This is what ENTs told me about tinnitus (twice)
When I first developed tinnitus, I went to see an ENT. I was basically told: āJust live with it. Thereās nothing you can do.ā That was it... šÆ 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: āThereās nothing you can do.ā And then this: āWe could cut the (middle-ear) muscle⦠but we donāt know if it will help. It might make things worse.ā 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. š¤·āāļø Now Iām really curious about you š 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? Letās share openly, please. I think this will help a lot of people here. šš