She tests at "functionally hearing" levels, not HOH, not mild or moderate. But I can tell you as her mother that she doesn't hear the way a typically hearing child does, so I think it's misleading to label her as either hearing or mild/moderate HOH based on those tests. Her doctors don't, her teachers don't. They consider her functionally deaf, but with access to sounds via CIs.
Her accommodations needed are different from a mild or moderate hearing child. She's a deaf child. When her CIs are turned on, coils are in firmly place, and there are no barriers to the sound, she has access to sound at the levels a hearing child would have. If someone is talking and she brushes her hair aside, moving the coil a centimeter to the left, she hears nothing. If her ski helmet moves the coil a centimeter to the side she goes from hearing me giving instruction 100 yards away to hearing nothing. She can hear conversations from the playground out a closed window as clearly as the teacher at the board, but if her batteries die in the middle of class, she hears nothing. It's very different from a 30db shift in degree of hearing when you take off a hearing aid. It's a 90+db shift. Her learning environment has to take into consideration that if she has a cold, if her equipment breaks, if the wind blows a certain way she can be participating with a 100db hearing loss. I agree with SR171Soars, that access to sound via CI is temporary and tenuous, it's not a permanent altering of a child's hearing state.
You know that I think the CI successfully provides my daughter with access to sound, but I think it is as important to understand the limitations: this tool does not make her hearing, nor does it make her mild or moderately HOH. She's deaf, with a tool that she picks up and uses to hear, and puts away when done.