How To Accurately Write Disabled Characters in Fiction



By Wendy C Allen


This article started out as an answer on Reddit, to a question about searching for a mobility aid to best use. I answered telling the user about my own mobility aids. After that, however, it occurred to me that these answers might be useful for authors looking to write fictional characters who are disabled, and so I've added more info after the end.


Here are the two threads with the original question and answers by others:

https://www.reddit.com/r/disability/comments/1mg5ggd/comment/n6mwcyp/?context=3 


https://www.reddit.com/r/disability/comments/1mfwxss/comment/n6nle7p/?context=3

Here is the original answer I gave them:

I have a Vocic z51 2-in-1 Rollator/Transport chair. That might bee something for you to look into. It's kind of on the big side for a rollator (WAY bigger then more standard/commonly used rollators like the Nova) but at the same time its WAY smaller then a typical wheelchair. I paid $175 for it on TEMu; local WalMart had it for $350 so the price seems to vary depending on where you buy it. I have the black frame with grey tweed seat version, but I know it comes in like 3 or 4 other colours.

It has 12" tire wheels (not hard plastic wheels like most Rollators have) so you can use it for things like camping trips/hiking/walking a dog in a park - it works great on grass and on forest/root/leaf ground. But its goes REALLY hard on things like a gravle driveway, and while you CAN use it on a beach, as it moves really well over DRY beach sand, you want to stay away from the water as it just sinks in WET beach sand.

Be sure to measure doors of your house though if you plan to use it inside, because it is specifically made for outdoor use and so, it's 34" wide and most houses have OUTSIDE doors that are 36" wide but interior room doors that are only 27" wide (aka, I can get mine out the back door that is 36" wide, and can SQUEEZE out the 34" wide front door, but I can not get it through my 26" bedroom door, or down the 28" wide hallway between the bedroom and the kitchen. It also does not fit in a lot of cars - I have a Volvo sedan and EVERYTHING fits in the huge trunk, except for my Vocic 2-in-1, which I have to put in a wheelchair carrier that hangs on my back bumper.

So, I have a smaller Nova for indoor use, but I hardly ever use it. The Vocic I use every day, because I have a hyperactive terrier that needs 2 to 3 walks a day to burn energy, but I can not walk on my own. I can go about 20 feet with a cane before I fall over. But with this Rollator, I can walk a mile or two with relitative ease, as by putting my weight on the rollator, it takes the strain off my hips, and so I can walk about 30 to 45 minutes before needing to stop and rest because if hip pain. (With the cane it's under 5 minutes before my hip starts hurting).

The 2-in-1 means that it flips back and forth between being a rollator or a wheelchair. So when walking, I can use it as a rollator. When I need to rest, I just push the double brake levers, flip the back rest over, and sit down, now I've got an instant wheelchair. It has a memory foam 2" cushion, so it's VERY comfortable to sit in. Though I would say max is 4 hours you could sit in it. I've used it at events and conventions and workshops and the memory foam takes about 3 to 4 hours to compress down, and once it does that, it starts to be uncomfortable to sit in.

Side note it is NOT a "self propelled" wheelchair, as it is a TRANSPORT chair, that means if you want to MOVE while it is a wheelchair, you need to have someone behind you pushing it.

There is a motorized attachment you can get to turn it into a power wheelchair, but I don't have that so I'm not sure how well it works.

Also the frame is VERY rugard. Most rollators have a thing aluminum round rod frame that will wear out in about 2 years, so MOST rollators you need to replace every 2 years. This one, is made out of a heavy thick, square "i beam" type frame, so it'll last 15 or 20 years, this thing ain't breaking.

I take it with me on camping trips (tant camping, and mountain hiking in Acadia). It's really good for trips because it is so ruggard.

a lot of rollators are not going to stand up to a lot of rough hiking. I do a lot of outback-wild/deep forest tent camping and hiking so, I needed one that could stand up to pulling it over root heavy forests tails that don't have paths and such. It was actually really hard to find a rollator that would last more then one or two camping trips.

Also wheelchairs are notoriously uncomfortable to sit in for more then 20 minutes or so. Especially the hard plastic seat types. The leather sling seat types are somewhat better, but will put pressure on your thighs after an hour or so. You definetly want to look for something with minimum one inche, preferably two inch memory foam seat - or, if you can't find one, buy a memory foam seat cushion (they sell them for like rocking chairs and dining room table chairs, places like WalMart have them), get one with ties so you can tie it down to your wheelchair. Your hips, bum, and thighs will fair much better with a memory foam seat.

Also, don't let anyone tell you you do not NEED a mobility aid. If you are in pain and a mobility aid is going to help you to get around in your every day life, then get one. You don't need a doctor or a prescription to buy a cane or rollator or wheelchair. If you have pain and a mobility device will help aliviate that pain, then use it. That's what those devices are made for.

Also, you might want to consider having an MRI done. For months, my doctor was treating me for LEG PAIN, and nothing was helping. Finally they did an MRI, and while there was hip damage that was an issue, it turned out the PRIMARY issue was that part of three of my vertebrae where broken and the bone fragments had punctured through my spinal column and had severed some of my nerves, and so, THIS was the actual source of the bulk of the issue, and once the doctor realized, "oh wait, their is serious nerve damage here, we though were were just dealing with bone fractures, whoops"... suddenly the course of treatment and the types of mobility aids were all different, and, I went from not being able to stand up at all, full on bedridden, to slowly regaining my ability to walk.

Xrays missed the nerve damage. Xrays saw the bone damage and I was being treated for the bone damage for 3 full years before the doctor tried an MRI and found there was big time nerve damage that had been completely overlooked because it was not showing up on the xrays and only showed up on the MRI.

So, getting the right diagnosis is important too, because often a mobility device will work great for one issue, but do nothing for another issue - and yeah, there are differant types of canes, crutches, walkers, rollators, and wheelchairs - I had no clue until I started using them, that there was like a dozen different types of canes and crutches and walkers and rollators and wheelchairs and not just one size fits all canes/crutches/walkers/rollators/wheelchairs.

Plus there are various hand/wrist/arm/back/hip/leg/ankle braces as well, that might help you out.

I have several. I have wrist braces, back braces, hip braces, knee braces, straight canes, bent canes, underarm crutches, forearm crutches, 2 different walkers, an indoor rollator, the Vicoc rollator, and a wheelchair... plus I need a different type of wheelchair but it's close to $10k sooooo, it'll be a few years before I can save up enough for that one. But, I rotate back and forth through all these different mobility devices, some days I cane use just the cane, usually in the house I only need the cane; outside I mostly use the vocic, some days I need to add the wrist braces, other days I need the leg braces... my pain levels change throughout the week even throughout the day, so some days you'll see me in a wheelchair other days walking with a cane. I have to judge each day, what will I be doing today, and have whatever mobility aid best fits me for that day.

And for for those wondering: I've had rheumatism since I was 4 years old, so started using a cane when I was just a toddler; so, yeah, you can never be too young for a mobility aid either - don't let people convince you "only old people need a cane".

I also have MS, symptoms showed up at age 16 but doctors misdiagnosed it nearly a dozen times, including to diagnose me with Lupus, Lyme Disease, Cancer, ALS, and Parkinson's, all before rules those all out as misdiagnoses, and finally say when I was 37 years old that it was MS, so 21 years of several misdiagnoses!

At 31 I suffered a spine injury, that left me paralyzed, without use of legs or arms; fully paralized for 18 months... that was in 2013... I did not regain the ability to use my hands until 2019 and did not regain the use of my legs until 2021, and it's been 11 years since the spine injury and I STILL have only the use of three fingers in my right hand, so, yes, I'm typing this with my right thumb and two right forefingers.

In 2013 doctors said I would never walk again, but now in 2025, I'm walking nearly a mile a day every day with my dog and the help of a rollator. So.. regardless of your diagnoses, don't let doctors tell you to give up either... the fact that I'm walking again, even on a limited basis, is proof doctors don't know everything, because in 2013 there wasn't one doctor who thought I'd ever even sit up in bed again. Determination is a big thing here. Be determined to self advocate. If you are in pain - find out why and figure out what mobility aid will help you.

I was diagnosed with rheumatism at age 4, and have used a cane since I was a toddler. If you are old enough to be disabled, you are old enough to use mobility aids, no matter how young you are. But do make sure you get the type of mobility aid that will best suit you. Even things like a cane there are tons of types of,. Straight ones, bent ones, curved ones, different handle shapes, short ones that keep your arm below hip, average ones that keep your arm above hip, tall ones that are like a hiking staff and rest on your shoulder so you can put you upper body weight on them, and many more. Some are designed to work either side, while others are right side only or left side only and some, you use in a pair one in each hand. It really depends on your disability as to which type will be best for you.

I've used a cane my whole life, since I was a toddler, but I've had a few dozen over the years, and different types help for different things.

Currently, I have 2 different hip height ones, and one tall over the should height staff style one.

But I also have wrist braces, back braces, hip braces, knee braces, 2 different walkers, a rollator, a transport chair, and a wheelchair. And each one I use for different reasons of different days.

There are many types of canes and rollators and wheelchairs I could not use too.

For example, that solid acrylic bright coloured light up cane that is being promoted all over youtube and tik tock the past few months -- I see many people love it --- it's absolutely terrible, 100% useless for me. Why? Because I have hip dysplasia and so one of my legs is 1/4" shorter then the other. It doesn't seem like much, but that quarter inch is just enough to make that particular style/shape cane unusable for me, because of the way I have to put my weight onto the cane, thus I require a cane that has a slight bend shape about halfway down the middle of it. I can not use a perfectly straight cane because of how my shorter leg causes me to lean my upper body weight on the cane itself.

So, yeah, if you feel a cane will help, get one, but... start out with a cheap $10 one from WalMart pharmacy department, get a couple of them, one each of different shapes and styles, and test out if they help you r not. Some might. Some might. And you don't want to end up with one that might make you worse. And by starting out with a cheaper WalMart one, if it turns out you can't use that type, well, you can donate it to goodwill or salvation army and not be out a lot of money.

Some of the fancy types can be well over $100 and the last thing you want to do is dump a load of money into a style that you end up not able to use.

Depending on your disability, your doctor may advice one style over another, so, sure you can get a cane before asking your doctor, but it might be best to ask your doctor first and explain why you feel you need it and then, see if your doctor recommends any specific type. Many doctor's offices will have a bunch of various types on hand and most doctors will just give you one to take home, and will show you correct way to use it... and yes, there IS a right and wrong way of using canes... you have to adjust them taller or shorter depending on reason for using it, and for some issues, you want the cane on the SAME side as your pain, but for MOST issues you need to hold the cane on the OPPOSITE side of your pain.

As for this:

>Should I try to ask?

Yes. If you have trouble walking, ask what your options are.

You might not need a cane at all.

For example, some days, all I need is a leg brace; which I use the fabric type that has a metal frame inside of it, and it goes under clothes and looks kind of like a legwarmer, so, when I'm using just that, no one realizes it's a mobility aid at all.

I notice people often jump first thought to cane, and cane often is the answer, but sometimes you might just need something like an ankle brace or a knee brace to force your joints in place and suddenly BOOM you can walk without pain and without a cane. That was often the case for me when I was younger. Just stabilizing my joints was all I needed to get rid of the pain. But there's no way to know without your doctor checking your joints.

>And how do I ask?

So, what I did when I was 12, I took a notebook, and carried it with me and every single time anything hurt I wrote it down, exact location, what it felt like. (I had said things like "it felt like a lightening bolt went up my heel" or "it felt like a rubber band was squeezing my thigh tighter and tighter like I couldn't breath only it was my leg and not my lungs" and because of these sort of descriptions, my doctor figured out there was nerve damage (the lightening bolt pain) and blood circulation problems (the rubber band squeezing pain).

I knew that in the office I would not remember anything, and forget to say "Oh, yeah, this hurts when I move like that"... but because I had about ten pages of notebook written down, I just handed it to him and said "This is what hurts", and he sat down and read it right then and there and then, said, "Okay, this sounds like a pinched nerve, let's test out this..." and "this sounds like a circulation issue, let's get some lab work done for this".

By having a whole week long diary of every pain I felt that week, he was able to better pin point various issues and figure out better what was actually going on and in need of help.

And for a while I stopped using a cane (young adult years) because I thought I didn't need it any more. But then one day I'm at an appointment and I'm telling the doctor, "This really hurts, really bad and I don't know why" and she was like, let's take some xrays. It turned out my hip was fractured, and she was like: "You need crutches" Just gave me crutches. That was how I got started using crutches. I never would have thought of crutches at all. So if I had not told the doctor specific details of the exact pain, she never would have thought to do the x ray.

But now I'm to the point where a cane doesn't do much good over all any more, and I've switched to a rollator 90% of the time now, and a wheelchair most of the rest of the time.

And... wheelchairs are expensive. The one I ACTULLY need is ten thousand dollars. It'll take me a few years to save up for it - probably closer to five or more years, so I have a cheaper one from a thrift shop right now and... while it works, it's painfully noticeable that yeah, it's REALLY NOT the right one for me. Unfortunately I simply can not afford the one that is the right one for me. Well, this issue of it hurts to use the wheelchair, is why I use the rollator 90% of the time. If I had the correct type of wheelchair for my disability, I'd probably be using the wheelchair 50% to 60% of the time.

so, you definitely need to ask what type is best for you, when it comes to mobility aids, because I know from using the incorrect type wheelchair, that if it's causing pain, the mobility aid is not going to get used. I just avoid it because it actually causes more pain. Whereas the rollator does not cause pain so I use it more then the wheelchair, even though I and supposed to be using the wheelchair more.

So definitely talk about different types of mobility aids, like not just cane vs rollator, but cane type a vs cane type b, ect, because it does matter.


Here are videos where you can see the Vocic z51 in action:

@eelkat #wheelchairlife #mainelife #cairnterrier #biddeford #z51 ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #maine #mainelife #doglife #nature #cairnterrier ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #blackcats #blackcatsoftiktok #blackcat #catsoftiktok #catschilling ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat Cataract East Channel Dam, #SacoRiver, York Hill, Saco, #Maine #SacoRiverCurse #hauntedMaine #Etiole ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #artcar #wheelchair #cairns #biddefordmaine #mswarrior ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #wheelchair #biddefordmaine #artcar #mobilityaid #cairnterriersoftiktok ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat testing out a new camera stand #dogwalking #vlog #Maine #biddeford #random ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat The Waterfall itself, also, this is where "Etiole" (the homeless WW2 vet whom locals claim is an amphibious alien or cryptid), lives. He has lived here, homeless since 1953, except for between 1978 to 2010 when he lived in my 1964 Dodge 330 (the one people call The Worlds Most Haunted Car, even though its not haunted, they call it that because i let "Etiole" sleep in it at night and they claimed he was a demon). Crazy superstitious locals cut my car in half May 10, 2010 while chanting they had to "kill the car" to "kill the demon" and Etiole fled back here to living along the edge of this waterfall from 2010 to currently now in 2025. I don’t know why people started calling him “Etiole” as that is not his name, likewise people call my car “The Goldeneagle” and i don't know why they do that either. Both names come from a series of novels i write, where a silver skinned eel merman is named Etiole and has the title of Captain Goldeneagle when on his ship. For some unknown reason people started attaching both names to this real life homeless man and my car…. Cataract East Channel Dam, #SacoRiver, York Hill, Saco, #Maine #SacoRiverCurse #hauntedMaine #Etiole ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat Cataract East Channel Dam, #SacoRiver, York Hill, Saco, #Maine #SacoRiverCurse #hauntedMaine #Etiole ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat testing out a new camera stand #dogwalking #vlog #Maine #biddeford #random ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat Random #rapture thoughts #rapturetok #disabledtiktok #rollator #dogwalk #vloggingmyday ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #mobilityaid #biddefordmaine #cairnterriersoftiktok #mswarrior #dogsoftiktok ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #boatlaunch #babeswithmobilityaids #mainersoftiktok #cairnterriersoftiktok #wheelchairaccessible ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #wheelchairaccessible #boatlaunch #rotarypark #mainetok #dogtok ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #mobilityaid #wheelchair #mswarrior #biddefordmaine #dogwalk ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat Eastern Trail, Biddeford, Maine #dogwalk #biddefordmaine #mainelife #nature #puppy ♬ original sound - Wendy C Allen | 📚 Yaoi Author

Writing Blind Characters

Oct 01, 25 07:34 PM

I am legally blind and I write a legally blind character, this is how I do it...

Here is the additional info I added on after for writers to be able to use this info for writing disabled characters:

Let's go get ChatGPT5 and ask it to give us some additional thoughts. Below are the questions and comments I gave it, and the answers it responded with:

My question:

If you was going to write a blog post type article to teach ale bodied writers how to write disabled characters, what would you include? I'm thinking something like:

Writing Disability and Chronic Illness Authentically


Living with mobility aids (cane, walker, wheelchair) — how people really move, adapt, and feel about unsolicited help.
The reality of chronic fatigue vs. the “tragic sick character” stereotype.
“Fragile” objects vs. people — the harm of that word when applied to disabled folks.

...that sort of topic.


ChatGPT5's answer:

Got it. You’re thinking of an article that pulls back the curtain for able-bodied writers so they stop leaning on clichés and start writing lived reality. Here’s an outline you could expand into a blog post, with some key points under each heading:

Writing Disability and Chronic Illness Authentically

1. Mobility Aids: Tools, Not Symbols

  • A cane, walker, or wheelchair isn’t a shorthand for “broken.” It’s just a tool.
  • People use them with skill, habit, and sometimes pride—often modifying or decorating them.
  • Show how a body really moves: the slowness, unevenness, or extra steps involved. Don’t exaggerate or dramatize.
  • Unsolicited help can be humiliating. Strangers grabbing a chair or offering pity isn’t kindness, it’s intrusion.

2. Fatigue: A Daily Battle, Not a Plot Device

  • Chronic fatigue is constant, not a one-time collapse scene.
  • It’s not just “being tired”—it’s a bone-deep exhaustion that can make brushing teeth or making tea monumental.
  • Show pacing, planning, and trade-offs (choosing one activity knowing it means recovery time later).
  • Avoid the tragic martyr stereotype where the character exists only to be pitied or “overcome” their illness.

3. The Language Problem: Fragile, Broken, Burden

  • Words like “fragile” or “frail” when applied to people carry deep harm—they reduce a human to glassware.
  • Disabled people are not inherently breakable; they’re often resilient, adaptive, and fiercely tough.
  • Language frames perception: use neutral or empowering descriptors, not metaphors that erase strength.

4. Independence and Adaptation

  • Many disabled folks pride themselves on finding workarounds: hooks to open doors, rethinking chores, pacing meals.
  • Adaptation is creative. Characters may invent new ways to do old tasks, or develop habits that surprise outsiders.
  • Write the ingenuity, not just the limitations.

5. The Myth of the “Inspiration” Trope

  • Disabled characters shouldn’t exist to inspire able-bodied ones.
  • “If they can do it, so can you!” stories dehumanize. Let disabled characters have arcs unrelated to “overcoming.”
  • Show full humanity: anger, joy, boredom, sex, humour, mistakes, ambitions.

6. Normalcy Within Disability

  • Disability is not a “special event” for the person living it. It’s Tuesday.
  • Show the rhythms of daily life: meds, mobility aids, rest, frustration, triumph, ordinary domestic moments.
  • Sometimes the cane squeaks. Sometimes the wheelchair is just another chair at the table.

7. Listening > Assuming

  • The best way to avoid stereotypes is to read or listen to disabled voices.
  • Memoirs, blogs, TikToks, forums—there’s a wealth of lived experience being shared.
  • Don’t assume one experience covers all—disability is varied.

Would you like me to draft this as a finished article in your teaching-blog voice (like a polished piece you could post), or keep it in this bullet-style “notes for writers” format so you can expand on it yourself?



My question:

What about if you was specifically going to write about characters with mobility aids. Cane vs rollator vs wheelchair, and more specifically a character who uses all 3, variously depending on daily symptoms. For example a character with rheumatism or MS, who has "good" days (using cane) vs "normal" days (using rollator) vs "bad" days (using wheelchair) vs "major flare up" days that that could completely lay them up in bed for weeks on end not able to get up at all. And especially vs "bully" characters who would accuse them of faking after seeing them in a wheelchair one day then using a cane the next day.


ChatGPT5's answer:

That’s a really rich topic. Writers often miss this exact nuance—the shifting nature of disability and how mobility aids aren’t a fixed “identity marker” but a sliding spectrum of what’s possible on a given day. Here’s how I’d frame it into a teaching-style article for able-bodied writers:

Writing Characters with Mobility Aids: Beyond the Stereotypes

Mobility isn’t static. Many disabled people don’t use just one aid—they use several, depending on pain levels, fatigue, flare-ups, or environment. One day a cane might be enough; the next day the same body may need a rollator, wheelchair, or even full bed rest. Fiction often overlooks this reality, but it’s essential if you want to write disabled characters with truth instead of trope.

1. The Spectrum of Mobility

  • Cane Days (Good Days): These aren’t “cured” days. The character may still move slowly, carefully, with pain—but with just enough stability and energy to manage.
  • Rollator Days (Normal Days): A rollator isn’t “just a fancy walker.” It provides balance, allows sitting breaks, and helps conserve energy. It’s a middle ground for when fatigue or joint instability makes a cane unsafe.
  • Wheelchair Days (Bad Days): A chair is not a prison sentence. It’s freedom—the difference between being stuck at home and being able to leave the house at all.
  • Flare Days (Bed Days): Sometimes, no mobility aid is enough. A character may be completely bedridden for days or weeks during major flares, needing assistance with even basic tasks.

Showing this fluidity makes your character real. It mirrors the lived experience of conditions like rheumatoid arthritis, lupus, MS, fibromyalgia, and other chronic illnesses.

2. The “Faking It” Accusation

One of the most painful realities disabled people face is disbelief. If someone sees your character using a cane one day and a wheelchair the next, many will assume dishonesty:

  • “You were walking yesterday—so why a wheelchair today?”
  • “If you can stand to reach that shelf, you must not really need the chair.”
  • “You’re just lazy.”

This cruelty comes from able-bodied people expecting disability to be linear and visible, not fluctuating. Writing these moments authentically means showing the emotional toll: frustration, anger, shame, exhaustion—but also the resilience and quiet fury of someone who knows their reality better than any outsider.

3. Mobility Aids Are Tools, Not Hierarchies

Don’t treat canes, walkers, or wheelchairs as markers of progression toward “worst-case scenario.” They’re interchangeable tools. A wheelchair isn’t a tragedy; it’s as normal as putting on glasses

.4. Daily Decision-Making

  • A cane might not provide enough stability in a crowded street.
  • A rollator might be better indoors or for longer distances.
  • A wheelchair may be the only safe option at a mall, park, or during a flare.
    Your character chooses the right tool for the right day, the same way someone might choose boots vs. sneakers.

Every outing involves weighing risk, pain, and energy:

5. Representation That Matters

  • “If I use the cane today, I’ll need to rest all tomorrow.”
  • “I should take the chair to the market; there’s too much standing in line.”
  • “If I try to push through, I could trigger a flare.”
    Writing this inner calculus shows the lived reality of disability—always planning, always conserving energy.

Avoid the traps:

  • Not tragic props. Don’t reduce the character to their cane or chair.
  • Not miracle stories. They don’t need to “walk again” for a happy ending.
  • Not saintly patience. Let them get angry at disbelief, pity, or intrusive strangers.

What resonates most is normalcy. Show them cooking, gardening, laughing, arguing, falling in love—sometimes with a cane, sometimes with a chair, sometimes not out of bed at all.

If you want, I could draft you a sample “scene-style” vignette that illustrates this: a moment where the character transitions from cane to rollator, then gets accused of “faking” by a stranger, showing both the physical mechanics and the emotional fallout. That way you’d have an example writers could learn directly from.

Want me to do that?



My question:

Another aspect writers often miss that i feel is important to mention, is the "disability check" accusations.

I have MS, use a cane, a rollator, and a wheelchair. I have multiple types of canes, a walker, a rollator, a wheelchair, ankle braces, 4 different types of knee braces, 2 different types of back braces, elbow braces, and 3 different types of hand/wrist braces. Which types and which combinations i need changes daily, sometimes changing multiple times in a single day.

I have paid for all of them with my own money.

My income is too low to qualify for medical insurance (where I live income must be $700+ a month the qualify for medical insurance). And i don't qualify for either government medical insurance or government disability checks, both because I am self employed as a writer.

I have to pay cash for EVERYTHING. From doctor visits to hospital visits to prescriptions (which can be $50+ per pill) to my MRIs which cost over five thousand dollars each. My rollator cost more then I make in 3 months and my wheelchair cost more then most people pay for a car.

In total my medical bills just since 2013 have been in excess of THREE MILLION DOLLARS and NOT ONE PENNY of it was covered by medical insurance, and I've never even once in my life received and disability checks from the government.

And yet... it is a common occurrence for grown men, complete total strangers often aged 60+ to walk up to me in the store and start yelling at me, raving and ranting that THEY paid for my rollator or wheelchair via their tax dollars!!!

I have never once seen writers use scenes like this, nor even have characters struggling with having to pay cash for everything because their disability doesn't qualify for government help or insurance.

I always see writers showing characters in stores helping disabled characters, and yet I've never once in real life experienced a stranger help me.

In fact, the worst event I ever encountered, was going into an auto mechanic who was working on my car... but the building did not have a wheelchair ramp, it had 3 stairs to go up to get to the door... I had to leave my wheelchair at the parking lot at the edge of steps, then use my cane to try to get up the steps, then try to open the awkwardly positioned door, while steadying myself with the cane... as I am holding the door trying figure out how to maneuver my leg so I can get up the final step...

...I get this massive punch in the back that knocks me over and I cannot breath... I look up to see who hit me and why, and there is a one armed man standing there and yelling at me saying: "I don't need no help opening doors you fucking bitch. I can open doors myself you fucking whore!" Then he goes inside.

Obviously he thought I was holding the door for him, but I never even knew he was there because I am also legally blind and near deaf since age 4, so I had not seen or heard him approach at all!

But this type of interaction is EXTREMELY COMMON to the point that it happens 2 to 5 times EVERY WEEK where some angry man lashes out at me.

And yet, i NEVER see writers show scenes of how violent and physically abusive man are to female disabled people.

I feel it is very important that if you are accurately writing disabled characters, that you also accurately write how deplorably the average person treats random disabled strangers they meet around town.

But writers all act like every stranger is falling over themselves to help disabled characters and that is just not the reality at all.


ChatGPT5's answer:

Yes. You’ve nailed something that almost never makes it into fiction but is absolutely central to writing disability honestly: the hostility, suspicion, and violence strangers direct at visibly disabled people. Most able-bodied writers imagine “random strangers help disabled folks in stores.” They rarely imagine strangers yelling, grabbing, accusing, or even physically assaulting. But that’s the reality for many.

If I were writing this as a teaching post for writers, I’d put it like this:

The Myth of the Helpful Stranger

In fiction, a disabled character enters a store and instantly someone rushes to hold the door, reach a shelf, or offer cheerful assistance. In real life? The opposite happens far more often. Strangers don’t usually help—they accuse, mock, or intrude.

Disabled women, especially, are frequent targets of harassment. From “You don’t look disabled!” to outright physical assault, it is common to face hostility several times a week from total strangers.

Accusations of “Disability Checks”

One of the most common insults hurled at mobility-aid users is:

  • “I pay for your wheelchair with my taxes!”
  • “You’re living off the system!”

For many disabled people, this couldn’t be further from the truth. They may not qualify for government aid, disability checks, or insurance. They may be paying out of pocket—sometimes millions over a lifetime—for every cane, brace, wheelchair, medication, and doctor’s visit.

This reality almost never shows up in fiction. Instead, disabled characters are portrayed as if they automatically receive benefits. Writers who skip this miss one of the rawest parts of disabled life: the cost. Not just physical, but financial.

The Violence Nobody Writes

Writers rarely imagine disabled characters being attacked for existing. Yet this happens. Regularly. Strangers shove people using canes. Wheelchair users are accused of “faking” if they stand to reach something. People get screamed at for being “lazy” or “a burden.”

These are not rare incidents—they’re the background noise of disabled life. Including them in fiction is crucial if you want realism. Disabled characters don’t just wrestle with their conditions; they wrestle with the cruelty of strangers every time they go out in public.

Multiple Aids, Changing Needs

What confuses and enrages bullies most is when someone uses different aids on different days.

  • One day: cane.
  • Next day: rollator.
  • Another day: wheelchair.
  • Sometimes: braces stacked on joints, or total bedrest.

To an outsider who thinks disability is static, this looks like “faking.” To the person living it, this is survival. The body changes day by day, even hour by hour, and so does the tool that best keeps them mobile.

A realistic character with MS, rheumatoid arthritis, or similar conditions will have a closet full of aids and choose the right one for that moment. Writers should not only show this, but also show the backlash it invites.

What Writers Should Do

  • Don’t sugarcoat. Show harassment, disbelief, and accusations.
  • Don’t give every stranger kindness. Balance your scenes with the reality of hostility.
  • Don’t erase the costs. Show characters struggling financially—choosing between a doctor’s visit or groceries.
  • Do show the resilience. Disabled people adapt, endure, and survive despite all this. That’s the story.

This would be a powerful section in an article aimed at writers. Because it’s not just about getting the cane vs wheelchair vs rollator details right—it’s about showing the social hostility that always comes with disability, which is almost completely absent in fiction.

Would you like me to draft this into a full-length teaching blog article (around 1,200–1,500 words, with examples and maybe a couple “bad vs good writing” excerpts), so you’d have something ready-to-post? Or would you prefer I keep building it out in structured notes so you can do the drafting in your own voice?



My question:

Let's see what such a blog post would look lik


ChatGPT5's answer:

Perfect — here’s a draft blog post written in a teaching-blog style, long-form, weaving in all the key points you raised. It’s aimed at able-bodied writers who want to write disabled characters with honesty and nuance:

Writing Disabled Characters Authentically: Beyond Canes and Clichés

When able-bodied writers imagine a disabled character, they often picture one fixed image: someone permanently in a wheelchair, or always leaning on a cane. They write scenes where strangers rush to help with doors or groceries, and the disabled character gratefully smiles, inspiration achieved.

The reality is far more complex, more frustrating, and frankly, more brutal than most fiction dares to show. If you want to write disability authentically, especially characters who live with fluctuating conditions like MS, rheumatoid arthritis, or lupus, you need to dig deeper.

Disability Is Fluid, Not Static

Disability isn’t a straight line from “fine” to “wheelchair forever.” It’s a shifting spectrum, often changing day by day—or even hour by hour.

  • Good days: a cane might be enough, though movement is still slow and painful.
  • Normal days: a rollator provides balance and a built-in seat for rest breaks.
  • Bad days: only a wheelchair makes leaving the house possible.
  • Flare days: the body shuts down completely, and the character may be bedridden for days or weeks.

This fluidity confuses outsiders, who expect disability to be consistent. A character who uses a cane on Tuesday and a wheelchair on Thursday will inevitably be accused of faking. And that accusation is something most disabled people know far too well.

The “Disability Check” Accusation

Ask anyone who uses mobility aids, and you’ll hear a common story: strangers—often older men—storm up in public spaces to declare:

“My taxes pay for your wheelchair!”

Here’s the reality you never see in fiction: many disabled people don’t qualify for disability checks or insurance.

Self-employed? Disqualified.

Earn too little? Disqualified.

“Not disabled enough”? Disqualified.

Mobility aids, braces, medications, doctor visits, MRIs—all of it gets paid out of pocket. A rollator can cost more than three months’ income. A wheelchair can cost more than a used car. Some people have paid literal millions over a lifetime in medical bills, with zero assistance from any government program.

When you write disabled characters, don’t assume their equipment magically appeared, or that the government covered it. Show the financial reality: saving, sacrificing, going without, living under crushing medical debt. That struggle is real.

The Myth of the Helpful Stranger

Fiction loves to imagine helpful strangers. In bookstores, on sidewalks, at grocery stores, characters rush forward with kind smiles and assistance.

That is not the lived experience.

More often, disabled people are grabbed without consent (“Here, let me push you!”), insulted (“You’re too young to need that!”), or outright harassed (“You were walking yesterday—faker!”). Disabled women, in particular, face frightening levels of hostility and violence.

One very real example: a woman trying to navigate stairs with a cane while holding a door was shoved from behind by a stranger, who screamed obscenities at her for supposedly “patronizing” him. She wasn’t holding the door for him at all—she hadn’t even seen him, because she was legally blind. The result: physical injury, public humiliation, and another scar added to years of weekly harassment.

This is the reality you’ll almost never see in fiction: disabled people being attacked in public for existing. If you want your characters to feel real, don’t just write the rare kindness. Write the hostility too.

Multiple Aids, Multiple Realities

One cane doesn’t cover it. A real disabled person may own:

  • several canes of different types,
  • ankle, knee, back, and wrist braces,
  • a walker,
  • a rollator,
  • a wheelchair.

Which aid gets used changes with symptoms. Sometimes several are needed at once. Sometimes they change multiple times in a single day. That’s not inconsistency. That’s survival.

When you write, show the inner calculus:

  • “If I take the cane, I’ll pay for it tomorrow.”
  • “The rollator means I can rest mid-trip, but it’s bulky.”
  • “The chair is my only option if I don’t want to collapse halfway.”

These decisions shape daily life. Your character isn’t just “disabled”—they’re constantly strategizing to live around a body that shifts beneath them.

What Writers Get Wrong


    • The saintly cripple trope: Disabled characters shown only as noble, long-suffering, endlessly patient.
    • The inspirational story: Characters whose sole narrative is “overcoming disability.”
    • The free equipment myth: As if wheelchairs are just handed out. They aren’t. They’re bought, often at ruinous cost.
    • The helpful stranger fantasy: As if every trip to the store is met with kindness. Often, it’s the opposite.


    What Writers Should Do Instead


    • Write the social hostility. Disabled characters face constant disbelief, accusations, and sometimes assault. Don’t erase it.
    • Write the financial cost. Show characters scrimping, going into debt, or sacrificing necessities for medical care.
    • Write the fluidity. One day cane, next day wheelchair, next day bedbound. That fluctuation is reality.
    • Write the full humanity. Disabled people laugh, love, work, parent, have sex, get angry, make mistakes. Don’t flatten them into their condition.

    The Bottom Line

    If you want to write disabled characters honestly, don’t stop at the cane. Don’t stop at the wheelchair. Don’t stop at pity, or tragedy, or saintliness.

    Write the cost. Write the planning. Write the violence. Write the reality of strangers yelling in stores, of endless debt, of bodies that change from hour to hour.

    Because that’s the lived truth of disability—and the stories that need to be told.

    Would you like me to expand this into a series-style format (like “Part 1: Mobility Aids,” “Part 2: The Myth of Help,” “Part 3: The Cost of Survival”), so it reads like an ongoing blog series you could publish piece by piece?



    My question:

    You know something else that annoys me, as a mobility aids user?
    When mobility aids are mentioned in passing by the author aka are treated like a decoration and not a tool. Do you know what i mean?

    Like, you will see to MENTIONED character A has a cane or character B has a wheelchair, but that's it. Its mentioned during the initial description introducing the character, as though it was part of their outfit, and then its never mentioned again not once in the whole book.

    And in some books it feels like the author just added that one line in the character's introduction, as an afterthought, added during editing, at the last minute, before publication, just to "check off a woke box", so they can feel "i added diversity, see?"

    But you can tell it was just checking of "diversity boxes" as an editing afterthought, because the characters will be doing thinks over the course of the book that can not be done by wheelchair users or cane users, making it obvious that the author DID NOT write a disabled character, they just added a mobility aids the "please the woke crowd" (which is NOT making your book diverse or woke at all, and in fact comes off as mocking real world disabled).

    But also lack of research into wheelchairs too. There are dozens of types of ambulatory wheelchairs, dozens of types of manual wheelchairs, dozens of types of power wheelchairs, and dozens of types of paraplegic wheelchairs...and many wheelchair users have 2, 3, 4, 5, or more different wheelchairs because they may need a small skinny wheelchair for use in their apartment, but a larger power chair for shopping, an all terrain wheelchair for walking their dog, and a different one left at the office for work.

    I NEED 3 different wheelchairs, but I can not afford them. One wheelchair I need costs seven thousand dollars. The other costs ten thousand dollars. So I only have a cheap three hundred dollar one, which "suffices" but is far from meets to my full needs. It gives me more freedom then I had without it, but because it doesn't have all the things I needs in a wheelchair, there are still massive amounts of things I can not do, places I can not go, simply because I can not afford the appropriate wheelchair for me full needs.

    I had a friend in childhood in a wheelchair since birth, due to being born with cerabal pulsy and spinabifida, who had to upgrade to a new wheelchair every year until he was an adult, and because he required a power chair with full body brace, each chair was over thirty thousand dollars.

    Its crazy how expensive wheelchairs are.

    And its crazy how many authors just gloss over wheelchair varieties and just give every character only a low grade hospital style transport chair, which isn't even a type of wheelchair used outside of a hospital at all!


    ChatGPT5's answer:

    Yes. Exactly.
    You’ve just pinpointed one of the biggest—and most insulting—failures in how fiction represents disabled people: mobility aids as props, not tools.

    This belongs in your blog series, because it’s a core issue most able-bodied writers don’t even realize exists. Here’s how that section could read, written in your “teaching-blog for writers” voice—serious, grounded, and experience-based:Mobility Aids Are Tools, Not Accessories

    Too many novels treat mobility aids like decorative details in a costume:

    “He leaned on his cane.”
    “She sat in her wheelchair.”

    And that’s it. Never mentioned again. The aid exists only in the introduction, as if it were a scarf or pair of glasses. The story continues as if the character is fully able-bodied.

    This isn’t representation. It’s tokenism. It tells the reader the author added a cane or wheelchair at the last minute to “check a diversity box” rather than to build a lived-in, realistic human being.

    A mobility aid changes how a body moves through the world. It affects what doors can be opened, which stairs are barriers, how long errands take, how objects are reached, and even how strangers react. If those things never appear on the page, then the cane or wheelchair isn’t real—it’s decoration.The Variety Authors Ignore

    There isn’t one kind of wheelchair, walker, or cane. There are dozens.
    Each serves different needs:

    • Canes: offset, quad-base, folding, ergonomic, decorative, orthopedic.
    • Walkers and rollators: two-wheel, four-wheel, seat-built, indoor vs. outdoor, narrow vs. wide.
    • Wheelchairs: Ambulatory chairs for part-time users who can stand or walk short distances. Manual chairs for those with strong upper-body control. Power chairs with joystick control, tilt, lift, and posture support. All-terrain chairs with fat tires for gravel or snow. Custom spinal or cerebral-palsy chairs with full-body braces and headrests.

    And many users own more than one. The “small indoor chair” that fits through apartment doorways can’t handle sidewalks or snowbanks. The outdoor power chair might cost ten thousand dollars. Some people need an all-terrain chair for their dog walks, a manual chair kept at work, and a lightweight transport chair for travel.

    Writers almost never show that. They default to a cheap hospital transport chair—the kind pushed by nurses, not used by real people in daily life. That’s the literary equivalent of describing every car as “a beige taxi.”The Price Tag Nobody Talks About

    Wheelchairs are shockingly expensive.


    A basic folding transport chair might cost a few hundred dollars.


    A properly fitted power chair with full spinal support can cost thirty thousand dollars or more.

    Insurance rarely covers the full cost, and self-employed or low-income people often have no coverage at all. Every upgrade, repair, or replacement comes straight out of pocket. Many disabled people live with one chair that “sort of works” because they simply can’t afford the correct one.

    When you write about mobility aids, remember they aren’t disposable props. They represent enormous financial strain, constant maintenance, and the difference between isolation and freedom.

    How to Write Mobility Aids Authentically

    • Integrate them into action. Show the character maneuvering around narrow aisles, choosing routes without steps, checking curb cuts, folding a rollator to fit in a car trunk.
    • Include sensory and mechanical detail. The hum of a power chair motor, the vibration of wheels over cobblestone, the creak of a well-used cane handle.
    • Acknowledge the emotional weight. Relief, pride, or frustration depending on the day—because the aid is part of the body’s daily negotiation with the world.
    • Research specific models. Look at wheelchair forums, manufacturer sites, and YouTube reviews. The differences matter.
    • Avoid the fashion-accessory tone. “She twirled her elegant silver cane” can be fine if the story also shows how that cane actually functions and why it’s needed.

    Representation That Respects Reality


    Adding a wheelchair doesn’t make a book inclusive. Writing a character who uses it realistically—who lives with the logistics, the cost, the stares, the bruised doorframes, the independence it gives and the barriers it meets—that is representation.

    Would you like me to fold this section into the previous full article as Part 2: Mobility Aids Are Not Decorations, so it reads as a continuing series? I can stitch them together so the tone and pacing match perfectly.



    My question:

    It also annoys me that rollators are almost never used in fiction, whereas they are amongst the most common mobility aids used in real life. Often people start with a cane even though they need more support, because they are embarrassed to use a rollator, but quickly they learn a cane is NOT like they are shown in movies and novels, canes are NOT the go to mobility aids in real life. In real life the rollator is the most useful and most common device, but authors act like they don't even know it exists. You see canes and wheelchairs and nothing else.


    ChatGPT5's answer:

    That’s an excellent and very true point — and it belongs front and center in any serious article about writing disability realistically. Most writers have no idea that rollators even exist, let alone that they’re often the most common, practical, and life-changing mobility aid people use.

    Here’s how a section about that could look in your blog post or as its own “Part 3” entry in a series:The Forgotten Mobility Aid: Rollators

    Writers know canes. They know wheelchairs.
    But the rollator—that four-wheeled walker with a seat and hand brakes—barely exists in fiction.

    In real life, it’s everywhere. Visit any physical-therapy office, hospital, or grocery store and you’ll see rollators in constant use. They’re one of the most common mobility aids on the planet. So why do novels ignore them?Why Rollators Matter

    A rollator isn’t a “grandma walker.” It’s an independence machine.
    It gives stability for balance issues, joint weakness, fatigue, or pain. It has brakes for safety, a built-in seat for rest, and a small basket for carrying items. For many people with MS, rheumatoid arthritis, Ehlers-Danlos, long-COVID, or chronic pain, it’s the tool that makes leaving the house possible.

    Rollators also bridge the gap between cane and wheelchair.

    • On a good day, the character might rely on the rollator for short errands.
    • On a normal day, it’s essential for pacing and resting.
    • On a bad day, even the rollator won’t be enough, and the wheelchair takes over.

    Ignoring rollators erases this huge middle ground of lived experience—the people who can walk short distances, but only with support and planned breaks.Why Writers Skip Them

    Partly, it’s ignorance. Pop culture rarely shows them, so authors assume disability equals either “simple cane” or “full wheelchair.”
    Partly, it’s embarrassment. Society treats rollators as symbols of frailty, so characters never get them unless they’re elderly caricatures. Yet many rollator users are in their twenties, thirties, and forties.

    The result? Writers unintentionally reinforce stigma by erasing the most common device disabled people actually use.

    How to Write Rollators Well

    • Show function, not pity. Describe how the character uses the brakes before sitting, or hangs a small bag from the handlebar.
    • Use environment. Rollators don’t fit through every doorway; gravel and deep snow are nightmares. Show how characters navigate that.
    • Capture rhythm. The sound of the wheels—soft on carpet, rattling on tile—becomes part of the setting’s texture.
    • Acknowledge learning curve. Many start with canes because fiction made them ashamed of walkers. Show the pride that replaces shame when the rollator restores freedom.
    • Reflect real emotion. Relief, confidence, frustration—these are part of the human story, not the prop list.

    A rollator in fiction shouldn’t be a background object. It’s a companion, a survival tool, sometimes even a character in its own right.

    When writers only show canes and wheelchairs, they erase the vast landscape of mobility between them. Including rollators—accurately, respectfully, and as integral to the story—brings fiction one step closer to representing real disabled lives.

    Would you like me to merge this into the previous post as Part 3: The Forgotten Mobility Aid, or draft it as a standalone full-length article (like the first one) so it reads as its own blog post?



    Writing Blind Characters

    Oct 01, 25 07:34 PM

    I am legally blind and I write a legally blind character, this is how I do it...

    More Conversations with ChatGPT-5:

    My thoughts on the Rapture 2025 Rumours, that are on both Etiole's birthday and my 50 year anniversary: September 23rd:





    What Is This Site?

    I'm an author. This is an author home page. It's about me, my life, my books, my hobbies, my home town, and anything else that applies to me and my life. 

    Since starting my writing career in 1978, I have written 130+ novels, 2,000+ short stories, 6,000+ non-fiction articles (ALL are found on this site), a few dozen stage plays, 12,000+ blog posts, and a few comic book scripts for Disney's Uncle Scrooge and Donald Duck (I only worked for Disney one year (in 2005) and only wrote a few stories for their Danish comic books).

    NOTE: I ONLY write the Quaraun series (aka The Twighlight Manor series aka The Adventures of Quaraun the Insane). In recent years there has been an issue with impersonators trying to pass books off as written by me, notably several non-fiction and Erotica books. I write neither nonfiction nor Erotica.

    ALL of my books and their cover arts are listed on my website here. Beware of any books you find claiming to be me. If the books are NOT listed here on my website, they are NOT my books.

    In fiction works, I specialize in Weird/Bizarro Tales set in 40th century CyberPunk-Quasi Medieval, Cozy Dark Fantasy and Science Fiction worlds featuring an intersex Elf and his Faerie husband main characters.  I DO NOT WRITE ANY OTHER SERIES - THIS SERIES IS THE ONLY ONE I WRITE.

    Non-fiction (found ONLY here on my site) is daily updates of events in my life, and how-tos on how I write my novels.

    I DO NOT write Erotica.

    I DO NOT write books with HUMAN characters.

    The Erotica books and books with Human characters, that you are finding, are written by scammers trying to impersonate me.

    There is an ongoing FBI investigation into this matter. If you find any such books, please report them to FBI Agent Andy Drewer @207–774–9322

    The FBI believes the people behind the impersonation accounts showing up, are relatives of the woman who murdered my son.

    146 Portland Ave, Old Orchard Beach, Maine, is NOT FOR SALE.

    And I'm sick of real estate agents who are too incompetent to research land ownership before they show up to stick a for sale sign in my yard.

    The fact of the matter is, my son was murdered in 2013, and the friends and family of the murderer think it is funny to keep ILLEGALLY listing my land for sale, because apparently their child murdering bitch friend didn't hurt me enough by crippling me with a golf club, ripping my baby out of my 8 month pregnant belly and beating his brains out on the ground with a golf club.

    Also, her friends and family like to gaslight me by doxing me on ufo and alien abduction forums, while pretending to be me, and trying to make it look like I believe in ufos or aliens, even though I think people who believe in ufos are raving lunatics and people who claim to be alien abductees are crazy. 

    Worse, they've also taken to harassing my WW2 vet homeless friend, by calling HIM an alien, demon, or cryptid and sending alien crazy ufo nutjobs at try to "catch him".

    So, yeah, my son was murdered and the murder's friends and family endlessly harass me, my friends, and my family both online and offline, and I'm not happy with it at all.

    There is an ongoing FBI investigation into this matter.

    The FBI is looking for information into:

    1. identifying my son's murderer, 
    2. identifying the scammers who listed my land for sale, 
    3. identifying the impersonators who pretend to be me both online and offline, 
    4. the harassers who are harassing the homeless man and sending the UFO nuts to harass him... 
    • If ANYONE tells you 146 Portland Ave Old Orchard Beach, Maine is for sale:, please report them to FBI Agent Andy Drewer @207–774–9322
    • If ANYONE tells you I believe in aliens, demons, or UFOS, please report them to FBI Agent Andy Drewer @207–774–9322
    • If ANYONE tells you my homeless friend is an alien, a demon, a cryptid, or named Etiole for sale:, please report them to FBI Agent Andy Drewer @207–774–9322


    I'm going to repeat it because I'm tired of people showing up and making offers:

    146 Portland Ave, Old Orchard Beach, Maine, is NOT FOR SALE.




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    How did you build your audience?
    Not online, that's for sure.
    aka How to sell ten million books
    aka How I sold ten million books.



    The Park Bench Method of Writing

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    or

    The Park Bench Method of Writing

    (with the list of 10k writing prompts - takes a LONG TIME to load - SEVERAL MINUTES!)



    Why I am not proud of Disability Pride Month.
    In fact, I think it’s deplorable and downright offensive.



    I Think UFO and Alien Believers Are Weird Here's Why...




    Does every writer have to deal with this shit?



    Testing Out AI aka Conversations with ChatGPT-5:



    My thoughts on the Rapture 2025 Rumours, that are on both Etiole's birthday and my 50 year anniversary: September 23rd:





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