Six plus months if you’re lucky!! Waitlists are more like two years where I amYeh that’s what got me. Speech wait lists are 6 months +, this entitled person puts a call out with the aim of bypassing that. So much wrong with that. Makes my blood boil
Exactly. I know she mentioned that they don’t know the extent of L needs right now. But it’s very sad that given they have resources and an architect that they haven’t approached the design with ideas of how to plan for the future. She’s just in denial though isn’t she.I still can’t get over the fact they haven’t design their house around Lus needs? Like they’ve employed architects and would be costing millions but didn’t get in anyone to actually talk them through how to set up their house for their disabled daughter?
She doesn’t want to modify her new house because she doesn’t want anyone with a disability living there. Lulu can live on the ground floor with a day/night nurse and the family can live their life upstairs! Truly that’s what I get out of her comments.Exactly. I know she mentioned that they don’t know the extent of L needs right now. But it’s very sad that given they have resources and an architect that they haven’t approached the design with ideas of how to plan for the future. She’s just in denial though isn’t she.
100 percent what I think.She doesn’t want to modify her new house because she doesn’t want anyone with a disability living there. Lulu can live on the ground floor with a day/night nurse and the family can live their life upstairs! Truly that’s what I get out of her comments.
That’s exactly my feeling as well. It all crystallized for me when she was talking about possibly keeping Lu in the guest bedroom downstairs instead of designing the whole home with accommodations.She doesn’t want to modify her new house because she doesn’t want anyone with a disability living there. Lulu can live on the ground floor with a day/night nurse and the family can live their life upstairs! Truly that’s what I get out of her comments.
Yes same. Just shows how disconnected she is. She’s got the night nurse for Luella and she looks after the baby who wakes what did she say, once a night?The worst thing she said is that Lu may end up living downstairs, that’s horrible. I honestly can’t get over her saying that.
She’s so fake. Just a smile for the camera.When she said all that and they didn’t know what the future holds after saying in the podcast Lu would NEVER WALK etc etc…(so she knows that she would need a lift in the future) it made me think the worst that it wasn’t worth putting in the accessibility/ mobility measures in for Lu..
But in recent stories she seems much happier to be with Lu. So that’s a nice thing to see. As Lu really is just poor joy!
Exactly !!!! She is the one who keeps saying she will never walk. So put the lift in already rather than spending millions on a custom build that is aesthetically pleasing but not functional for their familyWhy does she keep saying she doesn’t know what the future holds and also that Lu will never walk? If she knows she will never walk, why not put a fecking lift in now.
Denial is strong in this one. Devastatingly, life-alteringly strongIt’s just so sad. Imagine having all that money and resources at your disposal and not doing everything that you can for that child.
Saying they don’t know what she’ll need in the future is a cop out. Pathetic.
For someone who whinges about having no freedom, she sure has a lot of it...much more than your average mum.I thought she didn’t have a village? 3 events in 1 weeks..
She’s been out to more events in the last 2 or 3 months than I have in the last 2 years!For someone who whinges about having no freedom, she sure has a lot of it...much more than your average mum.
I love this. Thanks for sharing!A good article that Erin should read. From an adult's perspective, but the essence is the same.
Dear Mum: Love, your disabled child
We need to talk about those photos of me in the hospital that you keep posting on Facebook!thedlist.co.nz
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