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The (not so old) Crocks Cafe -Part 2

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  • I don't know about IS, but I would think it would purely be based on your income rather than household income?
    Hopefully someone who knows a little more will be along soon.
    http://www.direct.gov.uk/en/MoneyTaxAndBenefits/BenefitsTaxCreditsAndOtherSupport/On_a_low_income/DG_185670

    I have read a bit more and I don't think I'd be better off as I thought I might get an extra premium but it looks like my IS would be just under £80 and my ESA would be just under £100 but I think if I didn't have all the horrible stress of everything ESA entails I would seriously consider IS instead. However, I don't know how that would affect my mid to long term goal of being well enough to hold down a part time job.
  • Are you eligible for (what I think is called) severe disablement premium? My WRO mentioned this last week but I don't know any details of eligibility etc.
    I must go, I have lives to ruin and hearts to break :D
    My attitude depends on my Latitude 49° 55' 0" N 6° 19' 60 W
  • Are you eligible for (what I think is called) severe disablement premium? My WRO mentioned this last week but I don't know any details of eligibility etc.

    Thats what I thought but I then read you have to get high or mid rate care DLA, have no one claiming carers allowance for you and live on your own
  • OK, sorry about that. It just popped into my head as WRO had mentioned it.
    I must go, I have lives to ruin and hearts to break :D
    My attitude depends on my Latitude 49° 55' 0" N 6° 19' 60 W
  • Nothing to be sorry about, these things are very complicated
  • Indie_Kid
    Indie_Kid Posts: 23,097 Forumite
    Part of the Furniture 10,000 Posts Combo Breaker
    You can't get IS now if the reason you want to claim is due to being unable to work due to disability.
    Sealed pot challenge #232. Gold stars from Sue-UU - :staradmin :staradmin £75.29 banked
    50p saver #40 £20 banked
    Virtual sealed pot #178 £80.25
  • Understatement! *g*
    Hope you can find something that helps.

    I'm on the quest to find somewhere to live as I only have til 9th March here. *sigh* Wish for a miracle for me!
    I must go, I have lives to ruin and hearts to break :D
    My attitude depends on my Latitude 49° 55' 0" N 6° 19' 60 W
  • bigzippy
    bigzippy Posts: 4,034 Forumite
    Chest pains?

    DD gets those. The GP said it was nothing.

    Mind you, they also said that her fainting regularly is nothing.

    I think I need to be having a terse word or five with the GP....
    One doc told me it was nothing; another told me it was my ribs rubbing up against my sternum and causing scar tissue - which then gets inflamed (I have a lump that gets bigger and smaller on/around my sternum, been there as long as I can remember, and is more painful at some times than at others); and lately, when I said I couldn't take a full breath and was in tears when he asked me to and my peak flow was fine, latest GP said it was costochondritis - all thrown in with the HMS/fibro/ME/CFS.

    Can someone here answer my question?
    ...

    I shall phone the job centre on Monday but I hate phones and only have a mobile so it will cost a bomb.
    Imo you're better ringing BEL than Job Centre directly.
    "I am indelibly stained by hope and longing" - Nuts in May
  • SingleSue
    SingleSue Posts: 11,718 Forumite
    Part of the Furniture 10,000 Posts Name Dropper Photogenic
    Chest pains?

    DD gets those. The GP said it was nothing.

    Mind you, they also said that her fainting regularly is nothing.

    I think I need to be having a terse word or five with the GP....

    His chest pain they put down to his very mobile ribs.......I'm still not happy with that explanation (he also goes breathless with it but they say it is unconnected to his EDS or heart murmur) and we are going to be having another word about this.

    Also going up for his dizziness and fainting, the fact he needs (not just wants, actually needs) high cafeine drinks to stay upright and focused....someone else has mentioned POTS, so I am going to mention that to the doctor as it would explain an awful lot.
    We made it! All three boys have graduated, it's been hard work but it shows there is a possibility of a chance of normal (ish) life after a diagnosis (or two) of ASD. It's not been the easiest route but I am so glad I ignored everything and everyone and did my own therapies with them.
    Eldests' EDS diagnosis 4.5.10, mine 13.1.11 eekk - now having fun and games as a wheelchair user.
  • SingleSue wrote: »

    Also going up for his dizziness and fainting, the fact he needs (not just wants, actually needs) high cafeine drinks to stay upright and focused....someone else has mentioned POTS, so I am going to mention that to the doctor as it would explain an awful lot.

    I have relied on caffeine from about age 13, gradually getting worse as the higher my education levels became although eventually when I was on 6 to 8 cups of strong coffee a day and a couple of unbranded canned drinks I had to stop completely as they were becoming a problem, that was when I was 17. When I went to uni at 19 i gradually became dependant on it again and at one point I stayed awake for 37 hours working on a very important project and drank 16 cans and a fair few coffees, a normal person would still be buzzing after that much (plus a ton of sugar) but i barely felt it, and had my normal sleep patterns after. Now I don't have to be alert I don't drink that much, but if I have to do something that day I still need the caffeine to help. It's sort of another form of medication, so I know exactly how your son feels :(
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