I remember the most random things...
I remember the most random things...
No, not like that.
More like: Johnny says he’ll be here at three. Johnny shows up at 3:25. Kid is pissed he wasn’t there at 3.
Or: Hey, we might go out for pizza next Friday. Kid hears Friday=Pizza, and gets pissed because some other thing got in the way of pizza and didn’t hear the “might” part.
Nobody lied with the intent to deceive or mislead. Just life happens.
Ugh. Yeah, that sounds familiar. Never seen people send themselves down that cycle so hard. Get punished, unable to let go of the anger, get told to stop or more punishment, I don’t fucking care punish me, gets more punishment.
Sucks if you don’t understand it. People just need to be told to fuck off and cool down, then you can deal with it. In the heat of the problem ADHD makes it so much worse.
People self-diagnosing young children with ADHD is the dumbest thing.
Children are full of energy and easily distracted, people! That’s their whole thing!
How do you know it’s self-diagnosed? Children have diagnosable ADHD, and nothing in this post suggest this parent just randomly diagnosed their child.
ADHD is not the same as being “full of energy,” that implies a deep misunderstanding of the condition.
This comment said:
People self-diagnosing young children with ADHD is the dumbest thing.
Children are full of energy and easily distracted, people! That’s their whole thing!
Well, I’m closer to 40 than I am to 30 and only kinda figured out I had it like 2 years ago.
If you can function fine without meds then an official diagnosis might not be worth the costs and trouble. Self-discovery is a good thing though and there are many ways to do that, all are valid.
Another thing though is that the symptoms tend to get worse as you get older because managing the traits/symptoms associated with ADHD takes a lot of energy and after a while burnout becomes a very real possibility.
The only reason I noticed my own symptoms and ADHD traits is because of that. Had somebody suggested I had ADHD a couple years before that I would’ve said that there was no way. Looking back now though, it was there all along but back when I was younger it was easy to find and maintain coping mechanisms.
It gets tiring.
I don’t know how well you’ve got a handle on your symptoms, so it’s impossible to say.
In my case mine got worse within the last few years. A cortisol response to chronic stress, it felt like i lost all the gains of willpower and responsibility i had gained, and returned back to my struggles of my youth.
Finally accepted i needed help and am still finding my way, but i just feel more normal now. I never would have given in if i had some semblance of function, my old man’s stubborn distrust of doctors of any sort rubbed off i guess.
For me, it gets rid of the worst of the ‘static’ running around my noggin, let’s me focus without feeling like I’m flexing a muscle, and gives me a lot more oomph to complete tasks i gotta do without my brain flashing the danger sign.
Im just getting started mind you, perhaps I’ll find more changes as i get further along this trail
I was diagnosed in my mid 30s. I even managed a good grade on a physics degree, without assistance.
By my 30s I began to burn out. I got diagnosed mostly since I thought the meds would help. In practice, the CBT helped even more. For the first time I was talking to a professional who both could keep up with my thought process, and offer useful advice and methods. It’s helped me unpick a good number of maladaptations I had, and so free up a lot of mental resources.
It also helps to know that I am not a failed horse, but a highly effective zebra.
It definitely does.
I normally use a tank analogy. A tank is a shit vehicle for commuting, or distance driving. If you never even know you can go off-road, you’ll never see the benefits, only the costs.
The zebra analogy is the more traditional one however, and tends to ring with more people than my variant.
Because it’s a spectrum everyone is on. Clinical diagnosis asks “how many,” “how often,” and “is it causing problems” to locate a patient on the spectrum. That is, yes ADHD patients’ experiences are mostly common; it’s the rate of recurrence and their control of it that is not.
Also, many are undiagnosed so when I see comments saying “but that’s what it’s like for everyone, almost all of these memes apply to me” I sometimes feel I should ask how many apply, how often, and is it causing problems.
Relatable. My partner termed it best when he made the observation that I treat my environment like a matte painting in a cartoon. If I place something down and don’t make some kind of mental note it’s gone. Dissolved into the matte painting and requires playing a hidden object game to solve. Whereas if I made some kind of note even “that’s interesting” I will remember for weeks where something was.
Enfuriatingly “have you seen my…” sometimes gets answered with “have you checked the matte painting?” bloody lucky they’re cute enough to get away with it.
Oooh. How’d you make it so far without a diagnosis if it’s severe?
I got diagnosed at 40 because my son was diagnosed and I saw a lot of similar behaviours so figured why not.
I wouldn’t classify myself as severe and hell I make good money with a good career so clearly I manage it.
That said, I look at peers who got diagnosed young and regret I didn’t get the same. I struggle with RSD and specifically emotional regulation. Successful in everything but relationships which is arguably the most important thing in life. Where diagnosed peers got assistance and understanding I had a childhood filled of “do better” and “if only he applied himself” or “shut up”.
It’s disheartening.
That said, I’m happy for my son and hopefully he will have more success.
Hindsight 20/20 here too.
What’s important is we give our kids the tools we didn’t have.
I’m also working with autism diagnoses with my kids too. You got this. The universe doesn’t hand you problems it doesn’t think you can’t handle.
I got diagnosed young and didn’t get a lot of the support you’re talking about. It was more like they threw ritalin at me and expected me to be normal now. Also, Ritalin was terrible.
I think it has less to do with the early diagnosis and more with the public perception when the diagnosis was made. There’s more understanding now than before.
Yeah sorry when I said support a lot of what I meant was the understanding part. Simply having a diagnosis changes a person’s perception. That’s what I was lacking growing up as I’m sure many like me can attest.
Simply having the acknowledgement I’m different and maybe I’m loud in class for a reason that I’m not to blame could have helped with my at times crippling self awareness and internal criticism.
I’d argue a lot of my negative perceptions of myself and the world around me stem from having to grow up alone and struggling in silence for all those things neurotypical people take for granted.
Sometimes a simple label is support enough.
The contrast between these two states is unbelievable sometimes.
Behind the potted plant next to the TV, I saw it there last week!, I shout from the other room as my mum hasn’t even finished asking her question.
At the same time, I only remember what I had for breakfast because I’ve been eating the same exact thing for years now.
I’ve been eating the same exact thing for years now.
Ok, is this also an adhd thing, because I’ve been doing the same and people around me keep commenting on it.
What’s weird as someone who was diagnosed at 40 in comparison to my son at 8 a lot of this behaviour I see in him and not necessarily with me. I don’t know if this is because of the separate angle that people with ADD are consistently oblivious to what’s happening around them lol.
Like little dude will not sleep on some passing “commitment” I made to simply shut him up 3 months ago. 🤣