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@anonymousspaceman
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Yo just curious any of yāall autistic and hypersensitive to tastes and just donāt like water???? Or will only drink water from certain sources? Like if Iām not desperately thirsty Iāll only drink bottled water or water from one specific sink in my apt- all other water just tastes Bad, yknow? And water from those Brita pitchers is something I absolutely do not fuck w at all- shit tastes nasty. Reblog with your water preferences in the tags cuz neurotypicals always b tryna tell me that āwater has no taste itās just water and all tastes the sameā and I KNOW thatās bullshit
I'm not sure if I'm quite hypersensitive to taste, at least not in the extreme, though I do get all of my water from two towns over because the water from my house tastesā¦bleh. Kind of like if someone had added chlorine to it.
By "I get my water from two towns over", I mean that I take an hour out of every week to fill up a car full of jugs using my grandma's tap.
I also bring a large water bottle with me wherever I go, which used to include restaurants (because their water is always a wildcard in terms of quality and I only really drink water).
OOOOO IM WITH YOU ON RESTAURANT WATER. I havenāt gone to restaurants for a while due to covid, so I forgot all about restaurant water, but you really never knew what you were gonna get. Iād say that most of the time restaurant water tasted godawful, and Iād have to order something else to drink. But there have been a few rare times Iād gone to a restaurant and the water absolutely SLAPPED so hard I drank multiple glasses.
I admire your dedication to good water. And thatās actually a really good idea. Iām moving out of my parents place soon, but I think Iām gonna have to come back often to fill jugs of water as well. Because no water tastes as good as the water from my parents bathroom sink, absolute god tier stuff.
So it turns out that my parents apartment building is one of the only in the area which still has lead pipes. I for some reason thought that all lead pipes in my city were replaced before I was even born, and thatās what happened for the most part but there were some loopholes for some buildings that got to keep their lead pipes I guess. My sister only found this out recently because she works in waste management and had access to the documentation for some reason. My city is known for having some of the cleanest drinking water that you can drink straight from the tap so I never thought this was a possibility, but that delicious water that I drank alllll the time was lead water š« coooool
Does anyone else with autism/sensory processing disorder have an extreme aversion to eating leftovers? I mean, food that is prepared, refrigerated and then heated back up like food you take home from a restaurant or leftover takeout. For some reason I just canāt do it. There are exceptions, such as if I buy already prepared and refrigerated at a store, or if someone else heats it up for me and I donāt have to look at it or smell it before it is ready. Everyone makes fun of me or gets mad at me for being like this and makes me feel like I am spoiled or a baby or a drama queen and it would make me feel a lot better to know Iām not the only one
Itās been a long journey friends⦠but we made it
Thank you @lunamay3 for this wonderful discovery
Go get yall glow tangles!
The problem with Vyvanse, as Iāve said frequently, is that it takes a while to kick in. I have always had a really hard time getting up in the mornings, because there are so many little choices and steps involved in getting up ā what will I wear, what will I eat, I have to get out of bed, get my pills, get dressed, brush my teeth, give my cat her meds, etc ā that are death to people with ADHD. It takes me hours to get out of bed, and it was worse as a kid. I usually wake up around 9 or 10 and then am on my phone for 1-2 hours at least before I get out of bed and take my meds, and then itās another 1-2 hours before they kick in, which means all those tasks are still really hard because Iām unmedicated, and I often get distracted before I get around to what I need to do, so that by the time it kicks in Iām already way off track.
My psychologist was like, ok, well how about putting your pills by the bed, and then taking them as soon as you wake up, so that by the time youāre ready to get up itās kicked in? I said Iāve thought about it, but always forget to put them out the night before, and the process of opening 6 bottles and getting the right ones and getting a drink etc feels like too many steps overwhelming my brain so I justā¦donāt. But I got one of those pill boxes and prepoured all my morning meds for a week into it and put it by my bed with a drink, and so the past two days Iāve done that, and itās GREAT. Oh my god! When Iām done dicking around on my phone, Iām ready to go! I can justā¦get dressed! And eat breakfast! And plan the day! I imagine this is just what normal people do all the time without even thinking about how many micro steps are involved in everything about getting ready for the day, but I feel like I discovered a superpower. Itās amazing.
ADHD medication is really life-changing, and it makes me sad when I hear adults talking about how their kid needs it but theyāre not sure because they donāt want to āchange their personalityā or whatever and when Iām able I will actually jump in and tell them this. Itās not a quirky fun kid disorder where youāre just a bit bouncy. Itās not even about doing poorly in school. Itās about all these things normal people donāt even notice, like how fucking hard it is to get ready in the morning. When I was a kid I would for real sit on my bed for hours staring at my closet because I couldnāt decide what to wear or what to have for breakfast, because that choice paralysis is amplified a million times in an ADHD brain. My room was always a mess, I couldnāt keep track of anything. Schoolwork as a kid is bad enough, but if you donāt find workarounds, thatās going to be that person as an adult with bills and responsibilities. And a lot of us do find workarounds, but they only work to a certain point, and then youāre in high school or college or have a career or a kid and it fails and your life is a disaster. Itās a severe disability. My ADHD impairs my life way more than my chronic pain. And treating it is so simple. As far as psych disorders go, it is is the easiest to treat, with very high success rates, relatively few and mild side effects, it works right away, and most people respond to the first or second medication they try, unlike antidepressants, which take several weeks to see if theyāre working and often have to go through many classes of drugs to find the right one and the right dose. Give a kid with ADHD Adderall and they will improve, like, in twenty minutes. It doesnāt change your personality, unless by āpersonalityā you mean the crippling anxiety and low self-esteem that comes from feeling like a constant failure and being irritable all the time because youāre being overloaded by tasks you canāt manage. Itās not addictive as long as you take the correct amount, and ā this is an extremely important fact I want every parent and clinician to know ā untreated ADHD is itself a big risk factor for substance use problems, and yes, giving these people amphetamines or other stimulants will lower that risk significantly. Frustrates me how the guidelines often say donāt give it if the person āabusedā stimulants ārecreationally,ā because usually that term āabuseā has nothing to do with actual criteria of SUD but refers to anyone using drugs not prescribed to them, which, not surprisingly, a lot of people do as an unknowing form of self-medication. Youāre not going to get someone off meth and get them to get their life together if that meth is the only thing thatās been letting them function at all, and treating underlying disorders is a critical part of SUD treatment that gets overlooked because itās treated as a moral crime or a lack of willpower. Anyway thatās a digression but I have to say it every time I talk about ADHD meds because itās really terrible how many people suffer against this huge obstacle to their lives just because there are stupid stigmas about medication.
The rest of managing ADHD is about jerry-rigging workarounds like putting pills by your bed or putting all your clothes in bins under your bed because sorting and folding them is too much for you or writing notes using multiple different pens to make it easier to read or accepting that you can actually just eat all the individual parts of a sandwich separately if all the steps involved in making the sandwich is freezing you up. You really need both of these things, these modifications and medications together, because the life hacks wonāt solve the underlying problem and the pills wonāt suddenly teach you time management. But man, what a difference it makes when you actually get what you need.
Just went to the doctor for a physical and brought up how Iāve been concerned because I have horizontal ridges in my thumbnails and the internet says that means I probably have one of several life threatening conditions, and she took a look and immediately asked if I rub my thumb nails a lot. I said yeah I actually do cuz itās a stim Iāve been doing a lot lately, and she said thatās why. It makes total sense with the timeline of when I picked up that stim and the affected fingers, but I just canāt believe thatās the reason and I canāt believe she was able to pinpoint it instantly lol. And Im soooo relieved that it doesnāt mean Iām dying!!!
Yo just curious any of yāall autistic and hypersensitive to tastes and just donāt like water???? Or will only drink water from certain sources? Like if Iām not desperately thirsty Iāll only drink bottled water or water from one specific sink in my apt- all other water just tastes Bad, yknow? And water from those Brita pitchers is something I absolutely do not fuck w at all- shit tastes nasty. Reblog with your water preferences in the tags cuz neurotypicals always b tryna tell me that āwater has no taste itās just water and all tastes the sameā and I KNOW thatās bullshit
I'm not sure if I'm quite hypersensitive to taste, at least not in the extreme, though I do get all of my water from two towns over because the water from my house tastesā¦bleh. Kind of like if someone had added chlorine to it.
By "I get my water from two towns over", I mean that I take an hour out of every week to fill up a car full of jugs using my grandma's tap.
I also bring a large water bottle with me wherever I go, which used to include restaurants (because their water is always a wildcard in terms of quality and I only really drink water).
OOOOO IM WITH YOU ON RESTAURANT WATER. I havenāt gone to restaurants for a while due to covid, so I forgot all about restaurant water, but you really never knew what you were gonna get. Iād say that most of the time restaurant water tasted godawful, and Iād have to order something else to drink. But there have been a few rare times Iād gone to a restaurant and the water absolutely SLAPPED so hard I drank multiple glasses.
I admire your dedication to good water. And thatās actually a really good idea. Iām moving out of my parents place soon, but I think Iām gonna have to come back often to fill jugs of water as well. Because no water tastes as good as the water from my parents bathroom sink, absolute god tier stuff.
Source ~ FB The Chronic Couple
[Begin Image Description: Title "Dyscalculia: A Math Learning Disorder"
Various pastel bubbles:
Trouble recognising quantities without counting
Often needs a calculator
Trouble with mental math
May count with fingers
Struggles to keep score in games, often losing track of whose turn it is
Misplaces objects frequently
Gets lost easily
Has trouble telling time on an analogue clock
Difficulty remembering number related dates and facts
Misjudges how long it will take to drive somewhere
Frequently late
Difficulty sorting out directions (right from left)
End Description]
working memory bad š
ALTERNATE ENDING:
there are lots of coping mechanisms out there but this is the only method that (sometimes) works on my wretched brain. can't remember? predict the Future
Congratulations to Definitely Craig on being the funniest person alive.
To other autistic people, are you able to drive?
(Personally, I cannot. I havenāt taken the test, but I donāt plan to either, because I fear I would struggle on the road with parking, keeping the car between the lines when driving, knowing to keep my distance and remembering to turn on signals etc.)
I have my permit, and I really want to get my license. Especially since one of my special interests is cars. I donāt drive much though because I never have the opportunity, I live in a big city and itās easier to just use public transportation. On the rare occasion that I do drive Iām way too cautious because I have difficulty with all the complicated shit I have to remember like signals and stuff and with spatial stuff like you said, keeping the car between the lines and parking. Not being able to drive makes me feel trapped sometimes and I hate relying on other people to drive me places but Iām so terrified to learn.
Since I found this post again I just wanted to update since I just passed my road test a month ago, at 27 years old. I never thought I would get to this point. Iām still working on things like highways and still not comfortable driving alone, but my confidence and my driving ability have been improving drastically the more I practice.
I think what helped me was taking professional lessons. I couldnāt afford them so Iād given up on ever learning, but when I was gifted some lessons by a generous family member I figured what the hell, might as well try. And it made all the difference. Iām pretty sure my instructor was neurodivergent, we never talked about it but I could tell from how we interacted (the 15 minute mutual infodump session about Doctor Who that he pulled over to have and had to extend the time of the lesson for was the thing that clued me in lol, but there were also subtle things in our conversations that made it obvious to me). He understood my struggles with driving on a personal level and bc of his own experience with the same struggles was able to give me helpful tips on compensating for them, even with differentiating left and right, and helping me know how to deal with getting overstimulated and overwhelmed while driving. Also, this is the thing that really helped the most- he assured me that no matter how bad I did, There was no risk of harm to anyone because he could control the car from the passenger side if he needed to. He promised me it was just my fear holding me back, and then he took away the thing causing the fear, essentially. Knowing it was virtually impossible to fuck up, I just went for it, and I actually was way better at it than I thought I would be, including with all the things I mentioned struggling with in the last reblog. I practiced with my dad a lot between lessons and found that I felt pretty confident in my newly unlocked ability and the tips Iād learned, even when the car couldnāt be controlled from the passenger side. I donāt know if my experience was unique since the instructor was clearly neurodivergent and knew how to work with me, but the lessons really really helped me and I couldnāt have done it without them.
I still failed the road test twice, because the testers were a lot less kind and neurodivergent-friendly than my instructor, and some of them like to psych you out, but I eventually got a tester who seemed uninterested in all of that and just truly wanted to assess my skills, and he passed me.
I just went on vacation with my girlfriend and did about a third of the driving. Iām working on being able to do half or more of the driving in the future. Thatās something I would have never thought possible when I first reblogged this post. I am excited because as I improve more job opportunities and more freedom will be unlocked for me.
After two failed road tests a year apart with a whole pandemic in between them, I finally just passed my third today!!!!
I am actually a very good driver at this point, but Iām evidently not a good road test taker. I also kept having examiners who would psych me out so bad Iād mess up on very simple things- this last one, thankfully, actually seemed to be a decent person and not a hardass who just wanted to see everyone fail.
Iām so happy and so relieved itās over with and I never have to do it again!!!!!
So I finally introduced my girlfriend to one of my special interests (sea glass) and Iād say it went pretty well
Any autistic people have experience with gabapentin for anxiety??
My dr just prescribed it to me and said that autistic people tend to see better results from it than they do from ssris
I feel like Iāve seen mixed opinions of it online and I donāt know that much about it so if anyone has been on it what was that like?
To other autistic people, do you struggle with knowing when you're hungry?
I have no idea that Iām hungry until Iām ravenous and by that time itās too late to try and make anything that involves more steps than just throwing something in the microwave. I try to keep well stocked on frozen meals š°
Time blindness is the weirdest aspect of executive dysfunction and so weird as an experience to live with. Itās like you see the clock, the clock says 3pm, you look at the clock again and itās 3:02, then 3:05, and then you look again and itās 8pm and WHAT THE FUCK.
You donāt even need hyperfocus. But hyperfocus is like the Warp Speed:tm: version cause when that hits, itās 3pm and then itās the next day and why is the sun rising and when did i last eat and oh god i need to use the bathroom. And oh, also, youāre EXHAUSTED. The act of your brain tunnel visioning on something drains you (but thatās another topic).
Time blindness isā¦. having the general knowledge that today is Wednesday, and you need to do something on Thursday. Thursday is logically tomorrow, but the mysterious void of time is likeĀ āthatās like next week or something.āĀ Itās knowing you have to do something in three weeks on the 21st. And as the days creep closer, the 21st is stuck in a constant state of still being 3 weeks away, despite the fact itās now tomorrow.
Itās wild. ADHD is literally living in a constant state ofĀ āThere is Now. And there is Later.ā and thereās no in between; no dates, no times; no hours, weeks, or months. Itās just Now and Later, and oh god why is is X oāclock already!?
Maybe I DO have ADHDā¦.
god, no oneās ever succeeded at describing this for me before.
Reblog if you believe phone call anxiety is real and it isnāt childish bad behavior.
Trying to prove a point to this job helper.
Phone calls can be harder on your anxiety bc you cant pick up on the other persons behavioral cues as you talk with them
^^^^
After 10+ years of psychotherapy, almost all of my social anxiety triggers are now at a manageable levelāeven academic public speaking, which was my #1 worst trigger for most of my lifeāexcept for my phone anxiety. Itās literally the one and only thing Iāve never been able to significantly improve.
I have to talk the whole conversation through with my friends beforehand.
I have to get explicit confirmation from my friends that āyes, you really need to ring that person right nowā.
I have to write scripts.
I have to take anti-anxiety meds, or get drunk.
I only ever ring someone as the very last resort, when all other methods are unavailable.
I hyperventilate and cry afterwards.
Iām also a 28-year-old scientist with three degrees and a teaching position. Iām normally a logical (albeit emotional) person. But anxiety is not logical.
Anxiety is due to inability to correctly perceive threatsāmore specifically, due to both increased expectation and increased frequency of false recognition of threats in response to neutral stimuli (this is called āpessimistic biasā). Social anxiety simply means that this inability to correctly perceive threats is specific to social interactions, rather than generalised to all aspects of life. (For example, a resting facial expression or lack of verbal acknowledgement is more likely to be perceived as anger, disgust or rejection by a socially anxious person than a neurotypical person. But a socially anxious person is not particularly more likely to worry throughout the day that theyāve left their stove on.)
Therefore, socially anxious people learn to cope with this bias by becoming hypervigilant to social cues such as posture, hand gestures, nodding, eye contact, eyebrow position, mouth tightness, tone of voice, talking speed etc., and then using all the available information to attempt to be logical and ātalk down the anxietyā. We also learn to be high self-monitors, which means that we closely observe our audience and constantly (subconsciously) monitor their responses in order to ensure that they accept us and deem us āappropriateā.
But non-verbal social cues arenāt available during phone calls!
There isnāt any body language to read, or eyes to look into. You canāt monitor your audience for approval. They donāt follow the script you prepared. All you have is their voice, which is usually masked (everyone seems to have a āphone voiceā, ācustomer service voiceā or āprofessional voiceā) and distorted by the phone and is therefore useless. All of a sudden youāre back to relying on a single neutral stimulus, and the pessimistic bias kicks in, and you start to panic because youāre not getting constant feedback.
Itās a Recognised Psychological Thingā¢.
Phone anxiety (actually, phone phobia) is one of the most common, most recognised and most treated phobias in the world. Social anxietyāof which phone phobia is an extremely prevalent triggerāis one of the most common, most recognised and most treated anxiety disorders in the world.
Itās most definitely real, most definitely notĀ āchildishā, and youāre not alone.
also, if you have any degree of sensory processing disorder, difficulty processing language, or hearing problems ā which arenāt limited to just āvolume too quietā but also include things like being unable to pick out speech from background noise, or distinguish phonemes when someone has an accent or talks too fast ā then voice calls are legitimately REALLY DIFFICULT.
itās like trying to read semaphore in a snowstorm while having an allergy attack.
yes, that is hard.
no, itās not just you.
no, youāre not making it up for attention, being a baby, or lazy.
voice calls are simply not as good as text.
the fact that most businesses will not communicate via text is a combination of inertia and ableism, not a sign that everyone but you loves voice calls and youāre a weirdo. frankly most people kinda hate them unless itās a loved one whose voice you want to hear.