- Joined
- Oct 16, 2019
This Paige bitch can't die soon enough. I feel very bad for her medical team and anyone else who has to take care of her. That sullen expression she sports for most of her selfies makes her downright slappable.
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How she managed to pass the background test and stay at Disney is beyond me. White girl magic I guess.Ell Oh Ell. On a hunch I looked into the Osceola County, Fl. records too, since Skinwalker used to live there when she was in the Disney College Program. Shoplifting from Walmart, sentenced to a fine, impulse control classes, and community service, tsk tsk.
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Also heard through the rumor mill that her new black and pink wheelchair (which she modeled off of one belonging to someone who has a pretty devastating disorder and really cannot walk) has a 12" seat, which is usually for pediatrics chairs. I had noticed in the photos from when she picked up Hickory that she had a second cushion on her seat and looked like she had "outgrown" her original 16" Barbie Car
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But I didn't notice by Mothers Day she had a new, much smaller custom Tilite. The "I'm so thin I have to shop in the kids section" of wheelchairs.
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Sorry I'll stop, I just get excited because every time I bring this miserable sack of shit up one of her former friends drops new info into my inbox.
Please don't stop! Everything you post about her is simultaneously hilarious and horrifying.Sorry I'll stop, I just get excited because every time I bring this miserable sack of shit up one of her former friends drops new info into my inbox.
I seriously wish I could post even half of what people send me about her. Some of it is just so batshit and yet there are receipts. But I do not blame them for not wanting to risk that she figures out who is talking to me because wow, what a nightmare she is.Please don't stop! Everything you post about her is simultaneously hilarious and horrifying.
Mysteryelles; went to eye doctor, didnt bring medical records from an other doctor "forgot"Munchie move.
God damn Christmas came early for me.
So I had a little question for my Skinwalker leak. Back in early 2018 when she originally DFE'd and made everything private (lol how'd that work out?), Skinwalker made a vague post about how she had been diagnosed with something really serious, that she didn't even post about online. Then she came into IF and gave an apology for being such an OTT nightmare, realized she had gotten caught up in the drama of social media and always trying to compete with other "spoonies" for attention but she was seeking help for her problems and stepping back from the CI community now. Someone else (who was probably her tbh) later came into IF saying she had been diagnosed with GBS which caused the change of heart but she was doing really well, back at work, had seen that she was being dramatic and was now seeking far less invasive treatments and not making everything an end-of-the-world catastrophe.
This diagnosis happened when she was hospitalized for several weeks in Tampa Bay, and Jaquie came to visit her. The rumor that circulated after that was that Jaquie asked too many questions and made it clear she was going to "steal" her GBS diagnosis which made Skinwalker realize how terrible the social media was for sick people. Which, run through the standard bullshit filter, translates to "Skinwalker got a rare n' shiny and didn't want to share with Jaquie." Skinwalker did not like to be the skinwalkee.
I had over the years gone back and forth on whether:
1) she really had GBS as an unintentional consequence of munching. It's an autoimmune attack on your nerves following an infection and it's no joke. It can paralyze or even kill a person if they're not treated, and with her being the Skelly Who Cried Wolf maybe doctors delayed treatment thinking she was faking once again.
2) she used a positive autoantibody test from IVIG or something like that plus reported symptoms of tingling, nerve pain, and weakness in her limbs to convince a shady doctor to diagnose her with GBS when really she had peripheral nerve damage and muscle wasting from anorexia.
The last post I saw before she DFE'd was her whining because Disney was arguing with her over a single small disability accommodation, and a few months later Sadie was out and Hickory was in, which made me think the accommodation was related to something Sadie did. Maybe she lunged at a real service dog or was out of control at work or something.
Turns out the answer is even funnier. Disney fired her because she has no documentation of her diagnoses. She has the standard munchie combo from QMB, but when she kept claiming additional diagnoses and could provide no proof of them she was fired. She also was denied SSDI because of this. When she was in the hospital in February for a "GBS and kidney disease flare" she first told everyone she needed dialysis because she was in kidney failure, then changed it to that she needed plasmapheresis for her GBS when she was called on that lie. She told everyone she had kidney failure, heart failure, muscular dystrophy, and Parkinson's along with the other things she claims. Her parents didn't know anything about this and she lives with them and is entirely up her mom's ass all the time.
She uses two different hospitals and Dr. QMB so that none of her doctors know what she's claiming to who.
She is hella bulimic. I thought she was a hardcore anorexic and just exercised purged her TPN and g-tube purged what little she ate but naw dude, she eats tons of food all the time to the point where it is shocking to people, and it's one of the only things she can talk about.
And Mama Winig shows up with a walker and Sadie when she also wants to LARP as disabled. I knew about Sadie but not the walker.
Also, Amanda, since you read here, I see you deleted or renamed Hickory's instagram account, which i never even mentioned that I knew about. I actually only found it yesterday and was checking tonight to see if it was a new account that was gaining followers or an old one you abandoned. Clever girl. Anyway, have I not shown you that internet is forever? Here, let me show you how easy it is to recover your deleted facebook posts. I don't even have a facebook.
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Plasmapheresis is not usually used for GBS. IVIG is the go-to for GBS. Plasmapheresis is used for GBS’s chronic sibling: CIDP (Chronic Inflammatory Demyelinating Polyneuropathy).
Here’s the thing about CIDP. It’s not a diagnosis of exclusion. You have to show elevated proteins in your CSF via lumbar puncture to be diagnosed with CIDP. GBS can evolve into CIDP over time, or you can develop it spontaneously. The difference between GBS and CIDP is time. GBS comes on super suddenly and, with treatment, does resolve. CIDP is gradual (or is diagnosed when somebody with GBS doesn’t recover within a few months) and never resolves.
CIDP is a bit of an “orphan” disease. Not very many people really know about it unless they have it, someone they know has it, they work in neurology, or they are an infusion nurse. Many CIDP patients get misdiagnosed with something else (usually small fiber neuropathy or MS) because nobody knows about CIDP. There’s not a ton of research on it, either.
GBS is a bitch of a disease because you can just wake up one day mostly paralyzed. People die from it because it paralyzes your autonomic function, and it can move fucking fast. CIDP does all the same shit GBS does, but over the course of years. And the treatments can pause it or slow it down, but there’s no cure. There have been encouraging strides made with stem cell transplantation recently, though.
... and walks around on her skelly legs while carrying an armful of junk food. Wow. I love her she's magnificent.mutual friends with someone who was close circle of by Skinwalker. These are screenshot pulled and taken from a Facebook video in April and praying that posting these won’t blow my cover but wanted to share too good to keep for private. proof she does binge according to @Kate Farms Shill!
how convenient to forget MRIs that show a perfectly healthy brain for her four hour Neuro optho appointment.
I love how she just says a bunch of random shit but never actually posts that her doctors have said anything is wrong with her. With this appointment she left with the diagnosis of a lazy eye and long eyelashes???
my favorite thing is that she thinks her “eye flutter” is passing out. How does that even make sense?
CIDP is what Julian claims to have and presumably also what Skinwalker was going for. She was already on IVIG when she claimed to get the GBS diagnosis.
My theory on the dialysis machine was that she just happened to take a photo of one while in the hospital and posted it online claiming it was for her, or she found a photo of one someone else posted and stole it. This was the proof she provided.
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maybe her child’s lift vest is squeezing her body up and causing her eyelid to squint. Rare unknown sideeffects of wearing child life vests 24/7 as an adult.
Why is it that Julian claims CIDP yet doesn’t get ivig? My guess is he doesn’t really have it- possible it was suggested at one time so he ran with it. But it’s a dead giveaway to me that his dx is BS. The 2 people I know with CIDP have been ivig quite a long time.
Plasmapheresis is not usually used for GBS. IVIG is the go-to for GBS. Plasmapheresis is used for GBS’s chronic sibling: CIDP (Chronic Inflammatory Demyelinating Polyneuropathy).
Here’s the thing about CIDP. It’s not a diagnosis of exclusion. You have to show elevated proteins in your CSF via lumbar puncture to be diagnosed with CIDP. GBS can evolve into CIDP over time, or you can develop it spontaneously. The difference between GBS and CIDP is time. GBS comes on super suddenly and, with treatment, does resolve. CIDP is gradual (or is diagnosed when somebody with GBS doesn’t recover within a few months) and never resolves.
CIDP is a bit of an “orphan” disease. Not very many people really know about it unless they have it, someone they know has it, they work in neurology, or they are an infusion nurse. Many CIDP patients get misdiagnosed with something else (usually small fiber neuropathy or MS) because nobody knows about CIDP. There’s not a ton of research on it, either.
GBS is a bitch of a disease because you can just wake up one day mostly paralyzed. People die from it because it paralyzes your autonomic function, and it can move fucking fast. CIDP does all the same shit GBS does, but over the course of years. And the treatments can pause it or slow it down, but there’s no cure. There have been encouraging strides made with stem cell transplantation recently, though.
And even then, plasmapheresis is usually second in line treatment for CIDP in which IVIg is first in line for, as well as the aforementioned GBS. There are a few other treatments that can be used in line with either but I don’t want to go giving these munchies more ideas since a few seem to be lurking around the dx (or maybe I should just to see the potential shit rain down on them because I’m a terrible, terrible person). But yeah, it’d be fucking hard to get GBS while already on an autoimmune dose (which is much, much larger than a dose for something like an immune deficiency) and I could only see her getting CIDP if she had it prior to starting IVIg or it wasn’t in her system...or she was just getting a tiny dose of about 2mg for a non autoimmune disorder. Either that or she must have been very exceptional indeed and of great interest to neurologists and immunologists everywhere. Lie better, munchies.
Anyway! Who exactly is this Julian and why does their name show up everywhere? I can recall them showing up on LCF back when I lurked the munchie thread over there claiming that they were definitely not a munchie (sure, sure) and that Jaq had copied everything off them but their name seems to pop up everywhere. Just how many diagnoses does this person have and how do they know so many munchies? They seem like they’re potentially pretty milky but guessing they try to play it smart to keep nasty people like us off their radar?