@DressingForRevenge DTS1 also has 'mild' ASD - apologies if that's not the correct term! - essentially he doesn't qualify for any extra help at school, EHCP etc but is very limited in the food he eats, is a very poor sleeper and has other related issues. And if he doesn't eat regularly he will have an absolute meltdown
so yes, I completely hear all the "you must find time to eat well, look after yourself, do exercise etc" but he's often not asleep till gone 10pm and I am utterly shattered. He needs a good routine (and lots of exercise!) to keep him anywhere near calm, but that too impacts on my available time.
Incidentally my last office was only built in the late 1980s and still had no disabled access, incredible really! There were a couple of steps up to the front door and revolving door, neither of which would be suitable for a wheelchair. It's since been knocked down for housing, I think partly because of the £££ involved in making it anywhere near suitable for current DDA regulations.
@trytopullyoursocksup I prefer a small group but then my brain has turned to mush since having the DC, the less people to remember the better
and my goodness, the guilt around family mealtimes... I envisaged that we'd have lovely ones round a table (like the ones in Bread but less arguing, preferably!) but DTS1 is just a nightmare at mealtimes, he will physically gag if people are eating things he doesn't like. BIL & his wife used to be very sniffy if we let him watch his tablet for a bit at dinner time once he'd finished eating, just so we could have 10 minutes' peace to finish too - now they have a toddler they do exactly the same!
Well done on your great starts @Amisillyornot and @SeventyPounds 
I'm immediately put off by anyone agonising over a few pounds left to lose @RedDoughnut! I love an omelette too, recently invested in an omelette maker as I'm so terrible at making them. An excellent healthy option, I thought - then I realised it makes lovely toasties too 