- Joined
- Mar 2, 2021
Humans have done quite alot to derail "Survival of the fittest." How else do you explain the vast increase of retards and uggos.
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The only cases of this I can find are for complete DiGeorge Syndrome where they are born with no thymus at all.It's been awhile since I checked up on "gods brave little warrior Silas" and sure enough, he's still kicking. Well, not kicking but he's still breathing. They're talking about doing a thymus transplant, and to me , it's seems to be a sketchy sign when only one medical place does it. I sure wouldn't want to be doing it if I was a doctor, I'd rather do it on a child with a normal rate of recovery, rather than not be able to show any signs whatsoever.
He made it to six months, and his head is slowly forming a heart shape. Soon him and Luna can have mental playdates.
I’m betting there’s surgeons who’re studying how to fix his jaw. Are they going to break it, or are they going to go with a full replacement of it? I’d be worried about the muscles, but giving him the ability to close and open a jaw would be an immense help for him I feel. It might be a bit tricky to speak for a while for him though. My guess is the reconstruction surgeries are waiting until he’s stopped physically growing.It's so surreal to hear that clear and normal voice to that severely messed up face. What a trooper though, it really is amazing just to have survived that, let alone being able to still get so much out of life afterwards.
Yes it was. It had grown enough to disrupt the valves, from the R atrium. It was very solid, more so than the heart muscle in rigor. Irregular boundaries and deformation of the chordae.It's okay if you can't answer this, but I'm intrigued. Was it an angiosarcoma? What was the tumor like histologically?
People think DS is all smiling tards and it is not. My childhood acquaintance (of "I'm not retarded, I have Down syndrome, asshole!" fame) is very high functioning and lived in fear of developing dementia. It's really sad, because her family couldn't exactly lie to her and say it wouldn't happen, because she knew it could. There's no way to know if it will happen to her, and if it does, she understands what will happen. It's terrible.
I have definitely heard of people with DS, and other mental disabilities, getting organ transplants, BUT like "normal" people, they have to have stable housing, a support network, and understand what's happening to them.Yes it was. It had grown enough to disrupt the valves, from the R atrium. It was very solid, more so than the heart muscle in rigor. Irregular boundaries and deformation of the chordae.
The girl apparently was high functioning- she was well groomed and had been at the hospital for some time, I think they were attempting some treatment. There was a previous surgery with scars on the heart apparent but it failed to remove the entirety of the cancer or stop its growth. I don't think they place DS people on the transplant list, but I could be incorrect.
It was a truly bizarre thing to see.
That and he might be iffy to try anything to risky/extreme. I'd imagine for a lot of people with severe deformities who are always gonna look fucked, your main priority would be on keeping at least the functionality you have and trying to enjoy life.I’m betting there’s surgeons who’re studying how to fix his jaw. Are they going to break it, or are they going to go with a full replacement of it? I’d be worried about the muscles, but giving him the ability to close and open a jaw would be an immense help for him I feel. It might be a bit tricky to speak for a while for him though. My guess is the reconstruction surgeries are waiting until he’s stopped physically growing.
Yes it was. It had grown enough to disrupt the valves, from the R atrium. It was very solid, more so than the heart muscle in rigor. Irregular boundaries and deformation of the chordae.
The girl apparently was high functioning- she was well groomed and had been at the hospital for some time, I think they were attempting some treatment. There was a previous surgery with scars on the heart apparent but it failed to remove the entirety of the cancer or stop its growth. I don't think they place DS people on the transplant list, but I could be incorrect.
It was a truly bizarre thing to see.
There really aren’t any here. But if you want to read about a specific person, check out the Empathic Nutritionist thread, also in Beauty Parlor, which is a spinoff from this thread.I'm new to this thread. Can anyone give me some main players? I tried looking through but got kind of bored of all the medical talk.
Also I would recommend the now-closed-because-she-died Jahi McMath thread, and likewise the Hartley Hooligans one.
Not to Sperg but it's very real. It happens way too much.I’m mad at his parents. Who leaves a lit candle unattended around a sleeping toddler? That’s what happened to him, his blanket caught on fire.
I know it’s come up before in this thread the wards full of brain damaged kids from shaken baby syndrome, but I’ve also seen some takes out there in the wider world lately that shaken baby syndrome isn’t real. Thoughts?
I’m mad at his parents. Who leaves a lit candle unattended around a sleeping toddler? That’s what happened to him, his blanket caught on fire.
I know it’s come up before in this thread the wards full of brain damaged kids from shaken baby syndrome, but I’ve also seen some takes out there in the wider world lately that shaken baby syndrome isn’t real. Thoughts?
He's really a special young man. What a positive attitude for all he's been through.This dude came up a few years ago when facebook deleted posts cause of how he looked.
SBSK did another interview with him now that hes 18.
Spoiled because last time he made people actually sick in this thread to look at him:
He really does seem like a great guy and although I'm sure he doesn't want pity, I can't help feeling bad for him. I admire that he's able to have such a positive attitude, but it's still sad that his physical form has been so devastated. While it would be great if appearance didn't matter and it probably shouldn't matter, especially when someone is as kind and intelligent as this young man is, unfortunately looks do make a difference in how humans react to one another. Even when you realize on an intellectual level that he's just a normal person who just happens to have been in a very bad accident, on a visceral, instinctual level, it's all but impossible to totally ignore his horrific disfigurement.He's really a special young man. What a positive attitude for all he's been through.
I always felt so so bad for this kid. Hearing his old interview about wanting friends and stuff broke my heart.This dude came up a few years ago when facebook deleted posts cause of how he looked.
SBSK did another interview with him now that hes 18.
Spoiled because last time he made people actually sick in this thread to look at him:
I'll also add that transplants don't last forever, either. Their "shelf life" is pretty short so even if you make it through the infections and illnesses caused by the anti-rejection meds, you'll still need a brand new transplant after a while anyways.I posted this a while back, and somehow it disappeared, but here goes: Most people don't realize that organ transplant recipients often remain chronically ill, just in a different way than they were before. They are very prone to infections of all kinds, and certain types of cancer, on top of the "visible" side effects of the anti-rejection meds. I've definitely heard of people who were approved for a transplant, and asked to be taken off the list because they didn't feel it was worth it.
There is a girl who is featured on another forum here who is in denial about her kid having delays.A lot of Kiwi Farms users are proof of Shaken Baby Syndrome.