Sunflower :)
Member
And yet again, when she DOES book hotels to stay in with J they never use a travel cot/put me up bed etc. She doesn’t even use a bed guard. He sleeps with her. But he needs his padded cell when he’s at home. Because that looks good for the DLA and justifies Kiera’s right?!. And still she wants adaptations and still the Hun’s think her house is unsuitable for J and his mobility needs
That bed always makes me wonder, obviously I understand some kids with special needs actually need them, but for J, if he's as bad as she makes out with vomiting (which we know he isn't) he's probably terrified when he wakes up and feels ill. Plus, she's admitted to not hearing him wake up and sleeping in, meaning he's been alone long enough to fall back asleep by himself. I know all kids are not the same, but any child at that age, I've encountered needs at least 2hrs stimulation before falling back asleep. Plus, if I woke up felt sick, and got sick in my bed without being able to move I'd be crying too and I'm an adult. Imagine how frightened he must be in those scenarios.
Although, I remember reading an article years ago about kids in orphanages learn to not cry out if they need help because they learn that no one is coming to soothe them and I have no doubt that Kathleen has thought J this. I'm not judging the cry it out method, although I don't agree with it, I understand it works for others but not with a child who can vomit at any time and can't shout out 'mum my head hurts' etc. Plus she has him on nurofen that often during the day, it probably doesn't even cover pain if he had it.
I don't understand. Children have been taken off their parents for less negligence than she does. But there are so many health professionals involved with J, why is no one stepping in and saying this isn't right. She changes his meds every other week. She leaves him in soaked clothing and nappies falling off, enough for Instagram to notice. She starved the child into looking like a child from a third world country so he could lick a chip from a happy meal. Monetises him regularly. I don't know how she still has him in her fulltime care and isn't on supervised visits. I'd like to think if we went down that road of negligence, a family member would have a word, or the school or hospitals would get involved and social services would link in, for nothing other than our children's safety.
Sorry. I get into a rant so easily from her!