Just a quicky from me. Arm is much better. The bruise kept coming out for hours and it ended up being really big and black but the soreness went away after a while so it looks a heck of a lot worse than it really is. It's already starting to go yellow around the edges, so it's on the mend. I had to have another BT done yesterday cause the Pathology lady didn't realise there were two parts to one of the tests, so I had to go back and I said to her, Umm I think you will need to use the other arm and when she saw the bruise she felt so bad about it. I told her it was OK though but she kept apologising the poor thing, it wasn't her fault. So I have a slightly less bad bruise on the other arm cause she got them to send over a super fine gauge needle to redo the test. The meds are going great - I already have patches of normal skin on my back again which i am super happy about. For those that dont know much about psoriasis, in a normal person you re-grow a new layer of skin around once a month, for people with psoriasis, it regrows every 3 days on the affected areas. So the purpose of the meds is to attack it via the immune system, so the drugs slow down the cell growth of the skin production - the same way chemo is used to stop the tumour cells from growing.

Arte, you asked about handed-ness? None of the kids are left handed at all. Apparently only 9% of the population is left handed.

Nella, I will make mac cheese for Alister's dinner when we are eating something he can't have/wouldn't eat, but the rest of the time he eats what we eat. he actually prefers to eat the same as us or otherwise he throws a tanty and wont eat his dinner, so the nights he is having something different, I have to give it to him earlier.