You are so very welcome. It proves my 15 year battle with MAV hasn’t been entirely pointless. I just wish I’d had access to some guidance myself at the beginning however, as screens were a main trigger, I couldn’t have accessed a forum anyway, not for many months, and theonly way to obtain practical advice is from another sufferer. Medics just don’t get it, unless they have personal experience if vertigo themselves or close family member. Nobody does. It’s indescribable so you can lt expect they could.
Just as example of the ups and downs. I was feeling great last eve when I penned yr reply, went to bed, had a not particularly good night and woke up feeling totally rubbish balance-wise. After three virtually perfectly normal, ‘how I used to be’ days. Only good thing is, once you improve a bit, triggers more obvious and you can sometimes exert more control.
Oh, don’t worry about yours lasting 15 years. Highly unlikely. I went 12 years misdiagnosed and unmedicated, ‘lost in the wilderness’. (Extremely long story) . That hasn’t happened to you. Helen