▲ 401 r/mobilityaids+3 crossposts

My wheelchair has no push handles, and incidents like this are why:

One thing that still gets me is how comfortable some people are just moving wheelchair users.

I had a store-side supervisor at work come up behind me once and push my chair out of the way because I was blocking a gate.

I immediately said, “Not cool.”
He goes, “You were in the way of the gate.”
And I was like, “So say something.”

He genuinely didn’t think he had done anything wrong.

So I asked him, “What if I pulled you into my lap and pushed you across the room?”

“That’s different.”

At this point I was getting a little hot under the collar.
“How?”

He tried to answer a couple of times and just… couldn’t.

Eventually he gave up, and you could see that he was a little embarrassed because I think it finally clicked what he had actually done.

I wasn’t upset because another human being had touched my wheelchair. There are plenty of situations where I’m perfectly fine with someone pushing me.

Another time, another automotive tech, Al, and I were in the storeroom gathering a bunch of small supplies. He basically went, “Here, you hold everything and I’ll push.”

He didn’t formally ask me either, but the situation was completely different. There was mutual respect there. We were working together, it made sense, and I agreed to it. I also knew that if I had said no, Al would have listened and that would have been the end of it.

That matters.

The difference is that he didn’t treat me like an object that happened to be blocking his path.

If I’m in your way, tell me.

If you offer me help and I say no, respect the fucking no.

Just don’t walk up behind a wheelchair user, grab their chair, and decide for them where they’re going.

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u/CapVikSolo — 1 month ago
▲ 716 r/mobilityaids+3 crossposts

Story Time: “I KNEW you didn't need that wheelchair”

A woman said that to me with triumph and vindication in her voice after watching me transfer out of my wheelchair, load it into my Jeep, and get ready to drive to work.

Apparently, watching me do all of that independently was all the proof she needed.

“I KNEW you didn’t really need that wheelchair!”

I genuinely had no idea how to respond.

Apparently, being good at transferring out of my wheelchair meant I had secretly been able to walk the entire time.

I just stared at her, shut my door, and drove to work.

I think part of it was that I drove a normal Jeep with hand controls instead of a big modified wheelchair van. Somewhere in her head, that apparently meant my legs must work. Never mind that absolutely nothing she had just watched me do required working legs.

And, of course, ambulatory wheelchair users exist too, so her logic would have been ridiculous regardless.

Six years later, that moment still sticks with me, not because I didn’t know how absurd her conclusion was, but because it taught me something I’ve continued to see ever since: even having an extremely visible disability does not exempt you from the disability police.

People will still watch you transfer, drive, work, shop, or do anything independently and decide that those abilities somehow cancel out the things you cannot do.

I can’t tell you how many times since then I’ve had someone see me driving, rush to beat me into an accessible parking space, and seemingly decide that whatever disability I might have couldn’t possibly warrant that space as much as theirs.

We talk a lot about people with invisible disabilities being told, “You don’t look disabled.”
But sometimes, apparently, even a wheelchair isn’t visible enough.

Edit for context: I’m a T4 complete paraplegic with no voluntary function or sensation below my injury level.

u/CapVikSolo — 1 month ago
▲ 216 r/TheAccessClub+3 crossposts

I miss when leaving the house was just “phone, wallet, keys.”

I’ve had ADHD my whole life, so forgetting something on the way out the door is definitely not new for me. Disability has just turned that particular character flaw into a full logistics exercise.
A friend from work invited me to a wellness fair today at the Adams County Fairgrounds in Brighton. Not my yum, but I had no other plans, and I like to try new things, so I figured I’d tag along.
I couldn’t tell from the information online whether everything would be indoors or outside. Looking at pictures of the fairgrounds, it seemed like some of the booths might be set up on grass even though there are paved paths around the grounds, so I loaded my scooter onto the hitch carrier, just in case.
Then I realized I’d forgotten my sunglasses.
Whatever. Not worth going back inside.
Then I remembered my spray fan. It’s hot, and because of my SCI I can’t sweat below my injury level, so that one actually was worth going back for.
One important bit of context: there’s a single step between my kitchen and the main floor of my house. I can hop it in my chair, so it’s manageable, but it takes a significant amount of effort. Doing it once is no big deal. Doing it over and over because my brain keeps remembering one more thing starts adding up pretty quickly.
So, back up the step.
Grab the fan, sunscreen, sunglasses, and backup batteries for the fan.
Get back toward the car and realize that if I’m wearing my sunglasses, I need the case for my regular glasses.
Back up the step.
Then I realize I left the sunscreen up there.
Back up the step again.
Then I remember my water bottle.
Back up the step AGAIN.
Eventually I finally make it into the car with everything.
Between needing more stuff with me now, that one stupid step, and my lifelong ADHD tendency to remember things approximately twelve seconds after remembering them would have been useful, it can take forever just to leave the house.
And naturally, when I got there, the entire fair was indoors. So almost everything I kept going back for ended up being unnecessary.
But it could have been outside, and that’s the part that gets me. Disability adds this constant layer of contingency planning to completely ordinary things.
I miss “phone, wallet, keys.”

reddit.com
u/CapVikSolo — 1 month ago

Wheelchair Users: What small setup change made your chair noticeably better for you?

For me, a lot of it has been figuring out what I actually like versus what a chair is “supposed” to have.

For context, I’m a T4 complete with no core, so some of my setup choices are built around giving me stability without adding more chair than I want.

I currently use 52 mm skateboard wheels as casters. Definitely not for everyone, and I have eaten pavement a few times because of that choice, but I like how they feel and handle.

I also don’t use wheel locks; I like high side guards; and I prefer a pretty significant seat dump so the chair envelopes me more like a bucket seat. I use a comparatively low back for my injury level, and I like my feet tucked pretty far underneath me, with my toes roughly under my knees.

I have a few add-on accessories I’ll use depending on what the day has in store, but for the most part, I keep my chair pretty minimalist.

And one thing I am absolutely firm on: I will not use a sling back. Or anti-tips.

Obviously, none of these choices are universal. Different bodies, disabilities, balance, terrain, and priorities all change what works.

What small setup change made your chair noticeably better for you?

reddit.com
u/CapVikSolo — 2 months ago
▲ 28 r/mobilityaids+2 crossposts

What’s one small wheelchair setup change that made a surprisingly big difference for you?

For me, a lot of it has been figuring out what I actually like versus what a chair is “supposed” to have.

For context, I’m a T4 complete with no core, so some of my setup choices are built around giving me stability without adding more chair than I want.

I currently use 52 mm skateboard wheels as casters. Definitely not for everyone, and I have eaten pavement a few times because of that choice, but I like how they feel and handle.

I also don’t use wheel locks; I like high side guards; and I prefer a pretty significant seat dump so the chair envelopes me more like a bucket seat. I use a comparatively low back for my injury level, and I like my feet tucked pretty far underneath me, with my toes roughly under my knees.

I have a few add-on accessories I’ll use depending on what the day has in store, but for the most part, I keep my chair pretty minimalist.

And one thing I am absolutely firm on: I will not use a sling back. Or anti-tips.

Obviously, none of these choices are universal. Different bodies, disabilities, balance, terrain, and priorities all change what works.

What small setup change made your chair noticeably better for you?

reddit.com
u/CapVikSolo — 2 months ago
▲ 358 r/disability+2 crossposts

If you don’t need the extra space, please stop habitually using accessible spots when a regular spot is just as close

I’m a wheelchair user, and something that honestly feels inconsiderate is when someone who has a legitimate disabled placard but doesn’t need the extra space habitually uses accessible parking even when there are regular spots the same distance from the entrance, or sometimes even closer.

I’m not talking about questioning whether someone is disabled or deserves their placard. There are plenty of disabilities where minimizing walking distance is necessary, and that’s a completely legitimate reason to have one.

I’m talking about situations where distance is the accommodation you need, there’s a regular spot that provides essentially the exact same distance, and you still automatically take the accessible spot.

For me, the extra space isn’t just a convenience. I need enough room to actually get my wheelchair in and out. A regular parking space right next to the entrance might be perfectly usable for someone whose main concern is walking distance, while it can still be unusable for me.

Obviously, if the accessible spot is the closest option and you need it, use it. That’s what it’s there for. But if an equally close regular spot works for your disability, I wish more people would consider taking it instead of treating the accessible spot as the automatic choice every time simply because they have a placard.

I’m curious how other people feel about this.

reddit.com
u/CapVikSolo — 2 months ago
▲ 17 r/spinalcordinjuries+1 crossposts

Disability Tax: What’s Worth the Effort?

Something I’ve been thinking about since my last post is the difference between being able to do something and deciding it’s actually worth doing.

There are plenty of things I can do independently but sometimes choose not to because the extra time, effort, or hassle just isn’t worth it.

But the opposite is also true: there are things I choose to do even when they’re harder because they give me a sense of independence, normalcy, or just let me be a husband and dog dad.

Sometimes that means getting out of bed to go check something so my wife doesn’t have to. Sometimes it’s getting the pups out and fed, making my wife breakfast, or handling some little household task that would be much easier to ask her to do.

Could she do those things faster? Absolutely. But sometimes doing it myself is worth the disability tax.
I think independence is partly learning when to conserve your energy and partly deciding what matters enough that you’re willing to spend it.

So what’s something you do, even though disability makes it harder, because to you it’s worth the effort?

u/CapVikSolo — 2 months ago
▲ 100 r/spinalcordinjuries+1 crossposts

Disability Tax and the Unspoken Toll on Relationships

I’ve always valued being highly independent, but recently I’ve been thinking about how much inaccessible design quietly affects both me and my wife.

I spent some time helping my elderly parents while they recovered from surgery, and their kitchen really drove it home. Most things are stored high. I can use a grabber for pantry items, but plates, bowls, and glasses are another story. Twisting and reaching for even the bottom shelf of their upper cabinets aggravated my back around my spinal hardware badly enough that my mom noticed the redness afterward.

Our own kitchen is far from accessible, but we’ve adapted it around me. Most dishes and food stay low, usually on the second shelf of the lower cabinets so I don’t have to reach all the way to the floor. The fridge is arranged around what I can reach. I have an adjustable table for food prep.
What I hadn’t really appreciated was what that means for my wife. She is constantly bending, stooping, and storing things lower than would be comfortable for her because that makes them usable for me.

Our house also has a step into the kitchen and another into the sunroom. I can get over them independently, but doing it a dozen times a day adds up. I can cook dinner, but carrying plates across the step is enough of a hassle that I usually call my wife to come get them. Our laundry is in the basement. I can bump down the stairs and have an old chair downstairs, so I can wash and fold laundry, but hauling it back upstairs is such a process that she often ends up doing that part.

She’s away visiting family this week, and I’m doing everything myself. I can do it, but everything takes longer, and sometimes I just skip little things. Would I have liked a cold beer in a cold glass with dinner? Yep. Was it worth another trip over the kitchen step? Nope. Water it was.

And I still make those choices when she’s home because I don’t want to run her ragged. I’ll take the dogs out, shut off the lights, and do the normal spouse stuff even when the house makes those tasks unnecessarily complicated.

That’s the part of the “disability tax” I don’t think we talk about enough. Sometimes I pay it in time, effort, pain, or things I decide aren’t worth doing. Sometimes my wife pays it in extra trips, lifting, bending, carrying, or fetching. Sometimes the thing just doesn’t happen.

If I could design our home from scratch, I wouldn’t make everything wheelchair height. I’d want mixed-height counters, pull-out storage, an adjustable cooktop, a side-opening wall oven, roll-under workspaces, and normal-height spaces for her too.
To me, good accessibility is where universal design meets the comfort and access needs of both partners, so the home works well for both people instead of making one person adapt around the other.

u/CapVikSolo — 2 months ago