This is what ENTs told me about tinnitus (twice)
When I first developed tinnitus, I went to see an ENT. I was basically told: “Just live with it. There’s nothing you can do.” That was it... 😯 No guidance, no plan, no real support. Of course, it made me feel worse. Some years later, I went back, this time because of TTTS. (middle-ear muscle spasms that can be extremely distressing) Different doctor, same feeling. Again: “There’s nothing you can do.” And then this: “We could cut the (middle-ear) muscle… but we don’t know if it will help. It might make things worse.” Both experiences left me feeling: More anxious More confused And completely on my own Each time, it pushed me into a deep search for answers. Eventually, I figured things out… but not thanks to these visits. 🤷♂️ Now I’m really curious about you 👇 What was your experience the first time you saw a doctor for tinnitus, hyperacusis, TTTS, or something similar? What did they tell you? How did it make you feel? Did it help… or make things worse? Let’s share openly, please. I think this will help a lot of people here. 🙏💙