia Association is seeking a part-time Administrative Manager for the organization. Maintain lists, create flyers and social media postings, respond to emails, setup Zoom meetings, help organize annual convention, etc. This is a paid and fully remote position and the pay is $20 per hour. If you are interested, please contact info@misophonia-association.org

07/13/2025

07/11/2025

Founded in 2013. Annual patient and family conventions. Free Misophonia virtual clinics. Representing Misophonia and its unfolding position in the world and in medicine and in research. Clear of attachments to any particular treatment or therapy remaining neutral until Moore is uncovered in scientific research and time. Friendly and warm and kind and steady. Our association is run by volunteers. Unavailable library of all presentations and videos and interviews and clinics for only nine dollars a month and you can have full access. Free support groups on zoom around the country and world. Dedicated to our cause to find the cure.

07/10/2025

Today!!

07/03/2025

Reports from families who have a member who has Misophonia have led to discussions about the fact that sometimes siblings suffer. This can take many forms, including preferential treatment for the affected person or attempts to construct situations that are entirely for the benefit of that person, and this can lead to resentment and difficulties between siblings, even long into adulthood. This may be the same for families who have a child who suffers from a significant illness or condition and we’re curious to discover more about these feelings.

In my clinic, I developed 25 years ago forms for siblings to complete when a family is coming for a visit about the condition of Misophonia and I wanted siblings who were able to fill out a rating form on their perception of this sibling’s situation with regard to this particular condition .

Are there others here willing to explore this topic? To share their feelings and sometimes of course the feelings are filled with empathy and compassion, but are there other comments or concerns that can arise to help us understand how best to address these kinds of family constellations .

The child in this photograph is smiling and that might lead someone to think that there is some degree of happiness in this difficult setting, but I don’t really think that’s the case . Having the diagnosis of Misophonia in a family rarely makes other people feel happier.

These are real situations and real questions and sharing information about what you’ve thought of or used or tried or considered in your own journeys can really help other people . Sharing is part of the goal of the Misophonia Association and has been for many years.

06/29/2025

What would it mean to find a cure for Misophonia? What do you imagine that could look like? What would you most want in something that would improve this condition or its symptoms? Are there degrees of improvement that would be acceptable?

06/21/2025

We need professional providers of misophonia therapies, treatments or techniques for the Misophonia Association website! Must have professional certifications or professional degrees to qualif! Contact us at misoassociation@gmail.com for application. We seek global listings! There is a huge demand!

06/21/2025

Are you a provider for a Misophonia treatment? We are eagerly seeking your information to post on our website. We’ve had about 26 people on there for quite a while but we’d like to have 260 people on there. The only thing we ask, is you have professional credentials and that you’re working legitimately in the field of Misophonia and we would like to get your information and you can send it to us at Misoassociation@gmail.com.

We have an amazing number of followers and people that support our association which was founded in 2013 and recently one of our posts received65,000 views so we are heading in the right direction .

We do invite a small donation to help us pay for the site and We would appreciate that in order to be listed right now. We are offering a deal for three years for about $100 so that’s pretty good deal if you look at advertising costs and I know our current providers have been very happy with the referrals and people seeking treatment.

I started this field off 28 years ago when I had cases of Misophonia show up at my Audiology clinic here in Oregon and they didn’t fit any of the categories for tinnitus are hyperacusis and so I developed this understanding of this condition and I called it selective sound sensitivity syndrome or 4 S. Over the years I developed a yahoo support group with over 5000 people that had symptoms of this condition and that morphed into the first convention in 2013 and then the Misophonia nonprofit organization was founded in 2013.

We are completely a Volunteer group. We don’t take funds from the Association and we use all the proceeds to help put on the annual convention and pay for cost associated with running the nonprofit which are only a part-time communication Manager and Office Manager.

Please consider contacting us and let us help you connect with people that have this terrible condition and who might receive help from you and that includes anybody from around the world. It doesn’t have to be the US only we are seeking global connections and working hard for global awareness of this situation that happens all over the world and we want clarity and communication and true research that shows exactly what Misophonia is and what we can define it as and so forth into the future as we progress

Thank you and please contact us right away Marsha Johnson AuD president Misophonia Association

06/18/2025

Are you aware that people all over this planet develop Misophonia most often between the ages of 9 to 13 years old and more females than males?

The Misophonia Association has established relationships with other countries and their organizations for this condition . 28 years ago when I discovered this condition in my clinic here in Oregon and began to collect cases, it became clear that these cases were spread so widely that many people with Misophonia haven’t met another Misophone!

It can be very lonely to have Misophonia in this world, and our goal is to strive to bring people together in helpful and healthy ways to share and continue to further our efforts toward finding relief and eventually a cure .

We are currently associated with Misophonia organizations in countries like New Zealand and Malta and Australia and England and other places. It is absolutely incredible. How much the field has grown since 1997.

When we think of Misophonia, we must think globally and how to both raise awareness and raise funds for research as well as inform people with it as to the latest strategies for improving their lives . Wherever they live.

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