New Policies Emerge In The Wake Of Climate-Connected Disasters
This week, people across the United States continued to be reminded of the results of a shifting climate—with people in the Gulf states still recovering from Ida, northeastern states dealing with the aftermath of Hurricane Ida-induced flooding, and western states battling wildfires and smoke.
With climate-related disasters as a backdrop, President Biden announced a goal of shifting some 45% of U.S. energy production to solar power by 2050.
Kendra Pierre-Louis, senior reporter for the Gimlet-Spotify podcast How to Save A Planet, joins Ira to talk about those stories and more, including new calculations of the importance of minimizing fossil fuel extraction, to a successful sample collection effort on Martian soil.
Is Inflammation In The Brain Causing Alzheimer’s Disease?
The brain of a person with Alzheimer’s disease has a few hallmark traits. First, a buildup of plaques made of proteins called amyloid beta. Second, are tangles of another protein, called tau, within individual neurons. A third major indicator is inflammation.
While researchers have long thought brain inflammation was a byproduct of the disease itself, there’s a growing hypothesis that it might actually be a driver of the disease’s progression. That would help explain why researchers have found people whose brains are full of tau tangles and amyloid plaques, but with no outward symptoms of Alzheimer’s.
Research on animals has supported this theory. But finding the same evidence in human brains is harder. Now, a team of scientists, writing in the journal Nature Medicine, thinks they have it: time-lapsed images of patient brains showing tau tangles and inflammation spreading through the brain in the exact same pattern.
Ira talks to Dr. Tharick Pascoal, assistant professor at the University of Pittsburgh and the study’s first author, about this finding, and what it means for future research into Alzheimer’s therapies.
The World According To Sound: Ultrasonics
The mating calls of the katydid, a large insect, are ultrasonic, beyond the audible limit of human hearing. What if we could hear them?
That’s the focus behind a collaboration between the abstract audio podcast The World According To Sound and scientist Laurel Symes, the assistant director of the Center for Conservation Bioacoustics at Cornell University. In this recording, you’ll hear the sounds of one of her study animals—a group of katydids in a forest in Panama.
Bill McQuay, sound engineer and an audio producer at the Cornell Lab of Ornithology, slowed down Symes’ recording so you can hear a whole world of ultrasonic activity open up, from ultrasonic mating calls of katydids to the ultrasonic pings of bats echolocating their next meal.
The World According to Sound is a live audio show, online listening series, and miniature podcast that focuses on sound, not story. Producers Chris Hoff and Sam Harnett create intentional, communal listening experiences as a way to “reclaim autonomy in a visually dominated world that is increasingly fracturing our attention.”
This katydid recording and more are a part of their next listening series, an immersive listening party where audiences from all over the globe will be invited to experience a world of sound together, beginning in January 2022.
How COVID-19 Reveals Existing Biases Against The Disability Community
In early July, I visit Ingrid Tischer at the Berkeley apartment she’s shared with her husband, Ken, for the past 10 years. When I arrive, she’s already sitting outside at the top of a gently sloping ramp that leads up to the door. We’re both vaccinated, but we’re still taking precautions: masks, outdoors, and social distancing. That’s because Ingrid has a severe disability.
“I have muscular dystrophy,” she tells me, “which is a neuromuscular disorder that I’ve had my entire life because it’s genetic.” Muscular dystrophy is a progressive muscle wasting disease. It impacts her mobility, including her ability to walk unassisted. Ingrid says she’s most impacted by having a weak respiratory system and uses an oxygen device called a biPap to help her breathe. Earlier in the pandemic, her doctor told her that if she got COVID, it would likely be a death sentence. “I’d never heard my situation put in such stark, certain terms,” she says.
Ingrid is in her mid 50s, with graying brown hair and bright blue eyes. She leads fundraising for DREDF, a disability rights and legal advocacy organization. She’s also a writer — she’s written a draft of a novel and has a blog called “Tales From the Crip.” In addition to a brilliant title, the blog is full of her personal reflections about navigating a world in which the needs and feelings of people with disabilities go mostly unseen and ignored.
When COVID hit in the spring of 2020, Ingrid was terrified. Because of the risk of infection and smoke from the wildfires that summer, she stopped leaving her house entirely, developed severe anxiety and depression, and began noticing a host of new health issues.
Her feet and legs began swelling and breathing became even more difficult than usual. Her doctor worried she might be developing congestive heart failure, but told her to stay home rather than come in for tests and risk infection. It’s a common story. A recent survey by the disability advocacy group #NoBodyIsDisposable found that many disabled people have delayed medical care for over a year due to concerns about COVID-19.
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