When my wife Grace and I moved to Guilford, Connecticut, 18 years ago, we were grateful that it was a town where you could walk for a reason. To go to the library. To get a pizza. To get your hair cut. To some people, those may seem like petty things. But for us, they meant a great deal.

Last March, our lives were disrupted in many ways. We stopped traveling by plane and train. Our time with extended families was mostly restricted to phone calls and Zoom sessions. But the nearby disruptions were just as bad. Trips into stores were quick, no-nonsense errands. The rest of our lives within walking distance began to lose out in our risk-benefit calculations. After a while, the isolation began to feel normal. Now that I’ve gained immunity, it takes effort to rediscover the town all around me. Continue reading “Friday’s Elk, May 7, 2021”

The New York Times, May 5, 2021

Link

In early 2020, dozens of scientific teams scrambled to make a vaccine for Covid-19. Some chose tried-and-true techniques, such as making vaccines from killed viruses. But a handful of companies bet on a riskier method, one that had never produced a licensed vaccine: deploying a genetic molecule called RNA.

The bet paid off. The first two vaccines to emerge successfully out of clinical trials, made by Pfizer-BioNTech and by Moderna, were both made of RNA. They both turned out to have efficacy rates about as good as a vaccine could get.

In the months that followed, those two RNA vaccines have provided protection to tens of millions of people in some 90 countries. But many parts of the world, including those with climbing death tolls, have had little access to them, in part because they require being kept in a deep freeze.

Now a third RNA vaccine may help meet that global need. A small German company called CureVac is on the cusp of announcing the results of its late-stage clinical trial. As early as next week, the world may learn whether its vaccine is safe and effective.

Continue reading “This New Covid Vaccine Could Bring Hope to the Unvaccinated World”

The New York Times, April 23, 2021

Link

A panel of advisers to the Centers for Disease Control and Prevention has recommended lifting the pause on the Johnson & Johnson Covid-19 vaccine for all adults while adding a warning label about a rare but dangerous blood clotting disorder. But a central mystery persists: How might a vaccine that has been given to nearly eight million people cause the side effect in just a few of them?

There’s no clear answer yet, but Dr. Andreas Greinacher, a researcher at University Medicine Greifswald in Germany, is leading one effort to find out. At a news conference on Tuesday, he said that he had reached an agreement with Johnson & Johnson to inspect the components of the vaccine to see if it could disrupt the normal blood clotting process under certain rare conditions.

“We just agreed that we would like to work together,” he said.

Continue reading “A new study hints at a reason the J.&J. and AstraZeneca vaccines may cause blood clots in rare cases.”

The New York Times, April 23, 2021 (with Emily Anthes and Noah Weiland)

Link

The Food and Drug Administration ended its recommended pause on the Johnson & Johnson Covid-19 vaccine on Friday and will add a warning to its label to note the potential risk of rare blood clots.

The decision, which clears the way for states to resume vaccinations, came after a panel of advisers to the Centers for Disease Control and Prevention voted to end the pause in a meeting on Friday.

Continue reading “The F.D.A. ended its recommended pause on the J.&J. vaccine, clearing the way for states to use it again.”

The New York Times, April 16, 2021 (with Noah Weiland)

Link

The White House on Friday announced an almost $2 billion plan for expanding and improving the nation’s ability to track coronavirus variants, an effort that public health experts have said is desperately needed to fight against variants that could drive another wave or potentially undermine the effectiveness of vaccines.

Continue reading “The White House details a nearly $2 billion plan to enhance the tracking of variants”