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The Nice People Thread, No.16: A Universe of Niceness.

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Comments

  • Jackmydad
    Jackmydad Posts: 9,186 Forumite
    Tenth Anniversary 1,000 Posts Name Dropper Photogenic
    Pyxis wrote: »
    Can you not get flyscreens here? I'm sure I've seen them for sale in catalogues like Cooper's of Stortford.


    Dear God!
    So you've struggled for years on your own, probably to the detriment of your health, and they say you have attitude?

    image1.gifimage1.gifimage1.gifimage1.gif

    I just don't understand it. :(
    Act all helpless and needy, and you get help. Try your hardest to help yourself, and get a bum's rush. :mad:
    I've seen similar things happen over the years.
    People who make any effort to help themselves are not seen as "needy"
    Those who know that, make sure they're seen as being "needy"
    Sad but true.
  • GDB2222
    GDB2222 Posts: 26,462 Forumite
    Part of the Furniture 10,000 Posts Photogenic Name Dropper
    SingleSue wrote: »
    How about this for annoying. I am apparently borderline for a powered wheelchair from the wheelchair service, not because my level of disability is not bad enough but because I am stubborn and have a "will attempt to do stuff regardless of the cost to me" attitude. So, if I didn't push myself, was a drama llama and didn't push through, I would have comfortably met the criteria.

    A powered chair would change my life. It would give me some independence back, it would help with the isolation whilst the boys are away from home at uni but more than that, it would also stop the damage still being done by my having to attempt to do things just to do the basics of living.

    I did ask her what did she expect me to do when I am on my own, if I didn't attempt to do stuff, to fight against the pain and the dislocations, I would go hungry, thirsty and would be laying in my own toilet functions if I didn't!

    She did say she was going to ask for the adaptations to be enlarged to include widening doorways inside the home and I am to give her a call and go through the referral process again once they are done but that my biggest obstacle would still be my attitude.

    How frustrating. I think that there's a theory that it's better for people to make efforts. That's not a judgemental puritan sort of attitude. The idea is that pushing yourself around keeps you stronger and fitter, whilst having a powered chair means that your muscles get weaker etc.

    The trouble is that that may generally be true, but perhaps not in EDS cases, as you keep damaging connective tissue, which may become weaker rather than stronger as a result.
    No reliance should be placed on the above! Absolutely none, do you hear?
  • vivatifosi
    vivatifosi Posts: 18,746 Forumite
    Part of the Furniture 10,000 Posts Mortgage-free Glee! PPI Party Pooper
    Pyxis wrote: »
    Can you not get flyscreens here? I'm sure I've seen them for sale in catalogues like Cooper's of Stortford.


    You can get them, but they tend to be flimsy hanging ones. Mine are made from very stiff fibreglass. There is now a company in the UK now that does really good flyscreens (The Fly screen Queen), but now I've started getting my stuff in America and doing it "One Piece at a Time" I want them all to match. Though it does make me chuckle and want to break out in song to the tune of Johnny Cash.
    Please stay safe in the sun and learn the A-E of melanoma: A = asymmetry, B = irregular borders, C= different colours, D= diameter, larger than 6mm, E = evolving, is your mole changing? Most moles are not cancerous, any doubts, please check next time you visit your GP.
  • SingleSue
    SingleSue Posts: 11,718 Forumite
    Part of the Furniture 10,000 Posts Name Dropper Photogenic
    Storm!! Absolutely chucking it down and it is right over us.
    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.
  • antrobus
    antrobus Posts: 17,386 Forumite
    GDB2222 wrote: »
    How frustrating. I think that there's a theory that it's better for people to make efforts. That's not a judgemental puritan sort of attitude. The idea is that pushing yourself around keeps you stronger and fitter, whilst having a powered chair means that your muscles get weaker etc.

    ....

    That's what physios think. They don't like powered wheelchairs. They don't like recliners. They don't like anything that makes things easy. They want you to get up off your fat arriss and work those muscles. And pain is a good sign that you're doing the right thing.
  • vivatifosi
    vivatifosi Posts: 18,746 Forumite
    Part of the Furniture 10,000 Posts Mortgage-free Glee! PPI Party Pooper
    For Herts NPs who know the Hemel Hempstead area... plus anyone else who wants to see an amazing photo...


    https://m.facebook.com/groups/705244626157981?view=permalink&id=2283599774989117
    Please stay safe in the sun and learn the A-E of melanoma: A = asymmetry, B = irregular borders, C= different colours, D= diameter, larger than 6mm, E = evolving, is your mole changing? Most moles are not cancerous, any doubts, please check next time you visit your GP.
  • PasturesNew
    PasturesNew Posts: 70,698 Forumite
    Part of the Furniture 10,000 Posts Name Dropper Photogenic
    Where's that s0ddin' moon? Cloudy here I think...

    I can see small clouds... but I think there might be blanket coverage much much higher up.... that just looks like open sky, but isn't.
  • Pyxis
    Pyxis Posts: 46,077 Forumite
    Ninth Anniversary 10,000 Posts Name Dropper Photogenic
    Zilch moon, and zilch ISS. :(:(


    Cloud was far too thick. Not even a glimmer. :(



    And cool and breezy..... so much so that I had a strange thing on called a coat!


    Really annoying about that moon, though.
    (I just lurve spiders!)
    INFJ(Turbulent).

    Her Greenliness Baroness Pyxis of the Alphabetty, Pinnacle of Peadom and Official Brainbox
    Founder Member: 'WIMPS ANONYMOUS' and 'VICTIMS of the RANDOM HEDGEHOG'
    I'm in a clique! It's a clique of one! It's a unique clique!
    I love :eek:



  • SingleSue
    SingleSue Posts: 11,718 Forumite
    Part of the Furniture 10,000 Posts Name Dropper Photogenic
    antrobus wrote: »
    That's what physios think. They don't like powered wheelchairs. They don't like recliners. They don't like anything that makes things easy. They want you to get up off your fat arriss and work those muscles. And pain is a good sign that you're doing the right thing.

    Except when you have EDS, pain is the signal that you have taken it too far and have caused damage and is a very bad thing physio wise.

    It's why normal physios will not touch people like me, too much potential to be sued when (and it is when for most of them), they push it too far/treat us like everyone else and irreparable damage is caused.
    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
    SingleSue Posts: 11,718 Forumite
    Part of the Furniture 10,000 Posts Name Dropper Photogenic
    Pyxis wrote: »
    Can you not get flyscreens here? I'm sure I've seen them for sale in catalogues like Cooper's of Stortford.


    Dear God!
    So you've struggled for years on your own, probably to the detriment of your health, and they say you have attitude?

    image1.gifimage1.gifimage1.gifimage1.gif

    I just don't understand it. :(
    Act all helpless and needy, and you get help. Try your hardest to help yourself, and get a bum's rush. :mad:

    More that the can do attitude counts against me, that I will still try to push things and have quite given in yet. I'll meet the criteria when I have a I give up attitude and won't still try to walk around and do things.

    I don't understand it either but them's the rules...
    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.
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