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

A lot of the ones I run into it seems to be some sort of weird roleplay in their heads, but now that you mention the voices part, perhaps they think this day dreaming and pretend is literally a manifestation of another personality. It doesn't help that there is a sizeable enough population of fakers on the internet who are much older that have spread this misinformation and created entire support communities.

Also there's a lot of kids who just don't understand how normal emotions work so are easily suggested towards understanding them as being separate personalities.

Theres always been teenage social contagions but not on this level: I blame shitty 'parenting' and China in equal measure: fuck up the kids and you don't need nukes.
 
The girls introduced themselves by first name and then told me about their self diagnosed mental health issues

i wonder how many would continue to self diagnose if they were put in a locked psych ward for a few weeks.

serious mental illnesses are no joke and i'm kinda concerned that this sort of mentality fosters the conditions under which actual mental illness can develop. not that i have a clue about the mechanisms that cause mental illness, i understand that they are varied, there are many genetic and environmental factors, and they're poorly understood.
 
i wonder how many would continue to self diagnose if they were put in a locked psych ward for a few weeks.
I remember many, many years ago some tumblr did faker being made to take antipsychotics. One of her headmates killed all the others and left shortly after. It wasn't the one with the flying dog in her head (Jen?).
 
Eh they’ll grow out of it. I remember all the girlies who wanted to be different when I was in school went through a cutting phase or an eating disorder phase. Now they’re all fat “Christians” and having kids is their only personality trait. This generation isn’t too different, they just have more outlets to use it for attention seeking.


And the ones who don’t will keep posting for our amusement. Everyone wins.
 
Eh they’ll grow out of it. I remember all the girlies who wanted to be different when I was in school went through a cutting phase or an eating disorder phase. Now they’re all fat “Christians” and having kids is their only personality trait. This generation isn’t too different, they just have more outlets to use it for attention seeking.
I want to hope so, but I think this scenario is a little different. Back then it was just a casual song and dance, usually solo. Now this identity of being different is being driven by huge online communities. And these kids (mostly girls) are using them as their only close social interactions. Losing your entire "support group" can be a very scary idea for teens and young adults.
 
Back then it was just a casual song and dance, usually solo. Now this identity of being different is being driven by huge online communities. And these kids (mostly girls) are using them as their only close social interactions. Losing your entire "support group" can be a very scary idea for teens and young adults.
It's still probably better if a young girl's online friends focus on "having DID" than being FtM; it's legal to tell her "you don't have DID."
 
I want to hope so, but I think this scenario is a little different. Back then it was just a casual song and dance, usually solo. Now this identity of being different is being driven by huge online communities. And these kids (mostly girls) are using them as their only close social interactions. Losing your entire "support group" can be a very scary idea for teens and young adults.

Well the internet was a thing when I was in middle/high school but social media wasn’t as intrinsic to society as it is now. So it was going on then as well, just to a lesser extent. I think we can safely look at Tumblr as a closer representation of the long term impact online socializing and virtual validation have on young people. I think it has definitely increased the amount of people who hang onto those broken identities into young adulthood at the very least. But, I would argue that the people who keep going beyond, say, their very late teens to early 20s are actually mentally ill so they’d be wacky with or without social media. Maybe not the same kind of wacky, but wacky nonetheless.
 
It's infuriating. There's always something, and honestly I'd say a majority of these kids don't really know they're faking. Through either being easily influenced (as nearly all teens are), having some anxieties (as nearly all people do), and being badly misinformed about what a "symptom" is, and usually a combination of all of the above, kids are being led to genuinely believe they have a debilitating condition. Earlier on it was tourette's, now it's DID. DID itself is highly contested as a diagnosis, but I won't go into all that now.

Venting and some PL here but I've had to recently assist a family whose daughter was convinced she had DID because she had an inner monologue. She explained it to her parents as "voices in her head" and they were rightly concerned. Some light investigating later, no they were not "voices", she was just thinking. She saw online that the "voices" many people have while reading or thinking are a sign of DID. Kids are being taught to pathologize literally everything and it's miserable. Both the kids and their families usually have no idea it's all sociogenic and fabricated. What's worse is it's usually been so drilled into the kid that it's a real problem that they actually need counselling to essentially "deprogram" them/re-wire their thinking and coping mechanisms.
It's incredible how today absolutely everything is pathologized. The "norm" is that everyone is "abnormal", and that every abnormality is a potential disability, you're just somewhere in the scale. I know this started as an effort at - for lack of a better term, "greater human understanding/compassion" - not mocking or fear disabled people or people who are "different." I believe the internet and Dr. Google sent that concept into hyperspace, which sent both the acceptance->normalizing piece* and the list of Very Special Conditions further into the ether, and they keep feeding one another. Everyone now has or knows someone with a bona fide personality disorder, has a medicated mental health condition, or is "on the spectrum." Physical maladies/conditions are somewhat less commonly labeled/advertised, though not by much on the internet...but the culture of "fly your flag...fly all 56 of your flags loud and proud on social media where you can have your defects praised to bloat your ego so you increasingly crave that sweet attention that a regular-person life just can't compete with (that is, a real life that hasnt been designed, wheedled, or bullied into catering to your every sensitivity)" is just ridiculous at this point. And this zoomed upward just as zoomers did. Most aren't as deeply defined by/enmeshed or invested in it as the major and minor cows in these threads/terminally online are, but the baseline really has changed.

*
To the point you get Steph "Nitwit" Cianfriglia's insistent demands for de-stigmatising /glorifying paraphilias (and the people that have them) like everything else is/has been (her primary one being hybristophilia - serial killers, specifically; but also, though not really a term she uses, spectrophilia; some of her past behavior has been suggested to be somewhat pedophilic or ephebophilic as well). Steph also is very fond of listing out all of her Very Special Conditions as well as engaging in some of the most extensive self- labeling the world has every seen. I believe there is a Google doc she put together somewhere that may be the exhaustive (and constantly updated) list of how she "identifies," but she regularly includes various of them in her social media posting, some semi-medical and others merely philias and identities. Today it's "as a gnomekin..."; tomorrow it's "as an autistic a/demi-sexual transman succubus bxy-slut with exceptionally low empathy (pending formal diagnosis as NPD, haters), my fibromyalgia and facial asymmetry are my super-powers that allow me to meld more closely on the astral plane with my polycule's ghost serial-killer lovers; but here on Earth, those disabilities mean I am constantly being discriminated against, such as when our fascist anti-otherkin government demands I pay the $13 of my rent left over after their subsidy blood-debt to me and my Cherokee ancestors, and that is why you should buy this unreadable patch written in runes, lovingly hand-crafted using my own skin clippings to season the paint. Notes: 1) yes, they are unwearable because they can't be sewn on.. I know and I don't care. Support disabled artists!! 2) Since I have been asked several times, NO, tributes to Odin or sacrifices to Loki do not count as payment!!!
perhaps they think this day dreaming and pretend is literally a manifestation of another personality. It doesn't help that there is a sizeable enough population of fakers on the internet who are much older that have spread this misinformation and created entire support communities.
I think that's true. And not only that, but - specifically on DID - in some corners it's become basically a quirky tic: some talk - in seriousness - about being a "system". Even otherwise sentient-seeming people are out there chirping happily about their "system" because they can't understand that having "different sides to your personality," or " behaving in situation-appropriate ways" is not, in fact, literally manifesting wholly different people. I guess it would be okay (dumb, but okay) if they were being metaphorical...but they're not...Utterly literal, utterly stupid. It's along the same lines of saying "I'm a girl but I like baseball hats so I must actually be a boy!". Same lack of understanding of nuance, proportion, metaphor, or that labels aren't reality, but only a short-handed reference point. It's like they can't distinguish reality from language or label. And worse, then they argue (incessantly and often hysterically) that their retarded literalism is actually (literally) scientifically correct and proven.

Bit of a tangent bc not solely about munching, but I think the seeming rise in all of these phenomena is interrelated or at least the various pathologies share some overlapping sociological contributors.
 
I was recently ho-humming about how these girls are all the same and I never get to post anything exciting and different. It’s always the same zebra diagnoses, the same faux-activism posts like they’re all writing from a template. Every once in a while one pulls a funny ha-ha stunt I can laugh at but then it’s right back to POTS whining and anxiephylaxis. And then this one appeared. Jessica Riley d/b/a rollingonward, a decade long acid trip rabbithole I promptly fell down. Consider this my spooky Halloween special.

I’m going to write the first part of this one in the order in which I found material rather than a strictly chronological ‘her oldest social media is. . .’ because I feel it enhances the overall experience if you see how the material came to me. It took me a long time to decide whether this one was a very creepy munchie, a munchausen-by-proxy case, a case of FND and denial, or a genuinely disabled young woman who was sheltered to the point of not understanding the outside world, and in any case, I wanted other people to see it. So I sent her to my research buddies who agreed something was definitely fucking weird and worth looking into.
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Then I scrolled back to the beginning of her insta page and got to work. My formal intro to Jessica is in October 2018 when she’s dressed up like Snow White, wearing glasses that look like they’re sized for a child and sporting an unfortunate haircut that I’ve seen a lot of disabled kids get saddled with because it’s easier for their caretakers. You can kind of see that she’s in a high backed wheelchair with the head rest behind her. It also appears the dress has been cut in the back to fit her.
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In the second post, we have toys, hello kitty, and an IV pole with a feeding tube pump. At this point I’m thinking some kind of birth injury or congenital disease that left her with major physical and moderate intellectual disability.
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She really likes dolls, especially the American Girl collection, and has tons of them. Almost all of them are gifts or secondhand store/yard sale finds her family get for her. She plays with them, dresses them up, makes up little stories and acts them out.
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Seizures. She also really likes stuffies and has a big collection of them, all with names and characters
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“when I could draw, before the seizures took it away.” Okay, so at one point she had some artistic talent but because of seizures that’s gone out the window. I think that makes sense, yanno, epilepsy and/or the treatment thereof can fuck up fine motor skills and Jessica can’t draw anymore as a result, we’re cool.
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These people are.. odd. In addition to just the epilepsy it sounds like Jessica was sheltered as all hell. Just from little bits and bobs she’s said, they seem to live in the middle of fuck nowhere. Super Christian. Jessica was homeschooled. She has siblings that seem to be older. They don’t live in the family home and she mentions their spouses and children sometimes. It could just be a case where the other siblings lived relatively normal lives but the parents homeschooled Jessica because the local school couldn’t handle her disabilities or something.
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She makes her dad a hat on the rainbow loom and says she was capable of this because her left hand currently works. Usually it does not but when it does, she goes bananas with the hobbies and crafts. She hasn’t said what causes her hand to not work usually.
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First really good look at Jessica and at least part of her wheelchair. She reminds me a lot of the deafblind doctor but I think it’s mostly the vacant facial expression. She mentions her parents have gotten divorced and that it was very upsetting for her. She lives with her mother and only sometimes sees her father. She's also very very thin. Atrophy happens when muscles stop working so that makes sense.
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Still only posting about seizures.
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Here’s where I started thinking something wasn’t adding up. She posts these very intricate drawings she’s done on an etch-a-sketch of all platforms saying they’re old and she’s not capable of anything like this anymore. To be fair, the last one gives us a date: 2015. A lot can happen in four years. Still, that’s a whole lot of fiddly precise movement of those knobs especially since the last one was done on a miniature one.
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She can still color just fine. I know these are vastly different skills but it’s a lot of fine motor control.
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A semi-location, she tags Potomac Edison Electric in her post. They service Maryland and West Virginia.
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A birthday, January 28 although no age given.
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And here’s where shit started getting real weird. So she’s got this contracture in her left hand and that's why sometimes her hand doesn't work. Okie dokie. She also claims she has a head so small that any headband that doesn’t come in toddler sizes looks like a headscarf, and that her head is only 2” larger than her brother’s was at birth. In the hat photos, she didn’t look unusually small in comparison to her father who is presumably average sized. Very thn, yes, but my brain doesn’t go “oh she’s got some kind of proportionate dwarfism” or anything.
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Seizures, still the only diagnosis.
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She’s ethnically mostly Jewish even though she’s been raised fundie Christian. She took Hebrew as a homeschool elective because it would help with Bible study and was called a “dirty Jew” by others because of this. She didn’t find out she was ethnically Jewish until recently because her mother’s heritage was a mystery and I guess they did a home DNA test that revealed it. She claims she has a disease that is found among some Jewish communities but doesn’t name it. Brown curly hair only occurs in jews apparently.
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The dog used to alert to her seizures and fevers. We learn she also has a port.
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She sometimes needs supplemental oxygen. She’s having more seizures and is drugged to the tits. Finally some answers about what’s wrong with her: #dystonia #gastroparesis #autoimmunedisease #encephalitis #failuretothrive. Okay so FTT – she was sick and not growing right from when she was a baby but they didn’t know why. That makes sense and fits with the “she was sheltered because she was sick as hell” theory. Dystonia, don’t know why she has it but that explains the contracted arm. I guess epilepsy and the treatments for it can cause that? The other three, well, GP’s always going to give me pause but if she has a shitload of other problems then who am I to doubt that one of them caused GP? And encephalitis, maybe she had a bad infection or something and it just was shit luck or whatever. She's also implying she can't speak sometimes.
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She’s capable of smiling semi-normally sometimes.
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In the hospital and discharged with no solution. She tells us that in the past she had a gangrenous infection of her digestive system and it needed to be drained. So that’s really not great and sounds like it came very close to killing her. The glasses are kinda fucking with my head. In this photo it looks like one lens is much stronger than the other but it’s nowhere near as noticeable in other photos. I guess it's the filter effect she has going on because her cheek is also distorted but just, spoiler alert: her glasses will become a central character.
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We flip to the next post and she’s just complaining that they didn’t give her pain medication this time. She was begging the doctor to cut her open so the students in the hospital could study her. Totally normal response.
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And here she’s saying she was only 56 lbs at her last appointment and has lost weight since then, running her feeds at only 10mL an hour. 56 lbs is Lich Queen / Eugenia territory for someone who is of a vaguely normal height. It’s hard to get a good idea of height when she’s in the chair, but when pictured with other people, her size looks pretty normal relative to theirs. Again, I'd buy that she's short and atrophied but I don't know if I'm getting "toddler sized" from her photos.
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She likes reading even though her epilepsy sometimes makes her forget what she’s read. She prefers books for younger people because she relates more. Again I have to comment that relative to the size of her doll’s head her own head does not look too outside the bell curve to me.
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She is able to do an intricate marker drawing now even though she previously claimed her conditions wiped out her ability to do things like this.
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She’s so very childish and always asking how old is too old to X. She’s aware these things are for very young children and she’s considered by most of society to be too old for them. I wouldn’t say she’s insecure about it. More like she wants to make sure you know she is an adult with the presumed mental capacity of a child. And now it’s a bit creepy, right? It’s not really creepy until you know she’s self-aware.
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See in these pictures the glasses don't look particularly strong nor do we get the distortion of her right eye like we did in that one pic.
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She used to hand sew. That’s a different wheelchair in the pic, a manual, but she’s showing off old work so let’s assume it’s an old pic in an old chair.
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March 2019 we get a better rundown of her illnesses: a progressive demyelinating nerve disease (not specified which type), epilepsy, parts of her did not grow normally and she’s unusually prone to infection. She has autoimmune encephalitis (not specified if she’s talking about the Brain on Fire type or a different variety) and dystonia. She’s got no feeling from the waist down and can’t walk. She has a feeding tube because she has GP and she used to get IVIG through her port but her old doctor got in some kind of legal trouble and the new one won’t do IVIG. She can’t swallow or chew. She has a VNS for epilepsy so cool, I’ll believe she actually has that one. She’s full of cysts and has dead tissue inside her but they won’t do surgery to remove it – this is the “cut me open so they can study me” remark, I guess. She’s now under 50 lbs. She has “part of an extra chromosome” (I googled because it didn’t sound real but there are partial trisomies) and severe allergies set off by even just the smell of things. And her nerves are dying. She’s totally numb in some places and has nerve pain in others.
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She's just so incredibly strange. Sometimes she does this thing where she tries to make like she can't make eye contact and she's often trying to make it seem like she has no control of her facial muscles but man, look how tight her neck muscles are flexed in this first one.
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Other times she's smiling naturally, making eye contact, looks totally relaxed, and she doesn't have her arm contracted across her chest. But fine, it's another old pic because her hair is much shorter than it used to be. Also, if her hair is this curly, is someone straightening it for her now? Or is this some kind of chemo curl situation where it fell out and grew back in curly?
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Her parents got divorced and she has radically bad encounters with non-religious and religious people alike everywhere she goes, because apparently adults come up to SPED-looking adults in wheelchairs with harnesses to yell mean things at them about their parents’ divorces. The comments are getting increasingly weird and in one, she says her grandmother and four sisters grew up in a “chicken house” and were starved while the adults ate fine. At this point I’m considering that perhaps this is actually an ARG / horror roleplay thing and I’m just not in on it.
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She lives in Bittinger, MD down a very long dirt road in the forest. Not where I’d want to live if my kid was medically fragile with intractable epilepsy. It’s only 11 minutes to the nearest hospital from “downtown” Bittinger (inasmuch as there’s a downtown) but what if she needs an ambulance in this kind of weather? We know from Katie Stanina what happens if a prolonged seizure isn't treated.
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Her face muscles have a mind of their own and she can’t always smile. She found an old journal from 2013 when she first started losing functions. The doctors had no answers and ignored her. Sure would like to know the story there.
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She can’t hold her head up now and her hair falls out very easily, sometimes to the point of total baldness. Hairdressers said they can’t deal with her hair because it’s all frizz.
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The doctor who gave her IVIG was her neurologist and one time when she went for an appointment he was “in trouble with the law and man from the law with guns were there.” Presumably he was the one diagnosing and treating them if he was the one signing off on her IVIG and likely the one who got the VNS implanted as well. Did he just hand these things out to anyone like the neurologist equivalent of our friend in Clearwater? Every time I think I’ve landed on one side or the other I switch back. Anyway they’re looking into botox for her contracted arm.
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Well look who it is in her comments, Grandma Rose with the trach. Jessica could still be mostly telling the truth and Rose is just skinwalking. At this point, I'd guess Rose thought she'd stumbled on someone who was actually sick.
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She has enough motor control to do crafts like this. This weird guy who comments on every pic wants a video chat now but she says she uses a child’s tablet and it can’t be used for video calling. I guess that explains the potato photo quality but sometimes the photos are fine. And why a child’s tablet? Can instagram even run on a child’s tablet?
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Still looks to be of a normal size relative to other adults in her life. Her bed has the no-rolly-outy side things. She's also smiling mostly normally and it looks like her contracture hand is relaxed too.
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Someone is rude and mocks her in messages. She won’t tell people how old she is and says she normally takes days off the internet after bad seizures to get her brain “unscrambled.” #askenazijews. Funny that we just had a whole convo about how they embraced genetic testing to avoid shit like this.
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Next post, she’s had a bad seizure day and is on the internet just fine.
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Difficulty smiling several days after seizures. She uses CBD to sleep but not for seizure control.
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Everything she posts is weird. When it’s not about her health it’s about dolls or coloring books or some other extremely childish interest like showing off her Jojo Siwa hair bows.
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Doesn’t show off her writing so we can’t gauge the alleged inability to write clearly.
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After many attempts she’s found a doctor that will do botox for her fucked arm.
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Still claiming she’s under 50 lbs and that ideally she’d like to be back up into the 60s.
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No really is this like a role-playing game or a fetish thing? The Papatonton person is private but they’re on every post, spamming the same comments over and over again. Jessica’s lost more weight from constant vomiting but won’t say how low she’s down to.
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Botox is loosening up her contracture. She’s claiming the shirt is a kid’s size small.
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Her port failed and there’s liquid pooling around it. It needs to be removed. Repeats that she had a bunch of abdominal cysts and dead tissue but they won’t do surgery and says it’s because she’s now down to 46 lbs. Even just ignoring the absurdity that any adult woman is 42 lbs and not a dwarf or Lich-tier emaciated, wouldn’t a bunch of necrotic tissue just hangin’ out kill you?
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Uh so, based on the above, how old do you think she is? Fresh out of high school? Very early 20s? That was my guess, especially with being so devastated about her parents getting a divorce. She shows this Rainbow Brite toy which came out in the early 80s and says it was before her time. It belonged to her sister and she always sneaked it out of her sister's room to play with it. And like I said before, from her posts it sounds like her sisters are quite a bit older. This toy was released in 1983. That puts them at being around 40-45 right? That's quite an age gap. And now I need to know how old she is.
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I went back to look for clues and the only thing I could find was that in 2001 her parents thought she was too young for an American Girl doll and she surprised everyone by taking exceptionally good care of it. If you aren't familiar, American Girl dolls are not porcelain collector's pieces meant to look at. They're expensive at $150 a pop (I think back in 2001 they were more like $100), but they're vinyl dolls for kids to play with. Their feature used to be that they were based on different historical periods and each had whole book series aimed at young girls. They even operate a doll hospital for fixing dolls that got drawn on with marker or got chewed on by the dog or their hair cut off. Point is, how old could she have possibly been in 2001 that they didn't trust her with a doll meant for children?
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So I searched “Jessica Riley Bittinger MD” hoping to find some more info and oh boy. I found a facebook. She was born in 1990, making her 29 at this point in her instagram and eleven when they thought she was too young for the doll. So maybe she really is a tard and as a tater tot she had a history of doll abuse.
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Going through her facebook is as freaky as her instagram. As far back as 2012 (age 22) she was wearing a helmet in public. She was still thin but not quite so emaciated, not using a wheelchair, no contractures, and her face was fine.
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In 2013 she started a blog, thegirlwiththehelmet.blogspot.com. First few posts are boring. Bio states she’s been having seizures since 2007, so age 17. About when all our girls start claiming new and devastating health issues.
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A few days before her birthday she posts that she has been losing feeling in her left leg and they don’t know why. She’s tired of her epilepsy medicine but when they tried to take her off it under hospital supervision, she had constant seizures. She’ll be getting an AFO for the leg.
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She posts about it on facebook too.
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And about how she’s writing letters to prisoners in crayon. And now I’m just thinking this is a fetish. A weird, fucked up fetish she's making her parents play along with.
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She's getting an unnamed IV therapy twice a week but it's helping. Her seizures are down by half. We learn she hasn't had a seizure-free days since 2011.
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She turns 23. She’s smaller now and needs more help than she did a year ago.
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It’s so much worse if you read it with the fetish angle, oh god. She sees the Disney movie “Brave” and enjoys it but feels she shouldn’t because Merida is a bad girl who doesn’t listen to her mommy and daddy. She longs for princess movies about girls who are good and obedient.
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She claims her foot is the equivalent to a women’s size 1 which they don’t really sell, so she needs to shop in the kid’s shoe section.
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Her writing is generally very childlike and it’s way more apparent in these old posts than in the insta, to me at least. It sounds intentional, not like the way someone with a genuine disability writes or just bad inexperienced writing that has improved with time but like someone who wants to sound like they are much younger than they are. Three times a week her parents schlep her two hours to get hyperbaric chamber therapy and an unspecified IV therapy. She makes friends with the other people there but some of them stopped talking to her.
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Her foot is turning inward. She gets PT and might need a wedge for her shoe to correct for it. She meets a woman who has polio and sees so much of herself in this interaction.
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She can’t go outside unless someone takes her and keeps her from getting hurt.
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She’s worse than the last time this person saw her, implying she was much healthier at one point in the not-so-distant past.
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And here we get a date for the intricate etch-a-sketch art.
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At this point a friend of mine starts digging through her family’s socials trying to figure out what’s going on. She finds a childhood photo of Jessica with her siblings. She’s the oldest, so the Starlite toy was definitely secondhand or found in a dusty corner of a bargain shop that was offloading 10-year-old Rainbow Brite toys in the early 90s. I know it means little when they’re this young, but she’s also not disproportionately small compared to her younger siblings. if you go to the next oldest sister's socials you can find a birth date for her, December 1991 so almost exactly two years younger than Jessie.
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A later photo, she still looks fine. Gawky, but healthy.
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She also found this photo from around when she made her dad the hat and god in heaven look at her fucking legs. Okay, maybe she really does have some fucked up atrophy shit and her weight has gone down lower than I thought humanly possible.
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On the blog she’s complaining she can’t do the keto diet because she lost a pound a day when she tried it and she’s already in the “>2nd percentile for her age.” Do they have those percentile charts for adults? I only hear about them for babies and children. I mean I guess in theory they do but after a certain point height is more useful than age in determining the average weight, right? Like there’s not really a huge difference between the weights of 30 year old women and 35 year old women the way there is huge difference between a one year old and a six year old. She also calls her parents mommy and daddy when she writes about them all the time and it is very weird and I do not like it.
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Sister Katie is getting married while Jessie sits home coloring with colored pencils.
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Her wheelchair is from Ebay. She has an older one that’s very heavy but they’re buying her a “convaid type chair with self propelling wheels.” Convaid makes special needs strollers and highly supportive pediatric wheelchairs and do not have an adult line, but I guess she’s not saying it is a convaid, just similar to their products. The chair she was using at the time was too big for her, so also not something prescribed and fitted.
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She gets her chair. Again, she’s saying it’s like this Convaid pediatric chair.
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I just don’t get it. This whole weird thing with her with age. She wants friends who are much older and claims she got in a fight with a psychiatrist who told her that she needed friends her own age and a friendship with a 60 year old was “unhealthy and socially inappropriate” and called her insane and then ended the session when Jessica pushed back. The story about Cleveland is not parsing in my brain goodly, but apparently they assessed her and decided to send a counselor from Peds up instead of the adult counselor, which frustrated her because she’s an adult, just a different one.
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She tells us she’s been on some super restrictive diet for years and she feels this makes people not invite her to social events, not the fact that she’s a weird adult who acts like a child, plays with dolls, and whose only interactions with the outside world are at medical appointments. She talks about how these two college girls come down from New York to visit this clinic every other month. She’s said it’s two hours from her home in Bittinger. Best guess is it's in Pittsburgh since that's almost exactly 2 hours from Bittinger and only 3 and a half from Buffalo (3 from the southern NY border). But the fact that these girls are traveling that far just adds to my suspicion that it's some woo clinic and there's nowhere closer that will sign them up for whatever bullshit-water they're being infused with.
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Comparing seizures to purgatory.
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She has a seizure at PT and then stops going. This seizure description actually sounds like she has at least some understanding of how a seizure works. She has no memory of it, is totally unconscious, and needs to recover and sleep afterwards. But she also finds it amusing that after her seizures she wakes up in new place which sounds off to me.
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Her dad works at a paper mill and comes home smelling like turpentine but she likes it.
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Every post she makes, I’m just a little more confused and weirded out. None of the conversations she has sound remotely genuine. They sound like the kinds of things a child thinks adults say when they argue.
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Okay, since 2009 she’s been gluten-free, dairy-free, and peanut-free because of allergies. Shades of our autistic Froggy friend M.C. and her fake food allergies.
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Actually come to think of it her posts remind me a bit of Pixyteri. The thoughts aren’t quite connecting entirely and you need to read between the lines to try to tease out what she means by certain things. And even then you’re liable to go “what the fuck, Jessie?” Here's just a selection of shit.
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They’re now doing her hyperbaric chamber therapy at home. I googled and apparently this is something you really can rent for your home. Who knew?
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The story of how she almost died from going off her seizure meds in the hospital. She was on valproic acid for her seizures but her local hospital tried to switch her to keppra suddenly. Several days of seizures and rescue ativan later her family discharged her AMA and resumed the valproic acid which brought her back to baseline.
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But because she was getting nosebleeds they lowered her valproic acid dose and she’s now claiming 27 seizures in a day.
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A good look at her wheelchair, cropped to cut out some children.
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...what? I guess this is supposed to be poetry like the comment says, about getting unwanted medical advice from strangers, but the whole story of it is just bizarre.
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Another thing, I think it’s just part of her childish affectation but she refers to medical professionals as things like “the brace man” and “the eye man.” In this one she says her eye doctor says her vision should not have improved the way it did and her prescription is going down by a lot now. Mentioning she wears children’s clothing again.
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Her dad takes her in the hot tub and makes sure she doesn’t drown. If her seizures aren’t real (and I’m once again suspecting they’re not) her family still thinks they are and treat her as if they are. This is not a victimless crime.
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I’ll admit I fell in this trap reading this. She’s so weird and alien to me that I started reading everything literally right up until I read the 20 pounds of advice stapled to her chest and realized she wasn’t actually accusing someone of stapling shit to her when she was seizing.
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She was “friends” with Adalia Rose who was I think six at the time this was posted. She claims to have received letters from her. She claims everyone that talks to her and isn’t outright hostile is a “friend” though so don’t put too much thought into it.
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Like this. If this story about Mike is even remotely true, he thought he was being nice to a child and/or talking to a retard. Also she’s very very tiny and wears toddler headbands, but an adult man can goof in her helmet.
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One of her doctors was trying to give people scripts for MMJ across state lines.
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What woman in her 20s describes “tattling” on her siblings to “daddy?” Her siblings are at ages where they’re starting to get married, so they’re not like little kids running around.
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You know what it reminds me of? Like someone who is just learning a new language but doesn’t quite have an extensive handle on the grammar and vocabulary yet trying to write about their day. “We went to the fair. I pet a goat. I ate french fries. I met a girl. She liked the fair. I liked the fair. We smiled at each other.” Except we know she's American and only speaks English and this is likely all just an act.
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They’ve been adding Lamictal in the hope it helps with the seizures. They have to start low because of the valproic acid and raise the dose slowly.
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Her dad tried to hire a local doctor in Maryland to manage the care her out-of-state doctors were giving her so she could get MMJ, which her out-of-state doctors are willing but unable to prescribe. He’s shot down, unsurprisingly.
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Mommy and daddy tell her “no more lamictal!!!” She stops taking it.
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She wrote and illustrated a book about herself.
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This Elizabeth woman in the comments is the mother/primary caretaker of a young adult woman with severe disabilities. Seizures, needs a wheelchair with the harness, can’t talk, can’t walk, tracheotomy, significant risk of dying in her sleep on any given night. From what I can tell in a brief browse, she was diagnosed as a very young baby with infantile spasms of unknown origin, her mother has ruled out a ton of possible conditions but still doesn’t have an exact name for the disease her daughter very obviously has. I say this because Elizabeth has been blogging about her life and her daughter’s care -which includes a helmet and IVIG - since at least 2009 and in their earliest interactions on Jessica’s blog she talks about how she reads Elizabeth’s blog religiously. I think she was using it as inspiration. The other thing that struck me is Elizabeth was an English/French major with a firm grasp on poetry and literature and she writes like one, if that makes sense. Lots of metaphor, poetic turns of phrase, quoting the classics and whipping out the grad school big-money words no normal human ever uses like ‘palimpsest.’ Jessica wants people to think she has a child’s grasp on language yet her favorite blog is one written in gradschoolese.
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I also say this because Jessica has sent Elizabeth and her daughter drawings and letters she wrote (in crayon of course!) and by all appearances, Elizabeth doesn’t have an inkling that she’s playing into what increasingly seems like a healthy adult woman’s roleplay fantasy, cribbed in part from her own very ill daughter’s life.
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Lol is this just a way to get a do-over on her childhood? She dresses up for Halloween for the first time ever after a lifetime of being told it was the devil’s holiday, because mommy and daddy said it was okay now that she’s dying. She decides to be a pretty princess.
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Here’s a christmas picture of her younger sister, also to make a possible point. So her youngest sister, sometimes her dad refers to her as “Kelsey aka Charlie” on facebook but since Kelsey is a totally normal feminine-presenting woman, we thought Charlie was just a childhood nickname. But there’s a post in August about how Kelsey has cut off all her hair despite her mother’s protests. This photo is from December so there was ample time for this cut to grow out but it hasn’t. I think her sister’s requisite fuck-you-mom-and-dad was a gender people phase she has since grown out of.
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The blog post these came from was boring but here we also find another perfectly normal childhood photo. This is the sister that got married, the one who has a two year age difference between them. I'm not saying Jessie isn't small. She's just so obsessed with you thinking she's pocket sized that it's fun to discuss how big she actually is. Speaking of. . .
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MEANWHILE! I had just started digging through her accounts and was leaning towards “she’s got something wrong but is also just really fuckin weird” when my research friend found a picture of some ugly-ass shoes. They’re called Bobbi-Toads and the feature of them is that they have “toenails” embossed on the toe box that you can paint to look like a pedicure.
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Sound like children’s shoes? That’s because they are. She claims she wears a women’s size 1, which doesn’t really exist, so she shops for the equivalent size in the children’s department.
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If you go over to the Bobbi-toads website and try to buy yourself a pair you will see that these green fellas go up to big kid size 6 which is an adult women's 8. Mystery solved. Her feet are a normal size and she's buying kids shoes that happen to come in women's sizes.
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Except she also has a pink velcro pair. The velcro versions only go up to a little kid 1 which would be an adult women's size 3. Okay, so we have a woman who is, at the very least, fucking tiny. Maybe she’s not lying. Maybe something has gone incredibly wrong in this woman’s development and she really is a tiny little dwarf of a thing with a serious genetic condition and I am an asshole.
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They even featured her on their social media in them.
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This mystery brought the archiving to a standstill until we found they actually do make all their shoes available in adult sizes. You just have to contact them directly if the ones you want aren't available. If you scroll back up to the green shoes you can see that she's saying she did have to contact them to get two different-sized shoes because of her AFO. We are back to "relatively normal sized adult, but very very skinny". This side quest took us an hour to complete.
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Back to the blog. She sees a new doctor and is possibly getting referred to Johns Hopkins for her leg.
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She’s up to dozens of seizures a day again
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Sometimes she's taken to the hospital by ambulance and is discharged home before she even full regains awareness.
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In late January 2014 she tells us this tale of how she was having so many severe seizures the local hospital tried to transfer her to a larger hospital but she left AMA instead because now that Hopkins has been mentioned, that was all they wanted. Instead they booked a hotel room near Hopkins with an explicit plan to wait for her to have a seizure and then call the ambu so they’d take her there. She starts shaking in the hotel and they call the ambulance as planned but whoopsie poopsie! They took her to the University of Maryland because it’s also right there in downtown Baltimore, two miles from Hopkins. She has an “event” and is admitted for EEG, but the “event” is not a seizure. She has 100 more of these “events” while under obvs, one every four minutes. This plot totally and officially backfires when U Maryland says her seizures are psychogenic and orders her family to stop feeding her benzos like they’re candy all the time. This is not the first time she’s been told they’re psychogenic but she says this can’t be because she’s had “weird test results” and other things she wants to keep private. Back home she’s shaky and feels terrible. Welcome to withdrawal, enjoy your stay.
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So there we go. The seizures aren’t epilepsy, they're psychogenic. She starts posting about withdrawal and how she has the shakes. Yeah benzos don’t fuck around, kid. Although I have a strong feeling she either is somatizing because they didn’t believe her and/or cribbed this from Elizabeth whose daughter had to be temporarily taken off of the benzo Orfi which she had been on for many years for her real disease. If she’s really getting the shakes from WDs already then uh, that’s not a great sign and she’s lucky she didn’t have a real seizure for once.
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On Facebook she says the medication change actually helped and her leg is less numb and painful.
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She is MAD that you think she’s doing this on purpose. Well, I don't think FND is fake or something they're consciously controlling it and if anyone posted here has it, I'd guess it was Jessie.
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God, she looks so normal and age-appropriate in this photo. Again, hard to judge based on the positioning but she doesn't look remarkably smaller than her healthy sister, stature-wise.
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But then over on facebook we're still going full retard.
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Sounds like her “part of an extra chromosome” she was talking about on Instagram is actually just a gene mutation of uncertain significance and doctors already told her they don’t know if it’s doing anything. And that's if she's not entirely making it up.
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And the dystonia claim. She has been on valproic acid and having tongue spasms which caused her to stop eating. Mommy starts looking into side effects of this medication and stumbles on dystonia, then brings her to the doctor. The doctor gives her L-dopa and I guess flexeril and the tongue spasms stop and her leg isn’t as bad the next day. She also reports less seizure activity in the days that follow, from over 100 at Hopkins to 30 when she was home down to 4. She’s trying to be seen by the NIH now that Hopkins was a bust. And she wonders what the psychologist would say now that this medication has worked. Well, I'd guess he'd explain to you what the placebo effect is and how it influences FND but what do I know?
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She starts eating again because the l-dopa fixed her tongue spasms.
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She gets really invested in the Justina Pelletier case. Justina was a teenage girl who was admitted to Boston Children’s from the ER for stomach pain, having been recently diagnosed Mitochondrial Disorder by another Boston-area hospital. Staff at Children’s suspected she more likely had FND but her parents couldn’t accept the diagnosis and instead shopped her around to doctors all over the country seeking different diagnoses. They offered psychological care in the hospital which made the family chimp out and try to take her out AMA, The hospital got Massachusetts child services involved and a judge ordered her to remain in hospital and away from her parents who were not to have any knowledge of her medical treatments. Since the family lived in Connecticut they involved that state’s CPS department who agreed with Massachusetts that it was munchausen-by-proxy and she should remain separated from her parents. Under supervision at Children’s she was weaned off several of her treatments and improving, including resuming normal bowel function after her parents insisted she was fully enema-dependent, but because the parents proved they had changed their circumstances, their custody was restored and she was released. They promptly shopped her around to other doctors until they found one that would perform surgery to have her healthy, working colon removed. A docuseries aired about a year ago and from the chatter I heard (I never saw it) it was clearly aimed at making the parents look good but instead made them look like attention-seeking narcs who burned the kid out by pushing her to high achievements in school and multiple sports then refused to accept the FND diagnosis they got. One of the things I heard repeated a lot was that Justina acted much younger than her calendar age to the point of appearing mentally stunted or learning disabled, and that there’s a scene where she rides a horse that gives away that she has way more muscle control than they claim she does. That part I saw a clip of and she not only balances fine in the saddle but posts and even mounts the horse without issue all while claiming she can’t walk and is a fulltime wheelchair user. Regardless, Jessica sees a lot of herself in Justina’s story. The flags are so red sometimes.
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She has to get an electromyography done to see why her legs won’t work.
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She goes for her EMG and with her gait is mistaken for a cerebral palsy patient. Instead of the EMG, they do another EEG, I guess because they want to know if she can be taken off the valproic acid instead of adding treatment for dystonia.
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Someone who was helping me with this pointed out that unlike a lot of our girls, she seems to really not enjoy the appointments and hospitalizations. Her parents seem to be the ones captaining that particular cruise ship. I don't necessarily think they're MbP so much as I think Jessie really does have FND and the family can't accept a psychiatric diagnosis for what appears to be purely physiological issues. Possibly a side with jessie sucking it up and going along with what her parents want if it means her childhood continues indefinitely
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Here we get a photo of our heroine standing up next to normal-sized adults. Well, not really standing up. She's posing to make herself look smaller, bend knees and hips, rounded shoulders, hunched over, the same tricks the troons pull. It's kind of funny that after scouring all the social media accounts for her whole family, this was the only photo we found of her standing next to other people. From this, given that these men (a band call The Blind Owl) are all average height and there's objects we can assume the height of like the table, we guessed Jessie is right around the 5'0" zone. Short, but not the midget she wants you to think she is.
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She’s been drawing a ton of flowers with colored pencils. They’re pretty intricate with a lot of fiddly detail.
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The brace man tells her “no more cane!” She now has to use a walker or else they’ll make her use a KAFO.
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For the first time in three years she hasn’t had a seizure today.
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Were you feeling shades of eating disorder from her obsession with being tiny and shopping in the kids section? You win the kewpie doll! At her “fattest” (her word) she had to wear a size 0 from the adult section and that was “curvy” for her height. She hated it! Don’t worry, she lost weight and is back to the kids’ section so Daddy can carry her everywhere like the little tiny helpless baby she is. I don’t doubt she’s the runt of the litter. I just wonder if she’s been starving herself for so long she actually stunted her growth.
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The L-dopa is working, but not really. Doctors aren’t really sure why her leg isn’t getting better. Johns Hopkins refers her out to a Parkinsons and dystonia clinic to get to the bottom of it. Her non-epileptic seizure clusters might actually be dystonia episodes.
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She sees the dystonia clinic. They agree she has it but don’t know why. They’re switching her add-on medication (the muscle relaxer I guess) to try to fix it. She might need genetic testing to see what’s going on.
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She goes for a followup and he wants to do genetic testing to see if she has one of the two common genetic dystonia conditions, and if she does she might need brain surgery. Her L-dopa is stopped and she’s on another unnamed drug. The doctor says her seizures aren’t seizures or dystonia but he doesn’t know what they are. She insists they’re not on purpose. Also UMaryland called her out for having an ED and also put in her chart that she binds her chest. In another post she complained that a cross necklace she was wearing was lost when they cut clothes off of her at the hospital, so I’m gonna guess when they went to cut her shirt they found she had some kind of ace bandage/binding situation under it and correctly guessed it was to make herself look smaller and more child-like. The doctor tells her to eat but she DOES! No one believes her when she says she eats all this food and just can’t gain weight!
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They're replacing her AFO with a KAFO. She never mentions this again.
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She names the medication she was on, Artane (trihexyphenidyl), an antispasomodic used for dystonia. It made her hallucinate so bad she didn’t recognize her parents. The doctor apparently didn’t believe her because he wanted to keep her on the medication but she went off it anyway. She says she now can’t walk at all and she has difficulty chewing without the medication but at least she recognizes her family again. She’s still doing these very intricate drawings of flowers and frog art for Bobbitoads.
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She gets a shoutout in some religious mag. It’s just a “pray for this very sick girl” with no new info for us.
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She claims her knee is infected, but not injured. She claims she has to crawl to get around.
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And still obsessed with these “medical kidnapping” cases that she sees so much of herself in. This was 7 kids of a prepper homeschool family in Arkansas who were being fed “Miracle Mineral Supplement” by their parents. It’s an industrial bleaching agent retards think can cure everything when really it just strips your intestinal lining and makes you shit it out. Said retards believe these shreds are "rope worms" that caused the autism or whatever is ailing their kids.
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She shows video of her “seizures” to the neurologist who says akshully they’re simple partial complex seizures. So what she’s talking about is complex seizures, which are either simple, complex or simple progressing to complex. Simple is sometimes referred to as “aura seizures” and often progresses to complex partial seizures. They only impair one part of the brain (the temporal lobe) and people having them may remain conscious and perform bizarre actions on autopilot which led to another nickname, “impaired awareness seizures.” (This is all from google, I don’t actually know much about epilepsy.) In any case the Neurologist refers her to Hopkins – the pediatrics department! - and tells her she’s too complex and special for him. She had written a note of things she couldn’t discuss out loud that were upsetting her about her body and signed it “Please help me” and the tech read it and said “okay” which filled her with hope. The dystonia specialist also called back and said the tests they ran were negative. He says no to botox for her left hand because shes “too bent up already.” This is the first time she really mentions that contracture in her left hand and she’s still been doing these flower drawings up until now. She won’t be seeing that doctor anymore and will try again with someone else. Turns out he was telling them her symptoms couldn’t possibly be what she was describing, he didn’t believe the hallucination story, and she thinks he is a giant poopyhead!!!!
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She sees a new neurologist in February. This one refills her benzo scripts and is glad she’ll be seeing the movement disorder clinic at Hopkins. Later mommy says that Hopkins called back and are refusing the referral. They referred her back to the giant POOPYHEAD. Instead Mommy found yet another a new neurologist in Morgantown, MD who might be willing to do botox. So generously, she has FND and isn’t actually doing this on purpose but between her and her parents she won’t get treated for the real problem. Less generously, she knows what she’s doing and that if she keeps it up she gets to be a little itty bitty girl forever. Given how much she acts like a child, that’s where my lil compass needle is currently pointing.
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In this post about fracking she makes it clear why someone who has uncontrollable seizures and a movement disorder should not be living where she lives: it’s snowy and mountainous and because their “driveway” is a long dirt road, the parents used to have to cross-country ski pulling the kids a sled to get to the road when it was snowy. Now they have a tractor with a snowblower. Remember that she claims she needs a helmet and wheelchair with a chest harness for her safety because of the severity of her illness.
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In case you were wondering who she’s really been skinwalking, because of course there had to be someone: it’s a little girl named Amy whose mother’s posts she often shared. Amy was extremely sick her entire life with some kind of degenerative disease that caused epilepsy and other issues. She had the wheelchair with the harness, the helmet, a feeding tube, she fell when she tried to walk and acted much younger than her age and started having serious dystonia issues in 2012-13. As the years went by she developed ataxia, her speech declined, she lost the ability to chew and swallow, and she developed worsening cognitive impairments and dementia. There was tons of proof that Amy was sick: EEGs that picked up multiple kinds of seizures, MRIs that showed brain atrophy, but like Elizabeth’s daughter, no one could ever firmly diagnose her. She was tentatively diagnosed with half a dozen things including Lennox-Gastaut Syndrome, Batten Disease, progressive myoclonic epilepsy, and mitochondrial disease, most of which were subsequently ruled out. Amy died in 2018 at age 17 and her parents allowed Beth Israel Deaconess Medical School at Harvard University to do an autopsy and research on her remains. Postmortem, she was finally diagnosed with autosomal dominant Spinocerebellar Ataxia type 2 likely caused by a previously undiscovered gene mutation. Jessica developed a friendship with Amy's mother in the last years of Amy's life such that the mother was sending Jessie presents, including, apparently, one of amy's favorite dolls after she died.
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Isn't this a ride? Hold on to your hats because it gets weirder.
(edits were just grammar/clarity shit, sorry I write these things at like 5 am when I can't sleep)
 
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She wants friends who are much older and claims she got in a fight with a psychiatrist who told her that she needed friends her own age and a friendship with a 60 year old was “unhealthy and socially inappropriate” and called her insane and then ended the session when Jessica pushed back.
How many of these girls fight with psychiatrists? lol.
She has an “event” and is admitted for EEG, but the “event” is not a seizure. She has 100 more of these “events” while under obvs, one every four minutes. This plot totally and officially backfires when U Maryland says her seizures are psychogenic and orders her family to stop feeding her benzos like they’re candy all the time. This is not the first time she’s been told they’re psychogenic but she says this can’t be because she’s had “weird test results” and other things she wants to keep private
Benzo pass: REVOKED!
She gets really invested in the Justina Pelletier case. Justina was a teenage girl who was admitted to Boston Children’s from the ER for stomach pain, having been recently diagnosed Mitochondrial Disorder by another Boston-area hospital. Staff at Children’s suspected she more likely had FND but her parents couldn’t accept the diagnosis and instead shopped her around to doctors all over the country seeking different diagnoses. They offered psychological care in the hospital which made the family chimp out and try to take her out AMA, The hospital got Massachusetts child services involved and a judge ordered her to remain in hospital and away from her parents who were not to have any knowledge of her medical treatments. Since the family lived in Connecticut they involved that state’s CPS department who agreed with Massachusetts that it was munchausen-by-proxy and she should remain separated from her parents. Under supervision at Children’s she was weaned off several of her treatments and improving, including resuming normal bowel function after her parents insisted she was fully enema-dependent, but because the parents proved they had changed their circumstances, their custody was restored and she was released. They promptly shopped her around to other doctors until they found one that would perform surgery to have her healthy, working colon removed. A docuseries aired about a year ago and from the chatter I heard (I never saw it) it was clearly aimed at making the parents look good but instead made them look like attention-seeking narcs who burned the kid out by pushing her to high achievements in school and multiple sports then refused to accept the FND diagnosis they got. One of the things I heard repeated a lot was that Justina acted much younger than her calendar age to the point of appearing mentally stunted or learning disabled, and that there’s a scene where she rides a horse that gives away that she has way more muscle control than they claim she does. That part I saw a clip of and she not only balances fine in the saddle but posts and even mounts the horse without issue all while claiming she can’t walk and is a fulltime wheelchair user. Regardless, Jessica sees a lot of herself in Justina’s story. The flags are so red sometimes.
I remember that case, I didn't read into it so I thought it was a kid with mito being misunderstood. Sad her colon was removed for no reason. :(
I don't necessarily think they're MbP so much as I think Jessie really does have FND and the family can't accept a psychiatric diagnosis for what appears to be purely physiological issues. Possibly a side with jessie sucking it up and going along with what her parents want if it means her childhood continues indefinitely
What a weird dynamic.
Also UMaryland called her out for having an ED and also put in her chart that she binds her chest. In another post she complained that a cross necklace she was wearing was lost when they cut clothes off of her at the hospital, so I’m gonna guess when they went to cut her shirt they found she had some kind of ace bandage/binding situation under it and correctly guessed it was to make herself look smaller and more child-like.
Haha, I wonder if she learned that trick from her ex-gender special sister. UMaryland sounds extremely based, constantly calling out her shit.
In case you were wondering who she’s really been skinwalking, because of course there had to be someone: it’s a little girl named Amy whose mother’s posts she often shared. Amy was extremely sick her entire life with some kind of degenerative disease that caused epilepsy and other issues. She had the wheelchair with the harness, the helmet, a feeding tube, she fell when she tried to walk and acted much younger than her age and started having serious dystonia issues in 2012-13. As the years went by she developed ataxia, her speech declined, she lost the ability to chew and swallow, and she developed worsening cognitive impairments and dementia. There was tons of proof that Amy was sick: EEGs that picked up multiple kinds of seizures, MRIs that showed brain atrophy, but like Elizabeth’s daughter, no one could ever firmly diagnose her. She was tentatively diagnosed with half a dozen things including Lennox-Gastaut Syndrome, Batten Disease, progressive myoclonic epilepsy, and mitochondrial disease, most of which were subsequently ruled out. Amy died in 2018 at age 17 and her parents allowed Beth Israel Deaconess Medical School at Harvard University to do an autopsy and research on her remains. Postmortem, she was finally diagnosed with autosomal dominant Spinocerebellar Ataxia type 2 likely caused by a previously undiscovered gene mutation. Jessica developed a friendship with Amy's mother in the last years of Amy's life such that the mother was sending Jessie presents, including, apparently, one of amy's favorite dolls after she died.
I'm happy they at least found an answer but how vile to take advantage of a grieving mum for your own LARP.
 
I am only part way though The latest epic from @Kate Farms Shill and one thing stood out to me:
Why do her stuffed toys need to be repaired so often? I have an unusual number of the for a person of my age; none of them have required repair except t secure some worn or loose stitching, Any one got any idea wht this happens to her stuff repeatedly?

Edit to fix typos. Ambien. Not even once. Also, finally finished reading KFS magnificent post. I'm speechless, but still want to know about the stuffed toys.
 

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I really, really don't like the daddy stuff. Also, I feel like a broken record, but I will point out yet again that here we have here a chick with an eating disorder.

She's got a very affected writing style. You can almost imagine what kinds of books she reads: old-fashioned doctor and nurse romances (Sue Barton, Cherry Ames type stuff*), super-Christian moralizing novels for young adults, classics like The Secret Garden (fun with wheelchairs and chronic illnesses!), that kind of thing. She sometimes writes like an adult author who is trying (and failing) to write from the POV of a child-- very artificial, very affected, and without any of the spontaneity and accidental humor actual children have. The classic novel and Christian young adult writing influences come out when she tries for sounding like an old soul trapped in a child's body (she's teensy teensy tiny, you know): totally simple, totally innocent, yet capable of great revelations.

She's not as dumb as she wants you to think she is, because so many of her blog posts are following the same formula of opening with everyday experience --> middle is experience interpreted through eyes of child --> concludes with a briefly-stated Moral of the Story. I'm beating the word "affected" to death, but she incorporates stylistic things like refusing to use contractions, apparently believing that this makes her sound very young and quaint. In a related pet peeve, she also uses a lot of old-fashioned expressions that make me think she's hitting the 1950s teen dreck hard. She also loves passive voice, as is appropriate for a delicate young Victorian waif with daddy issues.

This blog is a goldmine, and I love it. I just know it's going to get much worse-- I feel it in my waters, as Jessica might say-- and I'm here for it.

* footnote: young adult fiction written for girls used to be really bleak. It was dreadful romance stuff with a lot of plotlines about dedicated nurses who ended up marrying doctors. When I read this thread, I can't help but think most of the thread subjects would eat that stuff up. Someone could probably hit the jackpot by republishing that stuff.
 
what? I guess this is supposed to be poetry like the comment says, about getting unwanted medical advice from strangers, but the whole story of it is just bizarre.
This is probably unrelated, but her wording reminds me of an old radio program. It's called The Nightmare, and there's a part where the narrator describes a man beating his chest in...
The narrator was having a seizure. It's based on his real experiences with them, too.
There's even a part where his style of speech shifts to be more childlike.

I am only part way though The latest epic from @Kate Farms Shill and one thing stood out to me:
Why do her stuffed toys need to be reapired so often. I have an unusual number of the for a person of my age; none of them have required repair except t secure some worn or loose stitching, Any one got any udea wht this happens to her stuff repeatedly?
That's...a good point. I also have a number of plush pals, and even the one I sleep with at night doesn't get damaged often.

Maybe they're getting mangled under her chair? :(
 
Another one has gone to the big ICU in the sky: Kim Stewart aka Queasy.with.a.smile
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No idea about this one, I recognize the name from being discussed on IFGW back in the day but I never followed her and know nothing about her. Account is private.

Edit: funeral has been announced. Some people on here have access to her private account and said she had a recent surgery but not specified what.
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