Inactive Chronically Jaquie / Jaquie Beckwith / Jaquie Blake, Husband Judd Beckwith, & Helper Dog Harlow - Instagram Famous, Self-Declared Genetic Anomaly, Munchied Herself to Death

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How often was Jaw purging from her feeding tube that she is so sooooper sick unable to sleep and vomiting all night. Oh but don't worry she stops vomiting in the day time when she' vlogging y'all! She wants that G tube bad, she will probably say the medical marijuana gave her a reaction or changed her personality which she hates.
 
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Ironic, she claims to have EDS and was able to get the pushrim grips on her wheelchair herself? I tried to put them on my wheelchair and my finger joints weren't having it. Typical AJ, only having certain illnesses when it's convenient. I also don't understand why she brought pushrim covers from a European company when you can get them with Amazon Prime. Also, pushrim covers downhill BURN like mad, hello friction! She barely even self propels, not sure why she needed them.

Also, it might just be where I live, but it's stupid easy to get diagnosed with gastroparesis. I went for a GI follow up with a doctor I'd never seen and she's like I read through your chart and it sounds like you have gastroparesis, have you considered a feeding tube? No GES done, just wham feeding tube. Speaking of GI issues, with all the Zofran and Compazine AJ uses, she's probably full of shit...add narcotics on top of that and she's probably good and backed up. Explains why she's so full of shit.

She uses being chronically ill as an excuse to do absolutely nothing. I'm the same age as her, diagnosed with EDS and POTS, I still get up everyday and go to school, go on dates, have fun, and not act like I've been surgically attached to my sofa. Oh...wait we all experience chronic illness differently *eye roll* I think the reason why she's not in the Facebook support groups for her illnesses is because she KNOWS she will get chewed out.
 
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She uses being chronically ill as an excuse to do absolutely nothing. I'm the same age as her, diagnosed with EDS and POTS, I still get up everyday and go to school, go on dates, have fun, and not act like I've been surgically attached to my sofa. Oh...wait we all experience chronic illness differently *eye roll* I think the reason why she's not in the Facebook support groups for her illnesses is because she KNOWS she will get chewed out.

I love how she explains away her illnesses with, "They can change from hour to hour and day to day." She is 22 years old and living like a 90 year old invalid because she is crippled by these "illnesses." Honestly, I think anyone her age would get fed up with being in the house all the time when there are much more fun things to do.

I honestly don't think her GP is as bad as she claims it to be. We've already seen that she eats crap when she's able to eat orally and that can certainly exacerbate symptoms. Dairy, for instance, is a huge no-no when you are throwing up and she eats ice cream whenever she doesn't "feel well."

And, did anyone notice her eyes in the vlog from today? It looked like she had red patches underneath them which makes me wonder if she was rubbing her eyes to make herself appear sick.
 
And, did anyone notice her eyes in the vlog from today? It looked like she had red patches underneath them which makes me wonder if she was rubbing her eyes to make herself appear sick.

I thought the eyes looked like she had done something to make herself appear to look like shit as well. How is she having relentless vomiting if she has zero oral intake like she says? If she's not eating, it should be relentless dry heaving, so she told on herself that she actually is eating.

I'm her age and I do get fed up with being in the house all day even when I have to be, I don't find being stuck home to be fun. She's got a wheelchair and a Smart Drive, makes it pretty easy to go out and live a little even when you're feeling like shit.
 
I also don't understand why she brought pushrim covers from a European company when you can get them with Amazon Prime. Also, pushrim covers downhill BURN like mad, hello friction! She barely even self propels, not sure why she needed them.
I didn't do an extensive search and I'm not sure if there are like difference sizes but I only found blue, black, or red ones. I'm 100% Jaq would order from another site only to get purple or pink. And that brings us to the reason she needs them, because she wants more colour since the more obnoxious the better.
 
But the blinking lights? For someone who is so 'sick' she doesn't care about other disabled people...like those with light sensitivity seizures.
Didn't she claim epilepsy at one point? Her chair is nauseating and this is a very good point that the flashing lights pose a great risk to epileptics. It's all about Jacquie though, she couldn't care less about anyone who has real illness. Look at the way she behaved in the hospital for her J-tube...
 
I’m legitimately shocked that Jaq decided she would tolerate the Compazine. That stuff is made of nightmares. They actually give it with Benedryl as protocol in the hospitals I’ve been in because so many people have issues with it. Apparently it gets you buzzed though so of course she’d be into.
 
Apparently it gets you buzzed though so of course she’d be into.
At this point she's not even hiding the fact that she's living weird hit to weird hit. A lot of the drugs she gets put into her system aren't even the same type of high/buzz.... she is just that much of a junkie that she doesn't give any fucks.
 
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I didn't do an extensive search and I'm not sure if there are like difference sizes but I only found blue, black, or red ones. I'm 100% Jaq would order from another site only to get purple or pink. And that brings us to the reason she needs them, because she wants more colour since the more obnoxious the better.

Rib Grips are the "official" brand of these, but they're like $300, guess she isn't as loose with her money as we thought. OR... the Patreon well is drying up since she was dropping Patrons left and right.
 
Rib Grips are the "official" brand of these, but they're like $300, guess she isn't as loose with her money as we thought. OR... the Patreon well is drying up since she was dropping Patrons left and right.
That's exactly where my thoughts were heading when she put those covers on her spokes to try to make cheap imitation Spinergy wheels. For anyone who don't know, they are high end wheels that cost around $900 with different color spoke options.

In my 13 years of wheelchair use I've tried to add some personality to my chairs (light up front wheels, colored spikes etc.), but she seems to be vomiting out kid coloured accessories that just scream LOOK at me! Even the way she added the second set of push handles that were set up really high compared to her back made her chair look like it was made for a very young kid. I noticed those have been removed. I wonder why, seeing how she claimed they were added because the ones that are a original feature of her chair were too short for Judd. A common theme with these munchies seems to be wanting to get as close to the image of frail cancer kid as they can with as many brightly colored accessories as they can collect, but without losing their hair of curse!

She also went on and on about the weight of her chair being an issue and how it had to be as lightweight as possible before adding many extra pounds of weight to it in unneeded accessories. The only way to be any more over the top at this point is for her to add a flashing siren to h chair t announce to the world that anyone within a 2 mile radius is in the presence of the munchie queen
 
I've seen grips around here; which I get. Your hands are on that 24/7 and it'll get hard to grib something so metal and hard all day.

But the blinking lights? For someone who is so 'sick' she doesn't care about other disabled people...like those with light sensitivity seizures.

I was thinking about that myself. She's in and out of hospitals. She's going to trigger someone into having a seizure. Heartless bitch
 
Hasn't she been shown to walk just fine with those shoe insert things? Why does she need a wheelchair in the first place?

She really can't keep her story straight, can she? She just does whatever makes her seem sickest.
 
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lol she doesn't feel up to vlogging after a night of being sick (complete with sick!face!) then continues to ramble about Harlow for a few more minutes. ok Jaq, sure.
 
Ironic, she claims to have EDS and was able to get the pushrim grips on her wheelchair herself? I tried to put them on my wheelchair and my finger joints weren't having it. Typical AJ, only having certain illnesses when it's convenient. I also don't understand why she brought pushrim covers from a European company when you can get them with Amazon Prime. Also, pushrim covers downhill BURN like mad, hello friction! She barely even self propels, not sure why she needed them.

Also, it might just be where I live, but it's stupid easy to get diagnosed with gastroparesis. I went for a GI follow up with a doctor I'd never seen and she's like I read through your chart and it sounds like you have gastroparesis, have you considered a feeding tube? No GES done, just wham feeding tube. Speaking of GI issues, with all the Zofran and Compazine AJ uses, she's probably full of shit...add narcotics on top of that and she's probably good and backed up. Explains why she's so full of shit.

She uses being chronically ill as an excuse to do absolutely nothing. I'm the same age as her, diagnosed with EDS and POTS, I still get up everyday and go to school, go on dates, have fun, and not act like I've been surgically attached to my sofa. Oh...wait we all experience chronic illness differently *eye roll* I think the reason why she's not in the Facebook support groups for her illnesses is because she KNOWS she will get chewed out.

Seriously? What changed? When I was diagnosed about ten years ago it was nothing like that. I really went through a lot of tests and studies and medications. And they always said try to avoid the tube unless there's no other option. That's what happens when something becomes an ailment du jour I guess.

I think a lot of these "muh gastroparesis" spoonies just have hurt tummies from all the medications they've duped doctors into giving them. They probably have terrible diets too.
 
Seriously? What changed? When I was diagnosed about ten years ago it was nothing like that. I really went through a lot of tests and studies and medications. And they always said try to avoid the tube unless there's no other option. That's what happens when something becomes an ailment du jour I guess.

I think a lot of these "muh gastroparesis" spoonies just have hurt tummies from all the medications they've duped doctors into giving them. They probably have terrible diets too.

I'm honestly not sure what changed. The doctor saw I had POTS and EDS and I'm guessing with the rise of munchies having POTS, EDS, GP, and MCAS she probably just made the assumption. She told me more invasive tests like an upper GI or GES wouldn't be necessary...I find that a dangerous way of practicing medicine, how can you make a potentially life altering diagnosis and consider such drastic things without doing anything to confirm or exclude the diagnosis. Heck, my cardiologist wouldn't do anything besides increased fluids and salt tabs until I had a tilt table test done.
 
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Also WHY does she always look so stoned? She looks like she's constantly toking it up and is high as a kite.

It's the combination of iv zofran and iv benadryl, taken together they give s high that could rival coke.

Didn't she claim epilepsy at one point? Her chair is nauseating and this is a very good point that the flashing lights pose a great risk to epileptics. It's all about Jacquie though, she couldn't care less about anyone who has real illness. Look at the way she behaved in the hospital for her J-tube...

Her chair would give me fits. If I had to look at her and her chair over the last five days I've been inpatient, I would pitch a fit.

Another thing with AJ and JanJan is how they're able to vlog and not violate other people's privacy. The way they whip out their cameras at any sign they're "ill" while inpatient is abusive to the other patients. What about all the ADA stuff they claim supports them, yet ignored the rest of us. Oh wait, only AJ and JanJan count, the rest of us just have to deal with it.
 
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