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

[large_farva]

K-Lee’s brother looks so fucking done with this shit, poor kid.

It could be because of the meat puppet lil sis, OR that he had a brain tumor mom refused to treat.

Found this:



From the post:

As for my son, we didn't find a hospital that could cure him. He had a rare large tumor in his Pons and Medula of the brain stem, and deep in his Cerebellum. He was too young for radiation. The tumor would 100% cause death if attempted to be removed because of the location. The craniotomy and biopsy were high risks. We were told chemo was the only option. We aren't against medications and have about 20 physicians and great medical teams we regularly consult with for all our family medical conditions, but we prefer to weigh options and consider all including natural remedies. We refused to listen to the big pharma propaganda in part because doing our own research we found out IF our son survived chemo, he had a 50/50 % chance of being sterile. We found another option. We chose to tell our son Jesus loves him more than we do. We heard the neurosurgeons, but didn't believe in them like we believed in Jesus. Without any pharmaceutical or surgical interventions, our son's large rare cancerous tumor stopped growing. 6 years later his character, balance, cognitive, etc showed symptoms of change. The MRI showed a change in density and color. Again we were pressured and told pharmaceuticals were the only option. We demanded another biopsy saying God already granted the miracle and wouldn't take that away. The biopsy showed the once large, rare, Gangliaglioma tumor, is morphing into abnormal brain tissue. Without any drugs but with God's natural remedies, preventions, and our faith, this year our son celebrated his 13th birthday here on earth with us, cancer free. Instead of giving to and promoting the big pharma driven entities, pease find a personal way to help all children in this drug infected, chemically altered world. Hug more, eat pure, plant trees, listen to others, spread hope, give testimony, share your soul, lean on Jesus instead of fearing death, and never give up!

Panera Bread celebrates partnership with Make-A-Wish Foundation

Meet Claudia, an 8-year-girl from Geneva who has a rare anemia. She loves to dance, likes to play with her pets and wants to go to Auckland Zoo in New Zealand. With help from customers at the Panera Bread on East Main Street in St. Charles, her wish will likely come true.

www.kcchronicle.com

archive

The Whistler family, formerly of St. Charles, traveled to Disney World, Sea World, Discovery Cove and Universal Studios – a wish the foundation granted for Nicholas “Niko” Whistler, his mother Kelly Whistler said.

“It was the best thing we’ve ever done,” she said.

Niko, 4, was diagnosed with an inoperable brain tumor at age 2, Whistler said. Because his three siblings are also disabled with rare diseases, she said, she and her husband often lived in “survival mode” and lived like single parents as they took turns at the hospital and at home.

She said the Make-A-Wish vacation helped them forget about doctor appointments and let them remember how to laugh, play and be a family.

Three siblings who are also disabled? This needs a closer look and much archiving before mom decides to DFE

the blog
mom's twitter - it's already private

Our Family of Special Needs, a Special Love

A blog about Kayli Whistler, who was born with Trisomy 18 (Edward's Syndrome).

trisomy18.blogspot.com

archive

Our oldest has Degenerative Disc Disease and has had 5 spine surgeries since he first broke his back (during a baseball game) when he was 14. He had MRSA, a staph infection resistant to antibiotics, in his spine and is allergic to the two antibiotics proven to fight MRSA....We almost lost him. God took control.

Our middle son has Autism (high functioning), ADHD (severe), Sensory Integration Disorder (doesn't feel pain), and EOE (allergic esophagitis). There is no cure, nor treatment for the EOE. It is enzymes deteriating his esophagus and causing scarring (high risk of cancer).

Our youngest son has an inoperable brain tumor in 2 parts of his brain stem (pons and medulla) and deep in his Cerebellum. He was diagnosed with Gangliaglioma (cancer) by CHOP, the Dean at Loyola, and many other reputable hospitals. He was too young for radiation, and it was inoperable (shape, location) so we put a port in and waited for it to grow more aggressively so we could treat ALL the cancer cells (it was thought to be our only hope!) The cancer grew slowly for about 6 months...then stopped! God has given us another miracle! The tumor is still there, but remains stable/not growing. Inexplicable in the medical world, but a miracle in our world!

so many miracles - let us archive all of them.

 

[Trombonista]

so many miracles - let us archive all of them.

This is now the official motto of this thread.

 

[sperginity]

ig: lilyslittlelungs
this baby isn’t exactly a “tard” but this mom PISSES me off. she goes on and on in just about every other post how much PAIN and trauma her baby had to go through just to keep her alive. one post she was doped up with morphine and fentanyl which she needed around the clock, because at only a few months old would try to RIP her tubing out because she was in pain. apparently the kid lived completely doped up for a long time, and the mom doesn’t let u forget it. someone asked a question how she decided to let her daughter live in such pain, and she rudely replied, which i’ve seen her do to quite a few people, especially other moms in similar situations looking for a bit of support or kind words from someone who has gone through it and she will barely reply with just a thank you, if that. she also loves to hashtag her posts with tons of little trophy tags, making it like a special badge, the more fucked up her kid is the more tags she can slap on there and show off, like it’s a fucking good thing??? searching some of those tags on ig, u find a lotttttttt of these moms, it’s a black hole. i can’t imagine having a baby hauling around all that damn tubing every single day. that is no way to live.

that kind of care taking probably fucked up her brain and mood permanently. It isn't anyone else's problem, but she might not have been as awful without the experience of the kid. I have a hard time getting mad at people who are probably just broken rather than purposely shitty (although there is of course room for both of those things in one person).

 

[Android raptor]

Personally I take a lot of the shit Kayli's mom says with a grain of salt when it comes to the maladies her kids supposedly have. She has huge munchie vibes IMO, like I think theres definitely something to the idea that's she's a longtime munchie that basically won the munchie lotto with Kayli.

And yeah I wouldn't doubt the boy is miserable. The only time his mom seems to acknowledge him is when she's going on about his supposed medical issues. Even Gwen mentioned Cal and his accomplishments occasionally.

If one of Kayli's siblings ends up putting a pillow over her head I can't say I'd completely blame them.

 

[Allo Vera]

ig: lilyslittlelungs
this baby isn’t exactly a “tard” but this mom PISSES me off. she goes on and on in just about every other post how much PAIN and trauma her baby had to go through just to keep her alive. one post she was doped up with morphine and fentanyl which she needed around the clock, because at only a few months old would try to RIP her tubing out because she was in pain. apparently the kid lived completely doped up for a long time, and the mom doesn’t let u forget it. someone asked a question how she decided to let her daughter live in such pain, and she rudely replied, which i’ve seen her do to quite a few people, especially other moms in similar situations looking for a bit of support or kind words from someone who has gone through it and she will barely reply with just a thank you, if that. she also loves to hashtag her posts with tons of little trophy tags, making it like a special badge, the more fucked up her kid is the more tags she can slap on there and show off, like it’s a fucking good thing??? searching some of those tags on ig, u find a lotttttttt of these moms, it’s a black hole. i can’t imagine having a baby hauling around all that damn tubing every single day. that is no way to live.

Neonatal care has come so far in the last 20-30 years but this baby is proof that, sometimes, it goes too far. This little girl would have died if she’d been born a generation ago. Instead, she gets to live a short life permanently attached to a machine. There are worse things than death, I really believe that.

 

[bigfart420666]

Neonatal care has come so far in the last 20-30 years but this baby is proof that, sometimes, it goes too far. This little girl would have died if she’d been born a generation ago. Instead, she gets to live a short life permanently attached to a machine. There are worse things than death, I really believe that.

i agree i feel bad for the poor baby. looking at her older posts when she was hospitalized the poor thing was absolutely miserable. and i don’t think she’s really mentally slow, so she knows what’s going on. it’s broke my heart a little bit and i just hope she’s a happy little girl like she seems to be in the moms pictures.

 

[Android raptor]

Isn't there also a baby in Texas that has some horrible, painful condition that even the medical personnel think should be allowed to pass? The one that the mom was legally fighting to keep hooked up and revived daily?

At least with the potatoes and anencephaly zombabies they can't feel much or any pain. Keeping a kid that can feel pain alive like that seems like a form of torture.

 

[bigfart420666]

bro.

 

[John Merston]

bro.

En Inglés, por favor.

 

[Daughter of Cernunnos]

Trisomy 18, Edward's Syndrome, causes severe to profound mental exceptionalism (among other things), so at best she's profoundly disabled with very limited mental function. At worst she's a vegetable to due the whole "without oxygen for 30+ minutes during a heart attack" thing back when she was a few months old. Even if she was to be "only" severely disabled the loss of mental function wasn't that great.


You just know the district can't wait for Kayli to finally die so they can be free from her cursed mother. Sadly, those thousands of dollars are cheaper than a lawsuit and less damaging than negative reputation that she could whip up with her followers.

"WITHOUT OXYGEN FOR 30 PLUS MINUTES AFTER A HEART ATTACK" THING! That is a hilarious way to put it and really shows how beyond delusional corpse parents are.

if you want nightmares tonight

Spoiler: NSFL

this is "talking"
View attachment 1252750

mom's voice is creepier than kayli
View attachment 1252752
There's more life in the beach ball

More life in the microbiota of the shit she's contaminating the pool with. She sounds like she's farting through her throat when she "talks".

I don't believe a word of that story. It's just too perfect. Poor me, pity me. Not to mention it's been posted elsewhere,. And even if it is true, surely when he was an infant, they could've given him just palliative care, instead of putting him on all those machines?

I remember when that was posted and it seems to have went viral. I totally agree. It sounds so fanficy to me. Like the person got passionate about the issue and wanted to influence others or society itself with legal reform. It's not just the feminists and SJW redditors that are retarded but they have a similar style of writing, histrionic, fake stories and capitalizing off whatever happens to be popular on that site atm.

ig: lilyslittlelungs
this baby isn’t exactly a “tard” but this mom PISSES me off. she goes on and on in just about every other post how much PAIN and trauma her baby had to go through just to keep her alive. one post she was doped up with morphine and fentanyl which she needed around the clock, because at only a few months old would try to RIP her tubing out because she was in pain. apparently the kid lived completely doped up for a long time, and the mom doesn’t let u forget it. someone asked a question how she decided to let her daughter live in such pain, and she rudely replied, which i’ve seen her do to quite a few people, especially other moms in similar situations looking for a bit of support or kind words from someone who has gone through it and she will barely reply with just a thank you, if that. she also loves to hashtag her posts with tons of little trophy tags, making it like a special badge, the more fucked up her kid is the more tags she can slap on there and show off, like it’s a fucking good thing??? searching some of those tags on ig, u find a lotttttttt of these moms, it’s a black hole. i can’t imagine having a baby hauling around all that damn tubing every single day. that is no way to live.

The baby is adorable. Her head his shaped wrong but she's not repellent to look at like Kayli, Lola, Clare etc. Maybe the mom has sadistic or munchie tendencies if she's that into bringing attention to the pain she let her daughter suffer.

bro.

lmao zika-wino tard baby.

 

[Opabinia]

bro.

That's the biggest Cabbage Patch Kid I've ever seen.

 

[large_farva]

Isn't there also a baby in Texas that has some horrible, painful condition that even the medical personnel think should be allowed to pass? The one that the mom was legally fighting to keep hooked up and revived daily?

At least with the potatoes and anencephaly zombabies they can't feel much or any pain. Keeping a kid that can feel pain alive like that seems like a form of torture.

That was Tinslee Lewis. I can't find anything. Mom's facebook profile is locked down, no groups or pages from the looks of it, some scattered posts sharing the same articles from early this year.
If she died, they didn't even post an obit, if she's still alive, mom's not inviting attention via social media.

 

[A Detachable Penis]

bro.

When real life mimics parody.

 

[Android raptor]

It's old but I came across this post where Kayli's mom whines about how not every medical personnel goes above and beyond to cater to her and keep her tater alive. Only God can decide how long Kayli lives, so apparently that means she needs to be artificially kept alive with modern medical technology as long as humanly possible.

It's been said a lot but we really need a Kayli thread.

 

[large_farva]

Getting into moms blog here's a few early takeaways-

Kelly believed Kayli was actually potty training
Until they finally realized it was a result of her fucked up anatomy.

-All links are archived in the link at the end-

http://trisomy18.blogspot.com/2013/01/our-miracle-girl-is-potty-training-and.html

I put her on her bathroom toilet. Within 2 minutes, she stooled and peed in the toilet!!! She is Amazing!!! I cheered for her, and she smiled! I told her what a big girl she is! More smiles!! Kayli never ceases to amaze me.... 32 minutes without oxygen and not only did she survive, but now she is potty training! WOW!!! Thank You God!!!

http://trisomy18.blogspot.com/2013/01/potty-training-doesnt-stop-at-home.html

I told the nurse how she is wanting to go on the big girl potty now at home. I told the nurse I could try putting her on the toilet here, to see if that was why she wasn't pooping in the hospital. Within 2 minutes of sitting her on the big girl potty, she peed, then pooped! lol I asked her if she was done, and she sighed out of her trach (meaning she has something to say). I waited, then asked her if she wanted to stay on the potty and she didn't sigh, just stared at me. I waited, then again asked her if she wanted to get off the potty....another sigh. Kayli is treading beyond anywhere we ever imagined she could!

Updates: Potty Training, Ketogenic Diet, Surgery in the morning

A blog about Kayli Whistler, who was born with Trisomy 18 (Edward's Syndrome).

trisomy18.blogspot.com

At least once a day, she is put on her toilet and within 2 minutes she goes on the big girl potty! This is a HUGE accomplishment, we never thought Kayli would be capable of doing!

Summary of Kayli's current medical challenges

A blog about Kayli Whistler, who was born with Trisomy 18 (Edward's Syndrome).

trisomy18.blogspot.com

Kayli's bladder was pushing organs out of placement, and sitting on her arteries. This caused stress on her heart, and pushed her into de-compensated heart failure.

All of this and more are archived at: https://web.archive.org/web/20190803023745/http://trisomy18.blogspot.com/
There are multiple examples of mom being a tyrant to doctors and nurses, constantly lording over them that she knows best for her tater.

 

[C@astrophica]

bro.

I assume this is another holoprosencephaly case? That would explain the cabbage patch doll head.

Most of the more severely affected children develop into inert meatsacks once they get past infancy. They have no muscle tone, and they're either brain dead or doped up on phenobarbital to prevent them from having 100+ seizures a day. Some of them have trachs. I have no idea why tracheostomies on these human husks are not considered a major breach of medical ethics.

 

[Toohottotrot]

Most of the more severely affected children develop into inert meatsacks once they get past infancy. They have no muscle tone, and they're either brain dead or doped up on phenobarbital to prevent them from having 100+ seizures a day. Some of them have trachs. I have no idea why tracheostomies on these human husks are not considered a major breach of medical ethics.

Because it would be unethical not too. And Its a way of stopping the countless prolifeers from ending your career because you trying to do what was right

 

[I hate children?]

I used to think Kelly was bonkers from grief but her blog seems to be a lot of bizarre lies to gain attention and con people into believing Kayli has a legitimate need for the expensive things they beg for . She learned really early to target fundies by claiming Kayli was reserected from the dead after she "passed away" for 32 minutes as well as making a big recovery from being dead for 33 minutes. I wish to hell I was joking about the "passing away" part but Kelly has posted on several sites saying Kayli passed away for half an hour and brought herself back to life and is recovering from being anoxic 32 minutes.

Some of Kelly's most outrageous stories include Kayli's cleft palate healing on it's own . Of course she made a point of saying it is unheard in anyone else but Kayli did it with the help of Jesus .

There is also some bullshit about Kayli having out of body experiences to visit other people and a metric ton of other garbage that makes Gwen look sane which is a hard task.

 

[Toohottotrot]

Her clerf plata fixed Itself but her clubfeet didn't and when surgerically corrected go back to there old position and the insurance company keeps paying for more

 

[WarpedTourWasFun]

The most recent article I've found on Tinslee Lewis was from the beginning of March, and it wasn't really about her, it was about the nurses caring for her and how emotionally difficult it was to care for her. The hospital has been having to provide therapy for the staff caring for her.