And so they should!!!!The NDIS would not fund what a parent would do to provide usual care for their child, they would fund care outside of this for example, respite - because Luella’s epilepsy may mean sleep deprivation or monitoring well in excess of what parents of children without disabilities would experience. It would not replace the parental care role ever. All government funded schemes have limitations.
she doesn’t want to be a parent of a disabled child so she has just decided not to. It’s sick