Thanks Michael! I've found your reply very reassuring. It sounds like you symptoms were much worse than mine, especially the H, but they sound very similar. I still hadn't found anybody with the same symptoms, especially the footstep hiss. My ENT said he'd never heard of that before, and sent me for an ultrasound. Of course that was a waste of time, apart from the fact that I find ultrasound tests quite relaxing
The pulsating T and the footstep hiss have been causing me considerable anxiety, especially since they seem so volatile and unmask able. The classic T hiss is my L ear can get quite loud but I can deal with it. It also fades if I listen to music. As you probably read, all music is distorted, flat and tinny, but in the last couple of weeks I seen (shurely "heard" -ed ) some improvement, at least on my Mac speakers (not brave enough to try any others...) Music is becoming a little clearer, and some top end is coming back. Now I can hear hi-hats and ride cymbals, albeit quietly. And the 16 kHz slider on the EQ now makes a tiny difference to what I can hear. People still lisp randomly though. And the H, which caused me to yelp in Sainsbury's when I scanned a tin of beans, is slowly getting better it seems. In the last couple of weeks, after reading one of your posts, I've been playing soothing sounds all night from a couple of old computer speakers positioned on either edge of my mattress, and I'm sure that's been helping.
As I said, your tale of recovery from such appalling symptoms has perked me up a lot. Although of course in 1996 I suppose you were quite young, whereas I'm 54 so my capacity for regeneration is probably degraded. That's one reason I chose to do HBOT. Even though it's beyond three months I'm still tempted to give it a few more sessions. Chatting to the stoic MS sufferers in the oxygen chamber was also uplifting. They were full of happiness, genuine interest and empathy.
Anyway, thanks again, it's amazing how a reassuring message (with real substance) can affect one's mood.