Community Tard Baby General (includes brain dead kids) - Fundies and their genetic Fuckups; Parents of corpses in denial

[One Man Bland]

I would have anxiety problems growing up in that stressful situation too. His brother is practically a dead ringer for Sloth, who always has people telling him how good looking and handsome he is all the time when he obviously isn't, and is also super autistic, practically non-verbal, and periodically shrieks and rages through the house. While always being told how special and amazing he is. That shit would fuck anyone up.

Honestly just living with constant autistic meltdowns alone is enough to fuck a lot of kids up, even if the parents aren’t contestant cooing about how sperging out makes their dullard special.

Imagine living in a house that just also happens to have been partially renovated to function as an old fashioned insane asylum and normal activities can be suddenly be interrupted by anything from endless screaming to hitting to demolishing object self-harming activities like biting and head-wall banging - often for reasons that aren’t well understood because most parents aren’t behavior professionals and can’t afford all the therapy required to hash out what’s going on, or the trigger is pretty much impossible to avoid anyways. And that’s not even getting into watching parents having to deal with tard strength when giving their super autistic kids medication because you can’t explain to them how to take it or what they need it for.

Like shit dude no wonder the twin goes to stay with the dad far away from that nightmare. It’s probably why a lot of the kids with extremely mentally disabled siblings gravitate towards friends groups that do a lot of sleepovers or let them stay away from home as much as possible.

 

[Android raptor]

On the flip side, there definitely are parents with disabled kids who treat them as the sole source of all their problems instead of treating them as super special miracles. This tends to hurt both the kid as well as results in the other issues in the family going untreated. In severe cases it results in the kid even being abused and being blamed for the abuse.

Like with the woman who adopted that boy only to abandon him. His issues were likely just a symptom of a larger problem, and instead of properly treating it they just scapegoated and abandoned him like he was a dog.

 

[AnOminous]

This actually doesn’t bother me because it’s a normal thing for parents to say, even when their kids are run of the mill ugly. He’s handsome to her because he’s dressed nicely and did something she’s proud of.

It isn't particularly notable for a child of normal intelligence to dress himself.

 

[Toohottotrot]

Another pisses is when the kids not a complete tard but is full of drugs to keep totally tard level benefits coming in and the animals get better medical care because they want him dead

 

[derpi]

Anyone have updates on this case with the baby in Texas that’s on life support and in CONSTANT PAIN? .-.

 

[Daughter of Cernunnos]

Malibu Ken did an interview with the kid, whose name is Harry, his twin brother and mother a few years ago and yeah, he's definitely not intellectually normal. He can say a few words, but he's obviously very delayed. They call him autistic, but at one time he would have been diagnosed as straight up retarded.
His brother reminds me of the brother of Sophia Weaver, the girl with the disfigured mouth and Cal Hartley, in that all of them seem to have been indoctrinated to believe that their siblings are just the most amazing people ever born. Sophia's brother kept saying how cute and adorable she was, Cal was convinced that his sisters were vital individuals,who could show and understand love, enjoyed going out and were the best sisters a guy could ever have. While Harry's brother claims that Harry is incredibly funny, intelligent, special..etc. It's interesting how the siblings of these potato and semi potato kids are so similar in that they can't just love them, but they all seem feel that they have a duty to extoll their virtues and tell the world how amazing they are, while at the same time insisting that their siblings are also totally normal and just like everyone else.

BTW, Harry's left eye and wonky eye socket aren't real. He was born without either and underwent a couple of surgeries to construct a socket which was then fitted with a plastic eye. I dont know what he looked like before the surgeries, but I can't imagine that his appearance was much worse than it is now, but even if there was some improvement, it still seems like kind of a pointless endeavor. I doubt the kid knows or cares what he looks like, so what benefit is there to have made him undergo multiple operations that are almost certainly painful, in order to be given a fake eye that can't see and results in him still being extremely disfigured?
Here's the interview where you can watch Harry pop his eye out and hear Chris asking him enthralling questions that he barely understands like, "Does getting kisses make you happy or sad."

The Purest Example of Love (Goldenhar Syndrome)

Harry is diagnosed with Goldenhar syndrome and autism. His twin brother, Oliver, has learned from Harry that love is something to be expressed through action...

www.youtube.com

What a dumb surgery. Glass eyes have to be cleaned regularly and replaced every 5 yrs and you can get infections if you don't take care of them properly.

 

[RebatsivePulsard]

What a dumb surgery. Glass eyes have to be cleaned regularly and replaced every 5 yrs and you can get infections if you don't take care of them properly.

Plus the fake eye is misaligned, has a poorly constructed eye socket, and most of the eyebrow on that side is missing. WTF they were trying to accomplish is beyond me.

 

[booklover]

Anyone have updates on this case with the baby in Texas that’s on life support and in CONSTANT PAIN? .-.

If this is the case I think you're talking about, there's another person on this board whose own disabled child was recently hospitalized at the same facility. This baby, the one on life-support, is in a room away from other patients, under guard.

Honestly just living with constant autistic meltdowns alone is enough to fuck a lot of kids up, even if the parents aren’t contestant cooing about how sperging out makes their dullard special.

Imagine living in a house that just also happens to have been partially renovated to function as an old fashioned insane asylum and normal activities can be suddenly be interrupted by anything from endless screaming to hitting to demolishing object self-harming activities like biting and head-wall banging - often for reasons that aren’t well understood because most parents aren’t behavior professionals and can’t afford all the therapy required to hash out what’s going on, or the trigger is pretty much impossible to avoid anyways. And that’s not even getting into watching parents having to deal with tard strength when giving their super autistic kids medication because you can’t explain to them how to take it or what they need it for.

Like shit dude no wonder the twin goes to stay with the dad far away from that nightmare. It’s probably why a lot of the kids with extremely mentally disabled siblings gravitate towards friends groups that do a lot of sleepovers or let them stay away from home as much as possible.

When I was in junior high, there was a girl a couple years ahead of me who was a vicious, vile bully who was just as ugly on the inside as she was on the outside, and (among other things) had a serious drug addiction, which we all knew she financed by sexually servicing adult men. When we found out that her much-younger sister had terminal cancer, it didn't justify any of it, but it sure explained a lot. In short, she was acting out.

 

[Crunchy Leaf]

Anyone have updates on this case with the baby in Texas that’s on life support and in CONSTANT PAIN? .-.

Still alive as of May 20, for legal reasons. https://www.fox4news.com/news/tinsl...-family-awaits-a-ruling-in-their-legal-battle

 

[Bubblez McGee]

What a dumb surgery. Glass eyes have to be cleaned regularly and replaced every 5 yrs and you can get infections if you don't take care of them properly.

I was checking out the mom's blog and she mentioned that they'd had the glass eye replaced because Harry's real eye had grown darker, so she had the fake one remade to match the color and also reshaped to fit better. However, after finding pictures of him before the surgeries, it was as I suspected, not only did the fake eye not improve his appearance, but I truly think he looked better before.

Prior to his surgeries, half his face pretty much just looked blank, as if someone was trying to practice the clone stamp in photoshop and cloned the skin of his forhead over the left side of his face and left a tiny remnant of a phantom eye. Afterward ,his face looks mangled and crooked with big frankenstein-like scars in his hairline. In pictures of him posing without the false eye, instead of a barely there hint of an eye, he's been left a red, raw angry, swollen pit. He reminds me of that kid with severe amniotic band syndrome who was born with no eyes.

Below are a few pics of of him before the surgeries. And then after the operation with and without the fake eye. Not only did he look better before, but he somehow seemed happier too.
I dont know how his mother can look at his before and after pictures and justify putting him through that. Maybe she thought his appearance would turn out better than it did or maybe she's delusional and really thinks he looks better now.

Spoiler

 

[Francis E. Dec Esc.]

I was checking out the mom's blog and she mentioned that they'd had the glass eye replaced because Harry's real eye had grown darker, so she had the fake one remade to match the color and also reshaped to fit better. However, after finding pictures of him before the surgeries, it was as I suspected, not only did the fake eye not improve his appearance, but I truly think he looked better before.

Prior to his surgeries, half his face pretty much just looked blank, as if someone was trying to practice the clone stamp in photoshop and cloned the skin of his forhead over the left side of his face and left a tiny remnant of a phantom eye. Afterward ,his face looks mangled and crooked with big frankenstein-like scars in his hairline. In pictures of him posing without the false eye, instead of a barely there hint of an eye, he's been left a red, raw angry, swollen pit. He reminds me of that kid with severe amniotic band syndrome who was born with no eyes.

Below are a few pics of of him before the surgeries. And then after the operation with and without the fake eye. Not only did he look better before, but he somehow seemed happier too.
I dont know how his mother can look at his before and after pictures and justify putting him through that. Maybe she thought his appearance would turn out better than it did or maybe she's delusional and really thinks he looks better now.

Spoiler

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He needs Dennis Hopper's ping pong ball eye from Waterworld.

 

[large_farva]

For the deformed kids that are intellectually normal, hearing people online / their relatives constantly call them beautiful/handsome has to be incredibly depressing. It indicates that people do not respect their intelligence, do not think they are mature enough to handle a cruel reality and are prepared to blatantly lie to them.

Speaking of these kids, there's an IG that's pretty gut-wrenching and not for the faint of heart. it's @ melissa_2010
The kid has epidermolysis bullosa, it's a fucking evil disease that robs the body of collagen, the proteins that hold the layers of skin together. If these children are even touched, blisters will form and skin layers separate easily. They look like severe burn victims. Mentally intact and trapped in a body that will keep blistering until a secondary infection or cancer kills them.

The account I found was unique because the mother TWO children with EB, along with what looks like a lot more kids. The older child with EB passed away at age 14.

Since she has two kids with EB, I suspect it's something she passed on to them. I'm curious if they had genetic counseling after the first child was born/diagnosed. This isn't something I would wish on anyone, it is the worst disease ever. It's a bit infuriating she went and had another child with EB.

I was checking out the mom's blog and she mentioned that they'd had the glass eye replaced because Harry's real eye had grown darker, so she had the fake one remade to match the color and also reshaped to fit better. However, after finding pictures of him before the surgeries, it was as I suspected, not only did the fake eye not improve his appearance, but I truly think he looked better before.

Prior to his surgeries, half his face pretty much just looked blank, as if someone was trying to practice the clone stamp in photoshop and cloned the skin of his forhead over the left side of his face and left a tiny remnant of a phantom eye. Afterward ,his face looks mangled and crooked with big frankenstein-like scars in his hairline. In pictures of him posing without the false eye, instead of a barely there hint of an eye, he's been left a red, raw angry, swollen pit. He reminds me of that kid with severe amniotic band syndrome who was born with no eyes.

Below are a few pics of of him before the surgeries. And then after the operation with and without the fake eye. Not only did he look better before, but he somehow seemed happier too.
I dont know how his mother can look at his before and after pictures and justify putting him through that. Maybe she thought his appearance would turn out better than it did or maybe she's delusional and really thinks he looks better now.

Spoiler

View attachment 1364753 View attachment 1364804 View attachment 1364816View attachment 1365099View attachment 1365101

It looks better before the surgery because once his adult teeth came in, it distorted his face even more.

Also, it's possible the kid was the one who decided he wanted the surgery for the prosthetic eye.

 

[John Merston]

Also, it's possible the kid was the one who decided he wanted the surgery for the prosthetic eye.

Given his mental exceptionalism, I doubt he had the capacity to make that decision.

 

[derpi]

If this is the case I think you're talking about, there's another person on this board whose own disabled child was recently hospitalized at the same facility. This baby, the one on life-support, is in a room away from other patients, under guard.

Still alive as of May 20, for legal reasons. https://www.fox4news.com/news/tinsl...-family-awaits-a-ruling-in-their-legal-battle

Thank both of you! I didn’t remember her name and the court docs don’t mention it @.@
Those doctors and nurses are going to need so much therapy after this

 

[Lackadaisy]

The kid has epidermolysis bullosa, it's a fucking evil disease that robs the body of collagen, the proteins that hold the layers of skin together. If these children are even touched, blisters will form and skin layers separate easily. They look like severe burn victims. Mentally intact and trapped in a body that will keep blistering until a secondary infection or cancer kills them.

That's enough Tard Baby General for today...

 

[GenociderSyo]

Epidermolysis Bullosa presents in many of insane ways. The organization for it refers to it as the Butteryfly Disease due to the skin being as fragile as a butterflys wing. Interesting note : The only way to prevent infection is bleach baths.....on open wounds....try not to cringe...

There are 3 types depending on what layer of skin it effects and one orphan type:
Epidermolysis Bullosa Simplex which affects the top layer of skin.
The mildest form, Epidermolysis Bullosa Simplex Localized, only effects the palms of hands and soles of feet and does not effect life expentancy.
The most severe Epidermolysis Bullosa Simplex Generalized Severe, affects all but the palms of hands and soles of feet. They tend to be missing nails and this effects the lining of hte esophagus so they require dilations to keep breathing. They tend to die by age 30 due to complications of EB.
Epidermolysis Bullosa Simplex Generalzied Intermediate is like the severe version, but the esophagus lining is unaffected. They have oculuar issues and malignant melanoma is guaranteed to be an issue.
There are 8 more subtypes that are too rare to go into.

Epidermolysis Bullosa Junctional which affects the mid layer of skin.
The mildest form, Epidermolysis Bullosa Junctional Localized, only effects localized areas as well as teeth enamel and nails. It does not effect life expentancy.
The most severe Epidermolysis Bullosa Junctional Severe or Herlitz subtype. Blistering effects every region of the body as well as the mucus membranes. They have blistering all their their mouths, esophagus and their digestive systems. The blistering leads to fusion of the fingers and toes, joint contractures and hair loss. Most do not survive their first year of life. If you feel insane enough to google it they come out as a giant blister baby and they are in constant and contiuous pain.
Epidermolysis Bullosa Junctional intermediate, or non-Herlitz subtype, is a milder form of Herlitz subtype. In some cases the blistering is only limited to hands, feet, knees and elbows and it may even clear up by infanthood being over. They do tend to have issues with hair and nails. The swelling of hte esophagus and scar tissues does not tend to life limit or cause breathing issues and they have a normal lifespan.
There are 5 more subtypes that are too rare to go into.

Dystrophic Epidermolysis Bullosa which affects the uppermost layer of skin.
Dystrophic Epidermolysis Bullosa generalized is milder then the recessive forms of dystrophic EB. Blistering ususally is only on the hands, feet, knees, and elbows. There is the scarring of EB, but less severe and nails are lost over time.
Recessive Dystrophic Epidermolysis Bullosa genearlized severe is the most common and most severe form. Infants are born with entire body blistering and areas of missing skin. The mouth, esophagus and digestive track are all effected. Scarring caused in the mouth and esophagus can lock the jaw shut and limit the openings of the airway. Progressive scarring fuses fingers and toes, causes loss all nail, contractures the joints, and since it effects hte eye as well it leads to scarring and cataracts leading to blindness. They are al very high risk of getting squamous cell carcinoma, which is an unusually aggressive cancer. Thier organs are also affected as well as their heart. They tend to die by 30 of cancer or other eb reason.
Recessive Dystrophic Epidermolysis Bullosa generalized intermediate is the same as RDEB gen severe, but does not tend to lead to fusion of fingers and toes or contractures. Death is still ususal by age 30 due to cancer and compications.
Recessive Dystrophic Epidermolysis Bullosa Inversa is similar to RDEB GEN SEV, but majority of skin loss and blistering is back of neck, back and torso areas. Can also cause though psuedosyndactly (that is the name for the fusion of fingers/toes) and hearing loss due to ear canal erosion.
There are 5 more subtypes that are too rare to go into, as well as another 4 recessive subtypes.

Kindler Syndrome, when your body hates you so much that you have all 3 skin layers effected at the same type.
All 3 severe subtypes of EB combined into Super EB, with photsensitivity as well. Affects inside and out with intestional, esophageal, urethreal, and very high risk of cancer. Sweet escape of death by age 30 due to cancer or compications.

 

[Android raptor]

I remember watching "The Boy Whose Skin Fell Off" years ago. Dude seemed like a genuinly likable guy, and the bit about putting a can of baked beans on his coffin just to make people at his funeral wonder why was pretty great.

 

[allthecheese]

The Tinslee story has become surprisingly hush-hush. You'll notice there are no new pics of her. Rumor is she's sedated pretty much 24hrs, so they rely on old pics where she looks more alert. Her mom will say stuff like she loves watching "Paw Patrol" and having her nails done, but we see no pics or videos. (And really, when this all started, she was like 6 months old, tons of parents will claim their kid "loves" a tv show if they turn towards the noise). The local advocate groups have really gotten quiet as well. There were previous allegations that Cook wasn't providing the right care, but you don't hear that as much. One that I haven't heard an answer on, is why she doesn't qualify for a trach. It seems like it'd be a lot easier than intubating around the clock, but there's probably more to the story.

 

[Bubblez McGee]

Speaking of these kids, there's an IG that's pretty gut-wrenching and not for the faint of heart. it's @ melissa_2010
The kid has epidermolysis bullosa, it's a fucking evil disease that robs the body of collagen, the proteins that hold the layers of skin together. If these children are even touched, blisters will form and skin layers separate easily. They look like severe burn victims. Mentally intact and trapped in a body that will keep blistering until a secondary infection or cancer kills them.

The account I found was unique because the mother TWO children with EB, along with what looks like a lot more kids. The older child with EB passed away at age 14.

Since she has two kids with EB, I suspect it's something she passed on to them. I'm curious if they had genetic counseling after the first child was born/diagnosed. This isn't something I would wish on anyone, it is the worst disease ever. It's a bit infuriating she went and had another child with EB.


It looks better before the surgery because once his adult teeth came in, it distorted his face even more.

Also, it's possible the kid was the one who decided he wanted the surgery for the prosthetic eye.

I first heard of EB quite a few years ago from a blog called "EBing a mommy"about a woman whose toddler had an exceptionally severe form of EB. It was so bad that the poor kid got blisters on his eyes which eventually sealed them shut and blinded him. He was the opposite of a potato baby in intellectual capacity in that he was actually intelligent and musically gifted. Because of his condition he had a trach fitted in his throat which rendered him unable to talk, but he was quite aware. He wasnt even three years old, but he could follow the rhythm of any song and drum along to it. But like I said, his form of EB was one of the most severe and he died before his third birthday. EB really is a horrid disease...even if it doesnt kill the victim in childhood, their life is usually spent in daily, excruciating pain.

As far as Harry, the kid with autism and goldenhar syndrome...there is no way he had the mental ability to make the decision to have the surgery himself. Check out the interview with him and his family on the SKBK channel which I posted a few messages back. He's all but non verbal and seems to barely understand anything going on around him. I'm sure that the decision to have the plastic surgeries came from his mom or perhaps from both parents, but definitely not from Harry himself.

I agree that his jacked up adult teeth did make his appearance look worse, but so did giving him a swollen meaty socket with no lid that sits way below his real eye and that contains a plectrum shaped plastic eye that cant blink, but only stares blindly ahead.

Given his mental exceptionalism, I doubt he had the capacity to make that decision.

Yep, the kid doesnt have the mental ability to choose his own breakfast cereal, much less consent to a major operation

I remember watching "The Boy Whose Skin Fell Off" years ago. Dude seemed like a genuinly likable guy, and the bit about putting a can of baked beans on his coffin just to make people at his funeral wonder why was pretty great.

I saw that a few years ago as well. The guy had a great personality, good sense of humor and tried to be upbeat most of the time. You could only tell how hellish his condition really was when his mother was removing his bandages and even though she tried to be as gentle as possible, when she got to the ones on his back, it hurt so bad that he was absolutely sobbing from the pain. As dedicated as his mom was and as cool as a personality that he had, she said that if she knew what condition he had before he was born, she might have made the decision not to have him. After he died his brother said that he was relieved that Johnny was now out of pain.

 

[GenociderSyo]

This documentary followed someone with EB because they thought he was going to die. He didn't but another child did. This before stem cell research had started helping those with EB. One scene he is holding a box in his hands and it slips back on his arm and thats enough to damage his skin.