DD is one of the early-diagnosis cases. She was dx'ed just before her 5th birthday. Yes, that's unusually young, but, in her case, there were other factors at play--namely, she was exposed to meth and other harmful substances in utero (she's not mine biologically), both birth parents had ADHD, and both older siblings had/have significant mental health issues, so I was a bit anxious/overly-pro-active making sure things were addressed sooner rather than later.
Our initial flags were things like:
--DD had no idea that Dora (or any show) was more than just the time between commercial breaks--she couldn't stay in one place long enough to see that there was a story in a TV show!
--Impulsivity was far beyond what we saw with other kids her age.
--She had no understanding of "sometimes": it was either black or white. So, if I allowed, let's say, Kool Aid at dinner one night, she was convinced Kool Aid was a dinner drink, and dinner drink only. (Talk about confusing when I tried to do something fun, like ice cream for dinner on a hot day, and she flipped out that we were having an afternoon snack-time food at dinner time!)
--Emotions were always in "black and white" as well--either she was super happy, or super sad, but there was no middle "it's an okay day, not good or bad" for her.
--Staying on-task for short, multi-step tasks was difficult. (I was having to help dress her at 5yo, because she couldn't work through how to get undies on if she had already put pants on, and couldn't remember to put undies on first.)
--She couldn't stay still long enough to fall asleep at night.
--If a task required concentration, she immediately deemed it "too hard."
We started noting these things when she was young--like 3yo. It was obvious there was just something "different" about her, especially when we compared her and her similarly-aged cousin to other kids around their ages. (Cousin is still "quirky" but doesn't have any diagnosis.) She needed her tonsils and adenoids out (she had frequent adenoid infections), so we did that first, right at her 4th birthday. We knew that often OSA (sleep apnea) can look like ADHD because kids with OSA don't get restful sleep. So, we did the T&A, and she finally started sleeping better. But, her impulsivity didn't improve. She still couldn't "be still" for *any* amount of time. Seriously, she couldn't be still long enough to go pee without getting it everywhere! At that same time, we knew that DD turned into a "demon child" when on Amoxicillin; when we did the T&A, she didn't need Amox all the time any more, so we thought that would help improve things as well. But, her impulsivity still wasn't age-appropriate. She was ran by a motor that just wouldn't stop, no matter how hard she tried to control it. And, oh so often, she would do something impulsive, not be in control of herself, then bawl when she got in trouble for it, saying that she knew it was naughty but couldn't *not* do it.
So, at her 5th birthday, it was obvious that she needed help to be successful. She was testing "high" according to the child psych we took her to by our report, but she couldn't "perform" for the psych, so it was hard to get an accurate picture. We just knew that she was obviously smart, but couldn't show it, because she spent so much energy just trying to keep herself and the impulsivity in check. I took the plunge, and started her on liquid methylphenidate. It was like the dark finally lifted, and I had this smart child who was learning at an astonishing rate, who people loved to be around, asking to have her over for play dates, listening (like old ladies stopping me to comment on how well-behaved she was!), who could be in control of her body. I hesitate to call it a "miracle" for her, but it was pretty amazing for our family!
We went through the whole PT-OT-Nutrition-DevPed-psych work-up when she was 5.5yo, and she was diagnosed with ADHD, anxiety, PTSD (due to issues before she came to me), and a few other things. The Dev. Ped recommended continuing on the medication that we had started.
She's now 11yo, and we're taking our first break from medication for the summer, at DD's request. She's doing "okay" without it, but we're only on day 3 or 4. We talked about it before we did it, both with her and her doctor. The doctor wanted the break so that DD could continue into puberty without it as much as possible to allow her body to grow naturally without "fighting" the medication. DD wanted a break from it because "other kids don't have to take medicine every day." We talked about how she would be getting lots of reminders about her behavior, and that she would need to keep a good attitude about it, as we only point it out to help her be aware of it so that she can work on being in control of __whatever__.
Personally, I wouldn't change pediatricians just because one office diagnoses ADD/ADHD more than another one. In this case, I don't think "old school" is a bad thing. Quite honestly, I think ADHD is WAY over-diagnosed, and often used as a catch-all when nothing else seems to fit. Kind of like an office where I used to work--the doctors had their 10 favorite diagnoses, and everyone got put into one of those until proven different. DD was initially diagnosed by her (old school) pediatrician, and then the Dev Ped concurred. If *I* switched because I heard that Group B was more likely to give an ADHD diagnosis because they "see it more", I'd forever be wondering if it's "really" what was going on with DD, or if it was the "easy answer" for the doctor to give to satisfy the need to name behaviors.
--Mimi
Mom to Lala (2004), Bonus Mom to Big Sis 1 (1991) and Big Sis 2 (1992)
Grammy to Big Kindy Kid (2011), Big Pre-K Kid (2012),
Grandbaby Appendage (2014), and New Baby Grandboy (summer 2017)