I’m afraid I do not know the answers to the questions.This system I have realised is going to do whatever it wants no matter what! Even as LPA we are have no voice with the GP - who has asked us to go through the home. The care home that said Dad didn’t need a profiling bed/ special chair / soft diet/ help feeding himself. The same end of life care home that specialises in dementia care who have served Dad notice. The care home who repeatedly told me he didn’t need CHC funding who now have requested the district nurse who told me that my Dad after being put on palliative care was fully capable of movement & didn’t need any extra help. Even in the safeguarding meeting this nurse insisted she’d had an interesting conversation with Dad only recently. Dads not able to communicate & we have been his LPA s since 2016 to ensure his needs & best interests are met! His dementia means he is in & out of sleep/ consciousness minute by minute.
This same nurse suggested as LPA I could overturn Dads wishes & the cod evils on the office of guardian documents!
So this professional has been asked by the home todo an apparaial for CHC funding
whatdoido I have to give my permission ??
Your poor dad! It is never ending isn’t it?
Don’t they have Duty of Care? Surely they have to keep him there until somewhere else is found??
I feel for you and I wish I could help you more..