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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Who is honestly this ecstatic to be presenting their medical supplies? She made it into a show and tell. Jaq, just look at yourself. This thumbnail is so embarrassing. Munchie alert!!!
 

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Who is honestly this ecstatic to be presenting their medical supplies? She made it into a show and tell. Jaq, just look at yourself. This thumbnail is so embarrassing. Munchie alert!!!

I could not agree more. It's really sad, honestly, that she thinks this is OK behavior. I have never seen anyone get excited over medical supplies - they are a necessity for some people. 22 years old and acting like a kindergartner in show and tell is not normal.
 
I could not agree more. It's really sad, honestly, that she thinks this is OK behavior. I have never seen anyone get excited over medical supplies - they are a necessity for some people. 22 years old and acting like a kindergartner in show and tell is not normal.
MOST people get the medical equipment they need to survive and don't give a fuck about aesthetics unless they have the time and money to do so. Go take a look outside and see how many people bedazzle their wheelchair. Money's on that you find none...unless it's a kid or another munchie. Sure, some people in wheelchairs get what we call 'add-ons'; bags/grips/etc to make being in a wheelchair more quality of life friendly. But you aren't going to be seeing people adding twinkling lights and neon pink plastic on each wire.

Most people are able to live day to day with their disease with minimal issue or distraction to others. You see someone in a wheelchair and you might look but then you don't stare too long or you come off as a douche nugget. But AJ WANTS people to look. It's no fun being a 'sick' munchie if no one is looking at you and giving you attention.
 
The only individual involved in this Munchie shitshow I feel sorry for is Harlow. Harlow is a good pupper and deserves an owner who'll take him to the dog park and throw frisbees for him and give him belly rubs, not some lunatic who'll dress him in a neon pink vest and make him spend his days hanging around in dingy waiting rooms. Judd made his bed, but Harlow deserves better.
 
I know someone in a wheelchair, not an OTT munchie king/queen, he has a severed spine. He is small, because he doesn't use his leg muscles, he lacks access to buildings and other important locations in his life because a lot of older buildings do not cater for wheelchairs and he absolutely under no circumstances "decks" out his wheelchair or draws attention to it. It really puts it into perspective someone who genuinely needs a wheelchair and has a severe, permanent disability, who is just trying to live their life vs. Adjustable Jaquie, who can just pick and choose when her symptoms will affect her that day, not to mention just hopping out of her wheelchair anytime she sees fit. It's a disgrace and should be taken off her, wheelchairs are not glamorous at all. She is very childish with her reaction to it, treating it like a toy. She could never handle being in a wheelchair full time- hence get rid of it.
 
Did you guys notice that in her "Proof IVIG Is Working" vlog that she said her IgG is now in normal range? Well, I went back and watched some of her vlogs from when she was in and out of hospital at the beginning of 2017 to see if there were any inconsistencies and surprise surprise, I found a gem! In her vlogs from Jan/Feb 2017 (she goes into detail in "Difficult Immunology Follow Up 1/24/17) she repeatedly says that it is her IgA and IgM that are low, and that her IgG is borderline. Can anyone who actually knows about this stuff weigh in on this? Like whether it would make a difference for her IgG to go from 'borderline' to 'normal range' and her IgA and IgM to stay low? And whether IVIG really does only target IgG like she claims in her vlog from the other day? Oh, and I can't forget to mention that in her recent vlog she says her IgG has "always been low" whereas in the vlogs from early 2017 she says it is borderline rather than low multiple times.
 
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Jaq and Jan are just so weird together. Like we're going to "our" doctor's appointment and like I constantly need to remind myself that they didn't become friends on like a chronic health support forum it's Paul and Judd that were friends and they both "randomly" have all these same super rare disorders and such fragile health. It's just so weird.
 
So, yesterday, Janiece was adamant that she and Jaq are not the same but then, today, she buys the same backpack for her infusion stuff. It wasn't available in her fave lime green color so she bought a purple "galaxy" backpack instead. WHY do they feel the need to accessorize everything? You don't need some fancy backpack just for your IV stuff - that's sick. Yeah, you two are the same in that you both need mental health professionals ASAP.
 
The only individual involved in this Munchie shitshow I feel sorry for is Harlow. Harlow is a good pupper and deserves an owner who'll take him to the dog park and throw frisbees for him and give him belly rubs, not some lunatic who'll dress him in a neon pink vest and make him spend his days hanging around in dingy waiting rooms. Judd made his bed, but Harlow deserves better.
Harlow probably needs an emotional support dog.
 
Jaquie looks ridiculous in that dress and her AFO's. I can't.

Plus, she's wearing sneakers which just throws the whole outfit off. The dress alone is pretty but with the knee socks and AFOs, she looks like a goofy overgrown toddler. Honestly, with how little she is using the AFOs for walking, I don't quite understand why she is even wearing them. They look ridiculous.
 
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."

I agree. I have idiopathic gastroparesis. I had to go through a feeding study before getting diagnosed after going from dr to dr with my inability to eat properly. The feeding study was time consuming, expensive and barf-inducing. I am forced to take the awful reglan which just terrible. I had a compound pharmacy make something for me that worked well, but my insurance decided not to cover it, so back on the reglan. That and Zofran is what's makes me able to eat most days. This is not a "cute" disease - it's all about being very restrictive with everything you eat but I can eat steak, chicken, etc. I can't eat veggies with skin or shells like corn, peas, not fatty fried foods, no heavy creams, etc. The only thing is that I don't get WHY anyone would choose to create all of these sicknesses for herself at so young. Those of us suffering would JUMP at the chance to be unshackled and just go L I V E this life we've all been given.
 
I agree. I have idiopathic gastroparesis. I had to go through a feeding study before getting diagnosed after going from dr to dr with my inability to eat properly. The feeding study was time consuming, expensive and barf-inducing. I am forced to take the awful reglan which just terrible. I had a compound pharmacy make something for me that worked well, but my insurance decided not to cover it, so back on the reglan. That and Zofran is what's makes me able to eat most days. This is not a "cute" disease - it's all about being very restrictive with everything you eat but I can eat steak, chicken, etc. I can't eat veggies with skin or shells like corn, peas, not fatty fried foods, no heavy creams, etc. The only thing is that I don't get WHY anyone would choose to create all of these sicknesses for herself at so young. Those of us suffering would JUMP at the chance to be unshackled and just go L I V E this life we've all been given.

That sounds awful. I've watched other vlogs of people who have GP and the suffering is obvious when it is not forced or faked. For someone to claim a horrible illness for attention, it does a great disservice to those who actually have it. Not to mention that some doctors become resistant to treating problems because people fake symptoms which makes it more difficult for those who have medical needs. Both Jaq and Janiece need to stop with the crap and get a life. Both of them think it's OK to parade around with unnecessary medical gear while others who are using it because they need it live life as normal as they can. It's a daily struggle for them to find normalcy and I'm sure they would be grateful to live the lives that these two are throwing away.
 
Did you guys notice that in her "Proof IVIG Is Working" vlog that she said her IgG is now in normal range? Well, I went back and watched some of her vlogs from when she was in and out of hospital at the beginning of 2017 to see if there were any inconsistencies and surprise surprise, I found a gem! In her vlogs from Jan/Feb 2017 (she goes into detail in "Difficult Immunology Follow Up 1/24/17) she repeatedly says that it is her IgA and IgM that are low, and that her IgG is borderline. Can anyone who actually knows about this stuff weigh in on this? Like whether it would make a difference for her IgG to go from 'borderline' to 'normal range' and her IgA and IgM to stay low? And whether IVIG really does only target IgG like she claims in her vlog from the other day? Oh, and I can't forget to mention that in her recent vlog she says her IgG has "always been low" whereas in the vlogs from early 2017 she says it is borderline rather than low multiple times.

Has she ever said anything about getting routine vaccinations, like flu and pneumococcal? If those are timed just right, they can temporarily cause her immune system appear compromised. Especially if she had the pneumococcal first, it can really cause blood work to go wonky. All her unethical all-in-one doctor had to do is get the "diagnosis" on paper and WhackJac gets whatever she wants.
 
Janjan has a new video about deaccessing her port. Any med-fags that can explain wtf that means?
Also why there are no jangly tubes like Jacky?

Has she just not reached super-spoonie status yet?
 
Janjan has a new video about deaccessing her port. Any med-fags that can explain wtf that means?
Also why there are no jangly tubes like Jacky?

Has she just not reached super-spoonie status yet?

Deaccessing means JanJan had been taught well by AJ to remove the needle to make it safe without having to keep it covered. A pretty is under the skin, with a line that goes directly to the heart. Leaving it accessed like many of the munchies do means they're deliberately exposing themselves to any and every gets and virus out there. If any of them get serious they'll just have another trip to the hospital.

JanJan will get the jangly tubes soon enough. She's a novice in munchieland, she needs time to adjust to the club's rules.
 
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Correct me if I'm wrong but didn't WhackJaq say the IV compazine helped much more than expected? Then she got some new med, never mentioned what it was. It's very very odd that she's only vomiting at night, sounds more like CVS than GP.

I'm still confused as to how she's throwing up so much because she claims she has zero oral intake.

None of her doctors trust her to place and remove her own NG and she doesn't know why...hmm sounds like they're starting to catch on to ya! She's trying to sound like a brave munchie for going without her G tube, just so she gets all the asspats when she gets another one.

Miraculously she can haul ass when there's a bee, of course she can because she's only putting on about her mobility impairments.
 
None of her doctors trust her to place and remove her own NG and she doesn't know why...hmm sounds like they're starting to catch on to ya! She's trying to sound like a brave munchie for going without her G tube, just so she gets all the asspats when she gets another one.

If I know our girl, though...once she's got a new idea for a "tool", she won't stop doctor-shopping until she gets it!
 
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