Can somebody give highlights of the asd video if they watch it. I don’t think I can go through listening to it again
Spot onThat video : she says the reason most people delay getting a diagnosis is denial.
i felt like commenting : honey did it ever cross your mind the reason your adamant to get one for your youngest is because you are in denial you are raising a brat ?
I’m so naive- never even occurred to me that you could claim money for autism. Sadly, I think your post is probably spot on.I wonder how much she claims for them having the autism diagnosis? Even if she is on the lower rate of DLA of £23.50 a week (£47 for both Will and Bella) it is a lot of money a month. I could be a bad person saying this but I reckon she is claiming the middle componment of DLA of £60 a week each child, as she probably put down they need supervision in the night, hence the stair gates being up.
It goes on care needs and from her videos it doesn’t look like any of them have extra care needs to warrant needing dla at any rate.I wonder how much she claims for them having the autism diagnosis? Even if she is on the lower rate of DLA of £23.50 a week (£47 for both Will and Bella) it is a lot of money a month. I could be a bad person saying this but I reckon she is claiming the middle componment of DLA of £60 a week each child, as she probably put down they need supervision in the night, hence the stair gates being up.
She may show on her videos that her kids don't need care but I bet you any money she says they do need help with everything. She defo is playing the system.It goes on care needs and from her videos it doesn’t look like any of them have extra care needs to warrant needing dla at any rate.
I get mrc for my son and has an ehcp and he definitely wouldn’t be able to hand 2 weeks in Disney land he can’t barely handle an hour in a supermarket,she definitely doesn’t seem to want to disclose what kind of support her children needShe may show on her videos that her kids don't need care but I bet you any money she says they do need help with everything. She defo is playing the system.
My son has asd and I think he is high functioning as he is able to talk and do things but he has no eye contact when talking I constantly have to remind him to loo at me even down to photo or video recording he will never be looking at the camera.
My son constantly wakes during the night and I have to shower him and he has no aware of personal care. He eats by himself but only food he likes otherwise I have to feed him.
I think if she wants to talk about autism and what it means when you have a diagnosis and what support you child will get she should go into more detail. My son attends a mainstream school but is in the asd base part which means he goes to the main stream for certain subjects and when he feels comfortable to be in the mainstream part. When he was not in the asd base he had a full time one to one who had to take him to the toilet remind him to go toilet wash his hand pull his trousers up things like that. I could go into full detail about the support he gets at school but I won't and I think that's what Rhi lacks. She trys to say she wants her kids to access the right support but what kind of support is that and what support do your kids get now in school and out of school coz I I have support out of school to.
Yes my son also has a ehcp and she has never mentioned this before. During half term we go a few days away to family house it's a 2 hour drive, in that drive he constantly asking are we there yet, takes his seat belt of and can't sit on his ass long enough. After 2 days there he starts asking can we go home now he wants his bed his wants his house he wants his TV ect. I don't think I could plan a 2 week trip to America any time soonI get mrc for my son and has an ehcp and he definitely wouldn’t be able to hand 2 weeks in Disney land he can’t barely handle an hour in a supermarket,she definitely doesn’t seem to want to disclose what kind of support her children need
Wales has a different system to England and have ‘statements’ rather than an ehcp. To qualify for a statement their needs have to be very complex so if attending mainstream schools they would more than likely be under the school’s ALN support with a 1:1 assigned if thought necessary.Yes my son also has a ehcp and she has never mentioned this before. During half term we go a few days away to family house it's a 2 hour drive, in that drive he constantly asking are we there yet, takes his seat belt of and can't sit on his ass long enough. After 2 days there he starts asking can we go home now he wants his bed his wants his house he wants his TV ect. I don't think I could plan a 2 week trip to America any time soon
Show us how they really cope. Unless they can cope and that's y she has never shown a bad side to her trips
I do agree. I am in the same boat as you. Its hard to get the money and you don't get a lot.Something to note re: benefits like DLA and PIP is that they absolutely do not hand them out like sweeties. I say this as someone who claimed DLA as a child and now claims PIP as a disabled adult. It isn’t easy money. This woman has many issues but I don’t think comments practically accusing her of benefit fraud are particularly fair.