What do you wish you knew at the beginning of your kids diagnosis?
My 8 yr old daughter very likely has adhd, we have a dr appt with her pediatrician next week to discuss a possible diagnosis and treatment, etc. I’m new to neurodivergence in general and have a lot research to do. She specifically has troubles with emotional regulation, outbursts, transitions, friendships, and plenty of anxiety.
I’m specifically wondering what you wished you knew in the beginning: things that might help me best approach the dr visit and things to bring up or ask for - or things to not mention! Are there niche symptoms you wished you recognized? Or therapies you wish you knew about that weren’t offered at the start? Any other “insider” info or advice from a parent who’s gone through this before? (Similarly to giving birth, for example, I feel like half the time women aren’t given all the options, and might’ve liked to know the options.)
In my experience, even good drs don’t have all the info or know to ask the right questions, etc. Thanks in advance!