
boss charles
3.6K posts

boss charles
@rockstopher2
My last account got suspended because I tweeted mean stuff at a food hall that got rid of their buffet




@DarrenEstes Fair point. But you assume that AMT-130 is a cure. I bet you that the patients will still have to go to neurologists, physicians, etc. for their regular check-ups even after AMT-130 has been administered. And at that point, where is the cost savings?



all because this douchebag @johnarnold doesn't think rare disease patients' lives are worth anything easy to say until it is your family member who has DMD, SMA, CF, HD, etc.

30,000 Americans are symptomatic with Huntington's disease right now. Another 200,000 carry the gene. There is no approved treatment that slows progression. None. AMT-130 showed 75% slowing at 36 months. The 48-month data drops this summer. If the numbers hold, the FDA will have to explain why it spent months calling this therapy "failed" instead of reviewing it. $QURE #HuntingtonsDisease #AMT130

There is no issue with physician-led hospitals- the issue is about the conflict of interest when physicians self-refer patients to their own hospitals. The data is clear: POHs tend to treat more commercially insured and healthier patients than full-service hospitals. In rural communities, this can leave rural hospitals with a greater financial burden, further threatening their ability to keep their doors open and keep 24/7 care available in their communities. Read more: fah.org/wp-content/upl…





@BillBrewsterTBB That is correct, more than one. Not only did it stop progression, the patients that I personally know actually got better. This is also backed by many doctors and other healthcare professionals. The patients are ready and willing to share their testimonies as well.

🗿 It’s not Shadow of the Colossus. 🐉 It’s not Monster Hunter. 🕷️ It’s not Dragon’s Dogma. But if our indie game reminds you of them… we’re probably doing something right. #screenshotsaturday #pixelart #gamedev




$QURE It requires forcing desperate patients with a 100 percent fatal genetic disease to undergo invasive brain surgery solely to inject a placebo, while withholding a therapy that has demonstrated 36 months of profound disease slowing.



I deeply agree with Emily Bender's main point: LLMs are useless, unless you want to offload cognition. (The other two usecases she suggests are rare special cases of the third.) Offloading cognition into machines has always been the purpose and application of computer science and AI.

Sorry to be the downer because this is an impressive story in some senses. But it is ~trivially easy to make a single mRNA vaccine. It's not hard. I cure mice of various cancers with various therapeutics all the time. I've made mice lose more weight in a month than tirzepatide does in a year. What is hard and expensive is proving its BOTH safe AND effective **in a randomized and controlled study in humans** while ALSO manufacturing it at clinical scale and grade. I am happy for this man and his dog. It is impressive. But y'all are overhyping it.


• According to the story, the dog's cancer has not been cured. • Absent all regulatory and manufacturing constraints, we could not just synthesize magic mRNA cancer cures. The technology is very promising, but it's not yet any kind of panacea. • The emergent system of regulators and manufacturers is indeed far too conservative, and small-scale experimentation is much harder than it should be. More people should read the first part of The Rise and Fall of Modern Medicine. Recommend @RuxandraTeslo, @PatrickHeizer for more.

Sorry to be the downer because this is an impressive story in some senses. But it is ~trivially easy to make a single mRNA vaccine. It's not hard. I cure mice of various cancers with various therapeutics all the time. I've made mice lose more weight in a month than tirzepatide does in a year. What is hard and expensive is proving its BOTH safe AND effective **in a randomized and controlled study in humans** while ALSO manufacturing it at clinical scale and grade. I am happy for this man and his dog. It is impressive. But y'all are overhyping it.


Sorry to be the downer because this is an impressive story in some senses. But it is ~trivially easy to make a single mRNA vaccine. It's not hard. I cure mice of various cancers with various therapeutics all the time. I've made mice lose more weight in a month than tirzepatide does in a year. What is hard and expensive is proving its BOTH safe AND effective **in a randomized and controlled study in humans** while ALSO manufacturing it at clinical scale and grade. I am happy for this man and his dog. It is impressive. But y'all are overhyping it.



