Yes, that is how it is for me. Because mine mainly disappeared once the ME went, I now have more going on in my life, so less time out. It is probably no worse, just less manageable at the moment. I will try earplugs, well at least one so I can hear what people are saying.

I remember being with friends in a dining room with a hard floor and lots of voices, some exceedingly loud, and so I had to cover one ear so I could hear what they were saying. I do remove myself from situations, but it has got to the point where I am not having any social life unless it is a one to one.
Yes, its getting into the habit I have the problem with. Pills morning and evening are fine. Add any in during the day such as an antibiotic, and unless something is hurting, I forget unless it is right in my sightline. Once I am there it is no problem. I try writing things down on my 'to-do' list, post it notes, setting alarms, leaving things in obvious places, but my butterfly mind which analyses and processes constantly, particularly with so many things to do at the moment, means all my senses are over ridden so I don't hear or see things. Any interruption then I am jiggered.

Working on my downsizing my responsibilities at the moment so less brain activity hopefully after March when my resignation from a Charity comes into force, and after May, when my OU module should be in. Have made myself extra busy as a distraction to cope with some grief and loss last year, so took on too much...