Misophonia Association

Misophonia Association Please help us by liking our page and coming to our annual convention.

Established in 2013, the Misophonia Association’s mission is to empower the misophonia community with education, advocacy, research, and support, with the long-term goal of finding a cure. We are here to help those who suffer from misophonia, their families, and medical providers, to recognize, support, and spread the word about the condition, to spark research, to gather force to make things happen for everyone.

📢 Big News: Registration for MisoCon26 is officially OPEN! 📢We are heading to Tulsa, Oklahoma from October 22-24, 2026, ...
04/10/2026

📢 Big News: Registration for MisoCon26 is officially OPEN! 📢
We are heading to Tulsa, Oklahoma from October 22-24, 2026, for three days of connection, cutting-edge research, and community support.

Whether you’re a long-time member of the Misophonia Association or joining us for the first time, MisoCon is the place to find your "tribe," learn from top experts, and discover new strategies for navigating life with misophonia.

Why join us in Tulsa?
✅ Hear from world-class researchers and clinicians.
✅ Attend focused breakout sessions tailored to your needs.
✅ Connect with others who truly "get it" in a supportive, trigger-aware environment.

Early Bird pricing is live through June 1! Secure your spot now and save:
👉 https://misophonia-association.org/event/misocon26-tulsa-oklahoma/

We can't wait to see you there! 🧡

Keep up with us
03/30/2026

Keep up with us

Our 2026 events calendar is here: more free misophonia clinics, Global Focus events to bring people around the world together, and MisoCon26 (our annual misophonia convention). 🎉Save the dates and join our community!

03/29/2026

End of March mind and heart exploration via probing questions for all of those who have Misophonia or who love those who have Misophonia.

QUESTION: what do you do or say when other people tell you they don’t believe in the condition of Misophonia?

Looking for a Volunteer or someone who can help use something like Canva or other program to help put together a book ab...
03/29/2026

Looking for a Volunteer or someone who can help use something like Canva or other program to help put together a book about Misophonia. All proceeds are going to go to the Misophonia Association. Please contact me directly if you are able to help with this project. Othtcdrjohnson@gmail.com

03/23/2026

Update on the recent global focus on Misophonia event that was held Saturday, which is hard to believe but was yesterday.

We had a wonderful time and we had nearly 100 people sign up and indicate they would come and it was wonderful to hear the three presenters from South Africa, Africa, and Australia, and Norway.

Will be posting this on our website, of course, and also here.

These events have been so rewarding and people have been so interested to ask questions and participate and we’re looking again for three or four more locations to showcase in this coming September 2026.

Please let us know if you would like to be one of those individuals or organizations. We hope to fill up our special website for this endeavor with dozens and dozens of presentations over the next few years.

Takeaways from this event included the fact that Misophonia is still a mystery disorder in most of the world. Too many people don’t even know the name. Access to treatment is limited or to even access to individuals who know anything about it is quite limited. It appears that many places that this condition is just treated as some kind of mental illness or emotional disorder.

We should not be discouraged by this news however, we should be feeling inspired to take up the banner of spreading Misophonia awareness and creating systems that can support the people who suffer with it.

We really need more regional support groups and in country in your own language organizations that can help you understand in your family as well.

This is a great area for volunteers so if you read this and you’re in a location that perhaps has little access to any of these kinds of things, let them Misophonia Association know and we will assist as we can at least in this endeavor.

Looking forward to even more progress in this 29th year of the journey.

Dr. Marsha Johnson Audiologist

Happening right now.
03/21/2026

Happening right now.

Global Focus on Misophonia is an international initiative coordinated by the Misophonia Association to promote cooperation, share knowledge, and increase global awareness of misophonia. Our mission is to support communities across countries through bi-annual virtual meetings, communication, and coll...

This is the lowest worldwide estimate.
03/20/2026

This is the lowest worldwide estimate.

Check it out
03/18/2026

Check it out

03/17/2026

Do you live in the UK and want to participate in a misophonia Clinical Trial?

At the University of Sussex, MRF-funded investigators would like to invite you to take part in their clinical trial (subject to eligibility) to test non-invasive, vagus nerve stimulation for improving misophonia symptoms.

If you would be interested in taking part, please complete the screener questionnaire which assesses your eligibility at this link:

The most powerful, simple and trusted way to gather experience data. Start your journey to experience management and try a free account today.

The most heartbreaking part of Misophonia is the moment the young child begins to suffer the consequences of this condit...
03/17/2026

The most heartbreaking part of Misophonia is the moment the young child begins to suffer the consequences of this condition.

The onset of Misophonia has been found to be between the ages of 9 to 13 for the majority of those who suffer with these symptoms.

These are very young children who don’t have the maturity or the capacity to analyze their situations and alert others around them as to what is exactly going on.

They react in the way a child reacts when they get stung by a yellow jacket .

They cry out, they get upset, they lose their tempers, they feel completely attacked and off-balance, and unable to figure out what to do to make it stop hurting .

And the worst thing is that they can’t go to the people they need to comfort because many times one of the parents is the trigger.

It’s really quite an unfair situation to inflict something like this on an innocent child . I have conducted hundreds if not thousands of interviews over 30 years with families who have had a child develop Misophonia and It often turns on almost like a light switch one day . Or you could say it was like a lightning bolt .

Many adults remember those moments when their Misophonia began and they can describe it quite accurately. That makes sense because that moment is a moment of extreme human trauma . And life is never quite the same after that moment .

We must maintain our efforts to gather up every bit of information we can about this terrible condition and distribute widely and keep it freely available and reach out to help others .

At the Misophonia Association we’ve been doing our part really since 1997 and the official association was founded in 2013, but it had been growing strong as a movement for the previous 16 years.

We don’t care who figures it out and figures out what to do about it. It can be anybody really we are not particular about it at the Association. We just want it to happen for the sake of these beautiful young people who become almost instantly miserable and unhappy, and it’s a very tragic situation.

We must maintain our hope and our strength and our efforts and carry on as best we can until that moment arrives! 

Address

1827 NE 44th Suite 130
Portland, OR
97213

Telephone

+15032341221

Website

https://www.instagram.com/misophonia_association/

Alerts

Be the first to know and let us send you an email when Misophonia Association posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Share