Published on 12, July, 2020
I have had to go to A and E and found the experience deeply uncomfortable. Lots of people noise etc.
I also have had to wait over a month and a half for a breathing issue to do with my throat. Despite my Gp saying it was urgent.
I got told many reasons why I had to wait so long. Inconsistency, a real pain with my suspected ASD. This prolonged agony got me thinking, do hospitals really understand ASD?
Think of their layout and lack of facilities.
Does anyone else think this?
I certainly agree, I had to go to A&E a couple of months ago and it was torture! I also had to return several times for follow up appointments and they were nearly as bad, although for the latter times at least I was given prior notice so I was able to plan accordingly. My biggest lifesaver is knitting! No-one bats an eyelid at me ignoring everyone else and I lose all track of time when following a pattern so I don't get stressed out at how long it's taking :)