I am really trying... but I am not sure I can "recover" from this more than once. I should of been more careful. Water under the bridge as they say. Every time it seems like things are going in a positive direction, T smacks me down again. Life can be cruel.
Hi Erika. I hope you're doing well. I saw that you mentioned your distortions came back. Did they go away a second time? I'm dealing with my own second round of distortions after beating the first.
Ive actually had 2 days of VERY calm and good tinnitus. Ive even manage to hammer down conrete stuff that you walk on with a rubber hammer (ofc with earplugs) and no spike! So nice being outside in the warmth and do "labour" and just be able to be to good use for once!
Hello are you still on clonazepam since you live in Gent have you talked with Dirk De Ridder about long term clonazepam usage for tinnitus , dysacusis ? thank you
I think about you often and wish I could have done more for you.
I was visiting your Facebook page at least once a year but I think it's been taken down now, it was my way of paying my respects since I don't know where or if you were buried.
I am getting more days where my tinnitus is not the first thing I think about in the morning. But it's still on my mind at least once a day. It's been more than 2½ years since it got worse.
My tinnitus is med induced not noise induced both ears multitonal same since 7 months only got worse what happens if i use clonazepam rest of my life it works for now why did you stop after 2 years
Interesting thought - Is Anxiety and Stress a possible precursor to T? As our brain undergoes whatever changes that ultimately causes T, do we experience it as a result? There seems to be a link, but I wonder which is the result of the other.
A very stressful week + louder noise exposure to music over a 2 hour period has left me with bad TTTS vibration in right ear/head. It's the worst in silence, especially when going to bed & waking up. Temporarily cuts out when I talk or hear external sound. It's only been 7 days since onset, but I'm already frustrated & anxious about it. Praying it goes away.
If they were still looking for further study subjects I would make the 800km trip to participate. I am frustrated at the responses from health professionals about my tinnitus. They dont get it. It would be good to have an objective measurement.
I know. I asked my tinnitus researcher about it. She was aware of the article. She reckons it has all gone quiet. Nothing further has been published by the Bionic Institute about fNIRS.
Hi @trevl I saw your post about bionics institute. It was in a different thread though, so I reply here. The fnri does not measure the sound. The sound is not really relevant in research as much as it is to the patient. Presence and severity is measured.
Urk. I was outside walking with a coworker and they saw someone on the other side of the street so the one next to me litterally yelled STRAIGHT INTO my ear at the top of hes lugns for the other person to come join us. I reminded him to not do like that and he just brushed it off with "oh i forgot". Think i got a spike from it. Was wearing my 35 DB earplugs luckily enough. Anyone experience something similair?