Rare with Flair

Casey Greer and Cassandra Mendez

Casey + Cassandra are a pair of best friends with the same rare disease. Their goal is simple: sharing their lives to showcase the beauty and normalcy in disability, while having fun together. They’ll also touch on accessibility, friendships, style, and everything in between as they live their best, rare, lives! For show notes, go to rarewithflair.com

  1. May 12

    "anyways, i'm disabled"

    hi hello hey — we’re visually impaired Hopefully this isn’t news to our audience considering we’ve made nearly 150 episodes of us yapping, largely about our blindness. We’ve done many an episode about disclosing our disabilities in different settings — jobs, friendships, dating, and learning how to say just enough without accidentally info-dumping on unsuspecting strangers. Even with the same jobs and friends, we still find ourselves disclosing all the time, but nowhere does it feel more constant than while dating. Cass is out there, and before meeting the love of her life, Case also often found herself playing what felt like a game: trying to disclose casually in a way that felt conversational instead of Serious™. Somewhere along the way, we realized we’d both become oddly skilled at finding ways to bring up blindness in nearly any topic of conversation. Naturally, we decided to turn it into an actual game. In this episode, we put our disclosure abilities to the test: can we find a way to disclose our blindness with any conversation prompt? related episodes For more episodes on disclosing, check these out: 14. life, love, & dating with a disability for our thoughts on dating way back in 2021 38. our jobs, discrimination, & unattainable goals on disclosing for work 44. the beginner’s guide to disclosing disability on disclosing in dating and beyond 97. how we stopped word-vomiting all our struggles on oversharing or disclosing too soon 114. please, read the room!!! on when to disclose vs. when to let it go 124. we’ve changed our minds?: our 5 year podaversary on the ways we’ve changed over the years, including disclosure and accepting help Case + Cass during Case’s bachelorette, 2026

  2. Apr 28

    we secured the grant: HPS conference 2026 recap

    hi hello hey… we’re not ready to be back Physically, we’re home, but mentally, we’re still at the Hermansky-Pudlak Syndrome Conference. This year was extra special because we secured a Grant—Newkirk, that is. Case’s fiancé, Grant, joined the conference chaos for the first (and certainly not the last) time, and it made everything even more fun. We get into the excitement (and vulnerability) of bringing someone new into a space that feels so unique to our community—and spoiler alert: Grant was welcomed with open arms. This year’s conference was on the smaller side, but still just as meaningful. We’re recapping it all—from our many involvements to our favorite moments. To everyone we saw—old friends and new—it’s always such a joy to connect with this community. HPS is just the first of three conferences we’ll be at this year, so stay tuned for more recaps in the coming months… some of which may turn into chaotic live episodes. Case + Grant (+ Cass) at the HPS conference, 2026 related episodes Check out past HPS conference eps to relive the magic 16. a family reunion with blood draws: the hps conference (2021): a primer on all things conference 66. hps conference: reuniting our community after four years (2023) 91. doctors at a bar, cute lab mice, & dancing dinosaurs: hps conference recap (2024) 117. few but many: hps conference 2025 Still on a conference kick? Enjoy other episodes where we recap conferences: 50. squinting in orlando: albinism conference recap NOAH 2022 98. rolling out the red carpet for the albinism conference NOAH 2024 120. still alive but barely breathing lmao: ats recap our time at the American Thoracic Society in 2025

  3. Apr 14

    passenger princesses: zero miles driven

    hi hello hey, guess who has the best job?? us, because we don’t have to drive! We’re all well aware of the perks of driving—the privacy of your own car, the freedom to go anywhere at any time—but what about the perks of being a passenger princess (or prince)? Driving takes visual, mental, and physical energy that we simply don’t have to spend, which means more room to save money, relax, and stay relatively safe. We also talk about the importance of finding ways to navigate semi-independently and encourage y’all to lean into it when possible—whether that’s public transportation, rideshares, or tapping into your broader community instead of relying on the same person every time. However you do it, we hope you flex those mental muscles and get creative if you’re feeling stuck. We had so much fun recording this episode—something about it felt like classic Rare with Flair. Don’t worry though, we’ll be back to our usual shenanigans next episode as we recap the 2026 Hermansky-Pudlak Syndrome conference! related episodes For more episodes where we talk about driving (or not driving), check these out: 23. two blind girls take a driving test: why we choose not to bioptic drive (+ a quiz that proves how little we know about driving) 65. feeling like a burden: a vulnerable discussion on how not driving makes us feel 111. lifting the burden: how we pay it forward: how we give back to those who help us out Case + Cass attempting to drive with their dads, 2019/2021

  4. Mar 3

    oops, all blindie moments

    hi hello hey, welcome to a normal day in our lives! If you’ve heard even one episode of our show, you know we tend to save some of our best blind/disability moments for the pod to really bring our lovely listeners into our world. Whether it’s helpful perspective for listeners without disabilities or catharsis for listeners like us, we usually pull out the wildest ones. What you may not know is that those big, shocking stories actually happen somewhat sparingly. The little moments? Those happen practically daily. They’re so normal to us that sometimes we don’t even think to share them with each other. This episode is a collection of those moments — the quiet, low-key, blink-and-you’ll-miss-it (well… metaphorically) blindie experiences that make up our actual, everyday lives. No dramatic plot twists. No public showdowns. Just the cozy, mildly chaotic reality of existing in the world as blind girls trying to find forks, navigate doctor’s offices, and keep it moving. Because this is what disability looks like on a random Tuesday. Case feeling attacked by the impossible “Magic Eye” book while Cass feels seen by the large print books display, 2026/2024 related episodes Ready for more story time, big or small? Check these episodes out: 31. too blind to be sighted; too sighted to be blind living in the “gray area” between sighted and blind. 40. this one’s tmi… some of our most unfiltered chronic illness stories. 52. our lives are just one long, awkward moment a series of uncomfy social situations caused by our low vision. 63. our uber funny rideshare stories some of our wildest (and weirdest) rideshare experiences. 79. our lives are one huge contradiction times we saw things we felt we shouldn’t… but couldn’t see things we should. 99. the unhappiest place on earth: discrimination at disneyland our humiliating attempt to get DAS at Disneyland in 2024. 104. did they really just say that?! a smattering of some of the most shocking things people have said to us 106. we’re delulu about what we look like in public why we can’t fake looking “normal” and the stories to prove it. 108. the wound that never heals: our discrimination stories the most deeply cutting discrimination we’ve experienced in our lives 112. a grocery delivery shopper yelled at cass?? chaos from the world of grocery delivery. 137. sorry, my brain was buffering stories of when our processing speed said “please hold.”

4.9
out of 5
84 Ratings

About

Casey + Cassandra are a pair of best friends with the same rare disease. Their goal is simple: sharing their lives to showcase the beauty and normalcy in disability, while having fun together. They’ll also touch on accessibility, friendships, style, and everything in between as they live their best, rare, lives! For show notes, go to rarewithflair.com

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