Thanks folks
(and for the heads up about Home DVD - might get that for Xmas too)
I'm looking into PIP and stuff, also I'm currently filling in a housing form - we've been on band B for a few years but the housing person suggested filling in a medical needs thing. I guess I'll be on sick pay for a bit and then ESA or something although it can be quite hard to get that for my condition apparently (includes ME which is basically an 'invisible disability')
A lot of people have asked if the home ed has made it worse, it's a fair question and TBH I really worried about it as well when we were deciding. But it's honestly been the opposite, unfortunately the timing this relapse (which was a long time coming) made it look otherwise. HE is proving really easy and fun, and it's flexible around my bad days. Yesterday we did all our stuff snuggled on the sofa or on the living room floor, it was great, in between 'lessons' they just played lego or played outside for a bit while I had a rest. Compared to dragging them to school (an hour round trip, on my feet, twice a day) when they didn't want to go - literally dragging DS sometimes, and the stress it caused as well as the pain (I would often collapse in tears after the school run), the rushing around etc, it really is so much better for me as well as them which has been a pleasant surprise TBH. :)