this post was submitted on 30 Oct 2023
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Asklemmy

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[–] [email protected] 88 points 1 year ago* (last edited 1 year ago) (14 children)

I have ADHD, and most people _mis_understand it. They are familiar with some of the symptoms, like that it’s hard to focus, but completely unfamiliar with others, like that having an hour appointment in the afternoon can basically block out your entire day. I rely on and even thrive with medication, but there’s a nationwide Ritalin shortage that has basically kept me from working for the past month while I figure out a new medication.

[–] [email protected] 31 points 1 year ago

having an hour appointment in the afternoon can basically block out your entire day

I feel this bullshit so hard. Nobody gets it

[–] [email protected] 20 points 1 year ago (1 children)

Came here to see if anyone had mentioned ADHD. So much misunderstanding. The name of it doesn't help either.

Sorry to hear about the Ritalin shortage. Going without meds for more than a week super sucks. (I'm on vyvanse though).

[–] [email protected] 13 points 1 year ago (1 children)

Call it EDD (executive dysfunction disorder) which is a part of ADD and you'll find more people want to know what it is and don't just assume.

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[–] [email protected] 16 points 1 year ago

The other one that people never understand is the hyper focus side of ADHD. If I get rolling on a task: 1, don’t stop me I will not get back on task. 2, I will forget that planet earth exists, food becomes an afterthought, and breaks, even restroom breaks simply don’t happen.

[–] [email protected] 14 points 1 year ago

At first I thought "no, but I'll read the comments. Maybe it'll help me understand my fellow man." Then the top comment was ADHD and I was like, " oh yeah I do have that lol."

[–] [email protected] 13 points 1 year ago

It’s super frustrating when people are like “oh sure I know about how ADHD works”, when in reality they skimmed the webmd or wiki page for it that mostly just enumerates various ways in which it may present, without even registering that the implications of how the symptoms affect my life.

[–] [email protected] 11 points 1 year ago

Appointment inertia is the worst. I can't do more than one appointment in a day. It's not like a cute lil 'oh it's so hard' thing, I literally cannot do the cognitive processing required to do more than one appointment a day.

[–] [email protected] 10 points 1 year ago* (last edited 1 year ago) (1 children)

people misunderstand it

are familiar with some of the symptoms

On that note, I want to mention that I have seen and heard of a lot of people (mostly online) who self-diagnose with ADHD. Believe it or not, extended social media use (I'm not sure if Lemmy falls into this, it mostly refers to places made to be addictive like TikTok, Instagram and others) has apparently been shown to cause some symptoms of ADHD. I'm just using this comment to tell anyone reading it: if you think you have ADHD or any other mental health issue, talk to a professional, don't self diagnose. It can be destructive to yourself to think you do or don't, without checking. If you have symptoms, talk to a professional. And I'm sure OP whose comment I'm responding to will agree with me on this. Thank you. And you will one day thank yourself too.

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[–] [email protected] 7 points 1 year ago (3 children)

having an hour appointment in the afternoon can basically block out your entire day

I'm curious...what do you mean by this? I don't have ADHD, but I do find it very difficult to relax if I know I have to be somewhere later in the day. Is it anything like that? Or is it something else? Just wondering!

[–] [email protected] 8 points 1 year ago

I’ve heard it’s related to time blindness. Basically I can’t become invested in a project if I know I’ll have to break out of it shortly. So if I have an appointment at like 1pm, I either have to start my day really early to make sure I can get like 6 hours of work done before noon, or start my day after the appointment and work into the night.

It’s a lot easier when I’m on Ritalin, but it’s still difficult to plan around.

That’s basically why I always schedule any appointment for early in the morning, if I can.

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[–] [email protected] 60 points 1 year ago* (last edited 1 year ago) (3 children)

laughcries in neurodivergent

What can you do though: People are idiots and I am one of them.

[–] [email protected] 23 points 1 year ago

High five from an ADHDer!

It's fucking hard to explain that yes, it's possible for me to look like I'm operating like a normal person... but choosing to live and work in a way compatible with my brain isn't laziness. The hardest person to convince was myself. Thankfully, now that I'm enlightened, I care a lot less what other people think.

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[–] [email protected] 51 points 1 year ago (10 children)

Achalasia. My esophagus does not squeeze food/liquid and it gets stuck in my esophagus. Since the nerves in the esophagus are dead (paraphrasing of course) this then causes the top stomach sphincter to not know food/liquid is coming and to open up. Instead, (pre-surgery) food/liquid piles up on top of the stomach and I would have to hope the sphincter would open up and let food in. I had times where I could not swallow water as it would just sit at the entrance waiting to be let in & would have to force myself to vomit as it started to hurt.

Post-surgery (heller myotomy with fundoplication) my esophagus is effectively a slip & slide and I rely on gravity to be able to get food down my esophagus and into my stomach. The top stomach sphincter has now been cut open and never closes anymore. They then stitch part of the top stomach lobe to the sphincter/ esophagus junction area to prevent stomach acid from backwashing.

Even if space travel for the masses occurred during my lifetime, I will never be able to go to space because I rely on gravity to get food to pass through my esophagus.

[–] [email protected] 18 points 1 year ago (1 children)

So you could say that because of gravity, you’re stuck on earth.

[–] [email protected] 10 points 1 year ago

I see what you did there and I am disgusted to say I love you for it. :D

[–] [email protected] 9 points 1 year ago (1 children)

Wow that sounds heavy, first time I ever heard of it. At what age you got it diagnosed and treated?

[–] [email protected] 12 points 1 year ago (1 children)

First Dr visit was sometime in 2018 with surgery in Q2 2019'ish. I would have been 37'ish when symptoms first started coming on.

From what I've read, only 1 in 200,000 have it so it took multiple Dr's to finally find one who said to me, "I was just at a convention last month and heard a talk about a condition like yours and just happens one of the top Dr's on achalasia lives here in our city." Few months later and I was scheduled for surgery and it's been worlds better post-surgery. :)

It definitely affects my life every day with what I can & cannot eat (bread is a nightmare) but I take it in stride and drinks copius amounts of water with every meal.

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[–] [email protected] 48 points 1 year ago* (last edited 1 year ago) (1 children)

Any type of neurodivergence is not graspable for the majority of people, as it would require high skills to think in somebody elses shoes.
Debilitating chronic fatigue is called being lazy and as I just found out very recenty I have cerebrospinal fluid leaks which cause these issues. Hope it gets fixed soon. And shoutout to the doctors trying to tell me it is in my head and doesn't require urgent care.

[–] [email protected] 9 points 1 year ago (1 children)

And shoutout to the doctors trying to tell me it is in my head and doesn't require urgent care.

Fuck those people... >:|

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[–] [email protected] 27 points 1 year ago (13 children)

A lot of people don’t understand bipolar disorder, or schizoaffective disorder specifically in my case. “Had” being incorrect, as it’s a lifelong illness.

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[–] [email protected] 24 points 1 year ago (1 children)

ADHD+Autism

Very annoying. Most ppl already struggle to understand ADHD. Now try to explain autism or what it feels like when you have both. But then again, I also don't fit in with the autism crowd cause my autism is just light enough that I recognize my mistakes but I can't fix them.

I mean tbf how could someone understand autism if I don't really understand it myself. How could I, I've been born with a warped brain, I have no comparison.

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[–] [email protected] 22 points 1 year ago

Cancer. Sure, people realize you undergo treatment for a while. You may be in the hospital for a bit. You're very sick but you do your best. Eventually (maybe) you get to some state termed "remission." You're probably no longer being admitted to the hospital at this point. So you're basically all better right?

No. Not at all.

There are lingering problems that vary among patients. It's hard to explain. Very few people understand what it's like to feel under the weather for days, weeks, months. To live with the fear of relapse. To wonder if the chemo you underwent will cause you to develop a secondary cancer later. To have bone damage from steroids. To have increased sensitivity (read: pain) in many senses/ places from the courses of radiation. To have to fight harder for jobs if you lost yours (or didn't have one) and now have a gap. You may be such a determined, hard worker, but it doesn't take much to be seen as a liability.

Even if someone thinks they understand, they really probably don't. You dont even fully understand what's happening—today you wake up and just can't. You're tired. You're trying but you're so tired.

I can't get too upset, I guess, with people who don't understand. But I wish they could. Things may get better, but they'll never really be back to "normal," whatever that even means.

[–] [email protected] 21 points 1 year ago* (last edited 1 year ago) (2 children)

I've OCD, if that counts (not self diagnosed. I've a proper diagnosis from a psychologist and was on prescripted meds for a long time).

Most people think you're just supposed to wash hands too often, or arrange things symmetrically, or just be a cleanliness and symmetry freak in general. But that's far from true.

OCD is of many types. The one where you are a cleanliness freak is also valid if you've it to an extreme level. Unfortunately, I don't have that. I've the less popular one with random "what if" intrusive thoughts that also have their own solid almost traums inducing anxiety to go with them. Fun stuff.

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[–] [email protected] 20 points 1 year ago (2 children)

Chronic migraine. People think its just a headache, but that's really just the most obvious symptom and least complex symptom. Family practice/generalized doctors know too little about it to recognize it. Everyone around you thinks you're just being dramatic. If they can push through a headache then why cant you push through a migraine?

Migraine is a cycle that lasts days. It has phases: prodrome, aura, acute, postdrome. The acute phase (the headache part) is just one phase. Sometimes the headache isn't even that bad, or long. Sometimes it lasts multiple days. Its a neurological disorder and, in a lot of ways, basically is like your nervous system short circuiting for a few hours or days. Triggers have a lot to do with severity, but there is also a lot of bad info about triggers too. With chronic migraine, you could avoid all triggers and still have 1-2 migraine events a month, and those events dont care about your calendar.

Because information is so badly shared and everyone (mostly unintentionally) gaslights anyone with migraine into thinking they're not suffering from a chronic condition, many of us go a long time before discovering useful information or getting diagnosed.

There are a ton of signs during the prodrome phase which, once you know what to look for, can help you avoid (sometimes) the acute phase by taking meds soon enough and focusing on avoiding known triggers. Even standard over-the-counter stuff can short circuit a lot of migraines before the most painful part. But also, some of the prodrome stuff alone can make working or completing tasks difficult. I often start having trouble speaking, get very tired, have difficulty focusing vision. General brain fog. This can be hours or days before an attack.

After the headache phase, the postdrome is often more brain fog, speaking issues, low energy, but also sometimes a euphoric state which can make getting back into your normal schedule really difficult.

I miss family events. I miss friend events. I have to cancel stuff all the time. I worry about scheduling things for fear of being in a headache phase. I've been lucky with employers being understanding, esp with the work from home setup and mostly DIY hours, but i absolutely couldn't work a job with shifts.

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[–] [email protected] 19 points 1 year ago (8 children)

I have a couple.

  • Celiac disease. Most people, if they’ve heard of it, believe it’s a physical intolerance to gluten/wheat similar to lactose intolerance. Or, many people think it’s semi-imaginary gluten intolerance and some insist it doesn’t even exist. In fact it is a serious autoimmune disease that affects about every system in your body, and can produce dozens of symptoms ranging from complete debilitation to mild discomfort. Hair loss, dry skin, chronic diarrhea mixed with constipation, anxiety, memory loss, brain fog, insomnia, extreme fatigue, slow growth in children, anemia, osteoporosis, and even more… plus can lead to other autoimmune diseases. Nobody knows what causes Celiac as 30x as many people have the genes as ever develop it, and it can start at any time in life.

  • type 1 diabetes. Most people have heard diabetes as the 24x as common Type 2 Diabetes, and believe diabetes in general affects overweight people and has something to do with eating “too much sugar”. That’s not quite right for type 2 but it also has nothing at all to do with type 1. T1 used to be called “juvenile diabetes” because it affected people from ages 0-25. However, they changed the name because they found adults could get it, which is what happened to me (called LADA). Type 1 and Type 2 are practically opposite conditions that both affect your glucose regulation and have overlapping effects. Type 2 is where your body puts out so much insulin, it stops responding to insulin, called insulin resistance. It can be reversed to some extent by diet and exercise. Type 1 is an autoimmune condition where your body destroy the cells that produce insulin, leading to no insulin in the body at all, which can quickly be fatal. Unlike type 2, there’s no lifestyle or diet correlation, only genetics.

[–] [email protected] 9 points 1 year ago

I find that the entire category of auto-immune diseases are a thing most people fail to really "get". Especially if it is even moderately uncommon.

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[–] [email protected] 19 points 1 year ago (1 children)

I have agoraphobia related anxiety. It causes me a great deal of stress and discomfort when I'm outdoors and away from a "safe" zone like my car or my house. I get panic attacks. You will never see me decide to go for a 30 minute walk outside.

It's such a difficult thing to explain to people that it's not social anxiety that keeps me from going to certain places, it's the fact that I have to physically move away from my comfort zones.

I'm not severely agoraphobic to the point of not leaving my house. I go to work everyday and go to stores and such. But my car is always nearby.

[–] [email protected] 7 points 1 year ago

Can relate in a way. Also, all of what you describe is probably going to be revealed to be one super large spectrum that nobody cared to map out.

[–] [email protected] 18 points 1 year ago* (last edited 1 year ago) (9 children)

I am living with chronic vertigo. I don't know if it counts as an illness, but having this condition has made day to day living rather difficult. I feel strange all the time, there's this constant swaying sensation, my head feels like it is wrapped in layers of gauze and on really bad days even my vision appears clouded. I can't stand for prolonged periods when even sitting down doing nothing much feels like a drag.

I appear outwardly fine though, and even my family members forget that some basic actions that they think nothing of no longer come with ease for me. Everything I do, even holding onto, say, a plate, when I am doing the dishes, I am doing it with utmost deliberate effort because the internal swaying sensations I feel have me thinking I am going to tip over any moment and I will end up dropping whatever I am holding.

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[–] [email protected] 16 points 1 year ago (10 children)

I physically can't burp. The muscles in my throat don't open to let air out. We had r/noburp on reddit, but I don't know if there's an equivalent here.

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[–] [email protected] 16 points 1 year ago (3 children)

Asthma. People expect you to have dramatic TV style throat closing episodes where you turn blue grabing your throat as you gasp and gag. For me, an episode is just sudden onset hypoxia. I'll feel my lungs get tight, but because I'm still getting some air it can be hard to tell I'm suffocating, especially if I'm distracted. When it happens, I have about 3 - 5 minutes to catch it. If I fail to catch it, I'll quickly lose balance, struggle to speak, I'll be unable to think, and finally my vision darkens to a dot, and then I black out. I can appear fine, and then out faster than anyone expects.

Once I get a puff, I'm fine in 10 seconds (minus some shaking from the medication.)

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[–] [email protected] 15 points 1 year ago* (last edited 1 year ago) (2 children)

Chroma disease, people don't get that when I'm burned out for the day it won't help to take a short break. Immunosuppressants are a bitch.

Edit: shitty Phone. Yes Crohn's

[–] [email protected] 9 points 1 year ago* (last edited 1 year ago) (1 children)

Crohns? That's what I have and "invisible disability" is an apt description.

[–] [email protected] 6 points 1 year ago

My Dad lived with diagnosed Crohns for 25 years. We covered for him as a family however we could. But you just don't get how debilitating it can be unless you're intimate with it.

As a kid I thought my dad was lame and a bore for not doing a lot of things I wanted. As an adult and having cared for him for most of the last 10 years, I realized he was a warrior that achieved more than any other in his body could've.

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[–] [email protected] 13 points 1 year ago (2 children)

I am a caregiver for a person with rare b-cell lymphoma (chronic illness, treated with a biologic drug rather than chemo) and I've noticed 90% of people don't understand what chronic cancer means. People can't really comprehend someone being better than on their deathbed but much worse than their "normal" health and energy level, and that state will never end. I think popular culture portrays cancer as either "about to die" or "in remission", rather than showing portrayals of the weird in-between state many patients find themselves dealing with.

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[–] [email protected] 13 points 1 year ago (3 children)

I used to have costochondritis which was an inflammation of the cartilage in my sternum. It would feel like a pressure on my chest that wouldn’t be relieved until I bent backwards to stretch and “pop” my chest. So occasionally friends and family would see me stretching and wonder wtf I was doing

[–] [email protected] 7 points 1 year ago

I had that for a few years. Scary at first, then mostly just annoying to explain: yes I'm having chest pain, yes I'm sure it's not a heart attack, yes my chest is going to make a noise.

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[–] [email protected] 12 points 1 year ago (2 children)

Had mono as a kid. Parents got mad that I was being lazy because I didn't get out of bed for two weeks.

[–] [email protected] 8 points 1 year ago

Had mono in uni, for 7 fucking months. Like any good idiot, I wrote it off as my period first, then just needing to chill a bit. Then I got worried and saw a doctor, who said "mono almost never lasts 2 months, we'll run some tests". And meanwhile I should work on my stamina and keep training.

After half a year I got a different doctor, who did the mono test and tadaa. Told me to sit and do nothing, doctors orders. 6 weeks later it was gone.

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[–] [email protected] 11 points 1 year ago (4 children)

I have a few, but the most commonly misunderstood of these… I don’t even know if it has a name. I’m just socially slow and people assume I’m an introvert because of it.

Made worse because schools put people in special education classes for social issues, they can’t comprehend for some reason that people just don’t all socialize the same way.

It’s not all that uncommon either if you believe in the statistic that the average person lies a hundred times a day. WHY do they lie a hundred times a day? Because of exchanges like this.

“Hello.”

“Hi.”

“Hey, how are you today?”

“Good, just finished washing the dishes.” (lie to keep the conversation alive)

Which means our society, by training people to value sociability more than friendliness, are breeding its own compulsive liars. And on a side note, that brings us to another ill people don’t understand, because people think compulsive lying is a “bad seed” kind of thing when our environment (and sometimes the rebound after being 100% honest for a long time) can make us that way.

[–] [email protected] 8 points 1 year ago (1 children)

It is completely 100% ridiculous to try to 'diagnose' you from this short of a description, but it could be that you're autistic to some degree.

Us autistic folks like to take moral issues a lot more personal, like having to lie. We're often at odds with societal standards. We may feel like we're socially slow, even though in my experience, it's usually just that we socialize differently. And we definitely overanalyze things.

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[–] [email protected] 11 points 1 year ago (1 children)

My experience with post-covid symptoms was really nasty and the doctors couldn't diagnose me. I actually wrote a big lemmy essay on it like seven months after it all started. I'm not sure how to do cross-instance comment linking, but here is the lemmy.ml link.

[–] [email protected] 9 points 1 year ago (1 children)

Thank you. Long Covid is exactly what prompted me to create this post. I've been having symptoms for 15 weeks (insomnia, brain fog, exhaustion). My primary care doctor was useless.

I've since discovered a lot of literature on my own that has validated my experience: that it's typical for general doctors to have no clue, they're still working on finding good biomarkers for the condition (it's not easy to test for), and I've learned a bunch about PEM (post-exertional malaise) and self-pacing / energy-management techniques to prevent the push-crash cycle that people with Long Covid experience.

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[–] [email protected] 7 points 1 year ago

People think I'm a drunk because of my rosacea.

Those are two completely unrelated aspects of myself.

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