Episodes
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Whether you're playing a game of poker or a taking a leap of faith with your future, everything has its risks and possible rewards. In this week’s episode, both of our storytellers share moments when they took a chance.
Part 1: Beatriz Perez’s parents want her to use her first pay check to gamble on the slot machines.
Part 2: Dave Piontkowski is on a winning streak in Vegas when his severe ulcerative colitis rears its ugly head.
Beatriz Perez: I'm a Mexican-American computer engineer working in Massachusetts. I thrive on finding new things to try out and putting myself outside of my comfort zone, hence my new interest for story telling. I have a deep passion for empowering women and young girls in STEM. During the weekends you'll find me traveling to a random country, crafting, working on a new project, or reading a good book.
Dave Piontkowski is an NYC based stand-up comedian who performed at the Edinburgh Fringe Festival in 2023 and 2024 with his one man show 3 Kidneys No Colon which he is currently touring with.
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In this week’s episode, both of our storytellers share tales about birds that had a big impact in their lives.
Part 1: Paula Croxson uses her neuroscience background to get rid of the pigeon family that has taken up residence on her window sill.
Part 2: As a new urban park ranger, Tim Lopez gets a call to capture a swan on the loose.
Paula Croxson is a neuroscientist, science communicator, musician and open water swimmer. She received an M.A. from the University of Cambridge and a M.Sc. and a Ph.D. from the University of Oxford before moving to New York to run a neuroscience lab. She changed career direction around 5 years ago to focus on public engagement with science, first at Columbia University and then at the Dana Foundation. She is also the flautist in alternative rock band Marlowe Grey and nerdy rock band Pavlov’s Dogz. The swimming is apparently for “fun”.
Tim Lopez is a storyteller and educator born and raised in Los Angeles. His stories have been featured on the Moth Radio Hour, KCRW in Los Angeles, and CBS Radio nationwide. He is currently an Interpretive Park Ranger at Channel Islands National Park, where he brings the stories of the natural environment and the history of California to life. He is also a Jeopardy! champion and is legally obligated to mention that fact as often as possible.
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Episodes manquant?
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When it comes to mental health problems, there aren't really "cures," but in this week’s episode, both of our storytellers share how they figured out what worked for them.
Part 1: Deandra Anjahlee decides to study psychology to try to understand what is happening with her mind.
Part 2: After all other treatments fail to treat Nick Caruso’s 25-year long depression, he gives transcranial magnetic stimulation a shot.
Deandra Anjahlee is a community centered educator, leader, and fresh storyteller. She is a proud Brooklynite with Caribbean roots. Themes of identity and equity ground her work on and off stage. She is passionate about creating safe spaces for intergenerational learning, growth and joy. Her storytelling evokes laughter, nostalgia, and encourages introspection. When she’s not on stage, you can find her sneaking explicit music in at your kid’s prom, or catching the last bits of sunlight in Prospect Park.
Nick Caruso is a proud Michigan native living in Brooklyn bliss with his amazing partner and a bunch of plants. He's a lifelong lover of comedy and cinema, an entertainer at heart, and a career writer/editorial director/multimedia presenter. Nick is passionate about the intersection of storytelling and education and is always on the hunt for professional (or not) opportunities to craft and communicate new, additive narratives. He’s also an ordained minister, amateur mechanic, and aspiring 'Wait, Wait, Don't Tell Me' panelist.
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This week, we bring you two stories about frustrations in the field, whether it's a failure to find dinosaur fossils or a struggle with a painful medical condition.
Part 1: Paleontologist David Evans and his team start to feel defeated after three days of searching fruitlessly for fossils.
Part 2: After cave geologist Gabriela Serrato Marks develops fibromyalgia, exploring caves becomes a challenge.
David C. Evans holds the Temerty Chair in Vertebrate Palaeontology and oversees dinosaur research at the Royal Ontario Museum (ROM). He is also an Associate Professor in the Department of Ecology and Evolutionary Biology at the University of Toronto. David is an Ontario-born researcher who is recognized as an authority on the rich dinosaur fossil record of Canada. As a curator, David helped develop the ROM's dinosaur galleries, and was Lead Curator of the major travelling exhibition Ultimate Dinosaurs. He has been featured on numerous television shows, and most recently, David was co-creator of the HISTORY series Dino Hunt Canada. David’s research focuses on the evolution, ecology and diversity of dinosaurs, and their relationship to environmental changes leading up to the end Cretaceous extinction event. Active in the field, he has participated in expeditions all over the world, including the Africa, Mongolia, and Canada, and has helped discover 10 new dinosaur species in the last five years- including the remarkable horned dinosaur Wendiceratops from southern Alberta, and the wickedly armoured Zuul named after the Ghostbusters movie monster.
Gabi is a science communicator with a passion for expanding inclusion in STEM. As a co-founder of Stellate Communications, she helps academics multiply the impact of their research and engage with new communities. She also co-edited Uncharted, an anthology of personal stories from disabled scientists (Columbia University Press). Gabi is based in Boston and spends her free time drinking iced coffee with her husband and two cats, Spock and Moose.
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Science can sometimes feel like an exclusive club that only certain people are allowed into. In this week’s episode, produced in partnership with the Allen Institute, both of our storytellers try to find their place in science.
Part 1: After getting accepted to a PhD program, Max Departee can’t help but feel like he’s not good enough to be there.
Part 2: Han Arbach is worried coming out as non-binary will ruin their scientific career.
Max Departee is a research scientist from the Pacific Northwest who has always had a fascination with the natural world. A curious nature and outdoor spirt led him to attend Montana State University where, between fly-fishing on local rivers and skiing the Rockies, he earned his Bachelors Degree in Biotechnology. Max's career and training as a scientist have taken him many places, from a PhD program in North Carolina, to a small Biotech Start-up in Washington, and back to his home town of Seattle where he now works at the Allen Institute for Brain Science.
Han Arbach grew up dreaming of becoming an astronaut after watching the space shuttle land at the military base their family was stationed at. As they continued to grow up and became a “frequent flyer” in the orthopedics department for various injuries, their aspirations shifted towards medical training. Encouraged by fantastic AP Biology and Chemistry teachers in high school they pursued a biochemistry major at Mount Holyoke College. Here they were encouraged by a chemistry professor to try out research. This fostered a newfound love for discovery and research, and with it a new dream career path of becoming a scientist. Han completed their Ph.D. in Biochemistry at the University of Washington studying tail regeneration and nuclear structure in tadpoles. They then did Postdoctoral work at the Fred Hutchinson Cancer Center using viruses as a tool to probe facets of cell biology. Now, they are a Program Officer at the Paul G. Allen Frontiers Group. Outside of work, you will find them raising two dogs with their partner, attempting to befriend crows, and being a poor but enthusiastic gardener.
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In this digital age, technology can connect us in ways we never imagined. In this week’s episode, both of our storytellers share stories of the weird and wonderful ways technology created new opportunities and forged new relationships.
Part 1: In an attempt to be seen as “cool” by his friends, Azhar Bande-Ali reaches out to the Steve Wozniak and invites him for coffee.
Part 2: Don Picard can’t stop using technology to keep tabs on his son.
Azhar Bande-Ali is a storyteller who likes his tales with a side of laughs. His award-winning debut solo show, "Curry and Catharsis," presented at the NYC Fringe Festival, won hearts for telling an Indian story hyphenated by an American upbringing. As a former Moth StorySLAM winner, he obsesses over story structure that leaves plenty of room for silliness to highlight the complexities of the human experience.
Don Picard has worked in the Boston area for 30 years as a software developer. He was a double major in Theatre Arts and Computer Science at Cornell, and chose to work as an engineer in order to be able to live in Cambridge and feed his family. Don enjoys telling live stories about his kids, husband, and extended family as it is fun, therapeutic, and allows him to exercise the other half of his college degree so he doesn't become bitter.
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Healthcare is often a tangled web of bureaucracy and inefficiencies. In this week’s episode, both of our storytellers share their experiences navigating its many flaws.
Part 1: Zoe Wisnoski’s takes matters into her own hands when her son has months of ongoing fevers.
Part 2: During the pandemic, epidemiologist Bryon Backenson becomes disheartened when the public stops cooperating with public health authorities.
Zoe Wisnoski is a seeker of stories, adventure, travel, and moments that stick with you. She stumbled into the world of storytelling through a training put on by Story Collider. Her passion for activism buoyed by a penchant for oversharing has finally found a home. Formerly a feminist policy analyst with a Masters in Public Policy from the Humphrey School of Public Affairs, now a full time - still feminist - mother, Zoe spends her time attempting to create joy amidst utter chaos. When her son was diagnosed with the super rare, to date minimally understood, genetic disease Tatton Brown Rahman Syndrome (TBRS), Zoe reoriented her educational and professional background to meeting his needs and volunteering with the TBRS Community, the nonprofit aimed at supporting families and advancing research for TBRS. In 2024 she joined the board of directors and continues to search for answers.
Bryon Backenson is an epidemiologist. He is currently the director of the Bureau of Communicable Disease Control at the New York State Department of Health. He and his team investigate, respond to, and research infectious disease outbreaks. He is also a professor in the University at Albany College of Integrated Health Sciences, where he teaches in the Department of Epidemiology and Biostatistics. When not thinking about disease, he spends his time hiking, fishing, and reading. While he talks about epidemiology and infectious diseases all the time in classes, meetings, and webinars, this is the first time he’s tried to tell his own story in this kind of format.
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In this week’s episode, both of our storytellers share stories about moments in life where they chose to put themselves and their wellbeing first.
Part 1: When Yves Jeffcoat is diagnosed with multiple sclerosis, she isn’t sure how to manage this new normal.
Part 2: Jameer Pond keeps ending up in relationships he doesn’t want to be in, so his therapist suggests he take a sex sabbatical.
Yves Jeffcoat is a writer, a podcast host and producer, and a yoga teacher. Her writing has been in The New York Times, Paper Monument, Lapham’s Quarterly, Art in America, The Bitter Southerner, and elsewhere on the internet and in print. She has hosted and helped create podcasts with iHeartRadio, Afropunk, and Hulu that reflect her interests in Blackness, history, healing, and resistance. She is currently the co-creator and co-host of On Theme, a podcast about Black storytelling in all its forms.
Brooklyn, New York born award-winning storyteller, director and interviewer Jameer Pond has spent his whole life walking in his passion; engaging with people through diverse storytelling. Throughout his career, he’s created viral series such as Buzzfeed’s Black People Try, co-hosted BET’s first morning talk show Black Coffee, directed several cover videos across Condé Nast’s array of publications, including Sir Lewis Hamilton and Simone Biles, and has won a Shorty Award. You can currently catch him traveling the world, telling his dynamic stories with The Moth.
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This week we present two stories about the inspiration behind scientists' careers.
Part 1: Kate Marvel's dream of being a genius takes her to Cambridge to study astrophysics.
Part 2: When Joe Normandin begins to question his sexuality as a teenager, he turns to neuroscience for help.
Kate Marvel is a climate scientist at the NASA Goddard Institute of Space studies. She uses computer models and satellite observations to monitor and explain the changes happening around us. Her work has suggested that human activities are already affecting global rainfall and cloud patterns. Her book Human Nature: Nine Ways to Feel About Our Changing Planet will be published in 2025 by Ecco Press.
Joe Normandin earned a B.A. in Biology with a Specialization in Neuroscience from Boston University, where he worked as an undergraduate research assistant in labs studying the behavioral genetics of sexual orientation in people and female sexual behavior in a rat model. He earned a Ph.D. in Biological Sciences - Neurobiology and Behavior from Georgia State University, where he explored how the brain regulates sexual reflexes. He found evidence of a brain circuit that provides an anatomical/functional basis for the oft-reported side effects of delayed orgasm in those taking antidepressants. He is now a Lecturer and Director of Undergraduate Studies in the Neuroscience Institute at Georgia State University. Dr. Normandin values the wonderful public education and support he received as a young gay man growing up in Massachusetts. Even with that education and support, he struggled with his identity as a gay person. In high school, a psychology class introduced him to neuroscience, which led to a search for research that he thought would validate his sexual orientation. This search set him on a path towards becoming a neuroscientist, and ultimately led to questions he explores in the classroom: Are people born gay? Does it matter? Dr. Normandin is also an avid gamer and has saved the universe many times.
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In this week’s episode, both of our storytellers share their experiences with online hate and the surprising lessons they learnt along the way.
Part 1: After debunking Bella Hadid’s treatment for chronic lyme disease, Fola Olusanya finds herself in a heated debate with another TikToker.
Part 2: During the pandemic, infectious disease researcher and science communicator Laurel Bristow receives a flood of hate mail.
Fola Olusanya is a PhD student at NYU studying computational biomedicine, and has been a producer with Story Collider since 2022. She is also a writer and content creator.
Laurel Bristow is an infectious disease researcher, science communicator, reluctant instagram baddie, and all around fan of tomfoolery. By day she creates public health education for general audiences and occasionally uses her free time and instagram to educate about infectious disease, and advance her personal vendetta against the cruise industry.
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In this week’s episode, both of the storytellers share stories about moments when life just wouldn’t let up.
Part 1: After giving birth to her second child, Julie Raskin doesn’t know how to handle his constant crying and need to nurse.
Part 2: As a new immigrant and surprise cancer patient, Emmanuel Paul navigates the complexities of the US healthcare system.
After Julie’ Raskin’s son Ben was born with congenital hyperinsulinism (HI), a condition that causes the overproduction of insulin that leads to severe hypoglycemia, Julie joined a dedicated group of parents whose children were also affected by the condition to found Congenital Hyperinsulinism International (CHI). Julie is the CEO of CHI and since 2010 she has led this active worldwide community of patients, their families and caregivers, expert clinicians and researchers, and professionals in the biotech field to fulfil CHI’s mission to find better treatments, prevent death and brain damage, and support HI families every step of the way.
Emmanuel Paul is an immigrant from Haiti. He is a Journalist. A cancer survivor. Emmanuel is a graduate student at Harvard Division of Continuing Education. He graduated in Accounting and Finance at Northeastern University. He also hold a double bachelors in Anthropology and Sociology at the Haiti State University. Emmanuel is the founder of CaribbeanTelevisionNetwork, an online news media serving immigrant communities from the Caribbean in the United States.
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It’s not always easy to make friends, but in this week’s episode, both of our storytellers take us on heartwarming and sometimes unexpected journeys to find true friendship and meaningful connections.
Part 1: Eva Chebishev gets voted “Most Organized” in first grade and struggles to fit in with her peers.
Part 2: Morgan Roberts is worried about how people will see her if she enters a high school math competition.
Eva Chebishev (she/her) is a microbiology PhD candidate in the lab of Dr. Ana Fernandez-Sesma at the Icahn School of Medicine at Mount Sinai (ISMMS). Her research focuses on the immune response to Dengue virus (DENV) with hopes of creating a safe, effective vaccine that is protective against all four serotypes of DENV. When she finally finishes this PhD, she aims to combine her enthusiasm for science communication and public outreach with her life-long passion for musical theatre. To this end, she recently had the incredible opportunity to perform in the limited, Off-Broadway run of “Lifeline” an original musical which tells the story of Alexander Fleming’s discovery of Penicillin and the ongoing, rising global public health threat of antimicrobial resistance. She was also an attendee of ComSciCon-Flagship-2024, a science communication conference for graduate students, and has guest starred on the podcast “Mattsplaining” by Matthew Storrs. Outside of the lab, she performs in, directs, and produces “The Sinai Story Project”, a student-run showcase of original stories from the ISMMS student body. Finally, she is a diversity and disability advocate for equal opportunities in science and would like to thank The Story Collider for this opportunity and her Story Collider Workshop instructors for helping her find and craft her story.
Morgan Roberts is a Mechanical Engineering major in her junior year at Boise State University. She is currently pursuing aerospace engineering and has had wonderful opportunities interning for various aerospace companies in the US and is hopeful to get more! She loves playing volleyball, reading, spending time with friends and family, and working in the machine shop on campus.
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This week, we're presenting stories from scientists who faced unusually difficult paths to science. We all know it's hard work to become a scientist. But for some folks, even getting to that point where you can pursue your science education can seem like an impossible dream.
Part 1: When Evelyn Valdez-Ward discovers that she's undocumented, she fears her dreams of becoming a scientist are over.
Part 2: Samuel Achilefu's experiences growing up during the Nigerian Civil War inspire his passion for science.
Evelyn Valdez-Ward is an undocumented, Latina, scientist and PhD student at the University of California, Irvine. For her thesis, she studies the impact of California's drought on the ways that plants and their soil microbes (fungi and bacteria in the soil) communicate and interact with one another. In addition to doing research, she's extremely passionate about advocating for undocumented students in STEM. She recently published her story "I'm an undocumented scientist fighting for my Dream" in Science, and was invited to speak at the March for Science rally in DC to advocate for Dreamers in STEM. She has been awarded a UCI's Dynamic Womxn's Award for Outstanding Social Justice Activist, and the Svetlana Bersahdsky Graduate Student Award for her lobbying and advocacy efforts. She plans to continue lobbying and fighting for her undocumented community after graduating, and work in science policy, where she can continue to advocate for both science and minorities in STEM.
Originally from Nigeria, Samuel Achilefu is the Michel M. Ter-Pogossian Professor of Radiology at Washington University School of Medicine. He also holds joint appointments as a Professor in Medicine, Biochemistry & Molecular Biophysics, and Biomedical Engineering and serves as the Chief of the Optical Radiology Laboratory (ORL), Director of the Molecular Imaging Center, Director of the Center for Multiple Myeloma Nanotherapy, and a co-leader of the Oncologic Imaging Program of the Siteman Cancer Center. His lab harnesses the power of light to develop methods for understanding, diagnosing and treating human diseases and is made up of biologists, chemists, engineers, medical scientists and physicists. He enjoys biking, playing tennis, and travelling. Samuel lives with his wife and they have two college-aged children.
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In this week’s episode, both of our storytellers have a passion for science that can’t be suppressed.
Part 1: As a zoo volunteer, Lisa Yeager adores sharing her love of the wild, but one zoo patron is ruining that for her.
Part 2: Anna yearns to be a scientist, but her strict mormon family doesn’t want her to become one.
Lisa Yeager started her career as an environmental educator and bookstore manager in Anchorage, AK. She shifted to build a career in project management after earning her MBA at the University of Washington. She currently works as a Program Manager for Fred Hutchinson Cancer Center where she works to bring innovation and transformational change to business practices and collaboration. Lisa built her life in Seattle after attending UW because where else are you within a day of ocean, sound, volcano, shrub-steppe, lakes and two mountain ranges? With 10+ years as an informal education volunteer at Woodland Park Zoo, she is exploring ways to translate her business background and a recent second master’s in biology to support climate change education and advocacy. She serves on the governing council for the National Network for Ocean and Climate Change Interpretation, and received a Cee-Change fellowship and grant funding from the North American Association of Environmental Education. She is a previous board member of the International Applied Improvisation Network. She is the co-founder of Yes and Nature Collaborative (climateconversations.net), which combines scientific data, communication theory, and improvisational theater techniques to help people have more effective conversations about climate change and nature.
Anna is a naturalist and aquatic entomologist. Going to school in Utah gave her the opportunity for a backyard mountain classroom. She got to learn about migration patterns of mule deer, moose, elk, and pronghorn through GPS collaring initiatives led by the Department of Natural Resources. Her coursework helped her learn how to identify all the plants and animals native to the desert, valley, and mountainous regions of Utah. Monitoring the restoration of a canyon after wildfires, flash floods, and debris flows bolstered her knowledge of the resilience of native flora and fauna to historical natural disaster regimes. She found purpose, love, and life in those experiences. Now Anna gets to connect to the parks and people within NYC, as well as challenge herself through a doctoral program studying the evolutionary history of stoneflies. These insects are fundamental to maintaining the health and balance of freshwater ecosystems, but many populations around the globe are experiencing substantial declines due to human interference and climate change.
*For privacy reasons, Anna’s last name has been withheld.
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Sometimes life throws a curveball and children end up being the ones looking after their parents. In this week’s episode, both of our storytellers share stories about times they needed to adult-up and take care of their parents.
Part 1: When Saloni Singh’s mother is diagnosed with terminal cancer, Saloni is unexpectedly shoved into the role of caregiver and matriarch.
Part 2: After her deaf mother has several strokes and begins experiencing hallucinations, Michelle Antonucci struggles to get her mom the care she needs.
Saloni is known as the ‘girl in the white headphones’ because she is happiest when she is sitting in a corner, her noise cancelling headphones playing classical music, her Mac open and words pouring out of her. Those close to her will tell you that she lives life in techni-color and feels everything deeply so it’s hard not to listen when she begins to tell you about it. Saloni’s storytelling skills were first noticed when she distracted an entire wedding party with a story she was making up on the spot that combined Snow white, Cinderella and Thumbelina as one character – she was 2. She hasn’t stopped since. In her words - “I’m a corporate rat by day, introverted writer by night. Stories find me and then I try to find the courage to tell them.” She has been writing for years but has begun sharing her stories only recently at various platforms like The Moth, Fresh Ground Stories, 7 Stories and Story Sphere. This was her first story at Story Collider.
Michelle Antonucci was born and raised in Greenwich Village, later moving to Queens and now Long Island with her wife Patty and dog/child Charlie. She says she is a true New Yorker, as she does not have a Driver's License! Michelle is proud to be a CODA and has spent her life assisting and advocating for her parents. She is very grateful for her wife who has been her rock throughout her mother, Karen's, health crisis. "I truly don't know how we made it through, my wife is amazing". Michelle's story of life as a CODA and the issues the Deaf experience in health care is not unique, and needs to be told again and again to elicit change. "I need to make all the tears mean something".
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Happy National Honey Month! In honor of Honey Month, we wanted to celebrate beekeepers and the humble honey bees. In this week’s episode, both of our storytellers share their adventures with beekeeping.
Part 1: When Julie Carrick Dalton goes to check on her bees one day, she notices something isn’t right.
This story was shared at the Urban Waggle, a live storytelling event in support of the mission and programs at the Urban Bee Lab, in Somerville, MA in November 2023.
Part 2: Jon Schulz thinks rescuing a neglected apiary is the perfect opportunity to expand his beekeeping business.
Julie Carrick Dalton is the Boston-based author of The Last Beekeeper and Waiting for the Night Song, a CNN, USA Today, Newsweek, and Parade Most Anticipated novel. A former farmer and beekeeper, she is a frequent speaker and teacher on the topic of fiction in the age of climate crisis. When she isn't writing, you can probably find Julie kayaking, skiing, or tending her pollinator garden. Her next novel, The Forest Becomes Her, hits shelves in May of 2025.
Meet Jon Schulz, a data center architect turned beekeeper. In his day job, Jon works to merge high tech subsystems to deliver consistent, reliable and secure solutions for his global customers. As a beekeeper, his fascination lies in the autonomous functions of honeybees that combine collectively to create a thriving colony. Recently, Jon and his wife Amanda launched Blackland Bees, an apiculture business focusing on honeybee rescue, education, conservation and pollination services. Jon and Amanda can be found managing beehives at local community gardens, designing pollinator landscapes for schools and churches, rescuing and rehabilitating bee colonies and supporting Blackland Prairie restoration projects. Jon received a Bachelor of Science Degree in Computer Science, while also studying business and Spanish, at the University of Texas at Austin. He is currently pursuing his Texas Master Beekeeper certification, through Texas A&M Agrilife Extension. Jon and Amanda both grew up in the Dallas area and returned in 2012, after living in Austin, San Antonio and Houston. They presently reside in East Dallas, along with their two children, and manage an apiary of nearly 2 million honeybees!
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We're diving back into our archives to bring you some of our most memorable and impactful stories and episodes we've ever shared on The Story Collider podcast. This week, we're presenting stories about passion for science that keeps us going, even in the face of overwhelming struggle.
Part 1: When Cailin Gallinger struggles with her gender identity in college, her volunteer position in a plant lab becomes a lifeline.
Part 2: In the midst of homelessness and abuse, Rose DF dreams of a life in science.
These stories do include mentions of suicide, rape, sexual abuse, physical abuse and domestic violence. In case you’d find them helpful, now or at any point in the future, we have some resources available on our website.
Cailin Gallinger is a Master’s student in the Department of Earth Sciences at the University of Toronto. She studies the geophysical processes of planets in our solar system, from impact craters on the Moon to volcanoes on Mars and beyond, and has performed in several scicomm events in Toronto, including the LGBTQ-themed Science Slam at Glad Day Bookshop and David Hamilton’s Solar System Social. She is currently soliciting submissions for a forthcoming zine, Corona, focusing on queer and trans scientists living and working on the margins, and hopes to continue combining her passions for both science and art in her post-grad life.
Rose DF is a born explorer with a passion for accessible and inclusive science and education. A first generation scientist born and raised in the Dominican Republic, currently pursuing studies in Biophysics. After opening up about her life for a feature in "Stories in Science" Rose's social media presence has increased since, and she now uses it to raise awareness in the topics of inclusivity and diversity in STEM as she constantly challenges some of the stereotypes associated with being an "non-traditional" academic and a Latina in the US.
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In this week’s episode, both of our storytellers share their experiences with grief and how they chose to say farewell to their dearly departed.
Part 1: When Sanjana Murthy misses her grandfather’s funeral, she struggles with the lack of closure.
Part 2: Paul Barach impulsively decides to walk the Pacific Coast Trail to escape the grief of his girlfriend’s suicide.
This story does include mentions of suicide. In case you’d find them helpful, now or at any point in the future, we have some resources available on our website.
New York City based Research Coordinator Sanjana Murthy is thrilled to be here. Her lab's work at Mount Sinai (Dept of Psychiatry, Center for Advanced Circuit Therapeutics) identifies neurophysiological biomarkers to improve treatment for depression. She holds a B.S. in Brain and Behavioral Sciences from Purdue University, where she curated shows for the TEDxPurdueU stage.
Paul Barach is a writer, storyteller, and thru-hiker from Seattle, Washington. A 2013 Moth GrandSlam runner up, his stories have been featured on Risk, Out There, and other podcasts. Paul has also been a featured guest on Deviate with Rolf Potts, Backpacker Radio, Zero to Travel, and Armchair Explorer. Paul has hiked the Shikoku Pilgrimage, Colorado Trail, and Pacific Crest Trail among others, bicycled the Trans-America Trail, and most recently completed the Annapurna Circuit in Nepal. He is the author of the travel memoir "Fighting Monks and Burning Mountains: Misadventures on a Buddhist Pilgrimage" and is currently working on a memoir about the Pacific Crest Trail, as well as a comedic novel about a vampire hunter who's sick of his job. Paul currently lives in Tacoma with his wife Michelle and their dog Izzy.
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Fanny, vajayjay, kitty, muff, coochie, hoo ha, lady garden – whatever you call it, in this week’s episode, both of our storytellers share weird and wonderful tales about their vaginas.
Part 1: When Milly McDermott is 15, she finds a grapefruit-sized tumor growing out of her vagina.
Part 2: After a guy she was dating tells Dawn Harris she has two vaginas, she can’t help but wonder what is going on down there.
Milly McDermott is a cartoonist, comedian, and show runner who has ran comedy shows in both the U.S. and in China. Milly began her comedy career after being diagnosed with a rare uterine cancer at the age of 15. She now runs comedy shows in New York City and continues to publish comic strips about her life.
Dawn Harris is a theatre major from Alabama, enjoying a lucrative career in an unrelated field. She has studied storytelling at The Magnet Theater and The Story Studio. Her early years in New York were spent studying improv comedy with The People’s Improv Theatre, The Magnet Theater, and The Upright Citizen’s Brigade. Dawn has been featured on the podcasts Love Hurts and RISK! (under a mysterious pseudonym) and has told stories live with Story Collider, Awkward Teenage Years and The Armando Diaz Experience. Adam Wade highly recommends her.
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Defining yourself as a person or as a scientist is no easy feat. In this week’s episode, both of our storytellers grapple with who they are and how they want to be perceived.
Part 1: After Fernando Cuevas flunks out of college, he’s worried he’s destined to be stuck at his dead end Best Buy job forever.
Part 2: When Sonia Rehal’s sister passes from complications caused by the rare disease lipodystrophy, she doesn’t know how to define herself in the absence of her other half.
Fernando Leonardo Cuevas is a Theoretical Mathematician by degree, Analytical Engineer by profession, and an avid fan of Brazilian Jiu Jitsu, MMA and pointlessly hard video games.
Sonia Rehal is currently an educator at McMaster University in Hamilton, Ontario and the director for Lipodystrophy Canada, and non-for-profit organization supporting lipodystrophy patients and caregivers. Being a lipodystrophy patient herself, her advocacy for awareness started young. Interested in understanding the pathophysiology of lipodystrophy, her postdoctoral training focused on lipid inflammation and insulin resistance in animal models of obesity. This journey has allowed her to travel the world and publish important research findings in highly cited research journals. More importantly, her academic career has given her a unique perspective to patient advocacy, highlighting how important disease awareness and research funding for prospective treatments and are for the lipodystrophy community. Lipodystrophy can vary in severity however these themes hold in common: Lipodystrophy is incurable, has inadequate medical treatment and affects multiple organ systems. Unfortunately, a severe form of lipodystrophy has affected her family and herself, losing both her mother and sister to its complications at a very young age. This loss has only further intensified her passion to support our rare disease community affected by lipodystrophy.
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