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

There’s some really interesting language in that article. Does this mean that Texas or Medicaid is tired of paying millions of dollars for a dead baby? Let’s see what the shit-for-brains mother has to say, shall we...
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Her Facebook account:
https://www.facebook.com/trinity.lewis.3551

Another FB account set up for Tinslee:
https://www.facebook.com/Tinslee-strong-104920111197389/

I really didn’t have time to dig around, but it’s very interesting to me that no new pictures have been posted of this thriving, “sassy” child. I mean, at least try to prove us wrong?

Anyway, here’s some random tidbits:
-I have no idea why she’s using the last name “Keaun”, but she does have another daughter named Tylee.
-Trinity’s sister is “Syme Lewis” on FB (her actual name is Symphony...no, really), age 24, has kids with a guy named Darius Harris.
-Another relative (possible sister) is Deme Reed (short for Demetra).

Who really cares about millions of dollars in hospital bills when you need that Louis Vuitton phone case, amirite?
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That baby has been on life support for so long that she's totally gorked. Look at her eyes. There's nothing there anymore.
 
Tinlee's mom is mad about reporters using her pics of the child she's torturing
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she looks like she's having a seizure in the video but I know dick all about that shit so medfagging is encouraged. Archive hates video apparently and I'm on my phone so if someone else can grab the video that would be nice as well.
 
Tinlee's mom is mad about reporters using her pics of the child she's torturing
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she looks like she's having a seizure in the video but I know dick all about that shit so medfagging is encouraged. Archive hates video apparently and I'm on my phone so if someone else can grab the video that would be nice as well.
Archive of Video:


Unsure if its a seizure but its definitely not coordinated movement.
 
The fundies that spout about DS being "survivable" only showcase the smiling babies and the high functioning adults that are able to work and play sports. They don't show the ones with severe heart defects that die before they are a year old, the nonverbal ones that are basically hormonal toddlers in adult bodies, or the ones that will still need constant care if they live longer than their parents.

and the ones with dementia.
 
and the ones with dementia.
More than 75% of people with DS will be diagnosed with dementia by age 65.

I knew someone with Down syndrome who is incredibly high functioning (she actually completed an associate's degree and lives independently with her boyfriend, who also has DS). The thing her family worries about most is dementia, because she's definitely capable of understanding that it is a possibility. She knows that it happens to a lot of people with DS, she's seen it happen to her friends, and she knows that if/when it happens to her, she won't be able to live by herself or work anymore. She actually wrote on Facebook pretty frequently about being an adult with DS and what her concerns were. We're out of touch these days but I'd love to know what she thinks of the anti-abortion bills. She was born in the mid-70s, before prenatal diagnosis was a thing. Her mom was in her 20s and went on to have two healthy children.

The unpleasant effects of Down syndrome don't end because a baby is born without a heart defect or ends up with better intellectual function than others with the same diagnosis. You can have the best possible outcome of anyone with Down syndrome, and it still shits on you in the end.
 
More than 75% of people with DS will be diagnosed with dementia by age 65.

I knew someone with Down syndrome who is incredibly high functioning (she actually completed an associate's degree and lives independently with her boyfriend, who also has DS). The thing her family worries about most is dementia, because she's definitely capable of understanding that it is a possibility. She knows that it happens to a lot of people with DS, she's seen it happen to her friends, and she knows that if/when it happens to her, she won't be able to live by herself or work anymore. She actually wrote on Facebook pretty frequently about being an adult with DS and what her concerns were. We're out of touch these days but I'd love to know what she thinks of the anti-abortion bills. She was born in the mid-70s, before prenatal diagnosis was a thing. Her mom was in her 20s and went on to have two healthy children.

The unpleasant effects of Down syndrome don't end because a baby is born without a heart defect or ends up with better intellectual function than others with the same diagnosis. You can have the best possible outcome of anyone with Down syndrome, and it still shits on you in the end.

I work in geriatrics, specifically in Alzheimer’s and Dementia care. I have seen people who one year ago were classified as early stage and now they’re so far gone they aren’t returning to the program I work at.

it is very sad because it doesn’t discriminate. Doctor, lawyer, nurse, teachers, engineers. It doesn’t matter.
 
Imagine how many actual living children could be taken care of with that $24,000,000. Welfare, food stamps, school funding, hell, funding for kids in foster care. Anything would be better than wasting money on such a cruel science experiment, keeping this terminally ill baby alive and in pain just because her mother is in complete fucking denial.
 
I work in geriatrics, specifically in Alzheimer’s and Dementia care. I have seen people who one year ago were classified as early stage and now they’re so far gone they aren’t returning to the program I work at.

it is very sad because it doesn’t discriminate. Doctor, lawyer, nurse, teachers, engineers. It doesn’t matter.
Yup. Any traditional cases of DS, where chromosome 21 is fully duplicated, have an extra copy of the gene APP, amyloid precursor protein. Cleavage of this protein gives you beta amyloid oligomers, some of which are insoluble and your body gotta do a lot of extra shit to try and get rid of those. Any small disfunction in clearance or cleavage is now even worse cause there's an extra copy of APP. Failing to get rid of the insoluble chunks is how you get beta amyloid plaques characteristic to Alzheimer's.

And the ones who don't get dementia either have protective alleles compensating or don't have full duplication of chromosome 21 and thus only have the usual copy number for APP.

Wait shit why aren't we using Downies to test drugs on the earliest stages of Alzheimer's?! One of the major reasons drug trials are likely failing is because by the time symptoms show up, it's too late to significantly prevent or reverse the cascading dysfunction. We literally can quickly see whether they have full trisomies with easy karyotyping, know precisely the causal agent at play (gene dosage of APP), and could even take the time to screen against other genes/alleles at play. This is literally perfect I am mad now.
 
Yup. Any traditional cases of DS, where chromosome 21 is fully duplicated, have an extra copy of the gene APP, amyloid precursor protein. Cleavage of this protein gives you beta amyloid oligomers, some of which are insoluble and your body gotta do a lot of extra shit to try and get rid of those. Any small disfunction in clearance or cleavage is now even worse cause there's an extra copy of APP. Failing to get rid of the insoluble chunks is how you get beta amyloid plaques characteristic to Alzheimer's.

And the ones who don't get dementia either have protective alleles compensating or don't have full duplication of chromosome 21 and thus only have the usual copy number for APP.

Wait shit why aren't we using Downies to test drugs on the earliest stages of Alzheimer's?! One of the major reasons drug trials are likely failing is because by the time symptoms show up, it's too late to significantly prevent or reverse the cascading dysfunction. We literally can quickly see whether they have full trisomies with easy karyotyping, know precisely the causal agent at play (gene dosage of APP), and could even take the time to screen against other genes/alleles at play. This is literally perfect I am mad now.
It's a great idea, Dr. Mengele, but good luck getting any IRB outside of like, North Korea to sign off on using disabled people for research subjects.

I'm just giving you shit, of course, but there are always Appswe transgenic mice! Bonus: they're cute little buggers.
 
A rubella outbreak was what changed the tide of American public opinion on abortion, because suddenly so many women were having severely disabled babies. I wonder what would happen if we had a similar virus now in the US. (Rubella is mild in adults).
 
A rubella outbreak was what changed the tide of American public opinion on abortion, because suddenly so many women were having severely disabled babies. I wonder what would happen if we had a similar virus now in the US. (Rubella is mild in adults).
Gene Tierney caught rubella from a fan while she was pregnant and her daughter was born premature and severely disabled if I recall correctly.
 
Fuck, Tinslee's mom is really shaping up to be mama Nails 2.0. Though at least Jahi was dead and incapable of suffering.

Tinslee and Luna are the tard babies that make me the most MOTI. Tinslee's mom might not be at fault for fucking her kid up like Robyn is, but forcing her to keep suffering is sociopathic. I really hope she just dies in her sleep or something soon, she's been hurting long enough :(
They don't even fucking visit her, the worthless scum.
 
You don't put a child as old as Luna in a helmet, so I'm guessing this was some time ago. I hear you on being half asleep.

"They are stackable for space efficiency"
Hahahahha

Yup. Any traditional cases of DS, where chromosome 21 is fully duplicated, have an extra copy of the gene APP, amyloid precursor protein. Cleavage of this protein gives you beta amyloid oligomers, some of which are insoluble and your body gotta do a lot of extra shit to try and get rid of those. Any small disfunction in clearance or cleavage is now even worse cause there's an extra copy of APP. Failing to get rid of the insoluble chunks is how you get beta amyloid plaques characteristic to Alzheimer's.

And the ones who don't get dementia either have protective alleles compensating or don't have full duplication of chromosome 21 and thus only have the usual copy number for APP.

Wait shit why aren't we using Downies to test drugs on the earliest stages of Alzheimer's?! One of the major reasons drug trials are likely failing is because by the time symptoms show up, it's too late to significantly prevent or reverse the cascading dysfunction. We literally can quickly see whether they have full trisomies with easy karyotyping, know precisely the causal agent at play (gene dosage of APP), and could even take the time to screen against other genes/alleles at play. This is literally perfect I am mad now.
We can't afford more Alzheimer's research because our system spends so much on keeping dead people "alive". 24 million bucks?
 
Gene Tierney caught rubella from a fan while she was pregnant and her daughter was born premature and severely disabled if I recall correctly.
I believe someone posted an article in this thread quite a while ago about a mother whose now-adult daughter is profoundly disabled as a result of congenital rubella syndrome. She was born prior to Roe, and her mom has become a crusader for abortion rights. Obviously, she can't do anything to help her daughter, who is institutionalized and doesn't recognize her, but she believes she can help prevent other kids from similar suffering. It was a sobering read.
 
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