I can't believe how many people can't feel the sound? I agree this is by far the worst part of loud tinnitus. For me, some of the shrill loud sounds bouncing around are felt in the ear and in the brain. It's as if I can feel the hyperactivity lighting up in the different areas.
Also, my ear drums seem to tighten in response to the loud beeps and screeching that the tinnitus produces. It's not just a sound for me personally.
I am so glad you changed your picture from the dog. Mixed together with your understandable angry words made me scared to comment on your posts.
However since you wrote so eloquently last week about your suffering you have been on my mind a lot.
You say you fight everyday, especially pushing the noise boundaries, I did that for 6 months with my medical induced T as I have already said.
I wanted to ask would you give my method a try? Which I adopted 7 months ago, briefly gentle sound exposure, reduce stress, relaxation, minfulness, cleansing foods. I do believe it can help. especially as they know T is made worse by stress and obviously T is stressful. You have nothing to lose and all my ideas are non toxic.
I saw a programme this week about people trying to get into work with disabilities, 2 guys had tourettes, both were sent to see an eminent neuro who knew that their ticks were worse in times of stress and under occupation, one guys ticks had come on after a sudden death, yet he had been normal and working over 30 years. When he was calm talking photographs his ticks stopped, the other found a role, actually tree felling and while working his ticks stopped.
I knew immediately this principle could work for us too. Especially as medical induced T is stressful and anxiety creating.