- Joined
- Mar 23, 2019
No discussion about tard babies can be complete without McKenna Rayne!

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No discussion about tard babies can be complete without McKenna Rayne!
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No discussion about tard babies can be complete without McKenna Rayne!
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Oh wait, yes I can, Michael Manuel first posted in this thread back in 2017 is still alive and just turned five.
It depends on how severe it is. Babies with the alobar (brain completely fails to separate) are pretty much doomed to a life of potato-dom. Babies with the semilobar (only partially separated) and lobar (mostly separated except a few areas) may have better outcomes.Thank god that baby only lived to 15 months. I can’t imagine what the horror of a child with holoprosencephaly would be like if it lived for years
It depends on how severe it is. Babies with the alobar (brain completely fails to separate) are pretty much doomed to a life of potato-dom. Babies with the semilobar (only partially separated) and lobar (mostly separated except a few areas) may have better outcomes.
Is the most severe forms of holoprosencephaly what makes those horrifying cyclops fetuses that are either stillborn or die short after birth?
A little powerleveling, but my parents were acquainted with a woman that ended up having to fly to Sweden to get an abortion after she had taken Thalidomide.Most alobar are stillborn or die shortly after birth. I think the survival rate past one week is 5 %. Semilobar and lobar are both devastating and there really aren’t good outcomes. The “less severe” end of horoprosencephaly is facial deformities, severe mental exceptionalism and life threatening seizures. There outcomes for all forms of horoprosencephaly are terrible and horrifying. It’s a classic “not compatible with life” birth defect.
Yep, this is the condition the cyclops babies have. Thankfully this is a relatively rare and severe form of it.
One was born in September in Indonesia. The doctors believed it was caused by mercury exposure and the rubella virus.
(Getting rubella during early pregnancy causes devestating birth defects. A rubella outbreak in the 1964 is actually one of the big factors that led to Roe v Wade decision. Rational people understood the need for abortion when facing catastrophic birth defects. )
It's far more varied than you thinkMost alobar are stillborn or die shortly after birth. I think the survival rate past one week is 5 %. Semilobar and lobar are both devastating and there really aren’t good outcomes. The “less severe” end of horoprosencephaly is facial deformities, severe mental exceptionalism and life threatening seizures. There outcomes for all forms of horoprosencephaly are terrible and horrifying. It’s a classic “not compatible with life” birth defect.
That picture is a better argument for abortion (especially late term abortion for situations like this) than anything I could ever come up with. I'm tempted to show my parents that picture because they constantly tell me how awful it is that people can have late term abortions, yet they don't seem to understand that most of those are for situations like that poor child in the picture.Those videos are nothing but a modern day version of a circus side show. The video with the extremely premature fetus named ''Heavenly'' said she died from Alobar holoprosencephaly. There are several types of holoprosencephaly and alobar is the most severe kind. Mathew Nel has semi-lobar holoprosencephaly, which isnt as bad as the alobar type , yet he's still extremely physically malformed and developmentally disabled, so imagine what the absolute worst form of the condition looks like. Nearly every fetus that has it dies before birth, but some live longer than Heavenly did , which brings to light the full horror of the condition. If you think an extremely premature fetus looks grotesque, then you should see what happens when a fetus with lobar holoprosencephaly gets to or near full term. They are nightmares made flesh. It was fortunate for all involved that the baby in that video didn't live. .
What these parents don't realize is babies that severely effected aren't supposed to be born, which is why most end in miscarriages and still births. Nature generally corrects its mistakes, but some stay just outside that border that makes a condition totally incompatible with life, and with the aid of modern medicine, instead of dying in the womb, these kids get to be born to lives of non sentience at best and severe misery at worst. Then their parents and other assorted fundies put these unfortunates on display and call them ''miracles.''
Children like Jaxon Buell, the Hartley sisters and Mathew Nel are basically errors that got past nature's editing tool. They aren't miracles... they are biological typos.
It's far more varied than you think
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It’s a classic “not compatible with life” birth defect.
Thank god that baby only lived to 15 months. I can’t imagine what the horror of a child with holoprosencephaly would be like if it lived for years....Oh wait, yes I can, Michael Manuel first posted in this thread back in 2017 is still alive and just turned five.
His parents spend their days in the garage they turned into an home ICU, using vibrating machines on him and running his oxygen while their gift from god lays inertly, unfocused eyes staring off into space. The birthday video the father makes is just sad, he’s really struggling to put on the blessed brave face after five years. It’s extra tragic because they seem like really nice, but terribly misguided religious folk.
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Kayli's Krusade
Kayli's Krusade. 10,416 likes · 22 talking about this. Kayli was diagnosed prenatally with Trisomy 18 (Edward's Syndrome). Kayli's Krusade is to change the worthless label attached to Trisomy! You...facebook.com
As requested in the Hartley Hooligans thread: The Kayli's Krusade page is where the mom claims they are a family of 10. Did they magically spawn four more children? Or does Mommy like lying?
A comment on the skydiving (lol) video also implies Kayli was born in 2005 according to some old blog post. So, I wouldn't put it past Krazy Kelly Whistler to lie about a lot of shit.
View attachment 720963
People who willfully keep sad flesh prisons like this alive should absolutely not receive government benefits, kickbacks or other forms of welfare. You're taking away from actual people with brains in need of medical care or housing or food stamps to sustain what's essentially a corpse with a heartbeat. You choose to keep your abomination, so pay for it.
I'm willing to bet lots of Jesus freaks wouldn't keep their Little Miracles if they didn't get government nurses and respite care!
Someone needs to put Kayli out of her misery.
His mother appears absolutely exhausted. That look she gives the camera is one of desperation and hopelessness. Whilst proud papa wanders around making movies and murmering the usual fundie bollocks.
But it is somehow "God's miracle" when you're able to keep one of these monsters alive via extremely expensive heroic medical interventions that deprive normal babies of limited resources.
So their fucking tard babies get kept alive at vast expense while real babies who have an actual future get raped out of their future to pay for some fucking tard baby.
I like how much we've evolved as a society. (/sneed) Now horribly deformed children with questionable quality of life are seen as gifts from God as opposed to the 1600s where the mother and father would be accused of witchcraft and burned at the stake for consorting with Satan and giving birth to a devil's child.Why? Why did they defy God so much?
God wanted these creatures to die.
?TFW it looks right at you
Some of those 8 miracles sound an awful lot like mbp on the mothers part . How does this child keep ending up with such drastic medication overdoses , botched procedures and other disasters ?![]()
Kayli's Krusade
Kayli's Krusade. 10,416 likes · 22 talking about this. Kayli was diagnosed prenatally with Trisomy 18 (Edward's Syndrome). Kayli's Krusade is to change the worthless label attached to Trisomy! You...facebook.com
As requested in the Hartley Hooligans thread: The Kayli's Krusade page is where the mom claims they are a family of 10. Did they magically spawn four more children? Or does Mommy like lying?
A comment on the skydiving (lol) video also implies Kayli was born in 2005 according to some old blog post. So, I wouldn't put it past Krazy Kelly Whistler to lie about a lot of shit.
View attachment 720963
People who willfully keep sad flesh prisons like this alive should absolutely not receive government benefits, kickbacks or other forms of welfare. You're taking away from actual people with brains in need of medical care or housing or food stamps to sustain what's essentially a corpse with a heartbeat. You choose to keep your abomination, so pay for it.
I'm willing to bet lots of Jesus freaks wouldn't keep their Little Miracles if they didn't get government nurses and respite care!
Someone needs to put Kayli out of her misery.
There’s zero chance they’re paying out of pocket for anything. If the government isn’t giving it to them, some church is.This video is cursed, forward to ten friends or you will die in seven days.
It looks like the poor child Schiavo-ed at 4 months, and lost the majority of her brain after a heart attack. I know the mother is steeped in denial, but it's dishonest to claim that doctors won't treat the child because of a chromosomal disorder. The kid is a vegetable. I hope they're paying OOP for most of this.