How To Accurately Write Disabled Characters in Fiction



By Wendy C Allen

f you are here looking for aliens, ufos, demons, cryptids, haunted cars, curses, Etiole, the wild man of old orchard beach, the goldeneagle car, the white monkey, or any of that other weird bullshit, you want this video:



...and after that video, you want these ones:

eelkat_red_scarf.jpgWendy Christine Allen, 2019, able to sit up in a chair for the first time in years, and able to raise up my arm and wiggle fingers. This was when I started playing Witcher 3 on Twitch as part of my physical therapy to regain finger movement. Playing Witcher 3 daily from 2016 to 2019, is how I regained the use of my thumb and two for fingers on my right hand... it is also why I stopped playing Witcher 3 in 2019, once I had strengthen my two forefingers enough to start typing again.

Wendy Christine Allen, Old Orchard Beach's Autistic Author, Artist, Illustrator, & Art Car Designer

Counting Down to the September 23, 2028 50th Anniversary of my first published book (September 23, 1978)

If you are here looking for The Twighlight Manor series, The Crystonite Wars series, The Wild Years series, The White Rock Asylum for the Criminally Insane series, The Twisted Tales series, the Captured By a MerMan series, The Space Dock 13 series, The Kats of Planet Ptarmagin series, the stories about Miss Citten the Eel-Kat, or the stories about Etiole... ALL of those series were combined and consolidated into The Adventures of Quaraun the Insane Pink Necromancer series in 2014, so ALL the different series, are now under one series title.

List of the published titles still in print:

The Index of over three thousand stories in The Pink Necromancer series

What the series is about, for those new here:

The introduction to The Pink Necromancer Series. 

If you want some stories to get you started in The Pink Necromancer series, reading these first will give you a good introduction to the 3 main characters:

My Elves Are JellyFish...and I asked Google AI and ChatGPT 5.6 what they thought of this.

As requested, my daily writing prompt series is now available print paperback editions on Amazon.

There are 20 volumes of this writing prompt series currently planned and in varying stages of finishing, hopefully all 20 will be published by the end of 2026. I likely will do a 2nd series of writing prompt books in 2027.

Coming soon (Nov/Dec 2026)... patterns for my slow stitched embroidery:

BoomFuzzy-scottish-phooka-faerie-kelpie-form-Wendy-C-Allen-felt-embroidery-art2
BoomFuzzy-scottish-phooka-faerie-cooney-rabbit-form-Wendy-C-Allen-felt-embroidery-art
BoomFuzzy-scottish-phooka-faerie-nuckalavee-form-Wendy-C-Allen-felt-embroidery-art4
12-dancing-princesses-trow-king-Wendy-C-Allen-felt-embroidery-art
BoomFuzzy-scottish-phooka-faerie-kelpie-form-Wendy-C-Allen-felt-embroidery-art14
green-witch-faerie-Wendy-C-Allen-felt-embroidery-art
BoomFuzzy-scottish-phooka-faerie-enchanted-pony-form-Wendy-C-Allen-felt-embroidery-art4
BoomFuzzy-scottish-phooka-faerie-nuckalavee-form-Wendy-C-Allen-felt-embroidery-art7
fishing-village-Wendy-C-Allen-felt-embroidery-art7
mermaid-Wendy-C-Allen-felt-embroidery-art7

The first of the Visual Novels/Video Games for The Adventures of Quaraun the Inane/The Pink Necromancer series is published and available on Itch.io, there are 3 more planned for release in 2026, 6 more planned for release in 2027, and the big 60-hour 80k word 150 page one (Quaraun Goes To the Fair) is planned for a 2028 release.

There is a Pink Necromancer card game and a Pink Necromancer board game, as well as a Pink Necromancer table top RPG supliment for Dungeons and Dragons, all in the works, and to be released over the next couple of years as well.

I shouldn't have to say this, but people keep contacting me, so apparently I do:

  • No, I do not believe in aliens. Stop contacting me to ask for alien information. If you believe in aliens, I think you are insane, retarded, or both.
  • No, my car is not haunted. I've debunked that rumour many times now. . Stop contacting me to ask for haunted car information. If you believe in haunted cars, I think you are insane, retarded, or both.
  • No, I am not connected to Stephen King. I didn't even know who he was until you idiots started contacting me asking about him. I had to look him up on Google to find out what you were even talking about! If you have questions about Stephen King, go contact him and ask him. I'm not him. I don't know him. I know nothing about him. I've never read one of his books. I've never seen one of his movies. I can't figure out why you people are even coming to me to ask about him in the first place!
  1. If someone told you I believe in aliens, if someone told you my car was haunted, if someone told you I was connected to Stephen King, you NEED to contact the FBI agent in charge of my son's murder investigation and TELL HIM WHO it was who told ou, exactly WHAT it was they said, HOW they contacted you, WHERE they contacted you... because it is a KNOWN FACT that my son's murderer is the one who started all these slanderous alien, haunted car, Stephen King rumours, and the FBI is trying to catch her.

If you have any information about my son’s murderer, please give it to FBI Agent Andy Drewer at 207–774–9322 of the Portland, Maine FBI office.

Do you know who this woman is?

On August 8, 2013 she drove a backhoe over my house. On November 14, 2013 she arrived at Southern Maine Community College and crippled me with a golf club and murdered my son. One June 24, 2016, days after my first attempts to walk again, she attacked me with a shopping cart at Scarborough, Walmart, reinjuring the Nov 14, 2013 injury.

She crippled me when I was 8 months pregnant, a woman with a golf club, severed my spine and bashed my baby's head in, I spent 9 years relearning to walk, and the FBI is 13 years into the murder investigation and not yet id-ed the attacker who crippled me and killed my baby, both violently with a golf club.

Complete details of EVERYTHING she did is on this page here.

Clairescreenshot.pngThe golf club woman who called herself Clair as she looked November 14, 2013. Her hair is a weird chin leangth pageboy (very Medival style cut) platinum blonde with wide brown/black dyed stripes in it (like a reverse of Lily Munster, but the stripes are several, almost like a zebra). I am 5'6" and she was a LOT taller then me, like closer to the height of a man; she had thin lips like a man, and large nose like a man... she COULD have been a man disguised as a woman, given the ease with which she severed my spine....she's is a LOT stronger then is typical for a woman). She was wearing a chambre blue denim "blazer jacket over shirt" and a button up mens shirt (possibly flannel) and blue jeans. The bulk of her yelling was focused on accusing me of being transgender, even while ripping my baby out of my 8 month pregnant belly and bashing his head in with a golf club.
zzzz999ClaireRed2016-screenshotThe Claire woman as she looked during her shoping cart attack at Scarborough WalMart June 2016, the attack with left me paralyzed and in a wheelchair. Her hair was dyed dark red, and she drove away in a gold Volvo 240 Station Wagon of a late 1980s/early1990s model, with a "458" on the lisnce plate.... If you have any information about the woman who crippled me with a golf club, please give it to FBI Agent Andy Drewer at 207–774–9322 of the Portland, Maine FBI office.
@eelkat part 9 of 10 #dogwalk around the block (Maine st, Elm st, South street, Bradbury st) #Biddeford #Maine #night #fbiinvestigation #truecrimetiktok ♬ original sound - Wendy C Allen | 📚 Author

If you have any information about the woman who crippled me with a golf club, please give it to FBI Agent Andy Drewer at 207–774–9322 of the Portland, Maine FBI office.

Good god! We just found out about yet another slanderous rumour this woman has been spreading? When does it end? How many more of these things are out there?

Video explains what else she's done ...

If you have any information about the woman who crippled me with a golf club, please give it to FBI Agent Andy Drewer at 207–774–9322 of the Portland, Maine FBI office.


The Goldeneagle World's Most Haunted Car - 1964 Dodge 330If you encounter anyone claiming my car is haunted, demon possessed, or somehow connected to Stephen King please give the information of who, when, where/location to FBI Agent Andy Drewer at 207–774–9322 of the Portland, Maine FBI office.
@eelkat part 7 of 10 #dogwalk around the block (Maine st, Elm st, St Mary's, Dunkin, South street, Bradbury st) #Biddeford #Maine #night #plannedparenthood ♬ original sound - Wendy C Allen | 📚 Author

If you encounter anyone claiming I believe in aliens or was an alien abducttee, please give the information of who, when, where/location to FBI Agent Andy Drewer at 207–774–9322 of the Portland, Maine FBI office.

@eelkat part 4 of 10 #dogwalk around the block (Maine st, Elm st, St Mary's, Dunkin, South street, Bradbury st) #Biddeford #Maine #night #library ♬ original sound - Wendy C Allen | 📚 Author

If you know who drove this backhoe over my house at 146 Portland Ave, Old Orchard Beach, Maine 04064-1520 on August 8, 2013 please give the information of who it is to FBI Agent Andy Drewer at 207–774–9322 of the Portland, Maine FBI office.

eelkats_house_before_after.jpgIf you know who drove this backhoe over my house at 146 Portland Ave, Old Orchard Beach, Maine 04064-1520 on August 8, 2013 please give the information of who it is to FBI Agent Andy Drewer at 207–774–9322 of the Portland, Maine FBI office.

I am sick and tired of people not giving a shit that my son was murdered!

I am sick and tired of jackasses making up rumours and lies about me and my car, calling me an alien abductee and my car haunted, just to try to cover up my son's murder!


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 Answering #questions about my #multiplesclerosis specific #vocic #z51 #wheelchair ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat Saco River beach at Rotary Park, Biddeford, Maine, taking Koko for a walk #wheelchair #multiplesclerosis #doglife #mainetok #disability ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #wheelchairlife #mainelife #cairnterrier #biddeford #z51 ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #wheelchairlife #mobilityaids #disabilityawareness #disabled #wheelchair ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat Martel Field at Rotary Park, Biddeford, Maine, taking Koko for a walk #wheelchair #multiplesclerosis #heatintolerance #mainetok #maine ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #maine #mainelife #doglife #nature #cairnterrier ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat Saco River at Martel Field at Rotary Park, Biddeford, Maine, taking Koko for a walk #wheelchair #cairnterrier #doglife #mainetok #maine ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #wheelchair #artcar #cairnterrier #doglife #mainetok ♬ 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 #artcar #cairnterrier #doglife #mainetok ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #wheelchair #biddefordmaine #artcar #mobilityaid #cairnterriersoftiktok ♬ original sound - Wendy C Allen | 📚 Yaoi Author
@eelkat #artistsoftiktok #arttok #artcar #authorsoftiktok #lgbtqia ♬ 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
@eelkat Saco River at Martel Field at Rotary Park, Biddeford, Maine, taking Koko for a walk #wheelchair #cairnterrier #doglife #mainetok #maine ♬ 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:

Interestingly, I have recently learned that there are people who read my site that were unaware AI was real, and actually thought I was the one typing up the replies on these! LOL!

LLM text generating AI has been a thing in the real world since at least 2019, because my earliest articles where I was testing out AI were published in 2019.

In 2019 I did an entire series of Quaraun short stories, fully written by Dreamily (https://dreamily.ai/) and AI Dungeon (https://aidungeon.com/) and wrote several articles throughout 2019 to 2021 on how to use those two AI programs specifically for worldbuilding and plotting Fantasy stories.

In 2021 I joined the beta test program for ChatGPT and was already using ChatGPT daily BEFORE it's public release in November 2022, and I had talked about it several times in several articles throughout 2021 and 2022.

When my 2016 Witcher 3 gaming rig died in 2023, I decided it upgrade from a gaming rig to a mini server rig that can run overkill level 8qwart+ self hosted offline AI’s via Ollama (https://ollama.com/). If you thought my 2016 gaming rig was a crazy overkill mega rig, it weren’t even a quarter the crazy overkill mega computer I’ve been running Ollama on since 2023.

With Ollama I now use over TWO HUNDRED different AI programs to write my Quaraun books, thanks to HuggingFace (https://huggingface.co/models?pipeline_tag=text-generation&apps=ollama&sort=trending) with Delirium being the primary novel writing AI program I use (https://huggingface.co/sam-paech/Delirium-v1)

I don't know how far before 2019 AI existed, but I know Deep Fake videos (https://en.wikipedia.org/wiki/Deepfake) of me were being published by friends and family of my son's murderer on YouTube as far back as 2014. So image, audio, and video AI is well over a decade old.

So, for those who were confused as to who I was talking to in these articles, here are some wikipedia pages that give you info on what this thing is that I am talking to in these conversations:

Why use AI to write?

Because even though I am too paralized to type anymore, I can still think.

You got to remember: I became bedridden with a broken spine in 2013, and was quadriplegic until 2015; regained some use of my hands in 2015, and have been relearning to walk since.

So I was not online from November 14, 2013 until late in 2016, and then was only online a couple of days a month on my own website, and not on social media again until 2018, but then again, only checking in my accounts once every 3 months or so so only posting about 4 times a year anywhere, because I was just too crippled still, to sit up long enough to type. So it wasn't until 2022 that I returned to posting "regular" aka once a week, and so I lost track of everyone I used to know online because of being 9 full years offline.

You got to remember, I LOST THE ABILITY TO TYPE in 2013, and STILL IN 2025 have nearly no use of my left hand, while only have the ability to use TWO FINGERS of my right hand.

Meaning I AM STILL UNABLE TO TYPE WITHOUT ASSISTANCE.

The VERY REASON I looked into using AI to continue writing my series of novels, was BECAUSE I had become a quadriplegic with no use of either my arms or legs in 2013. and while I had regained some limited movement in my arms and legs now, it is not enough to either type for more then five to ten minutes a day, nor enough to walk for more then a few hundred feet a day, yes, even still now in 2025, twelve years later.

After the 2016 surgery gave me the ability to speak normally, I set out to use Dragon speech to text software. The novels "Into the Swamp of Death", "The Vampire Leprechaun of Fire Mountain", and "GhoulSpawn and the Lich Lord's Lover", were written this way, speech to text with Dragon software (as you can tell when reading them, because NO EDITING was done to these 3 at all, and what was published was MY EXACT DIALECT aka typed by Dragon THE WAY I SPEAK and not the way words should be spelt.)

However, in 2019 I found out about advances in AI, and because of my unique disability situation, was asked to join beta testing for various AI programs geared towards writing novels.

I am STILL severely disabled and STILL not able to type with more then the two first fingers of my right hand, still now in 2025. Without the help of ChatGPT, Ollama, and Delirium, I would not have been able to return to writing my Quaraun series.

Even though I am still mostly paralyzed in my left arm, and mostly paralyzed in my right arm save my two first fingers, I have been able to write and publish twenty-two additional novels, novellas, and short story collections between 2019 and 2025 with the help of ChatGPT, Ollama, and Delirium, something I could not have done, had AI not existed, because without AI I simply can not type, because the nerves have not yet recovered in my hands from the November 14, 2013 golf club attack that paralyzed me.

So what exactly is it that I am doing here?

In the pink bordered blocks titled "My question:" I am typing my thoughts, observations, questions, etc.

After each pink question block, is a black bordered answer box.

In the black bordered blocks titled "ChatGPT5's answer:" the AI program is typing it's thoughts, observations, answers, etc. in response to what I said to it.

While there are lots of AI programs out there, the one I use on these conversations is ChatGPT. I started doing these ChatGPT conversation articles in 2023, publishing them a few times a week the entire of 2023, at first with ChatGPT2, then ChatGPT3, then ChatGPT3.5, then ChatGPT4.o, each article states which version is being used, so you can actually see the changes in how ChatGPT talks and reacts over each edition.

In all I have made over one thousand of these "conversations with ChatGPT" articles since 2023.

Since August 2025, the articles are using ChatGPT5.

If you would like to try doing this yourself, here is the link to ChatGPT: https://chatgpt.com/

So, let's go... let's ask ChatGPT some things and see what it has to say back...

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:

    This page was written by Wendy Christine Allen of 146 Portland Ave, Old Orchard Beach, Maine.

    All Rights Reserved.

    Note: there are likely spelling errors on this site, and I am unlikely to see the ... I fix them when I find them, but, there are many issues here...

    Note: English is not my first language, Shetlean Scottish is my native language, there are likly spelling and grammar errors, as I do not know American English and am attempting to write it by sounding words out.

    Many times that Americans think a word on my site is misspelled, often it is not misspelled, it is just I mixed up languages and wrote it in Scottish without realizing I mixed the Scottish in with the English. Also our grammar is somewhat reversed from English grammar so words that are seeming in the wrong order for American English, is usually because they are in the correct order for Scottish and I either put English words in Scottish order by mistake or was unaware English put them in a different order then Scottish does.

    For those unaware, Scottish Shetlean looks like this:

    American English to Scottish:

    a bit (piece) = a party --- EXAMPLE: "And some know a bit of Latin " > "And somme kan of latyn a party "

    a long distance from = A piece fae

    a piece of = the bit --- EXAMPLE: "The duck ate a piece of bread " > "The deuk ett the bit breid "

    about the banks (on the shore/at the beach) = aboot da banks

    accomplishments = kunnandi

    After = Back o --- EXAMPLE: " After Halloween" > "Back o Hallomas "

    alive (living) = kvikr

    Always on the move = Never aff o da go

    am I not = amn't I --- EXAMPLE: "Am I not invited? " > "I amn't invited? or Amn't I invited?"

    are = is --- EXAMPLE: "Are you going soon?" > "Is ya to be going soon?"

    autumn = dah haihst

    belong to = fylgja

    best = bettah moost

    betray (verb) = svíkja

    bewildered = villhyggjandi

    building = biggin up --- EXAMPLE: "building confidence in everyday use " > " biggin up confidence in ivvryday øs "

    built = builded --- EXAMPLE: "He built a new porch." > "Hims builded a new porch."

    cast a spell = hoodooed

    cat = kat (sounds like "caught") --- EXAMPLE: "Is it an orange cat?" > "Be he a o'jinn kat?"

    child = bairn

    church = kirk

    color = colour

    danger = hœttr

    daren't = darena

    daring = djarfr

    dark = dökk

    dark elf = Dökkálfr

    dark-elves = Døkkálfar

    darker = dökká

    do you agree = ,eh? --- EXAMPLE: "That's a fine looking woman, do you agree?" > "Dair's ah right bonnie lass, eh?"

    do you want to come too = ,eh? --- EXAMPLE: "I'm going to the store, do you want to come with me?" > "Me go to shope, eh?"

    each = eche --- EXAMPLE: "Which each person can understand " > "That kan eche man understonde "

    educated = lered --- EXAMPLE: "Both among the educated and the uneducated " > "As wel among lered as lewed "

    elf = Alfr

    Elf = Álfr

    Elf Home = Álfheimr

    Elf World = Álfheimr

    elf-advice = Ælfred

    elf-beautiful = ælfscyne

    elf-friend = Ælfwine

    elf-guardian (female) = Ælfwaru

    elf-guardian (male) = Ælfweard

    elf-powerful = Ælfric

    everyday = ivvryday

    eyelids = eye ledes --- EXAMPLE: "He closed his eyelids." > "Hims did shut hims eye ledes"

    fair = faire --- EXAMPLE: "Going to the fair." > "Done gone went to the faire."

    feild = felde --- EXAMPLE: "Standing in the feild." > "Stoodt in thems felde."

    further = ferther --- EXAMPLE: "I looked further." > "I dids lokid ferther."

    green = grene --- EXAMPLE: "Look at the green hedges and woods." > "Look see at thems heigges and holtz so grene."

    handsome = braw --- EXAMPLE: "He is very handsome " > "Him wicked braw "

    have faith = trúa

    Have no doubts about our doing it = Nae faer o wis

    Have no liking for this. = Hae nae brou o this.

    have not = ain't

    He knows how many beans make five. = He kens the laid frae the croun o the causey.

    He knows which side his bread is buttered on. = He kens whilk side his bannock's buttert on.

    Head for = Mak wye for

    head rope in fishing nets and lines = baak

    head to head = Be at the knag and the widdie

    horse fly = klegsie

    I = Me

    I Think = Me thinks --- EXAMPLE: "I think we're late. " > "Me thinks that we is late. "

    I wish you well for the future = Lang may yer lum reek (translation: Long may your chimney smoke)

    idiot = eejit --- EXAMPLE: "You idiot." > "Ya eejit."

    idiot = numpty

    if = iffy or yif--- EXAMPLE: "If you don't mind..." > "Iffy yas does no care mind...."; "If you'll stay with me long enough = "Yif ye so longe with me wil dwelle". "

    I'll be even with you = A'll see day aboot wi ye

    know = ken

    looked = lokid

    looked = lokid --- EXAMPLE: "I looked up." > "I lifte up me eye ledes and lokid ferther."

    magic = hoodoo

    naked = nøkkviðr

    needle = bodkin

    neither = nouther --- EXAMPLE: "Who know neither Latin nor French " > "That kan nouther latyn ne frensch "

    No = Nay --- EXAMPLE: "No, I don't think so. " > "Nay, me thinks not. "

    Nobody knew = not-knew nobody

    Noontide = Da heicht o da day

    NOTE: Extra words are often added. --- EXAMPLE: "Did you meet the new family next door?" > "Dids ya gets a chance to stop by and meets with thems new folk that move-ed in down yawn there next doors to ya, eh?"

    NOTE: Extra words are often added. --- EXAMPLE: "He went to Rite-Aid to pick up his prescription" > "Hims did go to that yawn there new fangled store the new folks call that Rite Aid place, to gets himself some of thems there pills what the doctor gone and tells him to take each morning, a-yep, hims did."

    old = olde --- EXAMPLE: "But educated and uneducated, old and young " > "Bot lered and lewed olde and yonge "

    orange = o'jinn

    out = oot --- EXAMPLE: "The cat wants to go out." > "The kat he do wants oot."

    outside = oot dair

    people = fokk --- EXAMPLE: "the people of Shetland " > "Shetland fokk "

    people = folke --- EXAMPLE: "Look at all those people." > "Lookie at all thems folke."

    poorly = febelly --- EXAMPLE: "Who know French very poorly " > "That kan frensch ful febelly "

    Recognising = Recognisin --- EXAMPLE: "Recognising the bilingual nature of Shaetlan speakers " > "Recognisin da wye at Shaetlan spaekers is bilingual "

    shield = skjoldr

    Since = For --- EXAMPLE: "Since that is your native language " > "For that is youre kynde langage "

    tell = telle --- EXAMPLE: "I'll tell you in English " > "In englysch tonge I schal you telle "

    the = da, de, or is not used at all --- EXAMPLE: "I went to the store" > "Me goes to da shoppe" or "Me goes to da shoppe" or "Me goes to shoppe"

    them = dem, dem dair --- EXAMPLE: "I went with them" > "Me goes wit dem dair"

    there = dair --- EXAMPLE: "I want those potatoes" > "Me be wanting dem dair tatetas."

    they = dey

    To where = whither --- EXAMPLE: ""Where you go, I will go." " > ""Whither thou goest, I'll go."

    understand = understonde

    understand = understonden --- EXAMPLE: "Some understand English " > "And somme understonden englysch "

    very = wicked --- EXAMPLE: "very good" > "wicked good"; "very bad" > "wicked bad"; "very cold" > "wicked cold"

    Where = Whither --- EXAMPLE: "Where is the restroom? " > "Whither is the privy?"

    Yes = Yea or Aye --- EXAMPLE: "Yes, I think so. " > "Yea, me thinks so. " or "Aye, me thinks so. "

    For anyone actually interested in learning my native language, the Scottish government has THIS listed as the official dictionary of our people:  https://static1.squarespace.com/static/61d7352954b7fd1c9dbdfef4/t/65ddb2749d5e0541a01009c0/1709027964496/Spaektionary_2024feb.pdf  

    The Scottish government provides this document to show our language in use: https://www.shetland.uhi.ac.uk/t4-media/one-web/uhi-shetland-images-and-documents/documents-/shaetlan/Shaetlan-Language-Plan-2022-Shaetlan.pdf 

    More information about our language can be found on this website:  https://www.iheardee.com  which is written in my native language.


    However, there is also other reasons why words might be misspelled, or why I might not understand someone when they speak to me.

    My grandmother Helen Ricker Allen, was from Unst, Shetland, Scotland, and she the one who raised me. She taught me to read and write, but it was Shetlain that she taught me. She died when I was 8 years old, and I was locked in a woodshed after her furneral, I escaped the woodshed 27 years later at age 31, and have been trying to learn how to speak and write English since then.

    It is a very great struggle.

    At age 37 I took remidial reading and speaking classes at Southern Maine Community College, but we are Gypsies and Gypsy men do not allow us Gypsy women to have education, and so, while at college, on November 14, 2013, I was beaten with a golf club, while I was 8 months pregnet, breaking my spine, hips, and knees, killing my baby and leaving me quardepaleic since.

    Now my primary focus these past 13 years has been on relearning to use my hand so I could type... as of 2023, I have regained the use of my right thumb, and first two right fingers, and after 10 years offline, I am back online due to I can use three finguers.

    I never went to school, so I do not know maths and numbers and sciences, and I do not know what else would have been taught to me in school. We are Scottish Gypsies and Gypsy culture does not allow females to go to school. Being born female was already a great sin, but my grandmother took great risk in teaching me reading and writing. At 4 years old I was punished by my Uncle Bruce for knowing how to read, by being beaten in the face with a cinder block brick, that broke my right jaw and left me with garbaled near-mute spoken words ever since.

    Because no one ever spoke words to be face to face from he time I was 8 years old until I was 37 years old (I escaped the room at age 27, but did not start college until 37), I have no training in how to vocally sound out or speak the words I write or read. I can read words, but I do not know how to sound out or say those words. I can write words, but I do not know how to match the written word against the spoken word. I struggle to associate spoken words at all, or make them match up with writen words.

    Esentially, written words and spoken words are two completly seperate languages in my brain, and I have difficulty understanding spoken words.

    If you say a sentance to me with your mouth, chances are very high I will have ZERO understanding of what you said and I will not be able to ander you.

    However, if you WRITE down that exact same sentabnce, I can understand you and can type a written responce to you.

    My doctors tell me this is a side effect of extreme isolation and neglect and lack of human contact during my toddler, childhood, teen, and young adult years, and that my brain never deveoloped to comprehend spoken vocal words due to no one ever speaking to me in over three decades of the first half of my life.

    While I can read and write, American English (somewhat) I do no know how words are sounded out, what they are supposed to sound like. I readand write by shape recognition, not by sound/vocal recognition, so when reading and writing I do no "hear the words in my head" as I am told most people do when they read and write. In other words... I see "c a t" and think "c-a-t" I do not think "cat" nor do I "see" an image of a cat, no do I "hear" the word cat spoken. I'm told that this is very rare and that most people read and write by sounding out the words and linking them to visual mind images, while hearing the sound of the word in their head. I neiher hear words in my head no see images of things in my head. I'm told this is what makes me both a speed reader and speed writer, because I'm not tripped up by hear sounds or seeing images in my head like nomal people would be doing... however, I'm also told this is why my spelling and grammar are very poor, because my brain is not hear the sounds of the words or seeing visual images of the objects the words represent, so my mind also does not register spelling and grammer errors at all.

    As I was only let out of the woodshed on Sundays to go to the Cape Elezabeth Ward Church of the August Stake of the Church of Jesus Christ of Latter Day Saints, I was never allowed to go to school or hospital either. No adults ever talked to me because I was evil for comitted the sin of being born female, so I never learned how to speak properly and do not know how to sound out words to say them.

    I was 42 years old, in 2016 when, while having an MRI for my spine, the doctors found out my speak issue was caused by a broken jaw as a toddler that was healed wrong because not being allowed to go to doctors. I had surgury to fix that, and since 2016 have been trying to learn how to use my jaw and touge so I can speak vocal words now.

    Since 2023 my primary focus shifted to relearning to walk. I can now, in 2026, sit up for 2 or 3 hours a day, and can sand with a cane for a few minutes, and can walk for around five thousand feet in 2 to 3 segments a day, with the help of pushing my wheelchair like a walker.

    As of 2026, with a slight return to using my fingers and legs, I am once again focused on trying to learn the American English, but I live in mortal fear of my uncles and male cousins, as they are so hateful of allowing me to have education.

    have no one to help me to know if I am doing words correctly, and as such, I have no way of knowing if there are spelling and grammar errors, but I asume there are, and I fix them when I learn them, but I do not know what I do not know and spelling American words is a thing I do bnot know.

    I have Low Fucntioning Kanner's Syndrom, also known as "RainMan Type of Autism" aka REAL and ACTUAL Autism, not to be confused with Aspergers, High Functioning Autism, or and of thr 861 illnesses on the Autism Spectrum. An Autism Spectrum Disorder is an illness that has symptoms similar to Autism but IS NOT Autism. If you have an Autism Spectrum Disorder, it LITERALLY MEANS you do NOT have Autism.

    I am medically diagnosed as "kanner's syndrome, actual autism, the rainman type, profoundly retarded autistic savant, with a general IQ of 73, and an writing IQ of 221" but they added that they did not know how to properly diagnose me as I am "technically a feral child" and they don't know "how much is the autism, and how much is simple horrific levels of abuse and neglect induced post traumatic stress disorder that will go away with proper socilization".

    It means I know how to write, I can write a lot, and it is next to impossible for you to teach me how to do literally anythig else because my brain only knows how to write and doesn;t know how to do anything else..
    There's a reason, when I do book signings, people are quick to say: "Okay, what's the joke? why is this stupid retard here? where's the real author? I know this retard isn't the author. where are you hiding the author, why is this fucking retard here"

    The end result is, I have near zero social interaction... my 3 years in college was the ONLY face to face interaction I have ever had with humans in my entire life, and I struggle deeply to understand MOST words used by MOST people when they ask me question. And so I suffer from a huge lack of understanding many words people say to me, how to translate those words into spelling, and how to translate what it is that has been said.

    The fact remains hat until there exists a human on this planet who is willing to sit down and teach me what words spoken line up with and match what words written, this deficent is unlily to improve. But the fact also remains, that I am simply far too profoundly retarded for anyone to even try to make any attempt at all even to speak a friendly "hgelloe" or "good morning" when passing me on the street, so I have lost all hope of anyone ever either being my friend, being willing to teach me how to match spoken words to written words, or how to speak to other humans.





    While there are around 20k pages on this website, most of them are blocked from search engines, with only around 800 of them available for appearing in Google/Bing/etc search results. The remainder can only be accessed via the various links found throughout this site. This was done deliberately on my part, and I did it because the bulk of the pages on this website are chapters from 138 novels and 423 novellas, so only the first page of each novel and novella indexed by search engines, and the remainder are linked in order, one page at a time, via clicking "next page" at the end of each. So if you are looking for a specific page from a specific novel, Google can't help you.



    Thank you for stopping by and have a nice day! ꧁✨🌸🔮🦄🔮🌸✨꧂

    And if it’s your birthday today: ִֶָ𓂃 ࣪˖ ִֶָ🐇་༘࿐꧁ᴴᵃᵖᵖʸ☆ᵇⁱʳᵗʰᵈᵃʸ꧂🤍🎀🧸🌷🍭

    Wendy Christine Allen 🌸💖🦄 aka EelKat 🧿💛🔮👻

    eelkat_red_scarf.jpg

    Wheelchair Fundraiser

    @eelkat

    i just found out there is yet another bizarre rumour going around. where are these wild rumours coming from? who is starting them? and why?

    ♬ original sound - Wendy C Allen | 📚 Author
    @eelkat

    since I've been flooded with hundreds of messages the past two weeks asking if I still own "the world's most haunted car", yes, and here it is, filmed today May 18, 2026… but my son Xavier is dead, i am crippled and given that people are AGAIN showing up calling my Dodge "haunted", calling my friend "an alien", calling me "transgender", and spreading wild defamation slander connecting me to Stephen King, I think I need to start taking down the contact information of every blogger, podcaster, youtuber, and social media account spreading these rumors, and sue every single one of them for CAUSING my car to be cut in half May 10, 2010, for CAUSING the backhoe that drove over my house August 8, 2013, for CAUSING my son's murder November 14, 2013, for CAUSING me to be crippled and in a wheelchair November 14, 2013, and for CONTINUING to CAUSE harassers to show up in person to harass me near daily, STILL now in 2026. EVERYONE telling you my car is haunted, telling you my friend is an alien, calling my car "the goldeneagle", calling my friend "Etiole", or trying to connect me or my car to Stephen King, is lying to you. They crippled me when I was 8 months pregnant, and a woman with a golf club, severed my spine and bashed my baby's head in, I spent 9 years relearning to walk, and the FBI is 13 years into the murder investigation and not yet identified the attacker who crippled me and killed my baby, both violently with a golf club and the FBI believes that it is friends and family of the woman who did it, are the ones who started and spread the rumors saying my car is haunted, saying I'm an alien abductee, saying all kinds of similar bs about aliens, ufos, ghosts, witchcraft, demons, and Stephen King connections, even though I don't believe in ghosts, aliens, ufos, demons, and had never heard of Stephen King before 30k of his fans showed up in my yard trying to find my car! FBI believes the backhoe driver and the murderer are the same person and it is a developer who wanted my land and so started the Stephen King, ghost, and alien rumors all in an attempt to drive me off my land, and when it didn't work they drove a backhoe over my house, and when that didn't work they crippled me and killed my son. Why are they doing this? How do I get them to stop?

    ♬ original sound - Wendy C Allen | 📚 Author






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    Get an email whenever Wendy Christine Allen 🌸💖🦄 aka EelKat 🧿💛🔮👻 publishes on Medium.

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    Do you know who drove this backhoe over my house at 146 Portland Avenue, Old Orchard Beach, Maine on August 8, 2013? If you have any information, please give it to FBI Agent Andy Drewer at 207–774–9322 of the Portland, Maine FBI office.

    My house at 146 Portland Ave, Old Orchard Beach, Maine, July 4, 2013, photo taken because we had just finished building a baby room on the back. vs My house August 8, 2013, when the same group of people (yes group, the golf club woman was not alone when she attacked November 14, 2013, nor was she alone with her second attack July 2016.) who murdered my son on November 14, 2013 at Southern Maine Community College and crippled me July 26, 2016 at scarborough WalMart,... they arrived the first time with a backhoe on August 8, 2013, that they used to drive over my house, during a time of day that I normally was home asleep... I had to work a different shift at the Waffle Cone Pizza Food Truck at George's Parking Lot by Bill's Pizza at the OBB Peir, that day, otherwise, I too would be at the bottom of a landfill, along with my house and everything I owned that was also in the house. I was 5 months pregnant at the time and have been homeless for just under 14 years, homeless ever since....

    ... which means it is now only a few weeks from the 14th anniversary of my son's murder. I was 8 month pregnant November 14, 2013, and a student ay SMCC, and coming out of the Buglight Lighthouse art studio after art class, when a still unidentifiedwoman wielding a golf club attacked me, severed my spine, while I was 8 months pregnant, triggered early labour, then killed my son minutes after he was born.

    While accusing me of being transgender, screaming "transvestite freak" and "look at that thing, that's Ken's son in a dress"... while I was 8 months pregnant.

    eelkats_house_before_after.jpgMy house at 146 Portland Ave, Old Orchard Beach, Maine, July 4, 2013, photo taken because we had just finished building a baby room on the back. vs My house August 8, 2013, when the same group of people (yes group, the golf club woman was not alone when she attacked November 14, 2013, nor was she alone with her second attack July 2016.) who murdered my son and crippled me, arrived the first time with a backhoe that they used to drive over my house, during a time of day that I normally was home asleep... I had to work a different shift at the Waffle Cone Pizza Food Truck at George's Parking Lot by Bill's Pizza at the OBB Peir, that day, otherwise, I too would be at the bottom of a landfill, along with my house and everything I owned that was also in the house. I was 5 months pregnant at the time and have been homeless for just under 14 years, homeless ever since.

    The backhoe driver returned November 14, 2013, armed with a golf club, used it to break my spine and smash my baby's brains out on the ground

    On November 14, 2013, my son was murdered. I was 8 months pregnant, leaving my college classroom, and just getting into my car, when 3 strangers, a man and two women, armed with golf clubs leapt out from behind my car screaming "kill or be killed, kill the transvestite freaks, kill them all before they kill us! look at that thing! That is Ken's son, look at how it's dressed! kill the transvestite freaks! kill or be killed"... while the bald man and the red haired woman chanted this over and over, the blonde woman, lunged with the golf club.

    She severed my spine, I am now a quadriplegic, and been paralyzed arms and legs, and in a wheelchair for 13 years now. She broke my hips, my knees, my legs, ruptured most of my discs, and shattered three of my vertebrae so bad that the shards of bone acted like glass and embedded themselves into my spinal column nerve bundle.

    The attack also triggered labour.

    My son was born in that parking lot, and he lived only a couple of minutes, before the deranged blonde woman, beat his head in and smashed his brains out, with the same golfclub she had just used to sever my spine and leave me crippled for the rest of my life.

    Realizing that I was not transgender, and they'd just murdered a baby, the man grabbed the 2 women and forcibly dragged them away to a 4 door white pickup truck, and they left me there to die.

    The FBI told me later, that a few weeks before this attack, and transwoman, had murdered a cis woman, in a parking lot, abou 20 miles away from where I was attacked. The FBI, believes that my attackers, had somehow found out I wrote transgender fiction, connecting my real name to my penname, (my father's name is in fact "Ken", and I do have a brother) and believed that I wrote transgender fiction, because I was myself transgender, even though I'm not transgender. The FBI, believes the attackers, thought I was my brother, pretending to be a woman.

    The FBI investigation, into my son's murder, has dragged on for 13 years, and still now in 2026, continues on, with the FBI, still not having yet identified my attackers, and only guessing at what their motive was.

    Thus we come to 2014, and the full swing change of the series I write. WHY my series, went from just a transman main character living life, to the full blown Mpreg genre series that it now is today.

    Before the attack, I had a chance of having a baby. I don't know. And because I'm in America, I'm too old to adopt. You have to be under 45 years old to adopt a baby. That is the law in America. I was informed this, when we tried to adopt, now that my injuries leave me unable to get pregnant a 9th time.

    Thus began my obsessively writing, my transman main character, pregnant. Always pregnant now. Every time. Every story. Stories that now fully focus on pregnancy, labour, miscarriages, babies dying, babies living, raising babies... the whole series, since 2014 has devolved into an outright baby obsession.

    Meanwhile, reborn baby dolls were suggested to me by my therapist, and have also become a deeply obsessive part of my life. Because 13 years ago my son was murdered minutes after he was born, because a transphobic bigot mistook me for being transgender, I'm STILL in a wheelchair, struggling to relearn to use my arms and legs, now 13 years later, and I'm still DAILY dealing with police officers and FBI agents who while they are trying to find my son's killer, they are also daily reminding me... oh, yeah, my son was murdered, literally ripped out of my belly, by a transphobe. Who still has not been located and walks free to kill again.

    The golfclub woman as she looked during the golf club attack at Southern Maine community college November 14, 2013. She is about 20 to 30 years older then me and would be around 75 to 85 years old now in 2026.

    Clairescreenshot.pngIf you have any information about the identity of this child murderer, please call FBI Agent Andy Drewer at 207–774–9322

    The golfclub woman as she looked during the shopping cart attack at Scarborough WalMart July 26, 2016. She is about 20 to 30 years older then me and would be around 75 to 85 years old now in 2026.

    zzzz999ClaireRed2016-screenshotIf you have any information about the identity of this child murderer, please call FBI Agent Andy Drewer at 207–774–9322

    The 2nd woman as she looked at both attacks, her hair goes all the way down to her knees. She is about 20 to 30 years older then me and would be around 75 to 85 years old now in 2026.

    Kendrascreenshot.pngIf you have any information about the identity of this child murderer's accomplice, please call FBI Agent Andy Drewer at 207–774–9322

    Do you know who these two woman who crippled me and murdered my baby, at Southern Maine Community College at 10PM on November 14, 2013, are, and what their connection to the backhoe that drove over my house is? If you have any information, please give it to FBI Agent Andy Drewer at 207–774–9322 of the Portland, Maine FBI office.

    I am a legally blind quadriplegic, and low verbal, I have also published 138 novels in the last 48 years. It's not as impossible as people think. The problem being blind and quadriplegic, medically have different meanings then how those two words are used medically.

    Fewer than 3% of all blind people see nothing. While 97% people who are classified as fully blind are able to see up to two feet in front of them. Legally blind means I can see more then two feet in front of me but not far enough to see twenty feet in front of me. In my case I can see about eight feet.

    Quadriplegic, has varying levels, it means having a damaged nerve bundle in the spinal column causing limited mobility of all 4 limbs, (in my case this was done by a women wielding a golf club, who also beat my 8 month infant's head to pulp on the parking lot tarmak, at the same time she severed my spine with the same golf club; both on November 14, 2013; the FBI investigation into my son's murder and my being crippled has gone on now for 13 years, a few weeks away from 14 years now, and the FBI has still not identified the killer or her motive). Contrary to popular misconception, quadriplegic does NOT mean ZERO movement, it means means limited movement, specifically in means unable to lift arms over head, unable to grip fingers around objects to pick them up, and unable to stand for more then 5 minutes to a time. Because there are so many thousands of nerves in each limb it is actually very rare for there to be 100% no movement, but how much, and to what extent varies by patent depending upon the specific point of injury to the spinal column.

    Meaning typing is still possible for over 60% of all quadriplegics.

    In my case, it was the lower spine that was severed, cutting off completly my ability to move my right leg, leaving limited feeling in my left leg, and an ability to stand but not walk, with crutches, for the first 9 years. I regained enough nerve growth in my legs by the 9th year to be able to take ten or twelve steps allowing me to get out of bed for the first time since the golf club attack; This in turn lead to me being able to start using a wheelchair, as I was able to sit upright for the first time as well.

    Because the shattered vertebrae bone fragments are broken off completly and embedded into the nerve bundle just above my tailbone, doctors were saying I would never walk again, but now at 13 years, I am able to push mu wheelchair like a walker, a distance of almost a thousand steps a day. Though doctors are still doubtful I will ever walk "normally" again, I have proven them wrong, when their said 13 years ago, that I would never walk again at all.

    But because of the placement of the damage to my spine, regaining hand use, was always thought possible, it was just a matter of waiting long enough for nerve regrowth, along side daily finger exercises. I was able to continue writing, after becoming quadriplegic, because I still have use of my right thumb, and 2 fore figures of my right hand. And can type 90 words per minute with those 3 fingers.

    I however have no wrist strength, elbow strength, or shoulder strength, so I am not able to form a fist, or lift objects, or brush my hair, or my teeth, all thing I have to have my caretaker do. But, those things are not needed for typing. Unfortunately, my pinky and ring fingers are "nerve dead" and drag over the keyboard, and cause horrific spelling errors and typos, which are incredibly frustrating to deal with.

    Unfortunately trying to edit errors myself, just makes the errors worse, because those same two fingers drag over the keyboard yet again. Prior to the golf club attack, I rarely had spelling errors; now I got more spelling errors then someone is learning English as second language. Editing is a challenge, that I've had to accept, I simply can not do myself, and I have to hire several editors to help with that.

    Low verbal means sounds can still be made, sounds that software programs like Dragon can be trained to recognize and translate, and type into full words. More then half my novels were typed with this method.

    I still have a long ways to go before I am anything close to being able to do the things I could do before the golf club woman beat my baby's brains out and shattered my spine. And you know what's more frustrating then how slow mu medical progression has been? The fact that it's been 13 years and the police and FBI are still coming up at dead ends as to who the woman who murdered my baby was, or why she even did it.

    My son's 14th birthday is only a few weeks away, but he didn't even get to live long enough to celebrate his 1st birthday, I don't even know why. And I can't wait to regain my ability to walk again, because regaining my ability to walk, means gaining the ability to go outside and start looking for my son's murderer myself instead of sitting at home trapped in a wheelchair waiting for the police and FBI to to find her. So, writing isn't a big priority for me anymore. I only write now, as a way to exercise my hands, in between relearning to walk.

    Never let a disability stop you. Plenty of writers, artists, athletes, do not let either blindness, speech impediments, or limited mobility hold then back from perusing their careers.

    Do you know who these two woman who crippled me and murdered my baby, at Southern Maine Community College at 10PM on November 14, 2013, are, and what their connection to the backhoe that drove over my house is? If you have any information, please give it to FBI Agent Andy Drewer at 207–774–9322 of the Portland, Maine FBI office.

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