Community Munchausen's by Internet (Malingerers, Munchies, Spoonies, etc) - Feigning Illnesses for Attention

Can you post a link or reminder of the username for those of us with shoddy memories?

@huge boobs thanks for more Tiffany detritus. Lentils, jerky, artichokes, fruit juice - none of this is recommended for gastroparesis! Why isn’t she just on a proper low-residue diet? Ah yes, because she’s making it all up and has no health professional helping her manage. If she needed all that crap on her wishlist it would be made available to her. I too am looking forward to this next arc.

@GhoulTori you do see plenty of OTTs claiming “undiagnosed autoimmune” and they are all hoping it is MS - I bet they couldn’t name two other autoimmune diseases. The relapse-remitting makes it easy for them to only have it on days they have adult responsibilities. It’s easy to test for but doctors won’t do a spinal tap without a good reason so they can claim they have been gaslighted and the meanie doctor won’t send them for diagnosis. HOW DARE YOU REQUIRE A DIAGNOSIS SELF DIAGNOSIS IS TOTALLY VALID OMG YOU ABLEIST SCUM!
We have patients report they have been diagnosed with MS but in reality an MRI showed brain lesions.
Which could be cause by: alcoholism, chronic cocaine, meth, or high dose adderall use, long term anorexia. Just all kinds of fun stuff besides MS but we have a growing number of young woman that really want that MS diagnosis.
I blame Selma Blair.
 
We have patients report they have been diagnosed with MS but in reality an MRI showed brain lesions.
Which could be cause by: alcoholism, chronic cocaine, meth, or high dose adderall use, long term anorexia.
Found out recently White Matter Hyperintensities are seen with chronic migraine as well. Seems like more and more conditions are getting added to the list of "reasons you shouldn't automatically assume it's MS."
 
I couldnt find anything about this bint elsewhere, but the absolute audacity of this bitch
Screenshot_20250730_233232_Chrome.webp

News article archive
 
Last edited:
Found out recently White Matter Hyperintensities are seen with chronic migraine as well. Seems like more and more conditions are getting added to the list of "reasons you shouldn't automatically assume it's MS."
You get them from other autoimmune diseases as well. They are a great example of a finding that in the right context can be serious but a lot of the time is treated as incidental.

Here’s another article from The Sun on the person above - Kae Burnell Chambers: Lies Exposed

She did an MA of Fine Art at Lincoln University where she researched Cospainting as treatment for mental health and fibromyalgia Research profile
 
One who isn’t worth a full timeline but made me laugh when I stumbled upon her: Cara (@cara_bowman12 on Instagram)

Claims Crohn’s, gastroparesis, and pots. Bio makes it look like she is a real influencer with an agency despite not cracking 75k views on any of her reels. All of her hospital content is her grinning at the camera with one hand under her chin like she thinks she’s cute and clever, but her complexion, thick long hair, and energy (plus obsession with looking cute for the ‘gram, which she makes a point to show in her videos) make it clear that she is not even remotely sick. Never gets much engagement (less than 10 comments per video), but the video that I stumbled upon (come to the ER with me) has comments disabled, which is telling given the rest of her engagement. She’s obviously healthy in the whole video and thrilled to be in the ER, constantly adjusting her outfit to look cute and then posing for her Instagram, and filming people who didn’t consent to be filmed (at least she kind of blurs them out?). Also talks about wanting a lot of foods that aren’t good for digestive issues (I only included the mac and cheese example, but there are others).

Given the angles of some shots, I’m guessing she’s an ED girlie who refuses to admit she has a problem, and purging/laxatives ate her go-to., though she occasionally tries to starve herself Easier to pass off as a health problem (Chron’s) and can claim gp to cover the attempts at starving herself.
 

Attachments

  • ScreenRecording_07-31-2025 19-22-52_1.mov
    109.5 MB
  • IMG_5037.webp
    IMG_5037.webp
    255.5 KB · Views: 138
One who isn’t worth a full timeline but made me laugh when I stumbled upon her: Cara (@cara_bowman12 on Instagram)

Claims Crohn’s, gastroparesis, and pots. Bio makes it look like she is a real influencer with an agency despite not cracking 75k views on any of her reels. All of her hospital content is her grinning at the camera with one hand under her chin like she thinks she’s cute and clever, but her complexion, thick long hair, and energy (plus obsession with looking cute for the ‘gram, which she makes a point to show in her videos) make it clear that she is not even remotely sick. Never gets much engagement (less than 10 comments per video), but the video that I stumbled upon (come to the ER with me) has comments disabled, which is telling given the rest of her engagement. She’s obviously healthy in the whole video and thrilled to be in the ER, constantly adjusting her outfit to look cute and then posing for her Instagram, and filming people who didn’t consent to be filmed (at least she kind of blurs them out?). Also talks about wanting a lot of foods that aren’t good for digestive issues (I only included the mac and cheese example, but there are others).

Given the angles of some shots, I’m guessing she’s an ED girlie who refuses to admit she has a problem, and purging/laxatives ate her go-to., though she occasionally tries to starve herself Easier to pass off as a health problem (Chron’s) and can claim gp to cover the attempts at starving herself.
Love it!

Maybe it’s just me, but the Venn Diagram of “felt cute might delete later” and “health emergency requiring an ER visit” should have zero overlap. As soon as it does, the munch is pretty much a given.
 
Claims Crohn’s, gastroparesis, and pots.
I'm sure this has been asked here before: but does any medically inclined Kiwis know if POTS a real disease, or one of those fake conditions like Mast Cell Activation Syndrome (?) I feel like every munchie on TikTok claims to have a POTS diagnosis (well, amongst their smorgasbord of diagnosis').
 
I'm sure this has been asked here before: but does any medically inclined Kiwis know if POTS a real disease, or one of those fake conditions like Mast Cell Activation Syndrome (?) I feel like every munchie on TikTok claims to have a POTS diagnosis (well, amongst their smorgasbord of diagnosis').
Tachycardia from standing up is a real thing. Having it happen markedly and often enough to be a problem or nuisance for someone can also be a real thing. Sometimes caused by medications or other disorders, often caused by deconditioning after prolonged bedrest (say if someone had been immobile due to a serious injury for a while). Also definitely accurate that it would be worsened by dehydration or electrolyte depletion.

As far as being a whole separate disease that is an untreatable lifelong disability- far more questionable.

It's an almost "variation of normal" phenomenon among teen and young adult females who fit a certain know it when you see it profile. Has been recognized for decades under various names. For a while they believed it was a "lite" version of mitral valve prolapse, but that was debunked. Might have hormonal aspects, might be some emotional biofeedback loops going on. It's a volatile life stage in multiple respects. It always used to be understood most young ladies would simply grow out of it.
 
There is genetic/inherited familial dysautonomia but that’s more heavy on the actually possibly dying than the I get a head rush and everything goes black that the social media girlies have.

I believe that some people developed inappropriate sinus tachycardia either after Covid or the Covid vaccination too but if treated it only lasts maybe 6 months. It’s under the dysautonomia umbrella too. A lot of those cases were seen in long COVID clinics or by private cardiologists.

And then there’s dysautonomia symptoms that can be caused by medication side effects. SSRIs can cause heat intolerance, some anxiety meds can cause blood pressure drops, etc. Or straight up anxiety attacks in general can last hours in people who haven’t worked on CBT skills - body can do funky things in attempt to compensate for fast breathing or heart rate etc.

Dehydration will almost always cause faster heart rate and possibly lower blood pressure. The social media dysautonomia girlies consume extreme amounts of sodium to create slightly elevated blood volume and I definitely believe the crash causes rebound effects. That’s why they feel terrible in the morning because they haven’t had anything to drink all night, then get up too quick to go to the bathroom.
 
POTS is real. The version you see on tiktok is insulting and dumb, and unfortunately the watering down of it to "my heart rate goes up when I stand up" means that a majority of people claiming it are fat, unfit, dehydrated, and/or anemic. Then they sit their fat, unfit asses in wheelchairs, it gets worse via deconditioning and they mooch off my tax money.

I knew a teenage student with POTS about ten years ago. It came on with puberty. It took months for doctors to figure out what was going on. She'd be out cold on the floor about once a week, and was a matter of propping her legs up and waiting for her to come around. She only got diagnosed after she broke her skull on the floor fainting. I wonder where she is now.

There was another, slightly older, student who used to throw herself on the floor and try to imitate her, except people find it incredibly difficult to fake a faint, and even more difficult to do so in front of paramedics. Which was incredibly funny and I'd give my lunch money to see that play out over again.

I also think a lot of "POTS" now is a kind of Shit Life Syndrome. If you're depressed and lie in bed or sit down all day, you decondition. You don't eat, you don't drink, you feel somatic pain from being depressed, you stand up, you feel even more garbage. Supported exercise and antidepressants would do wonders for a lot of the boilerplate POTS/EDS/GP chronic influencers. But you can't grift or get to play the sick role if you actually try to get better.
 
Supported exercise and antidepressants would do wonders for a lot of the boilerplate POTS/EDS/GP chronic influencers. But you can't grift or get to play the sick role if you actually try to get better.
This is a problem with "support groups", even for those with real illnesses. The dynamics of those places end up with a really perverse incentive to never recover.

Let's say it's a Facebook group for sufferers of African Bum Disease (the most dreaded illness amongst British 8-year-olds in the 1980s, largely spread by being "it"). African Bum Disease is incurable, but you can learn to live with it by making lifestyle changes and the right mental conditioning. So you have people who are stuck at home with horribly diseased bums, but they get to meet other sufferers (and the odd grifter pretending to have it) in this group and find a sense of community, people just like them. For many, these are their only friends, or at least they are the only friends who truly understand them and their lives.

So if you learn to cope with African Bum Disease, you no longer need the group. So you leave and lose all your friends. So it's better to stay in the group. It gets worse, though. There will be a large cohort of people who do recover, and leave the group. Those who can cope, and could advise others on how to cope, are no longer there. The people who are left, then, are those who are struggling. And the grifters who want to look as sick as possible. All these people give each other terrible advice that keeps them sick, and keeps them in the group. The very dynamic of the group is to skim off the people who could help others the most, and to concentrate and refine sickness and hopelessness.

The people who stay in the group the longest, and are the most prominent posters, are the ones who become admins or at least become leaders on a social level. And, given that staying in the group rewards failure to recover, these people are the biggest headcases who can't cope with their disease at all - and now they're the ones setting the rules. They have a HUGE incentive to not only play up how difficult it is to recover, but to actively prevent others from recovering. So when someone says that African Bum Disease can be mitigated by diet, exercise and a healthy mental attitude, those people are banned for "downplaying the seriousness of the illness". No, you see, African Bum Disease means that you can't work and need a power chair and a feeding tube and a GoFundMe.

That's before the munchies and grifters infiltrate the group. Their African Bum Disease is WORSE than yours - maybe like me they have 3 buttcheeks, that's 50% more bum to have disease in and frankly it's a miracle they're still alive. Those stupid doctors say they're faking and their third buttcheek is just their coccyx, so they have to see Dr. Feelgoodovic in Belgrade who will totally give you Ketamine for your African Bum Disease and if you don't get it you DIE! So now even the people who really do have African Bum Disease are competing with munchies and grifters to be the sickest and the most deserving of powerchairs and primo Serbian Ketamine. Of course, the munchies and grifters will want to become admins because they can abuse their powers for attention and self-promotion, so soon enough people pretending to be lunatics are running the asylum. Any good advice or questioning as to why they need speedballs to get up in the morning results in a ban. Nobody gets better.

This is why I think anyone with a chronic illness should steer away from "support groups" if they're not led and run by medical professionals. It's not just a case of some groups being bad, it's the case that these groups will inevitably become bad because of the dynamics within them.
 
Love it!

Maybe it’s just me, but the Venn Diagram of “felt cute might delete later” and “health emergency requiring an ER visit” should have zero overlap. As soon as it does, the munch is pretty much a given.
Hospital photo shoot posted on social media is an unmistakable clinical sign of MBI. If there are multiple such posts in their history, it's a 100% likelihood of either MBI or cluster B personality disorder (usually both, let's be real)
 
Found this article about her: Flowly Cara Bowman

Ah, and of course, she has a Daily Fail featurette: CLICK BAIT HEADLINE HERE

She’s insufferable. Who the hell walks into ED like she’s going on a photo shoot? Another one who got a bit sick with Chrohns as a teenager and now uses it to make up for her total lack of personality. Should introduce her to Ashley Carnduff.

Of course, she is fueled by GOD 🤮 “She believes she is being used by God to help others”.

Love this from her: “'Most days, I find myself bedridden and unable to partake in simple day-to-day tasks due to the lack of energy due to constant severe pain and the inability to eat a lot.” Yeah, really looks like it in your Tik Tok, love. Try harder at being a try hard.

She really really really wants you to know her tummy pain is super cereals guys oMG: “She wishes for people to comprehend the debilitating nature of these conditions, emphasizing that they are far from mere stomachaches.

'I knew absolutely nothing about vascular compressions when I first got sick. Now that I am more experienced, I wish more people knew and understood how debilitating these conditions are,' Cara said.

'They aren't just tummy aches that'll go away. There is very little research on them, so many go months, if not years, without a diagnosis.”

Cry me a fucking river.
 
I also think a lot of "POTS" now is a kind of Shit Life Syndrome. If you're depressed and lie in bed or sit down all day, you decondition. You don't eat, you don't drink, you feel somatic pain from being depressed, you stand up, you feel even more garbage. Supported exercise and antidepressants would do wonders for a lot of the boilerplate POTS/EDS/GP chronic influencers.
Without powerlevelling too hard, over the last year or so I have taken tips from posts like this, and can confirm that even just a bit more exercise and attention to nutrition noticeably improved several aspects of my life that had been blah.
 
I’m back with another dumpster fire from Reddit—not even sure where to begin with this one: https://www.reddit.com/r/dustythunder/s/EU8u19tbvG

The power leveling in the comments, the pearl clutching, and the blatant denial of how medical conditions work/the role of advocates? And the Lyme mention? Get me some popcorn, stat.
https://archive.ph/6OtQW

TL;DR: OP has a friend who's munched her way into a two month hospital stay and is trying to get OP and her mom to "advocate for her" because her mom is a narcissist. OP is skeptical of friend after witnessing a few pseudoseizures. Comments are from redditors.

My favorite comment
> People don’t end up in situations like this just for funsies. Something is deeply wrong, whether physically, mentally, emotionally, or neurologically, but no matter what it is, it is not your place to judge. Shame on you for masquerading as her friend. She deserves better people in her life.

I feel like this is a lot of what's wrong with society today - we're not allowed to judge or shame anyone, but it turns out that shame is what keeps people from doing shit like this.
 
The wording on the Dutch wheelchair stuff really reminded me of how that one woman who wanted to be an amputee with hooks for hands would write in her blog.
I’m super late here but you’re the one referring to FUCKING CAROLE WITH DORRANCE NO 5 STAINLESS STEEL HOOKS from 1996! Carole was later revealed to be a strongly haired old man troon who wheeled himself in his unecessary wheelchair around the Walmart pantys n socks department trying to get women to help him hook up his bra because he has DORRANCE NO 5 STAINLESS STEEL HOOKS for hands. God I miss alt.tasteless and how soft and naive I was back then.
 
Back