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Content provided by Casey Greer and Cassandra Mendez, Casey Greer, and Cassandra Mendez. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Casey Greer and Cassandra Mendez, Casey Greer, and Cassandra Mendez or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.
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Squid Game: The Official Podcast


Squid Game is back—and this time, the knives are out. In the thrilling Season 3 premiere, Player 456 is spiraling and a brutal round of hide-and-seek forces players to kill or be killed. Hosts Phil Yu and Kiera Please break down Gi-hun’s descent into vengeance, Guard 011’s daring betrayal of the Game, and the shocking moment players are forced to choose between murdering their friends… or dying. Then, Carlos Juico and Gavin Ruta from the Jumpers Jump podcast join us to unpack their wild theories for the season. Plus, Phil and Kiera face off in a high-stakes round of “Hot Sweet Potato.” SPOILER ALERT! Make sure you watch Squid Game Season 3 Episode 1 before listening on. Play one last time. IG - @SquidGameNetflix X (f.k.a. Twitter) - @SquidGame Check out more from Phil Yu @angryasianman , Kiera Please @kieraplease and the Jumpers Jump podcast Listen to more from Netflix Podcasts . Squid Game: The Official Podcast is produced by Netflix and The Mash-Up Americans.…
83. getting personal: recapping 2023
Manage episode 390579972 series 2880558
Content provided by Casey Greer and Cassandra Mendez, Casey Greer, and Cassandra Mendez. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Casey Greer and Cassandra Mendez, Casey Greer, and Cassandra Mendez or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.
Cass + Case give a year in review of 2023, walking through each season and sharing the highlights. They also share their hopes for 2024
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127 episodes
Manage episode 390579972 series 2880558
Content provided by Casey Greer and Cassandra Mendez, Casey Greer, and Cassandra Mendez. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Casey Greer and Cassandra Mendez, Casey Greer, and Cassandra Mendez or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.
Cass + Case give a year in review of 2023, walking through each season and sharing the highlights. They also share their hopes for 2024
…
continue reading
127 episodes
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Rare with Flair

hi, hello, hey, we’re talking all about guide dogs today! 🦮 Over the years, we’ve gotten lots of requests to make an episode all about guide dogs. Whether you’re seriously considering one or just curious about what it takes to get a working dog, this episode is for you! We’ve talked about canes plenty, and even compared pet dogs and guide dogs before, but we never dedicated a full episode to the topic, mostly because Cass is the one with experience, having worked with a guide dog for about eight years (now retired!), while Case hasn’t. So in this slightly atypical episode, Cass takes the lead and shares everything from how to know if a guide dog is right for you, to how to choose from the nearly 15 guide dog schools in the U.S.—each with their own unique approach and vibe. She also walks through the application process at Guide Dogs for the Blind and gives a peek into the incredible training that goes into preparing a dog to become a guide. Got more guide dog (or non-guide dog) questions? Send them our way at hello@rarewithflair.com and we just might answer them in a future episode! Want more cane or dog talk? Check these episodes out! 102. white cane hot takes 92. cass’ guide dog is retiring?! 48. mobility tools therapy sesh 13. ru & ro: guide dogs vs. pet dogs 2. canes, guide dogs, & faking disability Cassandra’s guide dog, Romana, snoozing onstage at the NOAH Con, 2022 show notes the National Federation of the Blind’s list of guide dog schools in the USA check out Guide Dogs for the Blind’s Orientation and Mobility Immersion program !Whether you’re looking to get a guide dog or not, this is a great opportunity to get much needed mobility skills you can learn more from this 20 minute podcast from GDB’s show, Central Bark watch the “Pick of the Litter” documentary by GDB to get more insight into the puppy raising process (and to enjoy some precious pups!). Look it up to see what current streaming options are available, or rent it for a small fee on Prime Video…
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1 122. taking quizzes like it’s a slumber party 41:28
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hi hello hey, ready to get cozy with us?? Longtime listeners know that personality quizzes hate to see us coming. We’ve always loved them, even as kids! So when Cass recently stumbled upon her old American Girl quiz books, we knew we had to bring them to the pod. In this episode, we each take a quiz from one of the three vintage books and find out just how well these throwback quizzes really know us. Spoiler: some results are spot on! And! The day this episode drops (June 24th) is Cass’ 28th birthday! Want to wish her a happy one or send us a question for a future episode? We’d love to hear from you at hello@rarewithflair.com . Check out our other personality quiz related episodes: 113. an instagram reel revealed who we really are 93. the great cardigan debate: our style roots 86. just a couple decisive, self-aware, water signs: revisiting personality types 18. personality types, astrology fails, & words of affirmation Case + Cass at the slumber party for Casey’s 30th birthday, 2022…
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1 121. ranking every disabled character we’ve seen recently 57:51
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hi hello hey, ready for some representation? A few years ago, we did an episode all about disability representation in media (with one of the greatest episode titles in Rare with Flair history), focusing specifically on blind characters in animated and live-action shows and movies. Since then, we’ve come across even more disabled characters (not just with vision impairments!) that we’re excited to talk about and rank for authenticity. This time around, we’re expanding our scope, and with that comes the understanding that many of these characters represent disability communities we’re not part of, like the Deaf community. While we can’t speak for those experiences, we’ll still share our perspectives as members of the broader disability community and approach each portrayal with curiosity and care. We had lots of fun talking about animated and live-action characters, but even included a book and toy, too! Did we miss any characters you love (or hate)? Send us an email at hello@rarewithflair.com and we’ll talk about it on a future episode! Case + Cass after the HPS conference, 2025…
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1 120. still alive but barely breathing lmao: ATS recap 1:05:15
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hi hello hey, we’re exhausted but invigorated! We know we say “this is a special episode” a lot (because, honestly, every episode is special to us). But this one really is: it’s only the third time in Rare with Flair history that we’ve recorded almost entirely in the same room! If you’re new here, you might’ve thought we always record together, but nope! With Case in Tennessee and Cass in Ohio, we’re usually recording from separate states. This time, against all odds (and at the cost of some sleep), we managed to capture a semi-thorough recap of our time at the American Thoracic Society (ATS) conference in San Francisco! This was Cass’s third ATS conference with the Hermansky-Pudlak Syndrome (HPS) Network, but it was Case’s first. The conference is a huge opportunity to connect with researchers, biotech and pharma reps, and organizations who can help us push toward a cure for the pulmonary fibrosis many people with HPS develop. There’s a lot of advocacy, booth-running, and behind-the-scenes hustle, and we’re pulling back the curtain to let you in on all of it. We hope you enjoy our chaotic, sleep-deprived, heart-filled recap of this fulfilling, jam-packed week! Case + Cass in their room at the American Thoracic Society conference, 2025 show notes Check out the reels (Youtube shorts) Case, Cass, and the HPS team made of each day at ATS! Day 1 recap Day 2 recap Day 3 recap Day 4 recap Case & Cass mention the podcast from the opening ceremony speaker called “ The Human Doctor ” so check it out! The host is a doctor who’s a wonderful storyteller, you won’t be disappointed!…
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1 119. we’re each other’s biggest influencer 1:05:19
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hi hello hey, it’s time for a little catch up on what we’re into lately! Once or twice a year, we like to take a minute (or an hour) to catch you guys up on what we’ve been up to aside from going to the Hermansky-Pudlak Syndrome conference and talking all things disability. On this edition of “What Are We Into Lately?,” we talk about the books, music, TV shows, hobbies, and lifestyle changes that have occupied our year thus far. Spoiler alert: we’re each other’s biggest influencers, and we fill you in on all the things one of us recommended that the other one has tried and loved. Have an idea for a future episode or want to comment on something we’re into? You can always send us an email at hello@rarewithflair.com , and we’ll answer it on the next episode (if you want us to, of course!). Cass with her tarts at a wedding and Case hula-hooping on the dace floor at the HPS conference, 2025…
hi hello hey, let’s go to the doctor! It’s been a hot minute since we did an episode on chronic health, but we’re BACK and ready for action! On this episode, we’re diving into what it really means to be your own advocate in the healthcare system, especially when you have a rare disease and a vision impairment. From the constant parade of specialist appointments to the exhausting task of explaining your condition to every new doctor (yes, we’ll gladly spell it… again), we’re sharing our lived experiences navigating medical systems that often aren’t built with us in mind. This episode pairs perfectly with a couple of others from our archive: 117. few but many: hps conference 2025 : our most recent ep, where we shared our reflections on meeting others with Hermansky-Pudlak Syndrome, connecting with researchers, and the joy of community 68. the nih has my colon! the research episode : a behind-the-scenes look at what it’s like to be the research subject, from clinical trials to NIH visits (including what it’s like to keep a jug of pee cold for a day) Cass at the NIH & Case participating in medical research, 2016/2023…
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1 117. few but many: HPS conference 2025 1:23:45
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hi, hello, hey—grab your popcorn, because it’s conference time! As many of you know, we’re two best friends with the same rare disease, living our best lives. We truly wouldn’t be friends without Hermansky-Pudlak Syndrome—or without this incredible conference. It’s where our friendship began, and where we reconnect with our amazing community year after year. We love soaking up the latest research from rising stars in science, catching up with familiar faces, and yes… there’s always some singing involved. Since we (Case & Cass) live in different states, this conference is also one of the rare times we get to hang out in person, making it extra meaningful. This year’s conference had a different vibe from previous ones, but it was still special in its own way. Come along as we recap the highlights! P.S. Don’t miss our episodes from past conference years, too! 16. a family reunion with blood draws: the hps conference (overview of the conference itself, 2021) 66. hps conference: reuniting our community after four years (2023) 91. doctors at a bar, cute lab mice, & dancing dinosaurs: hps conference recap (2024) listener shout-out We love getting mail from our listeners! This week, we’re sharing an excerpt from an email we received from Jeff L., a professor of cello at Texas Tech University who has low vision. He included a link to his YouTube channel , and we were especially wowed by his performance of Bach’s 5th Cello Suite where you can see him using assistive tech glasses to read his sheet music, and his talent truly blew us away. We’re so grateful to Jeff for sharing not only his music but also what the podcast has meant to him. It really means the world to us! Got a story to share, a topic to suggest, or just something cool you want to tell us? Email us anytime at hello@rarewithflair.com , and if you’re cool with it, we might read it on the show! Case + Cass partying at the HPS conference, 2025 show notes Case & Cass talk about Dare to be Rare , a nonprofit started by the HPS Network that sells clothes with the slogan to raise funds for rare disease research. The online store will officially relaunch May 16, 2025 so be sign up for their email list to be the first to hear about it! Cass mentions the Dare to be Rare jingle from 2017 (Youtube) written by Tommy Criblez of the band Ritual Talk (Bandcamp) Just for fun, Cass made reference to our episode 46. how we remember everything for how we are with dates Case is doing work on the HPS Network’s social media! Give them a follow on their various platforms: HPS Network Youtube channel HPS Network on Instagram HPS Network on Facebook Cass & Case mention Rick Guidotti, a former fashion photographer turned nonprofit founder of Positive Exposure . You can also check out Rick’s story in his Ted talk Cass gave a talk on how your iPhone could be a powerful assistive technology device on its own! Check out her slide deck (Canva) Cass mentions a short documentary-style video on the HPS Network at the American Thoracic Society conference in 2024 (Youtube). It’s a little over 20 minutes, but well worth the watch!…
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1 116. rare but radiant: our new and improved skincare routines 49:59
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hi hello hey, let’s talk about skincare today! Skincare has gotten really trendy online thanks to creators on TikTok and Instagram telling your which creams to use to make you look younger. While we’ve talked about makeup and sunscreen some time back, we haven’t done a full skincare routine episode. Even if you’re not a chronically online girlie, cleansing, sunscreen, and moisturizing are for everyone! Join us as we discuss our skin, and the products we’re currently using (as of March 2025) to make our skin a lovely place to be. Also, thank you to Johannah for the listener question that inspired this episode! If you have any thoughts or episode ideas, please email us at hello@rarewithflair.com ! Case & Cass getting their much-needed SPF at the NOAH Conference, 2024 show notes Cass mentions our episode on bleeding management, “let’s talk about blood” Case’s skincare picks: dry skin Morning: sunscreen: EltaMD Clear Mineral Face Sunscreen (Amazon) Night Cleansers CeraVe Hydrating Cleanser (Amazon) Murad Acne Control Clarifying Cleanser (Amazon) Makeup remover: Makeup Eraser reusable microfiber makeup removers (Makeup Eraser) Toner: Neutragena Gentle Daily Toner (Amazon) Exfoliator: Trader Joe’s Nourish Exfoliating Face Scrub Retinol (different products) use with caution!!! Moisturizers Neutragena Hydro Boost Water Gel (Amazon) Trader Joe’s Ultra Hydrating Gel Moisturizer Acne Neutragen Spot Treatment Pimple patches: Beekman 1802 Wicked pimple patches (Ulta) Lotion: Trader Joe’s Body Butter Cass’ skincare picks: oily skin Morning Sunscreen: Supergoop! (Re)setting Mineral Powder Sunscreen in Translucent (Supergoop) Cleansers CeraVe Acne Control Cleanser (Amazon) Typology L12 Purifying Cleansing Gel (Typology) Acne products Typology L39 Day Serum for Blemishes (Typology) Typology L61 Targeted Blemish Serum (Typology) Neutragena Stubborn Acne AM Treatment (Amazon) Moisturizer: Typology L41 Purifying Moisturizer (Typology) Night Makeup remover: Neutragena Night Calming Makeup Remover wipes (Amazon) Acne formula: Curology Custom Formula (Curology) Pimple patches: various from Starface Retinol acne peel: Murad AHA BHA Retinoid Clarifying Peel (Sephora) Lotion: Aveeno Daily Moisturizing Body Lotion (Amazon)…
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1 115. internet fan meetups, unicorn snot, & trying to see the jumbotron 1:03:42
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hi hello hey, ready to rock out at a concert? It’s no secret that we love music, especially seeing the artists we love live. This week, we answer a listener question from Delaney, a loyal fan of Jesse McCartney, about shows we’ve seen, artists we’ve met, and accommodations we’ve either requested or made ourselves to make the most of our show experience. Ever wonder how to go to a festival if you’re chronically ill? Cass takes us on her journey to enjoy the WonderBus festival for the three years she attended it. Which artist do you think Casey has seen the most? Guess you’ll have to listen to find out! Do you want your question turned into an episode?? Shoot us an email at hello@rarewithflair.com , and we just might! Cass at the WonderBus festival in Columbus, and Case at the Eras tour in Nashville, 2022/2023 show notes Casey makes reference to the time Kristen Chenoweth gave her her glitter when Case was just 14! For the full story, check out episode 7. thank you for the music Case & Cass mention high-fidelity earplugs to protect your hearing. Find some good ones in this article (NYTimes Wirecutter) Cass gives her “holy-grail” products that allowed her to successfully attend WonderBus while blind and chronically ill, and here are the keys to her success: Coolibar for UPF sundresses Wide-brimmed hat Unicorn Snot glitter sunscreen Camelbak hydration backpack DripDrop oral rehydration solution (electrolytes) Light blanket to sit on the grass (used the free one that she got on a plane)…
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Rare with Flair

hi hello hey, sometimes we can’t see things… and maybe that’s okay? Like most of our episodes, this topic was inspired by something in our real lives – in this case, a fantastic interview with Camryn Yule (YouTube) , a person with albinism who was in Wicked ! No spoilers, but Camryn talks about the need to “read the room” and be discerning about when to request accommodations, and when to let it go, to not hold up production in a fast-paced environment. This sentiment really resonated with us, and we knew we had to deconstruct it on the pod. Before you get worried that we’re not advocating for ourselves, we’re not recommending putting advocacy aside! We’ve talked about making sure you have what you need and disclosing in a variety of episodes, including: 108. the wound that never heals: our discrimination stories 97. how we stopped word-vomiting all our struggles 71. oversharing on facebook: our online advocacy journey 44. the beginner’s guide to disclosing disability 38. our jobs, discrimination, and unattainable goals 37. dear younger self: our advocacy journey 27. an engineer & an actress go to college 5. school days, accommodations, & finding the lunch table Instead of talking about times we haven’t advocated for our needs, we focus on the situations it’s absolutely necessary to make your voice heard, and say that anything beyond the necessary is up to your discretion. Sometimes, it’s okay not to see every little thing if the disruption of having your needs met doesn’t outweigh the benefit you get from seeing. Do you agree with us? Let us know what times are non-negotiable or completely skippable! Cass + Case on the High Line in NYC, 2024…
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1 113. an instagram reel revealed who we really are 48:43
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Case + Cass explore their personalities in a new way through the lens of personality tests from Instagram reels.
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1 112. a grocery delivery shopper yelled at cass?? 56:02
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Case + Cass talk about the grocery delivery services they use, shocking mishaps, and the kindest shoppers who went above and beyond.
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Case + Cass share how they pay it forward, from thanking friends for rides to showing care for loved ones in thoughtful ways.
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Rare with Flair

Case + Cass share their 2025 vision boards, their word for the year, and what they plan to stop, start, or continue in the new year.
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1 109. our wildest vision board dreams came true! 1:11:57
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Case + Cass review their vision boards for 2024 to see how their years measured up. They also give highlights of their year in seasons.
Case & Cass share frustrating discrimination experiences—rideshare denials, job stories, and some shocking, never-told moments.
Case + Cass chat about childhood video games, what they play now, and their tips for making gaming more accessible with low vision.
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1 106. we’re delulu about what we look like in public 55:10
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Case + Cass talk about how, despite their best efforts, they always look a little odd in public when trying to look "normal."
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1 105. case & cass’ carTWOon adventures 1:11:28
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Case + Cass talk about four more cartoons they've watched together in the last year and a half and plug other cartoons they've seen lately.
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Case + Cass share the uncomfortable, rude, silly, and ableist things people have said to them in public about their vision.
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Rare with Flair

1 103. live from columbus: recapping our amazing weekend 49:54
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Case visits Cass in Columbus! The two recap their jam packed weekend of candles, bookstores, bakeries, and the renaissance fair.
Case + Cass bought new canes and give their reviews. They also share hot takes on different cane styles and explain the benefits of cane use.
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1 101. cass has curly hair & case is running?! 59:19
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Case + Cass talk about what they've been into lately, including self-care, hobbies, side hustles, and media they've enjoyed.
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1 100. over one hundred hours of us yapping!!! 1:14:45
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Case + Cass celebrate releasing over 100 episodes and list their all-time favorites along with other episodes they’re proud of.
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1 99. the unhappiest place on earth: discrimination at disneyland 1:01:02
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Case + Cass share their humiliating experience trying to get the DAS pass accommodation on their recent trip to Disneyland.
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1 98. rolling out the red carpet for the albinism conference 1:24:58
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Case + Cass recap their time at the albinism conference in California. They talk about sessions they led and spending time with friends.
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1 97. how we stopped word-vomiting all our struggles 1:11:59
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Case + Cass touch on what oversharing looks like and how they used to give too much information about their health and life.
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Case + Cass talk about their bleeding disorder, how it affects them, and how they manage it. They also share some not-too-gory stories.
Case + Cass run through the things they’ve changed in their condos since early 2022 and how their homes have evolved to be more “them.”
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Rare with Flair

1 94. fear of photos or light sensitivity: the photophobia episode 58:23
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Case + Cass talk all about their light sensitivity, and how it affects them outdoors and indoors, including their favorite sunglasses.
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