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Tinnitus Relief & Habituation with Coach Frieder

Tinnitus Relief & Habituation with Coach Frieder

De: by Tinnitus Coach Frieder
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Hey Tinnitus Friends & Family, Welcome to the show all about tinnitus — the science behind relief, and how you can find the right approach for your unique situation. We dive into the latest science-based strategies, debunk myths about tinnitus cures, and explore effective treatments to help you find quick relief from ringing ears. 🌟 Ready to start your tinnitus relief journey? Visit my Linktree for all my best resources in one place: https://linktr.ee/outringtinnitus This podcast combines a scientific and myth-busting approach to tinnitus with deeply personal stories of living with single-sided deafness, tinnitus, and navigating life with a hearing aid. We’ve interviewed some of the world’s leading tinnitus researchers and practitioners, offering insights to help you understand and manage tinnitus effectively. Through my personal tinnitus relief framework, I’ve supported hundreds of people in reclaiming their lives and finding lasting relief. Whether it’s through our transformative online tinnitus community, 1-on-1 coaching, or our structured programs, there’s a path to success for you. 🎧 Learn more and take the first step: Join our supportive community: www.mytinnitus.club Explore my curated tinnitus resources: https://linktr.ee/outringtinnitus We wish you sound tinnitus relief and happy listening! Warm regards, Your Tinnitus Coach FriederAll rights reserved Higiene y Vida Saludable
Episodios
  • Episode 150 - The Hobby Tinnitus took from me (And how I claimed it back)
    Apr 3 2026
    Hey Tinnitus Friends and Family, Cycling was everything to me. And then tinnitus started. Suddenly, the one thing that used to give me peace became unbearable. Why I stopped cycling: First: I was exhausted. All my energy was going into coping with tinnitus. Googling constantly. Trying supplements. Obsessing over whether it was louder or quieter. I had nothing left for cycling. It felt like too much. Second—and this was harder: When I did try to ride after a couple of months, all I could hear was the tinnitus. I'd be cycling through a forest. Beautiful landscape. Birdsong. Wind. And all I could focus on was the ringing. It ruined the whole experience. So I stopped. I told myself: "Just until things settle." Weeks became months. Months became almost a year. I was waiting for the tinnitus to get quieter so I could enjoy cycling again. But it never got quieter. What losing it cost: Losing cycling didn't just mean missing the rides. It meant losing my reset button. No way to clear my head. No way to feel like myself. Life got smaller. ACT principle: When we abandon our values to manage our discomfort, the discomfort doesn't decrease—but the life does. I thought I was protecting myself by avoiding the thing that hurt. But I was actually making my world smaller. And the smaller my world got, the bigger the tinnitus felt. Because there was nothing else competing for my brain's attention. Just me and the ringing. The shift - what changed: The tinnitus didn't get quieter. It's still loud. I can hear it right now. What changed was my relationship with needing it to be quiet. I realized: I was waiting for the tinnitus to not be there before I could enjoy cycling again. So I made a decision: What if I went cycling with the tinnitus? Not waiting for it to go away. Not fighting it. Not needing it to be quiet. Just going anyway. So I got on my bike. And I rode. The tinnitus was still there. Loud and clear. But here's what shifted: I stopped making the ride about the tinnitus. I stopped needing it to NOT be there. I let it be there—like my heartbeat, like my breath when I'm cycling. And for the first time in months, I felt like I could enjoy this again. I could hear the tinnitus and feel the wind. The tinnitus and the movement. The tinnitus and the joy of cycling. What this is really about: This is what values-based living means. This is what Acceptance and Commitment Therapy (ACT) teaches: You don't wait for the discomfort to pass before you start living. You do what matters while the discomfort is present. And when you do that, your brain gets evidence: "I can do this. The sound is there, but I'm still me. I'm still living." That's when habituation happens. These days: I cycle all the time. Through forests. Along rivers. In complete nature. My tinnitus is there. Always. I can hear it. Loud and clear. But I don't pay attention to it. Not because I'm forcing myself to ignore it. Because I'm paying attention to something else. What's the thing you're putting on hold? Not a big question. A specific one. One thing you used to do that mattered to you. Cycling? Going to concerts? Reading in silence? Ready to understand where you are in your habituation journey? Take the free habituation quiz: www.habituate.online It takes 2 minutes and will help you: After the quiz, you'll get our free 4-day email course on ACT-based tinnitus habituation. Let me know in the comments: What's the one thing you put on hold? What would it take to try it again? I read every comment. New videos every Friday. — Frieder
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    10 m
  • Episode 149 - Everything I Wish ENTs Knew About Tinnitus
    Mar 20 2026
    Hey Tinnitus Friends & Family, After working with 700+ people with tinnitus, they all told me the same story: "My ENT said there's nothing we can do. Go home, relax, don't worry about it." And then they were sent home—alone, terrified, with no support. In this episode, I break down: What ENTs get RIGHT: There's no medical cure for most tinnitus (true) They rule out serious medical causes (important) They can help with underlying causes (earwax, TMJ, infections) Here's what I wish ENTs would explain: 1. Tinnitus is a nervous system condition, not just an ear problem The biggest suffering doesn't come from the sound itself—it comes from your nervous system's response. When your nervous system is in fight-or-flight, tinnitus becomes a threat. Your brain amplifies it, monitors it constantly, won't let it fade. ENTs treat ears. They don't treat nervous systems. And we can't hold that against them—but you need to know there ARE tools for this. 2. Loudness ≠ suffering I've seen people with very loud tinnitus who aren't bothered at all. And people with mild tinnitus who are suffering intensely. The difference? Not the decibel level. The nervous system's response. ENTs often give the wrong prognosis based on loudness alone. They assume louder = worse suffering. That's not true. 3. Isolation makes it worse When an ENT says "nothing we can do" and sends you home, you're left alone with a condition your brain perceives as a threat. That isolation activates your nervous system even more. Your brain thinks: "I'm alone with danger. This must be serious." ENTs don't mention that community and co-regulation are part of the treatment. 4. Habituation is possible—and it's teachable ENTs say: "You'll have to learn to live with it." But they don't tell you how. They don't mention: Acceptance and Commitment Therapy (ACT) — the most evidence-based psychological approach for tinnitus Nervous system work — teaching your brain that tinnitus is safe Community support — co-regulation with people who understand They leave you to figure it out alone. My tinnitus is 0% of a problem. Why? Because I didn't wait for it to get quieter. I lived my life despite it. What I wish ENTs would say: Instead of: "There's nothing we can do. Good luck." I wish they'd say: "There's nothing medical we can do to eliminate the sound. But you CAN habituate through nervous system work, ACT, and community support. Here are resources." Where to start: Take the free habituation quiz: www.habituate.online It takes 2 minutes and helps you Let me know in the comments: What did your ENT tell you when you first got tinnitus? — Frieder
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    12 m
  • Episode 148 - Why I Built My Tinnitus Club (And What Makes It Different From All Other Tinnitus Apps)
    Mar 13 2026
    At 19 years old, I developed severe tinnitus. I was terrified. Desperate. Completely alone. The ENT told me: "There's nothing we can do. You'll have to learn to live with it." And then sent me home. That experience is why I built My Tinnitus Club. I built what I needed when I was 19—and what I wish had existed back then. In this video, I'm sharing: Why apps, courses, and forums aren't enough What makes My Tinnitus Club different How community changes everything for tinnitus habituation Here's the problem with tinnitus apps: They treat tinnitus like a solo problem you solve alone. You download the app. Watch pre-recorded videos. Do exercises by yourself. Track progress on a chart. But when you're struggling at 2am—when your tinnitus is screaming and you think you'll never get better—the app isn't there. The algorithm doesn't know you're suffering. The pre-recorded videos can't respond to your specific situation. And that isolation? That's exactly what makes tinnitus worse. Here's what I've learned after working with 700+ people: Your nervous system doesn't learn safety from an algorithm. It learns safety from other humans. That's not motivational talk. That's neuroscience. We're wired for co-regulation—being around other people who've been through what we're going through. Apps can't give you that. But community can. Why I built My Tinnitus Club: When I was 19, I was born deaf in my left ear—so I only had one functioning ear. At 19, I damaged it at a concert. Severe, high-pitched tinnitus. I was terrified. I went to the ENT desperate for help. He said: "There's nothing we can do. Protect your hearing in the future. Good luck." No support. No resources. No follow-up. Just: "Figure it out on your own." So I did what most people do: Googled endlessly Read horror stories on forums Tried every supplement, sound therapy, supposed cure And I felt completely alone. Years later, when I became a tinnitus coach, I thought: "What if I had this at 19? What if I didn't have to spend years figuring this out alone?" So I built it. A safe space where people can: Learn the most effective tools for habituation (12-week ACT-based program) Be supported daily by real people who understand Never feel alone with tinnitus again I built what I needed when I was 19.
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    12 m
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