Noah of the Kelly clan

"Time moves so fast - one day its Monday, the next day its August" - Katie Brunwasser Profile pic courtesy of @prest0-art

[asexual-amanita]

Hey guys, this message is brought to you by insomnia and a mild concussion. I am going to be offline for a bit until I recover from said brain bonk. But don’t worry, I will return once my noggin is healed. I probably said that weird, but I’m lowkey really tired.

[noahkelly492]

Welp my phone is officially borked, guess we're in the dads old phone era now

Rust in pieces sweet Smasnug.

[prest0-art]

I wanna draw on my iPad but my charger wire broke 😭 😭 😭

[prest0-art]

I wanna draw on my iPad but my charger wire broke 😭 😭 😭

[noahkelly492]

RIP Presto's charging cable 2020-2026

[stellaxanderandzoeyfan]

Be blessed by maxizzy

[stellaxanderandzoeyfan]

Be blessed by maxizzy

[prest0-art]

Haven’t done any Doccy who stuff in a while

[noahkelly492]

Doctor whatsisface

[prest0-art]

Haven’t done any Doccy who stuff in a while

[noahkelly492]

Doctor whatsisface

[prest0-art]

Rough animation of my OCs (the brothers Edric and Bertram)

[prest0-art]

Small animatic from TikTok

[prest0-art]

Haven’t done any Doccy who stuff in a while

[not-xpr-art]

saw this post about how certain art can be triggering to people with epilepsy & anyone else affected by light and realised that the examples in the post accounted for literally a good 80% of my art...

so like i mentioned in my tags i have been going through and adding a #cw eyestrain tag to everything i think might fit that, but i think people should be aware that my art very often features bright & highly saturated colours and patterns, and often my alternative versions of artworks will feature glitch effects!

[stellaxanderandzoeyfan]

[prest0-art]

I know buddy I know

[noahkelly492]

Officially making this my new pfp (I had prestos permission)

[prest0-art]

Haven’t done any Doccy who stuff in a while

[autisticthoughtdaughter]

Autism is not an excuse, but it can be a reason as to why someone is acting a certain way.

I have told my mom about my autism when I had a meltdown, and she told me to not use it as an excuse. Excuse me but meltdowns are specific to autism, to people with autism. And I was having one.

That is the reason. That is not an excuse. I was trying so hard to improve and to lessen my meltdowns but once in a while I slip and have one. And I knew she knew that, she wasn’t being accepting and understanding.

I am so thankful that I have less meltdowns now. But I still haven’t gotten her nor my dad to understand that I am not using my autism as an excuse, I am explaining using my autism why I act a certain way.

People need to understand the difference between using a disorder as an excuse (Which barely happens anyway) and using a diagnosis to explain one’s own behavior.

[autisticthoughtdaughter]

I love having AAC, and the ability to access it at all times! I love not feeling pressure to use verbal, mouth words to express myself whenever!

But there is a couple of things that i don't like about being an AAC user, and being someone who can use it whenever she thinks that she will need it. I hate not knowing when i should, if that makes sense, need and use AAC. I hate having the fear of being fakeclaimed, of being told that i cannot use it because i could speak or was speaking as well as using it to communicate. I hate people. Especially when i am out and about using AAC.

People need to understand the nuances of being an AAC user, need to understand the nuance of needing something now but not using it later on and not using it after using it that one or couple of times already. I don't know how to help spread representation of verbal, and ocassional to part time AAC users. I dislike that we don't always feel comfortable using AAC out in the public because of outdated information regarding who can and who can't use AAC to help themselves.