Well, I should've realised that after my first 'virgin' year with the NDIS- things might get trickier!
Thinking of you @MaitlandGirl I think I just copped something like you have.
DSalmost-7 had his next 12 month plan approved, so I thought, via a phone call and supporting email from our LAC. I was so happy & relieved.
But no- I've since had correspondence (email letter and phone call) to say I need to provide support letters from every therapist/doctor he's ever seen. I freaked!
Now I've calmed down, it's actually not so bad. It meant I've had to harass his Physio, Play Therapist & OT to spend time writing up support letters. Thank goodness they're all well familiar with NDIS guidelines/practises and can knock up these letters quickly, without charging me much.
Also, as NDIS providers, they should want to protect their own income. Eg, Play Therapy is $165/week. Over 12 months that's nothing to be sneezed at. The Play Therapist damn well should spend time unpaid to secure that income. Luckily the physio agreed.
The issue seems to be I need to prove permanent impairment rather than permanent condition. All utter semantics. Imagine the child with cerebral palsy, unable to walk and in need of full care- why should you have to prove their condition hasn't improved in the last 12 months?
"Dear NDIS, I'm writing to inform you that a miracle has occurred, and our funding can be substantially reduced. The Pope has been informed and we've been praying to St Whatsherface. God Bless".
I'm on it, it's a bugger of a task though. Thank you for the vent!
Please join in with your own NDIS moans :)