1,768 karma · joined March 20, 2012
Anecdotally, I know a travel nurse who works in pediatric ICUs (PICUs). One shift a couple months ago, the overnight staff on her unit was >80% travelers. And this is in peds units that aren't as affected by COVID, because ~1/2 of the patients are cardiac babies with congenital heart issues. The only case I can see for not paying staff more to increase retention is that they can respond to a dip in cases over the summer, but that can't possibly be an 80% decrease in patients. Maybe they're waiting until travel rates come down to offer an increase in pay so their 1.2x salary offer is more enticing in comparison to the travel rates, but the current system is ridiculous financially. I did mention that we've seen first-hand that hospitals can afford to pay nurses $4k/week, though, and I'm sure I'm not the only one who noticed.
I'm also on the IACUC for my company, and I can assure you that we do care about animal life. We go to great lengths to ensure that research is being done in ways that maximize animal welfare to the extent that is possible. The FDA requires animal studies for safety and efficacy, and we can debate the morality of testing in mice, then NHPs before humans, but the system as it exists prioritizes de-risking first human doses as much as possible. Given that system, it is the job of the IACUC to oversee and approve every procedure done to an animal in the facility or in our company's name at other facilities. It's a big job that, at least at my place, is taken very seriously by researchers and up the chain of management.
They have good disease induction in their control groups, their targeted mRNA therapy shows pretty remarkable efficacy, and they show they can diversify a little bit with respect to the target.
These models are a little too "furry test tube" for me for this application. They work by injecting an antigen, either a short version of the myelin oligodendrocyte glycoprotein (MOG) peptide or the myelin proteolipid protein (PLP). The mouse makes antibodies against that antigen, and those antibodies also attack those antigens in their natural environments, leading to demyelination in the CNS. Well their mRNA for the MOG model makes more MOG peptide, giving the antibodies another target so they don't cause demyelination. In the human condition, there are multiple antibodies against multiple targets, so I'm not sure this is as relevant as they're suggesting, unless I'm missing something. I do want to add that this paper has a ton of work in it, and it looks pretty high quality as far as I can tell.
None of this is to say there's no value here, I'm just not sure what target they would make an mRNA for to treat human MS based on this paper or how they'd identify and test that target to get FDA approval to move into trials.
There's an Association of Art Museum Directors. Usually, the consequence for selling art to pay bills would result in that museum being censured by the art museum directors. They announced a couple months ago that they are allowing a 2 year reprieve from those censures due to COVID.
At the federal level, there are a few bills being introduced to deal with qualified immunity or other aspects that need addressing. These may not go anywhere, but more pressure may have an effect on that. Also, hopefully next time there's a massive economic downturn, officials remember that not supporting individuals makes the whole nation a powder keg, ready to spawn riots in all 50 states.
There's also historic precedent that protesting has a lasting change.
Is that believable? Sure, but locking arms is also a common thing during protests. The road was already blocked off and cars weren't going through. Also, they fired CS into crowds of protesters blocks away, claiming that they think the protesters are coordinating by secure communications and instantaneously turning violent across the city. Most of it seems like bullshit, and even if it's all true, locking arms on one side of a closed street is not at all unusual. They should have arrested the one guy hitting the glass and let the protest continue.
By the way, they used this event to justify the curfews that haven't been raised since then.
Any officer paying attention would know you won't be punished unless you act particularly egregiously like the one officer in Louisville reassigned to desk duty (big whoop). Add on the amount of animosity stoked by the president toward media for the past 4-5 years, and it really doesn't take a simultaneously coordinated effort to have this outcome.
Part of the trouble is that there seems to be a lot of variation in symptoms in people who test positive.
I suspect HomeKit integrations like "if the door unlocks, and it is night, turn the light on" will break.
What is way more common is that scientists from around the world, mostly funded by public money produce research that might implicate a particular pathway or target for a particular disease. Scientists in companies see those publications and try to verify the result, then make a drug for it. The process of making the drug, testing tens of thousands of compounds, making sure efficacy and safety margin are maximized, running clinical trials, and producing the drug with good yields is almost always done by companies.
The government can do stuff like funding studies on new uses for off-patent drugs, fund various parts of that development, and reduce regulatory burden to tilt the economics for companies to make drugs for a disease, but that mostly happens to do stuff that wouldn't happen in the normal system in which companies have to make money making drugs.
Disclaimer: I work in pharma, but in biology, not anywhere near the budget-making
I don't hate the idea of bounties, but someone has to decide what bounties to offer, and the current system for deciding that is whether money can be made in that area. It's not perfect, but at least broadly it means that there is an incentive for treatments for conditions that affect a lot of people and ones with a high cost of disease without treatment.
The thing I could see easily being missed by bounties (or maybe worse, being subject to being lobbied by pharma companies with a drug in the chamber) is drugs that start for one indication, but pivot or expand to another, and drugs that are second or third in class. There is undoubtedly some value to a second in class drug that is more efficacious and safer, and line extensions are also helpful for expanding the use of a drug in market.