Any mums of kiddos with cp?

My 6 month old has been diagnosed with very mild CP. He starts birth-3 and p/t next week. I have no idea what to expect with this diagnoses. If it’s mild like they’re saying, is there a good chance p/t will be enough him to help him live a pretty normal life? Is there a chance it could get worse yet? The neurologist didn’t tell us much other than another mri at 1 year unless they p/t decides he needs one sooner. Now that I’ve had a day to think about it I have so many questions but they are so busy they don’t really make appointments just to answer questions 😬