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

Just saw an incredibly dumb take from a munchie changing their tube dressing saying that because they're on creamy, delicious Kate Farms™️ they can still be kosher, but that it's unfair that there are no kosher TPN formulations for the extra special girls. I feel like if your god has made you that fucked up that you actually need TPN he's not going to care that milk and meat touched or whatever.
 
Just saw an incredibly dumb take from a munchie changing their tube dressing saying that because they're on creamy, delicious Kate Farms™️ they can still be kosher, but that it's unfair that there are no kosher TPN formulations for the extra special girls. I feel like if your god has made you that fucked up that you actually need TPN he's not going to care that milk and meat touched or whatever.

Would assume it's more of a mitzvah to assure your health then worry about mixing meat and milk.
 
Just saw an incredibly dumb take from a munchie changing their tube dressing saying that because they're on creamy, delicious Kate Farms™️ they can still be kosher, but that it's unfair that there are no kosher TPN formulations for the extra special girls. I feel like if your god has made you that fucked up that you actually need TPN he's not going to care that milk and meat touched or whatever.
...which is why they need to have their PICC replaced with a dual-lumen, one milk and one meat.

But seriously, these days the lipids are soybean oil, right? Mixed or not, TPN seems like it'd be pareve, but I'm neither Jewish nor a pharmacist. To my understanding, the barrier to making it kosher would just be for them to have one of those certifying rabbis suit up and visit the facility to stamp it as OK.

Anecdotally, observant Jews are just fine with everything up to and including prophylactic heparin; it's the weird storefront schism Protestants whose church has only been around for five years and they're the first person to need some pig juice so there isn't an official position on it yet, and their pastor can't answer texts until he gets his break at the car stereo store.
 
any illness-related social group will inevitably be dominated by munchies

A pre-eternal-September oldfag in other part of the internet taught me this. Any sort of "self help" or "issue-centered" community is going to end up this way for a simple reason.... the successful people don't tend to stick around. The most active members are going to be the people doing the most and having the least result. The successful people get what they need from the community and leave with little impact- they may even just have been invisible lurkers. In general.

... that was from a while back and saved in drafts but I still think it's worth posting.



I'm sure if someone really needs TPN it's fine that it isn't kosher/parvere/etc al.
But what about all the women ITT on TPN and also drinking Starbucks frappes?

I feel like pretending to be sick to get out of the religious requirements is not the same, and that is what many of the more straightfoward malinger-type munchies are doing.

...Though I know it gets complicated with the ones that start actually falling ill due to whatever they're doing with their lives. Guess only God can judge us.
 
but don't think there are genetic illnesses passed down only through the maternal line.
You can have illnesses passed on BY the mother in three ways:
1. The gene is contained in the mtdna (the mitochondria has I think 13 genes.) most ‘mitochondrial diseases’ are actually coded for by nuclear genes but if it’s a gene in the mitochondria it’s only passed from mother to offspring, both male and female. (There has been one case at least of male mitochondria being passed down.) stuff like MILS and NARD
2. Dominant x linked - actually this one can be from males or females but if the mother is affected male or female children will be and of the father is affe ted only girls will be.
3. Imprinting disorders where the dodgy imprinting is from the mother.
I can’t offhand think of a genetic disease passed on solely by AND solely TO females. If anyone knows one, do say
 
You can have illnesses passed on BY the mother in three ways:
1. The gene is contained in the mtdna (the mitochondria has I think 13 genes.) most ‘mitochondrial diseases’ are actually coded for by nuclear genes but if it’s a gene in the mitochondria it’s only passed from mother to offspring, both male and female. (There has been one case at least of male mitochondria being passed down.) stuff like MILS and NARD
2. Dominant x linked - actually this one can be from males or females but if the mother is affected male or female children will be and of the father is affe ted only girls will be.
3. Imprinting disorders where the dodgy imprinting is from the mother.
I can’t offhand think of a genetic disease passed on solely by AND solely TO females. If anyone knows one, do say
Wouldn't something like PCOS count? I know they're still investigating any genetic links.
 
You can have illnesses passed on BY the mother in three ways:
1. The gene is contained in the mtdna (the mitochondria has I think 13 genes.) most ‘mitochondrial diseases’ are actually coded for by nuclear genes but if it’s a gene in the mitochondria it’s only passed from mother to offspring, both male and female. (There has been one case at least of male mitochondria being passed down.) stuff like MILS and NARD
2. Dominant x linked - actually this one can be from males or females but if the mother is affected male or female children will be and of the father is affe ted only girls will be.
3. Imprinting disorders where the dodgy imprinting is from the mother.
I can’t offhand think of a genetic disease passed on solely by AND solely TO females. If anyone knows one, do say
The only thing I could think of that kinda fits requires a lot of bad luck and good luck. An x linked dominant gene with partial penetrance. Like brac1/2 abnormalities. In a hypothetical situation where the faulty x chromosome is passed on from the mother each generation and the males are lucky and the females are unlucky it would appear like only females get it. Males can get breast cancer and the penetrance of brac1/2 hereditary breast cancer is high but not 100% so it would be unlucky but possible. It still wouldn't be a female only maternal hereditary disorder but it would at least appear that way

There are a handful of diseases that only woman get like pcos, ovarian cancer, etc but if they are x linked you can also get it from your dads x chromosome. There are also some where although men lack the equipment to get the disease the genetic abnormality still effects them but just in a different way
 
Next part of Jessica soon, but first. Dani Marina was recently discharged from Penn without her central line or TPN and has been tantruming all over the place. She got herself admitted to a hospital again and was filming nurses and generally being a pest, when she suddenly DFEd. Normally this would be nothing, Dani deletes her accounts all the time. But it's the reason she quit that's amusing. Someone found her fake boyfriend's real wedding registry from May of this year:
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Which some idiot on a sock promptly sent to Dani. If this was you, consider drowning yourself in the nearest available body of water.
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Proof that's the right guy: here's the only photo she ever shared of them together from like 2014.
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And here's some pics from 2015 from facebook. She used to tag him all the time but I have no proof of that handy.
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And here's Cynthia Liptak.
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Formerly Cynthia Cicmansky. Old facebook details and yearbook pic match.
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LMAO DANI YOU INCORRIGIBLE RETARD.
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Dani will always be my least favorite munchy. I don't know if it's the disturbing fake unintelligible baby voice or her gross greasy unkept appearance (and home), but something about her seriously icks me out.
For me the ickiness comes from her seemingly complete lack of understanding the asthetics of social media and her having never figured out a filter or angle or to clean one corner of her gross space to film in. Clearly she developed that peculiar personality disordered love of being in-patient.
 
Next part of Jessica soon, but first. Dani Marina was recently discharged from Penn without her central line or TPN and has been tantruming all over the place. She got herself admitted to a hospital again and was filming nurses and generally being a pest, when she suddenly DFEd. Normally this would be nothing, Dani deletes her accounts all the time. But it's the reason she quit that's amusing. Someone found her fake boyfriend's real wedding registry from May of this year:
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Which some idiot on a sock promptly sent to Dani. If this was you, consider drowning yourself in the nearest available body of water.
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Proof that's the right guy: here's the only photo she ever shared of them together from like 2014.
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And here's some pics from 2015 from facebook. She used to tag him all the time but I have no proof of that handy.
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And here's Cynthia Liptak.
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Formerly Cynthia Cicmansky. Old facebook details and yearbook pic match.
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LMAO DANI YOU INCORRIGIBLE RETARD.
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Just gotta state the obvious; pathetic.
 
So, for reasons unbeknownst to me, this appeared on my FB feed: https://petition.parliament.uk/peti...PfVWCNta6lh4JY43jNHRUMrShs7nYaXmzSjqReJQyTbUQ

Some of the comments reek of munch:
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Some of the profiles reeked equally of munch, but unfortunately didn't have very much, no hospital photos etc, looked for them on instagram to no avail and no details of instagram accounts on their fb pages.

FII accusation:
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Text reads: "
False fii ( fabricated induced illness) accusations is something that is too easily thrown at parents of SEN children and children with certain medical issues. This is recognised in new ( basw) social worker guidance , for instance, where it is highlighted that families affected by me cfs, ehlers danlos, autism, pans pandas etc ( our family is impacted by several of these conditions) are being particularly targeted due to masking of symptoms at school and the array of symptoms involved, as well as due to the lack of wide spread knowledge of these conditions and how they present.
My friend has shared this with me; her family have been catastophically impacted by this. My family were also targeted with insinuations of fii at a time when we were desperately in need of help; my mum and I had to counteract every false insinuation and fund for a private immunologist ( two private drs had diagnosed and treated my son due to there being no local specialists)to attend an appointment to counteract this. The fear and added pressure on our whole family due to this, over 6 months, at a time when two family members were desperately ill and where arbitrary, unachievable expectations in terms of school attendence and threats of being taken to court were thrown at us, was unbearable. Each member of my little family has trauma brought on by this. Children are being incorrectly taken from their families due to uninformed ( no knowledge of medical and Neurological conditions) hunches. I have signed this petition. Families are scared to reach out for help with this threat hanging over them"

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Also on second look, her full name is Rebecca Farr-Barron, she has a twitter that may be a source of munchies: https://twitter.com/FarrBarron

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Text reads: "#LongCovidAwarenessDay. We’ve been asked to post something in black & white we miss… this video is from my 1st festival out of Lockdown July 2021, I was so excited for things to be opening up again, to start being able to see friends & family again, to explore London again, to DANCE, go to galleries, start Art courses again, to plan holidays, but I, like many others, have ultimately stayed in our own Lockdown as a result of #LongCovid.
I think it’s important to raise awareness of Autonomic Nervous System Dysfunction (or #Dysautonomia) and #POTS (Postural Orthostatic Tachycardia Syndrome) today. A lot of us have Orthostatic Intolerance (i.e we struggle being upright) as a result of Covid – essentially all those automatic functions that happen when you stand up to make your body adjust to the gravity change (i.e. circulation, blood pressure & heart rate etc) aren’t working – the blood literally drops & pools in our legs so we have less blood in the core of our bodies, so our hearts have to work much harder to pump the little blood that’s there around – hence we have very elevated heart rates on standing & very high amounts of adrenaline in our systems. My heart rate jumps to 130/140 just getting out of bed in the morning & can jump to 170 just standing too. I also have wildly fluctuating blood pressure on standing & it drops so low the longer I’m upright, that I’ll faint. I was advised it’s too dangerous for me to walk. That’s my goal, to get walking again.
Aside from all this some of the other debilitating symptoms a lot of us face are: constant dizziness, sensation of being on a swaying ship, vertigo, balance problems, severe chest pains, sensory overload & vision problems, severe insomnia (linked to the raised adrenaline), anxiety (adrenaline argh), migraines, numbness, alongside the more known symptoms of fatigue, brain fog & cognition problems & breathlessness. Dealing with one of these would be tough enough, but experiencing them all at the same time plus the fluctuating & unpredictable nature of them – it’s a very un-fun rollercoaster ride we’re on.
Lots of love & hope to anyone else suffering with #LongCovid & let’s hope more support is coming."

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I debated not including their names to avoid potential DFE in case anyone better at research than I wanted to dig in. If this was a mistake please let me know. I have SS without names and if I'm past the edit time I'll ask a mod if they can anonymise.

Sorry that I don't have any great hospital pics or such to share for these, they barely constitute Munchausens by Internet, but I couldn't resist posting after seeing some combo platters in the wild.

Edit: formatting cos i is retard.
 

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Petitioning the UK government for preferential treatment in a public healthcare system is so retarded. They only care about keeping the majority of people healthy for the least amount of money.

It always annoys me when people like that get told it's somatic, induced, fnd, etc and respond with something along the lines of "educate yourself" or "drs aren't up to date with current research". Yeah there are people that get misdiagnosed and yeah there are some doctors who graduated med school decades ago and don't keep up to date but these people are just upset they didn't get their desired diagnosis. A normal person when diagnosed with with somatic or fnd will either learn to cope or try to get treatment for that. If they comply with treatment and don't get better then the doctor is more likely to reevaluate. If you just cry about the diagnosis, don't accept it, and don't comply with treatment then you won't progress. These people seem to forget that a lot of medicine is about starting with the most likely, attempting to treat it, then moving down the list. If you aren't even attempting treatment then you won't progress. People forget that a lot of things are reached by excluding other things. A good example is dermatology. GPs usually suck at derm unless they have an interest in it. So if you have a non specific rash and they aren't sure what it is they start by excluding fungal. Then if antifungal cream didn't work they move to steroids. You don't want to be the guy that gave a steroid to someone with a fungal infection and made it worse. GP will usually only refer to a dermatologist if they've exhausted the tools in their tool box.



They also forget that countries with a public health care system tend to have systems set up to prioritize population health rather than individual health. The entire system is set up to take the most cost effective way to keep the majority of the population healthy. A lot of the time treatment is cheaper than tests by orders of magnitude. So when the ministry of health has strict criteria for ordering tests and tries to limit unnecessary testing it leads to a health system where doctors are indirectly incentivized to just treat the most likely diagnosis then if that doesn't work either order a scan/test or just try the treatment for the next likely diagnosis. They'll only really deviate from the working down the list approach if there is something potentially life threatening near the top of the list of likely culprits, in which case they'll order a test to rule it out. In a public healthcare system, a referral for a specialist or scan can be denied if the gp hasnt tried everything in their scope first. To keep wait lists short, quite often the referral gets denied with instructions like "try (x treatment) for 3 months then try again if no improvement". A chronic incurable but not immediately life threatening disease isn't a priority to a public healthcare system. Youll have to play the game to meet criteria for referrals. If you got health insurance at least a year before you starting munching then you could go private and then whatever ails you becomes a priority. Bitching to the government won't suddenly make it a priority. The government and health ministry only care about getting the most bang for buck.



If they were smart they'd just play the game. Accept the diagnosis, at least appear to comply with treatment, wait a while, then go back. Eventually they'll move down the list and get the diagnosis they want.
 
Now that the site's stable on clearnet again: part 3 of Jessica Riley d/b/a rollingonward. In part 2, Jessica found a new neurologist who finally ran the tests she needed to diagnose what turned out to be a rare progressive nerve disease. She had a port placed for IVIG treatments, a VNS placed for her seizures, and a feeding tube because the nerve disease caused dysphagia. She was finally properly fitted for a wheelchair and got botox to help her contractures. And then we met her doctor, who has been tried and convicted for prescription fraud and sued for falsely diagnosing people with said rare progressive nerve disease for profit. He’s been stripped of his medical licenses and spends his days filing batshit pro se lolsuits. Since he’s been out of the picture, Jessie’s back to trying to find a good doctor who believes her and that means looking the sickest she’s ever looked.

Sorry this took so long. Didn't mean to leave everyone hanging, just had bad internet for a week.

On June 16, 2019 she posts this picture saying her hair just plumb fell out. She woke up on Father’s day with hair all over her pillow and none on her head. She claims copper builds up in her blood stream which limits what supplements she can take but she can’t remember what this is called. A quick google says it’s called hypercupremia and it’s usually caused by a genetic condition called Wilson’s disease. If she had it, she’d need chelation therapy to keep her copper levels down or else her liver would be totally fucked and she’d turn yellow. She never mentions this again.
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Because she was getting IVIG so often for so long she claims to have gotten blood donations from over 200k people. Both of these pictures are from June 19 and she's lost most of what remains of her hair between them.
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Over on facebook she says her hair fell out in days instead of months this time. So those wigs and hats she was wearing on facebook were apparently covering up "mysterious" gradual hair loss that is not gradual this time.
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she blames it on the radiation from X-rays and other imaging. She tells people she had a piece of her port removed from her heart and right “hipatic” artery. Your hepatic artery is in your liver. Did a piece of it migrate through her heart and end up there? Is that why her liver hurt? But your liver doesn’t have pain receptors. Why was no one concerned with the fact that she had chunks of port catheter cruising around in her blood vessels for weeks? I'd say it was just a lie but she showed the broken-off piece in a specimen jar. I’m so confused.
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On the 21st she has a bandana to cover her head. Whoops, guess someone told her if her hair fell out from medication and radiation she wouldn’t have eyebrows either so now those are gone.
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Rose is sending her presents.
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She gets crocheted disney princess wigs because it's not like they make age appropriate head coverings for small-framed adult women or anything.
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I think you were a bored munchie sitting home with nothing to do and not getting enough attention so you pulled it all out so the general public would assume cancer. Just a hunch. Factitious trichotillomania, what will these girls think of next?
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She claims her vision is so bad she can’t see her own face in the mirror without her glasses. I don’t know. Sometimes her script looks kinda strong, other times not so much. A lot of it is just the angle of her face. When she’s got the fake neck contracture shit it looks like the script is very weak but head-on it looks stronger which totally tracks. There’s also just a weird story she told forever ago, about how she went to the eye doctor and found out one of her eyes had radically improved and the eye doctor thought that her old script must have been a mistake on his part because there was no explanation for how her vision could improve like that. Everything about this is weird.
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She’s balder than bald now and wearing headbands with big flowers on them like an actual baby.
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Her grandma buys her a bald american girl doll to match her totally unintentional hair loss. This family is so strange. I get why they make bald dolls for little girls who are undergoing chemo or who have alopecia or whatever to make them feel better because look, dolly doesn't have hair either! But she's an adult. If your hair all fell out one day would you want people buying you shit to commemorate it?
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She and Rose talk about how great dying young is gonna be. Munchausen by internet has an uncomfortable venn diagram overlap with doomsday suicide cults.
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She gets new glasses. My first thought was “wow those are small looking frames.” Yep, because they’re Paw Patrol glasses made for little girls. 1) they make normal glasses for little girls that are just scaled down versions of adult glasses and don’t have cartoons on the ear band and 2) the optician can resize adult frames to some degree and often will do so free of charge.
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Notice me, Jojo Siwa! Reminder that this chick is now 29.
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She'll be resuming botox for her crippled arm after a long time without. Again I want you to notice the positions of her pointer finger and thumb.
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She also wears Build-a-Bear glasses to show off how teeny tiny of a baby she is. I mean, they’re made to fit stuffed bears with large, wide heads and they don't fit on her face at all but do you i guess. Very exciting that you can get doll accessories to stick to your face.
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Talking about her many life threatening allergies which include someone eating peanuts in the vicinity, secondhand smoke, surgical drapes, and most feeding tube formulas. Her mask saves her.
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At the end of July she has an appointment with a new doctor. They discuss her hair loss and her insurance issues and about getting her into a palliative care clinic for rare and incurable disease. Her hair loss is now because she doesn't get enough calories and is malnourished. She repeats that she weighs only 46.2 lbs. She also says she has grand mal seizures every week requiring emergency meds but "normally the state only gives you four a year." Lol did you get cut off from your benzos again? She's not afraid to die!
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I do wonder how she's managed to keep her eyelashes beautifully intact through all this.
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Her broken port is finally removed on August 1. I wonder if all her contractures and shit disappear when she’s under anesthesia or has she spent so much of her life bent in one position that she’s not faking anymore.
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She smells of rotten meat but it’s healing. I think part of the reason she likes the potato camera, other than the “I am an innocent baby and can only use a children’s tablet” factor, is it acts as the ultimate filter to hide signs that she’s not actually a small child.
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She starts leaning into Messianic Judaism and repeats that she found out she was Jewish after doctors started asking if she could be. Now it’s “well over a decade ago” that this questioning started even though she only mentioned it recently for the first time. Also repeats that she was called a dirty Jew for learning hebrew which just sounds like she's looking for oppression points.
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Back to complaining about constant seizures. Her head looks distinctly shaven rather than pulled sometimes.
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Not too sick to play with dolls. Seizures slowed her down though.
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In August 2019, she announces that her feeding tube pump has been taken away due to her inability to keep down any formula and her ineligibility for other surgeries because of her very special anatomy none of the doctors understand. I suspect what happened is she’s still dealing with fallout from losing her father’s insurance coverage. It’s hard to tell if she even still has a tube since she never shows it off and the only proof we had that she even got one was the pump.
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Seizures are increasing again. There is no next step for her.
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She has anaphylaxis at a party because of the smell of peanuts. She’s too small for grown up masks and needs a toddler-sized one from China. She claims her head circumference is only 19 inches.
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So with an actual numerical value to look into, I asked Dr. Google. There I learned that akshully there’s not that big of a difference in head size between a kid and an adult. It’s surprisingly hard to get info about this but I found an achondroplasia website where they said that by the time a healthy person is 3 they’ve reached 90% of their adult head size (in achondroplasia they hit their full adult head size by that age, neato). A few other websites suggested 21" is the average for women. I'm honestly kind of surprised by how little your head size changes.
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Either way, Vog believes her when she says their mask was bad and broken and sends her new ones.
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Her fake stroke face makes me laugh a lot. Yes, I can also do this to my face with very little effort, and as people pointed out you can see her straining the muscle on the side of her mouth to keep it taut Caption also funny. Stop complaining that you can’t eat gluten, celiacs! I’ve had an eating disorder my whole life!
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A crazy man got loose in the hospital last time she was there and punched someone else hard enough to spray blood all over the walls. This was god watching over his favorite little baby girlchild. No concern for the person who got his blood sprayed across the hospital.
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She’s blocking all you silly gooses who say mean words. Oh no the jig is up fellas. Pack it in.
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This girl was just born too late. A few centuries ago she could have been a fasting-for-jesus anorexia miribilis case and people would have lined up to have her pray for them.
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Her brother is married now, but still all she does is sit in mommy’s house coloring in her coloring books and playing with her dollies. She also uses it as another chance to brag that she fits in child sizes.
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Be thankful you get to go out because she’s been sitting around the house refusing to go anywhere for years. It’s quarter to covid but she doesn’t know that yet.
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As soon as her hair starts growing back in it mysteriously falls out again. Eyelashes still fine. What a mystery.
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A christmas miracle. She can draw again.
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She shows off her oxygen to let us know she might have congestive heart failure. She never mentions this again, nor do we ever see her oxygen cannula attached to anything. I tried to see what her dad posted but it was just a prayer request.
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She's back to drawing and writing neatly.
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She gets a Valentine’s card from a boy! A boy with Downs Syndrome who she’s been sending cards to. Nope, not gonna think too hard about the implications there.
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She was always taught divorce meant your life was over but now that she sees her mother actually happy she's reconsidering.
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She can start a very important medication for her seizures again. Benzos are back on the menu!
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She wins dolls in an art contest meant for children thanks to her tard LARP.
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Once again, claiming she needs kid shoes. Once again, we find these came in adult sizes as well.
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FTR someone who is much better at judging things like this estimated her shoe size was about a women’s 7 when we were on the original Shoe Quest. I am bad at gauging things like height and weight from photos so I leave this here, make of it what you will.
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She’s trying to get diagnosed with polio now. Still saying there was no response on the EMGs she had on her legs that we now know were done by a complete fraud.
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Before I found the fraud, though, I was trying to find out whether FND patients actually don’t have a response to EMG. I couldn’t find that information at least in part because I couldn't understand what i was reading, but I did find this helpful chart of the most common functional focal dystonias: unilateral downward lip-pulling (the stroke face thing she does), plantarflexion of the ankles (her turned-in ankle), and contraction of the hand that spares the pinching grasp, which we can see in how her index finger and thumb are mysteriously spared in hers.
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Here we get a good look at the hair regrowth. It’s patchy, but my assumption is still that she’s pulling it and it’s finally long enough in some places for her to get at it for another round. Her life is such a loop of sitting on her mommy’s couch playing with dolls that covid does not affect her in any way. She already never left the house or saw anyone outside her family and a few doctors so social distancing is her status quo.
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Oh jesus. Pixielocks used to do this years ago. I guess liquids are fine with her GP after all. And her dysphagia so bad she can only swallow a quarter of a teaspoon of honey consistency. Wouldn’t liquid be worse? Like they sell thickeners at any drug store specifically for people with dysphagia.
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This is like the fifth time she’s specifically made comments about how people get offended when she doesn’t know what something tastes like. How often do people ask this? She supposedly doesn’t eat, doesn’t leave the house (so it’s not like people are asking her how a restaurant is after she said she went there) and she never posts abut food other than mentioning what she doesn’t eat because of her deadly allergies – gluten, dairy, and peanuts, +/- eggs which she often forgets.
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Besides, in other posts she insists that as a child she was told she was never allowed to refuse food because it was impolite and as a result had to eat things that I legitimately do not believe anyone ever fed her including two raw eggs on wonder bread. This goes back to what I was thinking about her being like tism-tier picky eater as a child and being made to eat things she didn’t tolerate. No I don’t really think she was fed raw eggs on bread, but how far of a leap is it from “raw” to “sunny side up with whites that haven’t fully set” or "scrambled but not cooked through"?
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She orders a wig and lets us know it’s a #childrenswig #juniors
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HOW DARE U??? Apparently other people have been questioning her claims
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Someone else died.
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She’s doing those diamond painting things, which again is a lot of fine motor control and more specifically, the ability to see tiny objects and manipulate them properly into equally small places on a canvas using a tiny number to see where each goes. She’s talking about color blindness because some of the colors look the same to her.
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Uh, I guess one of the sisters is going through a suicide phase.
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We hear her voice. Again, it’s just giving me Gypsy Rose vibes. Might as well be singing "Angels Among Us".
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Shitting on the magic jesus will heal me and buy me a mansion people.
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Vaguepost prayer request. Some things are worse than her parents getting divorced. You don't say.
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She got covid. Thankful she has oxygen but the photo she doesn’t even have a cannula in. I don’t really think she’s got home oxygen, just cannulae. Maybe her quack prescribed that too and she just has a stock of cannulae left over, maybe she took some home from her ICU stays or orders them on amazon or something, but we never see her oxygen tanks or a concentrator in her room or anything. It’s just the cannula on her face. She also doesn't chimp about the oxygen shortages that happened at the peak of the pandemic.
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I know the divorce thing is another part of her child-like affectations or an extension of her very fundie upbringing where divorce was the worst thing ever, but man it does get to be weird. It’s been two years and she still brings it up constantly.
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Insurance fucking with her tube. She only gets a change every other month even though she has a history of needing them monthly if not more because she's special, so she (read: Mommy) has to pay out of pocket when she breaks them. She can't get her botox, no one is checking her VNS, yet mysteriously she's survived. A neurologist tells her not to come into the office because she'll die based on her own description of her health. She'll be using oxygen more after a different appointment.
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In September 2020 she’s finally able to get her botox again and it works.
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Epipens, seizures, and pain.
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Seizures make her stutter.
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Seizures make her voice go away.
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Aww man don’t ruin one of my favorite songs you goblin.
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We're all terminal! Some of us are just running towards it at a sprint for internet attention.
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She can’t use candles safely so don’t worry, this clearly fake candle is fake. She is of “Jewish and Catholic descent” now. Lol @ acting like catholic is an ethnicity. I understand why Jews are largely considered an ethnicity - insular communities with genetic fuckery to prove it and inherited religion - but the most catholic countries on earth are like, Italy, Poland, Haiti, and the Philippines.
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Posting only for another mention that she’s so teeny tiny people can carry her everywhere like a baby. I have spoken to a lot of wheelchair users through this hobby and not a one would be comfortable being carried unless it was an absolute emergency like “the building is on fire, every accessible exit is blocked, and you will die if you don’t let me carry you out of here.”
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Claiming she wears the shoes her sister did at age 5. Lamenting that everyone else has a life while she sits at home playing Jesus's favorite cripple.
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Suggesting she once had a collaboration with Bobbi-Toads to make a pair of shoes called Rileeze and Jojo herself owned a pair. I can't find any proof these shoes ever existed.
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Claiming her hair fell out again and is now growing back in red.
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She makes this Jewish christmas ornament for her very Christian mommy. The text is her mom's maiden name, Durst, in Hebrew. Mommy must be so happy that after raising her daughter ultra-Christian she's now insisting they're Jewish.
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The holidays are hard but she's a fighter.
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Daddy takes her out for an adventure in her new stroller she got for christmas. I promised you we'd come back to the stroller.
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It's a Kool-Stride Special Needs Jogging Stroller with a maximum capacity of 150 lbs. It's meant to fill the gap between children's strollers and adulthood for people with special needs.
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Here are some other pictures of adult-sized humans riding in one.
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She puts a temp tattoo on her head saying everywhere else is way too skinny to fit it. She even bedazzles it.
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Another perfectly normal baby pic.
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She is now 31.
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I swear this girl makes up fights that never happened for attention
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She’s feeling pressure to pretend everything’s okay when it’s really not.
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Ooh more backstory. Because she was so tiny and not growing as a kid they took her to different doctors. It sounds like some doctors correctly said she wasn’t getting enough nutrition to grow and others chalked it up to endocrine issues. Her family was offered growth hormone treatment but declined. She later learned all her food issues were from severe allergies. I don’t know, fellas. I’m still getting the vibe that she was just an ultra-picky eater who was forced to eat things she didn’t like and developed a whole eating disorder because of it.
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Anaphylaxis, epi pens, oxygen. Still hasn’t proven the latter is connected to anything.
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Oh come on, even if her head is really that small I’m sure they make a variety of wigs for children and they’re not all blonde Alice bobs with bangs.
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But it makes one of her followers send her a new, brown wig to wear instead. She has this whole community of weird 45-year-old doll ladies hanging around and they all send her stuff all the time. Doll stuff, coloring books, hats, whatever she mentions “needing” or wanting a doll lady soon provides.
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She got rubella from the MMR vaccine as a kid and her doctors don’t think she should get covid vaxed as an adult.
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Her father takes clear pics of her instead of her Barbie tablet from 2003 or whatever the fuck she uses. We can see she has nice thick hair regrowth in her eyebrow and her eyelashes still look fine. She's also claiming this shirt is an adult size small but on her it's a dress.
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Another seizure, this time she says that she doesn’t stay off the internet after them anymore because they're so frequent she’d never be able to connect.
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Daddy takes her to the playground. Yeah I totally believe someone who needs a full support wheelchair with a chest harness, has many contractures, and is always a breath away from a seizure can sit independently on a swing set.
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She can apparently still do art just fine because she wins a contest for this bluegrass fest.
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Her older dog is sick. The younger one needs to be supervised when he’s around Jessica because shes a tiny small and fragile baby.
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She totally didn’t mean to take this photo where she’s making direct eye contact with the camera despite turning her head to the side. She was just reading on her tablet and accidentally hit the camera button. Honest! One of her relatives is on a vent from covid, but this post is all about how Jessie has terrible lungs and needs oxygen because she desaturates down to the 50s. Lmao no the fuck you don’t. In 2009 a blood oxygen saturation of 54% was recorded by a team of researchers who climbed Everest without supplemental oxygen. It was newsworthy at the time as before then, values that low were unheard of outside of cardiac arrest. One of the wild parts about Covid that made it such a mystery at first was that people were getting down to these ridic low incompatible with life levels of oxygen sats without showing the typical signs of respiratory distress. It was called "happy hypoxia" because they should have been comatose or at the least in extreme respiratory distress but instead they'd be chatting with hospital staff and fucking around on their phones.
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Anyway. Her aunt is doing better.
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She gets a reborn doll and specifies it’s not too heavy for her to move. Once again, she gets a present sent to her by some Jesus-loving weirdo adult who spends her days caring for fake babies.
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Here she says she was born somewhat prematurely and had a “selkie coat.” I’m guessing she means lanugo, which is the downy hair commonly seen in premature babies. I hope the rest of the story about her dad stealing it and rubbing it on his hands is some folkloric reference I'm blissfully unaware of.
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Leaning harder into her jew larp with Hebrew practice. Nice neat lettering for someone just learning the language.
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She’s been doing a lot of book review type content now. The first one is an American Girl book meant for like 9 year olds and it’s about a kid with HIV. Second one she says the real Patch Adams himself gifted her (??) and the last one is about a woman with cerebral palsy who uses an assistive device to communicate and of course she relates to all three.
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She still mostly reads books meant for very young children.
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She's all about the stroller now because apparently a full support wheelchair fitted for her just wasn’t giving off enough tater vibes for her. But also her glasses. Ohhh her glasses. I refuse to believe anyone prescribed these for her. Of course, you can get secondhand glasses fairly easily at thrift store or whatever.
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But I’m actually guessing she ordered them from something like Zenni where they let you manually put in values for your script and don’t require verification from a doctor. Zenni operates pretty much entirely on the honor system. You can scan in your prescription, but I made this one by scrolling through the available values and clicking where ever I felt like, no proof needed.
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It will tell you if you select too small or too large of a pupillary distance value which is cool, because I didn't feel like looking up my own script to see what a normal value was there and the warnings were helpful in determining one. Both of my first choices, it told me that was absurd so I settled for 60. It had no complaints at 60 and prompted me to continue.
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And there we go. Without seeing an eye doctor I can order a pair of super strong spex that are orders of magnitude stronger than my actual prescription with values that possibly make no sense. I guess they do this because normal people want to see and are at a low risk of lying to get super strong glasses that will fuck their vision.
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These are such a huge change from her last pair.
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She mentions in that post that she had an article come out. I actually found it right around when I found her facebook and it’s a real doozy. Total retcon, she’s now saying she had migraines, fainting spells, and absence seizures from childhood and grand mal seizures by the time she was a teenager. She also says she was diagnosed CIDP and dystonia by 20 and just woke up one day unable to walk, when per her blog she didn’t even start having any mobility symptoms until her mid-20s and didn’t stop walking until she was like 25 which is when the fake CIDP was diagnosed. Now she can use both hands but has limited coordination. The story of the Patch Adams book at least makes sense; her dad met an employee of Adams’ clinic through a Bluegrass charity he works with. But she’s also now working with something called Project Yes, making kids with actual problems feel bad because she has it worse off than them.
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There’s a video involved. I love how she says you might think she’s a normal kid but never admits she’s over 30. She says she still has the tube and can only eat blended foods if she feels like it. She didn't want the tube but she got it because Mommy and Daddy wanted her to and she didn't want to die before she met her nephew and she still questions if she should have just let herself die then. She describes why she lost her ability to draw, which is something like an etch-a-sketch being erased by her seizures. She also mentions in this video that her last hospital roommate was deaf-blind.


This is the only other video on her dad's account that features her. This was after some bluegrass thing called DelFest got cancelled for covid.

She has a new doctor working on her contractures. She can’t see his face due to her vision loss but she can feel his spirit. Alright, Hellen Keller.
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This is one of the reasons I initially put her in the “not faking” bucket. In addition to everything else she’d proven she had like the supportive custom wheelchair and the VNS, these giant cokebottle glasses reminded me too much of Katie Stanina and I thought, “there’s no way she’s faking this. She had to have some serious fucking genetic whoopsie daisy or a birth injury.”
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A “confession”: she’s actually legally blind and can only see bright colors and light but her body just improvised and that’s how she’s been able to read and do diamond art without being able to see anything. She just sees things differently than you do and has forgotten what things actually look like but her brain filled in the blanks and that’s why she can still do all these things. She stays in the line with her coloring pages by feeling where she’s already colored. For some reason I find blindness to be the most egregious of all her lies.
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Claiming to wear a girls’ size 6 or 7. I find it funny that if you look at old photos of her from before she got the chair she was hunched over forward claiming her back is twisted like that and now she's always leaned backwards.
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Now she’s really doing the deafblind doctor eyes. Her bracelet says something about an MRI, that she has a VNS implanted, and that she has a feeding tube.
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She’s going to wear the same dress for 100 days. Children’s size, of course. Don’t worry, mommy will hand-wash her dress for her every night.
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Suddenly showing off the box for a magnifier she claims she’s had for years and always used.
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I love these posts where a single mean poopoo comment has warranted a public response to let people know they’re totally not bothered at all.
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She gets the dress and proves it’s in a kid size. The dress only goes up to girls size 10 but it's meant to fit like a baggy potato sack. Yes, they do make the same dress in adult sizes.
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Claims she’s only had three haircuts in her entire life because it just falls out. Doubt.
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She is in so much pain but lidocaine patches fix it.
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She didn’t know she was blind and she could only see someone holding up their fingers a foot from her face with her good eye and not even that with her bad eye, but she could totally do intricate beadwork on tiny bookmarks because they were colorful and she “remembers some sort of order things follow” on a craft she just got that she never did before.
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Now claiming she’s only 42 lbs and could have sized down to a kids 4 because she only has a 20 inch chest. I just don’t even know anymore fellas.
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Calling out the EDS girls with their feeding tubes and huge smiles.
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She can make the bookmarks by carefully placing tiny rhinestones on a sticky pad, but she has to ask people what the finished picture is because that she can’t make out.
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Back to the fake strokeface. Her dog is dying and it’s all about what the dog did for her.
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ANGRY MUNCHIE!!! Someone has disrespected the house of Mommy!!!!! She can’t talk about it though.
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She gets way more attention from the doll-obsessed jesus ladies when she complains of seizures all the time, even though she allegedly has them daily.
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Apparently she hasn’t heard of the revolution known as “audiobooks” and is still claiming that despite being blind she thugs out reading the bible using a magnifier and solving it like a puzzle. There’s apps you can download that will give you audio of the entire bible in any translation you want and you can switch between translations at any time. You can also read along and zoom in the text as big as your screen will allow.
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Now claiming she can wear size 5T which is toddler sizes. I’ve never seen anyone mention their clothes size quite as often as this one does. Notice her hand is nice and relaxed.
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Next photo: she remembers her contracture because it’s botox day.
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She's also been working on the totally real-looking contracture in her foot.
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Claiming she can’t feel her legs so it doesn’t matter if she keeps them warm or not.
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Back to pretending she can’t focus on the lens because she’s blind.
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Her whole family has covid. She was exposed but doesn’t have it.
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Coloring (and shading!) by faith alone.
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I don’t have cancer but I am bald and I had a port and had to go to a cancer center! That’s kind of the same thing!!!
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"I might just be ridiculously thin."
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She gets an iPad. Goodbye potato tablet.
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Surprised these big growned up socks fit my tiny little girl feet, teehee!
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She’s been doing this 100 day same dress challenge and now she’s admitting that even though she sits in a chair all day and only occasionally hand washes it, the dress is falling apart.
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Open-pollinated squash and melons are notorious for crossbreeding and making edible but unpalatable mutants. This thing was probably more akin to a very large zucchini or a bland pumpkin when they cut it open than any melon worth eating.
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She rubbed skin off her bony knees but it’s okay, she can’t feel it anyway.
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For a while she’s just endlessly posting about this hideous dress and all the cute children’s clothing and accessories she pairs it with. Funny that in this one she can make eye contact without her super thick glasses, innit? Even with increased seizure activity.
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And she can still do this.
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She completes the challenge and gets her reward: another ugly dress by the same company.
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All her siblings are gone and moved out, her father is off living his new life, and she’s still just stagnating in Mommy’s house. Must be the epilepsy’s fault.
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Her vision is getting even worse, so she claims she’s teaching herself Braille now.
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And now she can make braille cards with her diamond painting shit.
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She finally returns to her blog to talk about it and about Patch Adams and the inequities of life.
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To the people who told her that she couldn’t teach herself braille in just a few days, you were totally wrong and she’s jesus’s most specialest blind girl.
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And images like this with the text superimposed and no alt text in the caption can’t be read by a lot of screenreaders. So there’s that.
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And she can still make direct eye contact with the camera lens without her glasses on. Her hair is growing back nicely, no patchiness.
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First attempt at makeup. She totes can’t see what she’s doing but mommy says it looks fine!
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Really? No one gonna point out these pics are an accessibility nightmare for blind people?
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Now claiming she’s so blind she can’t even tell what time of day it is and wakes up in the middle of the night thinking it’s day time and makes noise until Mommy comes to care for her like a baby.
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Yet she can set things up like this and know she’s staging and photographing it properly. I know people who have been blind for a very long time can adapt, but she’s only been claiming she’s blind for a few months and wants us to believe that the reason she’s so capable was she simply had no idea she was blind and just adapted.
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On her blog, she dances around what happened to the good compassionate doctor who heard her cry. She doesn't have a neurologist anymore because all of them are bad unlike the good doctor who served time in prison for running a diagnosis shop and pill mill.
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And that's where we'll stop. Man I say it all the time but covid was really the go big or go home for our girls. So many of them just faded away into obscurity but others were like our girl here, finding new ways to make sure everyone knows she's way sicker than those people dying on ECMO machines because their lungs failed.

edit: fixed a dropped image
 
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She’s trying to get diagnosed with polio now.
That's very vintage of her.
I hope the rest of the story about her dad stealing it and rubbing it on his hands is some folkloric reference I'm blissfully unaware of.
Her dad stealing it would be a pedo reference, bc they did that to the ones they wanted to marry.
Claims she’s only had three haircuts in her entire life because it just falls out. Doubt.
I guess we just have to ignore when she posted her hair on sm for yrs.
Now claiming she can wear size 5T which is toddler sizes. I’ve never seen anyone mention their clothes size quite as often as this one does.
Maybe it's an ED thing. I know Ashlich likes wearing kids clothes.
 
Suddenly showing off the box for a magnifier she claims she’s had for years and always used.
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Don't we all keep the boxes of our daily-used Harbor Freight Tools in pristine condition for storage, even when we're removing and replacing the tool inside it multiple times a day?

They don't sell that exact model any more, but it's under-$10 Chinesium.

I'm amazed that by the time she got to (incredibly) fake blindness, she'd whittled her audience down to just the ones who'd believe it.
 
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