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

[Allo Vera]

Trisomy 13 is even deadlier than trisomy 18, right? Are there any fundies with trisomy 13 spuds out there?

I was intrigued, so searched #trisomy13 on Instagram.

The answer is an emphatic yes.

 

[large_farva]

I was intrigued, so searched #trisomy13 on Instagram.

The answer is an emphatic yes.

Any trisomy disorder can be full, in which it affects every cell has the extra chromosome, or mosaic, where only some cells are affected. This is likely why there are hashtags for some of these more severe trisomy disorders showing living babies/children.
/sperg

 

[bigfart420666]

I was intrigued, so searched #trisomy13 on Instagram.

The answer is an emphatic yes.

that’s really sad, most of those babies look cute

 

[booklover]

The couple in the left-hand picture, lower left corner, displaying their baby bump knew their daughter had T-13 almost from the beginning, but they chose to continue the pregnancy because they wanted to have her for as long as possible. She went into labor a couple weeks before the due date, and the baby lived 60 minutes. They're expecting another baby now, and AFAIK this one is normal.

Also AFAIK, they are not excessively religious although I suspect they are nominal Catholics. Their You Tube channel is called "The Moran Family". They are about as far from LOLcows as you could get.

The Moran Family

Welcome to The Moran Family! My name is Brittany. I’m a stay a home mama. Married to my high school sweetheart, Benjamin. We have two beautiful girls, Laylah...

www.youtube.com

 

[A Detachable Penis]

So there's a small proportion of Downs cases that are inherited in a recessive manner (25% of it occurring). Now the challenge is to find some fundie parents who keep popping out the downs.

 

[The Husbando Collector]

So there's a small proportion of Downs cases that are inherited in a recessive manner (25% of it occurring). Now the challenge is to find some fundie parents who keep popping out the downs.

Start by narrowing down where the most inbreeding is and you'll find your answer.

 

[TheWhiteRabbit]

idk i get the sense that the mikayla girl was more of a burden. she reminded me of lola tbh.

it’s really hard for me to believe that she was normal like as normal as my baby, and then just became a potato to the likes of the hartleys? it’s so hard to imagine that scenario.

Her parents had her when they were still teenagers. The mom said that she kept noticing weird spasms McKayla was having when she was a few months old that eventually led to a diagnosis of lissencephaly. The family never tried to make her seem like she was anything more than she was & basically just kept her as comfortable as possible. The mom had to make videos explaining that McKayla wasn’t mentally a 10yo just in a broken body but a newborn in a 10yo’s body. People would cry in the comments that McKayla was left on a couch in a quiet, dim room & excluded from family activities. The mom again had to explain that laying on her couch in a quiet room is what was comfortable for her, explaining again that she didn’t have the mental function to process hardly anything. When McKayla died, people again bitched in the comments that she started giving McKayla’s things away too soon. Mom had to explain that the family was well aware that this would happen sooner or later & that they’ve basically grieved McKayla’s whole life for the child she would never be & the future she’d never have. I can’t stand the “mY KiD’s DiSaBiLiTy MaKeS tHeM sUpErHeRoEs NoT pOtAtOeS” type parents so seeing a parent with compassion yet a solid grip on reality like McKayla’s family was refreshing.

Another one I used to crack on but have changed my opinion of is Beth, the 5yo with severe Pfeiffer Syndrome (Beth’s Journey on fb) & her family. Her mom is pretty open about hating that Beth has special needs but loving her daughter.. if that makes sense. Beth is a happy, smart little girl who got dealt a bad hand with a fluke genetic defect but her family doesn’t seem to use that as a constant crutch. She’s overcome a lot & I think that’s mostly because her parents work with her & for the most part, don’t make excuses for her like the majority of special needs moms.

Edit: Sorry for the super late reply after others had already fully explained the situation. I haven’t been on here for a bit so I was playing catch up on the several pages I was behind.

 

[allthecheese]

Her parents had her when they were still teenagers. The mom said that she kept noticing weird spasms McKayla was having when she was a few months old that eventually led to a diagnosis of lissencephaly. The family never tried to make her seem like she was anything more than she was & basically just kept her as comfortable as possible. The mom had to make videos explaining that McKayla wasn’t mentally a 10yo just in a broken body but a newborn in a 10yo’s body. People would cry in the comments that McKayla was left on a couch in a quiet, dim room & excluded from family activities. The mom again had to explain that laying on her couch in a quiet room is what was comfortable for her, explaining again that she didn’t have the mental function to process hardly anything. When McKayla died, people again bitched in the comments that she started giving McKayla’s things away too soon. Mom had to explain that the family was well aware that this would happen sooner or later & that they’ve basically grieved McKayla’s whole life for the child she would never be & the future she’d never have. I can’t stand the “mY KiD’s DiSaBiLiTy MaKeS tHeM sUpErHeRoEs NoT pOtAtOeS” type parents so seeing a parent with compassion yet a solid grip on reality like McKayla’s family was refreshing.

Another one I used to crack on but have changed my opinion of is Beth, the 5yo with severe Pfeiffer Syndrome (Beth’s Journey on fb) & her family. Her mom is pretty open about hating that Beth has special needs but loving her daughter.. if that makes sense. Beth is a happy, smart little girl who got dealt a bad hand with a fluke genetic defect but her family doesn’t seem to use that as a constant crutch. She’s overcome a lot & I think that’s mostly because her parents work with her & for the most part, don’t make excuses for her like the majority of special needs moms.

Edit: Sorry for the super late reply after others had already fully explained the situation. I haven’t been on here for a bit so I was playing catch up on the several pages I was behind.

Heaven help you if the Spoonies or Munchies catch wind of a parent treating their kid like the baby they truly are mentally. They'll immediately equate their (fake) disabilities with the real ones, and say that they more accurately speak for the kid than the parents who have been caring for them their whole lives. The comment section on any article about growth attenuation is a hotbed for this. They'll insist the parents just haven't tried hard enough to communicate with their children, to get their authorization to do any surgery, that an expensive computer or eye gaze would magically unlock the voice that just must be in there because they say it is.

 

[Allo Vera]

This is a first for me - seeing a special needs fundie mama using her Instagram fame to promote a Kellogg’s product.

The child lying in the infant chair is six years old. Non-verbal, barely conscious in the majority of photos she posts. Has a lethal form of dwarfism: rhizomelic chondrodysplasia punctata.

 

[The Husbando Collector]

This is a first for me - seeing a special needs fundie mama using her Instagram fame to promote a Kellogg’s product.

The child lying in the infant chair is six years old. Non-verbal, barely conscious in the majority of photos she posts. Has a lethal form of dwarfism: rhizomelic chondrodysplasia punctata.

Yeah, because the thing that I want to think about while eating is a child trapped within their own deformed and slowly rotting body complete with what can be described as a soupy substance at best where the brain is supposed to be. Yeah, that sounds like a pleasant breakfast time thought.

 

[large_farva]

This is a first for me - seeing a special needs fundie mama using her Instagram fame to promote a Kellogg’s product.

The child lying in the infant chair is six years old. Non-verbal, barely conscious in the majority of photos she posts. Has a lethal form of dwarfism: rhizomelic chondrodysplasia punctata.

I was just about to post about this one, she baby talks to him constantly and it's a tad annoying, he looks about hartley level aware for the most part but smiles on occasion.
Another case of doctors telling someone their baby would be incompatible with life, only to be met with "in your face!, I'm making him survive because he is my warrior!"

 

[Allo Vera]

The funny thing about her is the endlessly sunny, positive way she writes about him. I mean, whatever gets you through the day I guess, but for the longest time I assumed he was of average intelligence and able to speak. But no. He’s severely mentally impaired, sleeps most of the time, suffers from seizures and is constantly in hospital with respiratory issues. He has enough awareness to smile but that’s about it.

 

[eternal dog mongler]

People would cry in the comments that McKayla was left on a couch in a quiet, dim room & excluded from family activities. The mom again had to explain that laying on her couch in a quiet room is what was comfortable for her, explaining again that she didn’t have the mental function to process hardly anything.

This is what annoys me the most.

Yes we have your non-verbal autistic son in physical restraints. He's fine and calm now. No, this is not medical abuse. He was trying to rip his Foley out.

People have very deep, emotional reactions to management of people who are different. Especially when it comes to kids.

 

[A Detachable Penis]

Another mother of a kid with rhizomelic chondrodysplasis punctata. This one writes a letter to the doctor who had the audacity to suggest hospice for what is usually a fatal diagnosis.

Like, congrats? As if doctors can magically know that your child lucked the fuck out with a less severe mutation or enough other genetic factors to protect against being dead. Especially for a rare disorder that may have not even had the genetic causes known when her daughter was born (a lot of disorders have recently had their mechanisms discovered due to better and cheaper genetic testing).

Also, from what I can gather, all the severe cases appear to be obvious in a fetus during ultrasound. The above case may not have been because it is less severe.

 

[Android raptor]

Looks like Sarah recently whined on a podcast about those evil pro-choice doctors that wanted her to abort her inside out baby. I haven't listened to it but I wouldn't be surprised if she's changed more details in the story like she's done in the past.

Still hasn't publically posted any pics of what the fucked up inside out baby looked like in full though (wonder why)

 

[WoofWoofDog]

I was just about to post about this one, she baby talks to him constantly and it's a tad annoying, he looks about hartley level aware for the most part but smiles on occasion.
Another case of doctors telling someone their baby would be incompatible with life, only to be met with "in your face!, I'm making him survive because he is my warrior!"

Yes! When Jude smiles it looks like he is seizing. So sick of all these parents saying their kids are "warriors" when the kids had no choice in the matter. Who would want to be having seizures all day?

another RDCP one is "Life Lessons with Jake & Jordyn" on Facebook. Mom and Dad have TWO kids with this condition. Like the Hartleys, they knew this was a possibility after it happened the first time.

 

[Extra Dainty Gorl]

Yes! When Jude smiles it looks like he is seizing. So sick of all these parents saying their kids are "warriors" when the kids had no choice in the matter. Who would want to be having seizures all day?

another RDCP one is "Life Lessons with Jake & Jordyn" on Facebook. Mom and Dad have TWO kids with this condition. Like the Hartleys, they knew this was a possibility after it happened the first time.

Correct me if I'm wrong here, but isn't there a 1 in 100k chance of it happening to start with? And generally happens in people with no known family history of it? So they probably thought "oh, we had one with it, so the next one/ones will have almost no chance of having it?"

I could be wrong, this is the result of hasty googling of it.

 

[WoofWoofDog]

Correct me if I'm wrong here, but isn't there a 1 in 100k chance of it happening to start with? And generally happens in people with no known family history of it? So they probably thought "oh, we had one with it, so the next one/ones will have almost no chance of having it?"

I could be wrong, this is the result of hasty googling of it.

This says the parents had a prenatal diagnosis with Jordyn, the younger one.

Meet Jordyn | Rhizo Kids Ohio

rhizokidsohio.com

 

[C@astrophica]

I was just about to post about this one, she baby talks to him constantly and it's a tad annoying, he looks about hartley level aware for the most part but smiles on occasion.
Another case of doctors telling someone their baby would be incompatible with life, only to be met with "in your face!, I'm making him survive because he is my warrior!"

She sounds like Miss Sally from Romper Room. She addresses Jude's "fan club" that way.

I feel so bad for the "rhizo kids," most of them look like little broken dolls. Apparently this condition causes painful joint contractures among other horrible things.

I don't think it's easy to detect in utero because it's so rare. All they can usually tell you is that the baby is measuring small. So I don't blame the parents for carrying to term because they don't know what is in store for their poor child. I do have a problem with all the heroic treatments some parents put their "warriors" through.

 

[large_farva]

She sounds like Miss Sally from Romper Room. She addresses Jude's "fan club" that way.

I feel so bad for the "rhizo kids," most of them look like little broken dolls. Apparently this condition causes painful joint contractures among other horrible things.

I don't think it's easy to detect in utero because it's so rare. All they can usually tell you is that the baby is measuring small. So I don't blame the parents for carrying to term because they don't know what is in store for their poor child. I do have a problem with all the heroic treatments some parents put their "warriors" through.

they knew in utero that the fetus had severe skeletal dysplasia and would likely be incompatible with life, they chose life - a life of agony