Plus: What Gaslighting Really Means, and Why It’s So Damn Hard to Spot
Gaslighting isn’t just lying. It’s psychological warfare dressed in charm and fake concern. It’s the friend who tells you you’re overreacting when you’re reacting exactly right. The partner who says you imagined the thing they absolutely said. The doctor who calls your symptoms imaginary while your body screams otherwise.
It starts small. A twisted comment here, a rewritten memory there. And suddenly, you’re doubting your gut, your grief, your own damn mind.
Let’s call it out.
What is gaslighting, really?
Gaslighting is a form of psychological manipulation in which someone causes you to doubt your perception, memory, or sanity, often to maintain control, avoid accountability, or protect their ego. The term comes from the 1938 play Gas Light, where a man dims the lights and convinces his wife she’s imagining it.
It can happen in romantic relationships, friendships, families, workplaces, doctors’ offices, anywhere power is abused and truth is twisted.
11 Signs You’re Being Gaslit
You feel like a shell of who you used to be Dull. Confused. Exhausted. A little lost. And quietly wondering if you’re the problem.
You constantly second-guess yourself You used to trust your gut. Now you rehearse your words before you speak and apologise even when you’re not sure why.
They rewrite the past You remember what happened. They insist it didn’t. Or it happened differently. Or you’re misremembering. Or too sensitive.
They dismiss your feelings “You’re being dramatic.” “Stop overreacting.” “You’re too emotional.” Translation: they don’t want to deal with what you feel.
They weaponise your insecurities You opened up to them. Now they use it against you — subtly or not. In arguments. In jokes. In gasps and eyerolls and “I was just kidding.”
You feel like you’re walking on eggshells You shrink before you speak. You manage their moods. You try to keep the peace by disappearing yourself.
They blame you for everything If they’re angry, it’s because you provoked them. If they lied, it’s because you were too difficult. Nothing is ever their fault.
You’ve started to believe you’re “too much” Too emotional. Too sensitive. Too needy. Too exhausting. That’s not an accident. It’s a strategy.
They isolate you from others Sometimes subtly, sowing doubt about your friends or implying you’re better off alone. Sometimes, overtly punishing you for having support.
They flip the script during conflict You bring up something that hurt you, and suddenly you’re defending your tone, your timing, your memory. The original issue vanishes.
You find yourself making excuses for them To your friends. To your therapist. To yourself. “They’re just under a lot of stress.” “They had a rough childhood.” “They don’t mean it.”
“It’s Not Always Screaming and Slamming Doors”
Gaslighting doesn’t always look like abuse. Sometimes it’s soft. Quiet. Delivered with a gentle tone and a hand on your shoulder. “I’m just worried about you.” “You’ve been really sensitive lately.” It can come from people who say they love you, and sometimes, maybe, do.
That’s what makes it so dangerous. And so hard to name.
If any of this feels familiar, you’re not imagining it. That voice inside you, the one that’s been flickering under all the doubt? That’s still you. And you’re not crazy. You’re waking up.
There’s a moment, maybe you know it, where someone asks too much, again, and instead of speaking, your body screams. Your jaw tightens. Your stomach turns. You smile and say, “Sure, no problem.”
I used to think being agreeable made me good. What it made me was exhausted. And resentful. And invisible.
This is about the messy, liberating art of setting boundaries, even if your voice shakes, even if you’ve never seen it modelled, even if it costs you people who only loved the version of you that said yes too often.
Where We Learn to Over-Give
We don’t come out of the womb clutching a to-do list and an apology. That’s learned. Most of us were raised to be good girls and boys, to not make waves, to share even when it hurt. And if you’re someone who’s lived through trauma or chronic illness, the habit of over-giving becomes a survival strategy. We give more, so we’re not abandoned. We stay quiet so we’re not punished. We work twice as hard to prove we’re worth the space we take up. Then there’s the capitalist cherry on top: if you can do more, you should. Productivity becomes morality. Rest is suspect. And boundaries? Selfish. That’s the lie they sell us so we’ll keep bleeding ourselves dry.
What Happens When You Don’t
The body keeps the receipts. Fatigue. Resentment. MS flares. Migraines. Rage that simmers under your skin until it boils over or turns inward. When you don’t set boundaries, your body will eventually do it for you. And the people who benefit from your lack of boundaries? They’re not going to suggest you take better care of yourself. They’re not going to set limits for you. That’s your job. Without boundaries, you become a ghost in your own damn life, present, but not really there.
Boundaries Are Not Walls
People get twitchy around boundaries because they mistake them for barriers. But boundaries aren’t walls. They’re bridges with toll booths. They say, “You can come closer, but here are the terms.” Boundaries allow love in, real love, not the manipulative, shape-shift-until-you’re-pleasing kind. You can say, “I love you, but I don’t take work calls after 6 PM.” Or, “I care about you, but I’m not your emotional landfill.” Boundaries are not ultimatums. They are clarity. And clarity is kindness, even if sometimes it sounds like fire.
What Saying No Can Sound Like
Saying no doesn’t need to come with a PowerPoint presentation and a side of guilt. Sometimes it’s just: “No.” Or: “That doesn’t work for me.” Or the power move of silence. You don’t owe an explanation for protecting your peace. And yes, you’re allowed to say no to people who love you, people who raised you, people who expect the old version of you to show up on cue. Every no is a yes to something else. A yes to your body. Your time. Your sanity.
Expect the Pushback
You will be called selfish. Dramatic. Cold. Especially if you’re a woman, or someone socialised to be the fixer, the feeler, the forgiver. But hear this: you’re not selfish. You’re sober now. You’ve sobered up from the belief that you must earn your place by disappearing. Some people won’t like the new you. Let them leave. That’s not a failure, that’s a filter. The ones who stay? Those are your people. Those are the ones who can love you with your spine intact.
Boundaries for Chronic Illness & Energy Management
If your body is already fighting battles no one can see, your boundaries are your armour. Cancel the plans. Turn off your phone. Say, “I can’t do that today” without a TED Talk. You don’t owe anyone an explanation for how you manage your health, your pain, your rest. Boundaries aren’t just emotional tools; they are survival gear. Especially when every decision costs energy you can’t afford to waste.
Personal Note
For me, learning to say no started with getting sick. MS didn’t just strip my nerves, it stripped my tolerance for bullshit. I don’t have the energy to please and perform anymore. What’s left is a very raw, very real version of me. She’s not for everyone. But damn, she’s finally for me. And with that came loss. I lost a lot of people, people who were only around for the good times, for the easy yeses, for the mountains of emotional support I used to give without question. When I got sick and started drawing lines in the sand, some vanished overnight. Boundaries have a brutal kind of clarity. They show you who’s in your corner because they love you, and who was only there for what they could get.
I was walking, just walking, and suddenly the signal from my brain went silent like a dropped call. It’s the second time this has happened to me. It’s really strange because it takes a moment for the signal to reconnect, and during that moment, which feels far longer than it actually is, my arms flail about trying to find something to grab hold of, even though it is an entirely pointless exercise. I hit the ground hard, narrowly escaping hitting my head against a brick step. I’ve torn the same calf muscle four times. I know the pain intimately, like a pain you thought you’d outgrown but still clings like smoke to your clothes.
But this isn’t about the fall. Not really. It’s the shrinking in someone’s eyes when I say, “I have MS.”
Multiple Sclerosis.
You’ve heard the name. Maybe you’ve seen a celebrity wear a ribbon or a TikToker do a day-in-my-life with a cane and a glossy filter. But unless it’s in your body, or someone you love is limping through this mess, you don’t really know.
So let me tell you.
MS is a full-time job I never applied for
Multiple Sclerosis is an autoimmune disease where your body, your own beautiful, broken, fiercely trying body, decides to eat away at your nerves. The myelin sheath that protects your neurons gets attacked, and like frayed electrical wires, the signals get patchy. Delayed. Disrupted. Or gone entirely.
It’s not predictable. It’s not curable. It’s not one-size-fits-all. No, yoga and oat milk matcha spirulina chia smoothies are not going to cure it. Yes, I’ve tried.
But more to the point, it sure as hell isn’t funny.
For me, it means:
Pain that stabs and twists like barbed wire in my calves.
Spasticity that locks my legs in place like rusted bolts.
Hands that stiffen and fingers that won’t move.
Fatigue that isn’t “tired.” It’s “my bones have been replaced with concrete and I can’t lift my arms to wash my hair.”
Brain fog that makes me lose my train of thought mid-sentence, or forget words like “kettle” and “Thursday.”
Vision blurring, numb hands, trouble swallowing, and the occasional delightful surprise of losing control of my own limbs.
Painful electrical pulses that shoot through your body, anywhere, any time, every day. The ones I rarely talk about out loud.
And let’s not forget the big daddy of dickheads. The hug that crushes your lungs and stabs you in the chest if you try to take a breath or move before it’s done torturing you.
And stress? It pours gasoline on all of it.
Stress is not just a trigger; it’s a loaded gun
When I’m stressed, when life delivers too much grief, too many bills, too many people expecting me to perform wellness like a broken-down show pony, my symptoms flare.
I lose strength. I lose sleep. I lose pieces of myself.
The problem is, the world doesn’t see the flare.
They see me cancel plans. They see me slow down. They see me quiet. And instead of understanding or patience, I get comments.
“Must be nice to lie in bed all day.”
“You don’t look sick.”
“We all get tired, you just have to keep going.”
“Are you sure it’s not all in your head?” >> No fucking shit, Sherlock! Look at my MRI, my head is full of it.
This is not your punchline
I’ve heard the jokes. Seen the memes. Watched people laugh about forgetting their keys and say to me, “Oops, maybe I also have MS!” (Yeah, not funny.)
I’ve watched people roll their eyes when I say I can’t drive today because my left foot won’t lift properly. I’ve had colleagues act like I’m milking it. I’ve had doctors talk over me, then prescribe yoga and mindfulness when what I need is a damn MRI. I’ve had strangers verbally attack me because I parked in a disabled zone.
I’ve seen pity turn into boredom. Sympathy into silence. And let me tell you: nothing hurts like being dismissed when you’re already fighting your own body just to exist.
What I want you to know
I didn’t choose this.
MS took my ability to dance, to sing, to be spontaneous. It took my certainty. It took the version of me that used to trust my own body and enjoyed life. It took the me that loved to be spontaneous, adventurous, playful. But let me tell you, it didn’t take my fight. I will not sit down and be quiet. I will keep going. I will keep fighting. It did not take my voice.
And so I’m using it.
To say:
Please stop downplaying invisible illness.
Please stop measuring someone’s pain against how well they can smile through it or hide the shit show that’s going on inside them.
Please stop expecting people with chronic conditions to perform gratitude like it’s a damn talent show.
Chronic illness is hard enough without having to fight for legitimacy and dignity.
And I’m tired. So fucking tired. Tired of fighting. Tired of barely surviving. Tired of pretending I’m fine when I’m hanging on by a thread. I don’t get to rest. I don’t get to fall apart. I have to take care of myself, every meal, every bill, every damn decision, in a body that betrays me and reacts to everything I do or feel. And no one sees the cost.
I’m still here
I am still here. Still trying. Still waking up in this fucking body I didn’t choose, but have no choice but to live inside. Yes, there is a lot wrong with me, no, I don’t enjoy it, and no, it’s not funny.
Sometimes I cry from the pain. Sometimes I scream from the frustration. Sometimes I laugh, because if I don’t, I’ll unravel completely.
But I am here. Bruised, exhausted, aching, but here.
And if you’re reading this and you have a chronic illness too, I see you. You’re not lazy. You’re not faking. You’re not alone.
You’re carrying a battle inside your body that most people can’t even imagine.
And you’re still here, too.
What about you? Have you ever had to defend your pain? To justify your limits? Tell me. I’m listening.
I recently got suckered by a local sparkling drink that looked like it belonged in a wellness influencer’s fridge. You know the type, soft colours, botanical flavour, “low sugar,” “no colourants,” “crafted.” It practically whispered, “I’m healthy, babe.”
And I believed it. Especially because it featured one of my all-time favourite flavours: elderflower. I didn’t question it. I sipped it like it was liquid virtue.
Then I read the label. Twelve grams of sugar. Three teaspoons in one small can.
For someone managing chronic illness, inflammation, and fatigue, that’s a problem.
What happened?
I got healthwashed, misled by clever packaging that makes something seem healthy when it’s not.
These drinks use phrases like:
Botanical
Low Sugar
Guilt-Free
Plant-Powered
Inspired by Nature
But they’re often hiding more sugar than you’d expect, or loaded with fruit concentrates and additives that don’t belong anywhere near a “clean” label.
Here’s what to watch out for:
“Low sugar” still adds up. In South Africa, it can mean up to 5g per 100ml, so a 300ml drink can still sneak in 12g of sugar.
“Botanical” is branding, not nutrition. It’s marketing fluff. It doesn’t mean the drink is good for you.
Always read the back of the label. Ignore the pretty front. Flip it. Check the sugar per serving and the ingredients list.
Sneaky red flags:
Serving size is 100ml, but the can is 300ml
“Fruit juice concentrate” or “cane sugar” listed early
Claims like “natural” or “artisan” with no real context
My takeaway?
Even products that look healthy can mess with your health, especially if you’re sensitive to sugar, trying to reduce inflammation, managing symptoms, or lose weight.
This isn’t about guilt. It’s about knowing what’s in your food so you can make choices that support your body.
Because sugar has a sneaky little habit of dressing up in wellness drag.
Ever been healthwashed? Tell me your sneakiest “thought it was healthy” product below
Don’t Tell Me I’m “Too Sensitive.” You’re Just Too Cruel.
It happened in front of a Starbucks. Like so many little violences do. I was inching my car into a disabled bay, my legs trembling, fatigue coiled behind my eyes like a migraine ready to strike, when a woman dripping in costume jewellery appeared. Finger raised. Voice already sharp with judgment.
“You can’t park there.”
I told her I could. That I had a permit and that I have multiple sclerosis.
She scoffed. “Those things are fake. You can buy them anywhere.”
“Really?” I thought to myself, “Where?” Probably would’ve been easier.
Then she looked me in the face and said: “Multiple Sclerosis doesn’t count.”
Let me repeat that. Multiple Sclerosis doesn’t **ing count.
Well, clearly I need to have a little chat with my world-class neurologist. Obviously, this woman knew something he didn’t.
I wish I had a clever comeback. Something surgical and savage that would’ve left her sizzling in a puddle of her own ignorance.
But I didn’t.
I just stood there, vibrating with rage, with shame of her making a scene in public, of her filming me on her phone, with that old, sick feeling in my gut: Here we go again.
My nervous system wasn’t built for public debate. And yet, here I was. My body on trial in the middle of town. I just wanted a coffee and to sit down because getting out in the world is an ENORMOUS treat for me these days.
The Price of Looking “Fine”
When I was first diagnosed, the man I was dating didn’t believe me.
“You’re not actually sick,” he said. “You look fine.”
As if illness only counts if it disfigures you. As if I must drag a wound behind me like a Victorian ghost to be believed.
He cheated on me with two of my friends and later dated a woman with a more obvious illness. I did start to question if he had some kind of bizarre fetish or if he just needed to feel more masculine by having a damsel in distress on his flabby arm. Who knows, people are weird. Once, with godlike certainty, he said: “Maybe you just don’t get to have love.”
I didn’t believe him; I’m not that messed up. But that’s what the world teaches you when your illness hides under your skin. That, unless your pain is public, photogenic, and can make people tilt their heads with an “oh, you poor thing” look, it doesn’t count.
That your nervous system, your actual lived experience, is somehow up for peer review.
Welcome to the Performance of “Okay”
Women are taught from the beginning to make pain look pretty. Smiling through cramps. Working through grief. Performing resilience like it’s an effing TED Talk.
Throw chronic illness into the mix, and you’re cast in a very specific role:
Be brave, but not bitter.
Be strong, but not messy.
Be informative, but not angry.
Be disabled, but not inconvenient.
God forbid you feel things. God forbid your body doesn’t cooperate.
The Ableism Hidden in Wellness Culture
Let’s talk about the billion-dollar lie that says you can “heal yourself” if you try hard enough.
Green juice.
Yoga.
Mindset.
Detoxes.
Energy work.
The whole “optimise your nervous system” cult that pretends trauma and illness are just bad habits you haven’t outgrown yet.
I’m not knocking genuine care or ritual or pleasure; I love a magnesium bath as much as the next exhausted woman. But I am calling out the violence that happens when the wellness world gaslights the sick. When it blames you for your symptoms. When it markets recovery as a brand you can buy if you hustle hard enough and stop being “negative.”
Sometimes a body is just broken. Sometimes it’s just tired. Sometimes it’s never going to be better, and that doesn’t mean you failed. It means the system did.
I Don’t Owe You My Pain Performance
I don’t owe you visible suffering. I don’t owe you explanations. I don’t owe you a limp, a wheelchair, a medical file, or a teary TEDx talk.
I have MS. It’s real. And whether I’m collapsed in bed or laughing at a party or, God forbid, standing tall in a disabled parking space, I’m still sick. I’m still fighting. And I’m still not here to make you comfortable.
Stop asking women to shrink their pain into something you can digest.
Stop calling us “too sensitive” when what you mean is, “I don’t want to feel implicated in your reality.”
My nervous system is not a fucking debate club. It’s not up for peer review. It’s mine. It’s sacred. And sometimes it hurts like hell.
And Still, I Rise. Not to Inspire You. To Save Myself.
The best part? That ex who told me I didn’t get to have love? He was wrong. So wrong it’s almost funny. I found someone who didn’t need proof to believe me. Who didn’t treat my illness like an inconvenience or a prop. Who holds space when my legs fail and holds my hand when they don’t.
What About You?
Have you ever been asked to prove your pain? Have you swallowed your symptoms to make others more comfortable? What would it feel like to stop performing and just… be?
You don’t owe anyone your broken parts. But if you feel like sharing, I’m listening.
I’ll be sitting at my laptop, working, writing, answering emails, maybe just thinking about writing while actually scrolling through memes, and then poof… I disappear.
Not slowly, like that cosy afternoon nap you give yourself permission for. I mean one second I’m here, and the next, gone. Like someone unplugged my brain. Then just as quickly, I jolt back. Blink. It’s over. The dog’s still asleep. The kettle’s still humming. But I’m sitting upright at my computer, wondering: Did I just fall asleep while working? And it happens more than once; these strange glitches come in clusters. I can be pulled out of them if the phone rings or if someone touches me, like my nervous system is waiting for a jumpstart.
I’ve had a few of these episodes now. They’re not dreamy or floaty or warm. They’re hard and fast and jarring. And they scare the shit out of me.
When you live with MS, every weird body glitch carries a question mark. Is this just MS doing its daily chaos routine? Or is this something new? I am always scared of something new because in my support group, my fellow spoonies will say, “It’s never just one disease,” or “Once you’ve got one, you’ll get more.”
Please, no.
MRI (Eventually) Incoming
I haven’t actually made the appointment yet. I know I need to. But I’m still in the bureaucratic limbo of:
A. Figuring out whether my medical aid will cover it (spoiler: only a portion, yay South African healthcare).
B. …I forgot what B was. I genuinely had it a minute ago.
Anyway. MRI, neurologist, those are on the horizon. Somewhere between the load shedding schedule and the next cup of tea.
And I’ll admit it: I’m nervous. Not because I expect a terrifying result. I’ve already got a brain with white spots and a spine full of screws and wires. But I need answers. And the options on the table are… not exactly comforting.
Here’s the shortlist:
MS fatigue, aka “lassitude,” which is a fancy word for soul-sucking exhaustion that hits like a tranquillizer dart. It’s not “you need a nap” tired. It’s “my brain is melting” tired. I don’t know how to explain it to people who have never experienced it. Closest is, imagine you’ve been awake for 142 hours and your veins are full of cement.
Microsleeps, which are tiny, sneaky, involuntary naps that last mere seconds but could happen while I’m sitting, reading, or, terrifyingly, driving.
Narcolepsy, which I don’t think it is, but hey, add it to the menu of potential plot twists.
Or, worst case, seizures, though mine don’t come with confusion or post-episode fog, so that seems less likely. Still, it’s on the board.
What’s the difference, anyway?
I did some digging because I’m me, and medical rabbit holes are my weird comfort activity. Here’s the deal:
MS Fatigue: Creeps in slowly, can last days, weeks, months (yup), worsens with heat or thinking or breathing. It’s not fixed with sleep; you just have to wave a white flag and collapse.
Microsleeps: Happen instantly and briefly. You might not even realize it’s happening. They often show up when you’re bored, tired, or doing something repetitive. Like, say… staring at a screen trying to earn a living.
Sleep attacks: Similar to narcolepsy, these come on fast and can make you collapse mid-sentence. (Not happening here, thank god.)
Seizures: Usually longer, often come with confusion or memory gaps. (Not me. I come back online almost too fast.)
So what’s happening with me? I don’t know yet. But I do know this: it’s unsettling. So much so that Bugsy seems to pick up on it and he lies next to me quietly till I’m back before carrying on with his 18th zoomie of the day.
The Mental Load of Not Knowing
This is the part they don’t tell you when you’re diagnosed. Not just the disease, but the never-ending detective work. The constant second-guessing. The mental calculus of “Should I worry about this now or later? Or never?”
It’s exhausting. And honestly? Sometimes it’s lonelier than the actual symptoms.
But I’m trying to do the responsible thing. See the doctor. Get the scan. Ask the questions. Start taking rest breaks (who has time for this?) and hydrate (not so easy when your throat muscles are experiencing spasticity).
Things I need to do:
Rest with intention: Schedule quiet breaks, not just flopping on the couch. Phone off, eyes closed, even if it’s just 10 minutes.
Temperature matters: I keep a fan close by. Heat makes it worse.
Bedtime boundaries: I HAVE to get stricter about bedtime; even though I want to binge British murder shows till 2 a.m., I simply can’t. A good night’s rest is imperative.
Talk to my doctor: Not Google. Not Facebook. Not an Ai medical app. Get actual help.
I’ll update you if/when the MRI happens. I’m claustrophobic and terrified of going in that damn thing. Maybe there’ll be news. Maybe it’ll be “just fatigue.” Maybe I’ll get a fancy new Latin diagnosis to add to my collection. Who knows?
In the meantime, I’m still here. Still working. Still trying. Still curious.
