My neice has CP aquired at birth from birth trauma (placental abruption at term) and they knew from the get go that she would have CP to some extent but only time would tell the severity. My niece has a neurologist and she was having a lot of scans and tests done to determine her level of brain damage and by 3 months she was seeing a phsyiotherapist 2 times a week to help with muscle tone and core strength. When she was 12 months she was accepted into CPEC (Cerebral palsy education centre) run out of Monash down in melb and as far as I know my sister doesn't pay for a cent of it as she got a govt funded place I think. She attends there 3 times a week. She does have to pay for some equipment but there is funding available to help with costs of that as well as various charities. I really think that waiting till she's 2 would be detrimental to her as they need to get onto it now, the earlier the better really.

I think you should give CPEC a call and explain the situation to them and they could help put you on the right track in terms of costs and treatments etc.