Show Notes
If you've been looking up some Oscar-nominated short films to watch before the awards show, you may have noticed one called "Jane Austen's Period Drama". Seeing this in theaters inspired Kate to finally release two interviews with indie artists - one feature filmmaker, and one novelist - who have released work about their period pain! Novelist Grace Daly, Bram Stoker Award-nominated author of The Scald Crow, has experienced debilitating symptoms from her endometriosis, adenomyosis, M-CAS, EDS, and POTs since she was 11, and has struggled to get doctors to take her seriously or treat her. She's woven those experiences into a classic haunted-house story with many twists that is SO FUN to read! Find the Scald Crow by Grace Daly anywhere that books are sold, or order on bookshop.org here: https://bit.ly/4uehIlD Filmmaker Brooke H. Cellars had period pain so excruciating it made it impossible for her to finish college or hold down a full time job. It took her 20 years to finally get diagnosed and treated surgically for endometriosis. Post-surgery, with hormone treatments to manage the endo, she was able to finish college and begin a career in writing and directing. Her feature film The Cramps: A Period Piece blends her real-life experience with a "darkly colorful", campy 80s aesthetic. Watch the trailer on youtube here: https://bit.ly/4cziaER __________ CRAMPED episodes are intended for informational and entertainment purposes only, and are not medical advice. Support CRAMPED by joining the Patreon at https://www.patreon.com/c/CRAMPED See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.
More from CRAMPED
This whole year, I've been secretly working on a 6-episode audio series about the Magic Wand Study - and now it's out! I teamed up with DB from Sex Ed with DB, and CRAMPED Season 1's sound designer Kelly, to make this deep dive into Magic Wand's 1000-person IRB-approved pleasure study, one of the biggest studies ever done on pleasure in people with vulvas. Here's episode 1 for your aural pleasure - head over to the Pleasure People feed to listen to episode 2 (out now as well!) and subscribe to listen to whole series.
Kelly Ripa has a podcast called Let's Talk Off Camera! It dives deep into Kelly's life, candidly discussing her marriage, family, career, and how she manages to juggle it all in the public eye. I hope you check it out and that you enjoy it as much as we do.
Deb's story sounds like a lot of crampers' stories: she was on birth control, started having pain and GI issues, and sought answers from her doctor. Despite doing her research, she ended up getting a surgery that not only didn't help...it made her pain and other symptoms worse. After finally getting the help she needed, she created a resource to empower endo patients to choose an experienced excision specialist - the Wulf Women directory. Wulf Women website: https://wulfwomen.com/ Deb's IG: https://www.instagram.com/wulfwomen/ Deb's Tiktok: https://www.tiktok.com/@wulfwomen
Maybe you've heard - if you've got ovaries, you've got a whole new organ! Well, "new" as in "recognized by science for the first time since the 1800s". It's been in there, doing stuff, this whole time. So what's the deal with the Rete Ovarii? What's it doing in there? Why did this organ get "mysteriously orphaned" after its discovery? And how do you minimize coffee jitters when dissecting a fetal mouse's ovary with tweezers and a microscope? I ask all these questions and more to Dilara Anbarci, PhD post-doc and author of the research paper that's going viral. Rediscovering the Rete Ovarii - Dilara's paper: https://pmc.ncbi.nlm.nih.gov/articles/PMC10659334/ Dilara's Instagram: https://www.instagram.com/somethingaboutdilara/ Dilara's TikTok: https://www.tiktok.com/@dilaraphd?lang=en
You probably saw the news: the condition formerly known as Polycystic Ovary Syndrome (PCOS) is now Polyendocrine Metabolic Ovary Syndrome (PMOS). So...what does that mean exactly? Why did the name need to be changed? And why did it take 20 years to actually make it happen? Dr. Helena Teede, the Director of the Monash Centre for Health Research Implementation in Australia, has been leading this effort. She gives us the lowdown on why PCOS was a medically inaccurate name, how the name of a condition can make it harder to diagnose patients, and how she lead 22,000 people worldwide in a collaborative process to re-name a condition that hundreds of millions of people experience. More info on PMOS at: https://www.askpmos.org/