Podcast
A Friend for the Long Haul: A Long Covid Podcast
Hosted by A Friend for the Long Haul · EN
Are you struggling with Long COVID-19, ME/CFS, chronic illness, or disability? "A Friend for the Long Haul" is a Long COVID podcast that aims to be a supportive companion. This podcast offers insights, humor, and shared stories within a community that understands. Each episode features a Long COVID patient or ally to help you feel less isolated, because you are not alone.
13episodes
Episodes
Newest firstAll episodes
The Spoonie Plant Guide: Low-Maintenance Houseplants for Spoonies ft. Megan Wages of Fancy Free Nursery
1w ago00:36:20Tap to summarizeWelcome to S04E09 of A Friend for the Long Haul - A Long Covid Podcast. This episode is part two of my catch-up chat with Megan Wages, my second-ever podcast guest, first wave Covid long hauler, co-owner of Fancy Free Nursery in Tampa, Florida, and the guest of last week's S04E08, Running a Small Business as a Covid Long Hauler with Megan Wages. In this episode, we talk about plants! I've become a plant lady in the last 6 years, and I've noticed that my plants tend to tell me a lot about how I'm feeling. First I noticed that the downstairs ones were fine. The upstairs ones were so sad. Turns out there's a reason for that. In Part 2 of this two-part episode, we get into the actual plant content. Specifically: what should a spoonie with limited energy, unpredictable symptoms, and a complicated relationship with energy actually grow?The answer is: more than you think. Megan walks through her spoonie-approved plant list, propagation tips, why your Calathea's attitude is not your fault, and the thing fluoride in tap water does to your spider plant. She also answers listener questions live, talks about soils, orchids in wine decanters, and the surprisingly emotional experience of a plant that keeps coming back no matter how badly you've neglected it.There's also a spider plant baby giveaway. Alysia won. She lives in a basement apartment and this is probably the perfect plant. I wish I had the spoons to get to the post office and send it to her. One day, my love!!! I promise!IN THIS EPISODE:Snake plants and ZZ plants: the spoonie ride-or-diesZZ Raven: the black plant for the goth baddiesPothos propagation and the hormone tip nobody talks aboutWhy I am a self-described prop lifterThe "teats" moment (you'll know it when you hear it)Ripsalis: if spaghetti became a plantSpider plants and the fluoride problemBurgundy rubber tree, Tineke, and the fiddle leaf fig blue sky tipOrchids in wine decanters: the lab aestheticAlocasia: pretty, finicky, spider mite magnetsWhy Walmart plants are a gamble (the fish department story)LECA: the water-to-soil bridge methodYour plant's health as a mirror for your mental healthListener questions answered Spider plant baby giveaway 🌱LISTENER QUESTIONS ANSWERED:Tara's 20-year fiddle leaf fig: how to help her thriveMonstera propagating in water: when and how to move to soilCan you bring an orchid back to life?Best plants for a low-light basement apartmentYou can find MeganFancy Free on InstaMegan on TikTokA Friend for the Long HaulA Friend for the Long Haul on Insta and TikTokSubstack: https://f4lh.substack.com/The podcast playlist on SpotifySupport this PodcastI'm a disabled lady doing this whole podcast on my own. If you would like to support the podcast, please subscribe and follow, engage with my posts, comment, and share episodes that resonate with you! Those are the biggest ways you can support me and my work.If you'd like to get some of my merch, check out my Bonfire shop! All proceeds are funneled back into the podcast for tech or used for community care and mutual aid. I don't keep the proceeds.I do have an Amazon gift registry that update for the summer each year. We are a blended family of 6 and all of us have disabilities. Some of our kids have complex medical issues as well as intellectual and physical disabilities, and we're increasingly neurodivergent. Summers get emotional, kids get boring, and the parents work from home without a "village" or the luxury of childcare. This summer gift registry keeps us afloat. ---If you'd like to be a guest on the show or suggest a guest, please use this form! https://forms.gle/q9wiV6mQ4G3SMBu99 Thank you for listening to and supporting A Friend for the Long Haul!
Transcribe →Running a Small Business as a Covid Long Hauler with Megan Wages
2w ago00:21:16Tap to summarizeWelcome to S04E08 of A Friend for the Long Haul - A Long Covid Podcast! I'd like to share that this will be the first installment of a change to the podcast: shorter episodes! Longer recordings will be chunked into more digestible episodes, for all our spoons.Six years ago, my friend Megan bit into a raw onion to see if she could taste it. She couldn't, and that's how her long covid story starts. She was my second guest on this podcast, and in this segment, she's back to give us an update on how she's feeling and to talk about what it's like to run a small business with your spouse when you get sick. Megan is the co-owner of Fancy Free Nursery in Tampa, a first wave long hauler, and we discuss:Long covid friendshipsPerimenopauseGLP-1s (anecdotal! talk with your doctor! don't judge other people! don't compare yourself!)Running a plant shop and floral nursery during lockdownHow plants saved the shopBusiness collabsUsing and running social media when you're your only teamBranching out into silk floralsYou can find MeganFancy Free on InstaMegan on TikTokA Friend for the Long HaulA Friend for the Long Haul on Insta and TikTokSubstack: https://f4lh.substack.com/The podcast playlist on SpotifySupport this PodcastI'm a disabled lady doing this whole podcast on my own. If you would like to support the podcast, please subscribe and follow, engage with my posts, comment, and share episodes that resonate with you! Those are the biggest ways you can support me and my work.If you'd like to get some of my merch, check out my Bonfire shop! All proceeds are funneled back into the podcast for tech or used for community care and mutual aid. I don't keep the proceeds.I do have an Amazon wishlist that I add everything I need or randomly like to and you can 100% track my state of mind, hyperfixations, and fears looking at it. ---If you'd like to be a guest on the show or suggest a guest, please use this form!Thank you for listening to A Friend for the Long Haul!
Transcribe →Finding the Magic in Surviving: Tarot, Self-Efficacy, and Reclaiming Joy with Megan Hamilton
3w ago00:48:45Tap to summarizeWelcome to season 4 episode 7 of A Friend for the Long Haul - A Long Covid Podcast! What can tarot have to do with rebuilding your sense of self after chronic illness? More than you might think.I sat down with Megan Hamilton, a professional tarot reader, speaking coach, musician, and host of the Embracing Enchantment podcast, for a conversation about identity loss, the grief of realizing you can't go back to who you were, and why the safety we thought we had was maybe never quite real to begin with.Megan introduced me to a concept called self-efficacy, which is the idea that keeping the promises you make to yourself, even tiny ones, builds the kind of trust with yourself that actually sticks. We talked about why celebrating a small win is genuinely neurological rewiring, not toxic positivity. And somehow we ended up at a very personal confession about how long I sometimes wait to go to the bathroom.We also got into tarot as a tool for accessing truth you can't reach through thinking alone, why ritual doesn't have to be elaborate to be meaningful, and what it actually looks like to find magic inside a life that's been turned upside down.Megan is one of those people who makes you feel immediately at ease and then quietly rearranges how you see things before you've realized it's happened. This one is for anyone who is learning, slowly and imperfectly, to treat themselves like someone worth taking care of.Find Megan's podcast information at embracingenchantment.com and follow Embracing Enchantment wherever you get your podcasts. If you'd like to book a reading with Megan, or work with her as a coach, check out https://www.impactwitch.com/ Resources & mentions in this episode:Mundane Magic by Molly Donlan (Megan mentions "pub day" for this new book. We recorded this a few months ago and I've been delayed in releasing new episodes because of my TBI symptoms.) Self-efficacy: concept introduced by psychologist Albert BanduraConnect with A Friend for the Long Haul:Email: afriendforthelonghaul@gmail.comLong Haul Line: 720-432-9368Substack: f4lh.substack.comMerch: Bonfire shopAmazon storefrontAnd on Instagram at both https://www.instagram.com/impactwitch and https://www.instagram.com/embracingenchantmentpod This show is just me. One AuDHD, queer, disabled lady with multiple chronic illnesses and one very mildly decent mic. I do everything you just watched with no team, no network, and no budget, which is either impressive or unhinged. Possibly both. If this episode meant something to you, I'd appreciate your kind support by sharing it with someone who would also enjoy it. You can also leave a review wherever you're listening, spoons permitting. It genuinely changes what this little show can do. There's also merch and a chaotic Amazon wishlist that help loads if you want to support that way. Okay. That's it. Low budget, high love, always. I'll see you next time.Connect with Beth:Email: afriendforthelonghaul@gmail.comLong Haul Line: 720-432-9368Substack: f4lh.substack.comMerch: https://www.bonfire.com/store/a-friend-for-the-long-haul/My Amazon WishlistVenmo: @afriend4thelonghaul
Transcribe →Rooted in Community: Art, Disability Justice, and Growing Something Beautiful with Amaranthia Sepia
Apr 2801:00:54Tap to summarizeWelcome to season 4, episode 6 of A Friend for the Long Haul - A Long Covid Podcast! One of my very favorite people is back on the pod: Amaranthia Sepia, co-founder of Sista Creatives Rising, commissioned seed packet artist for Sista Seeds, and now digital media manager for the disability and design podcast Down to the Struts. Amaranthia is a 26-year-old Black, disabled, neurodivergent artist and organizer based in New Hampshire, and in this conversation we get to really dig into her story, not only as a creative behind Sista Creatives Rising, but as an artist whose work is rooted in her family's gardening history, her love of Black women and the land, and her own hard-won journey toward self-preservation and community.We talk about her stunning seed packet illustrations for Sistah Seeds, founded by Amirah Mitchell. From the website: "In 2021, Amirah founded Sistah Seeds to connect black and brown growers to our culturally-important seeds. Sistah Seeds is one of a small but growing number of black-owned seed businesses in the U.S., changing the landscape of the seed industry. Together, we are part of a multi-ethnic, multi-national movement of farmers and seed-keepers, working to preserve our heritage and create a strong agricultural future for our communities."We also talk about hydroponics, healing, and how growing food for her mom during a health crisis sparked something lasting. We talk about Amaranthia's new role at Down to the Struts, how an unexpected $3,000 Social Security notice lit a fire under her to pursue additional work, and why remote, disability-justice-rooted employment is the difference between thriving and burning out.We also discuss what it's meant to find a vibrant disabled community online after years of navigating bullying, racism, misogynoir, and ableism...including the assumption that being homebound automatically means your life is sad and small. (Spoiler: it absolutely does not.)We also talk about Lilette, the tiny blue masking frog who has become the mascot of Sista Creatives Rising and might just end up in a children's book. No promises. But also maybe.Links mentioned in this episode:Sistah Creatives Rising: sistahcreativesrising.comSista Seeds: sistahseeds.comDown to the Struts (podcast on disability & design): downtothestruts.com Sista Creatives Rising on Instagram (for Lilette merch & links)The Sistas Uprising Fund micro grantsMentioned or featured in this episode:Katrina Dreamer (my pacing buddy, ep. 1, season 2 & season 3)Lissy Donovan (long hauler and business owner, ep. 9, season 3)📞 The Long Haul Line: 720-432-9368! Call or text to share a story, suggest a guest, or just say hi!📧 Email: afriendforthelonghaul@gmail.com📬 Substack: f4lh.substack.comI'm also on Instagram.A Friend for the Long Haul is a low budget/high love production made by a disabled one-woman operation. If it means something to you, share it with someone whose earballs need it. Thank you!You can support this podcast by checking out:My online shop full of long covid merch (tees, bags, etc)Sending me something useful from my Amazon gift listSharing episodes, reels, and my unhinged memesThank you!
Transcribe →A Friend for the Long Haul - A Long Covid Podcast: Strangely Optimistic, A Long Covid Film by Nina Storey
Apr 1200:22:43Summary readyHi! This bonus episode of A Friend for the Long Haul - A Long Covid Podcast was recorded in the spur of the moment on our phones, so it's nowhere near studio quality! I literally called Nina to see if she was free, and she was in a parking lot with Bubsie in the backseat. ---What if dark humor and salt could help shine a light on the often invisible world of Long Covid, chronic illness, and disability? Nina Storey, a long hauler who is a singer, songwriter, and comedy writer, decided to create a short film capturing the unpredictable reality of living with Long Covid. Despite the struggles and a very tight deadline, Nina's film, Strangely Optimistic, is a powerful testament to finding joy amid chaos, and it was all crafted in just five days for the 13th Annual Easterseals Disability Film Challenge. In this bonus episode of A Friend for the Long Haul - A Long Covid Podcast, Nina shares the story behind her dramedy and how her personal experience with Long Covid motivated her to push for greater awareness through storytelling. We discuss how she balanced creative vision with her physical health, why representation in media for invisible illnesses matters, and the key role humor plays in survival and advocacy. We speak of the strength of those of us living with chronic illness and disability, the power of community support, and the importance of authentic, unfiltered stories in changing perceptions. This isn’t just about Strangely Optimistic, it's about reminding us all that even in our darkest moments, humor and authenticity can pave the way for connection and understanding. If you’re living with chronic illness, caring for someone who is, or simply want to learn how storytelling can be a form of advocacy, this conversation offers inspiration and practical insight. Nina’s journey shows us that visibility is also about giving voice to the unspoken and challenging the stereotypes. And the occasional fart joke doesn't hurt.Find Nina’s film at https://www.strangelyoptimisticmovie.com or on the Easterseals Disability Film Challenge YouTube channel here: • Strangely Optimistic - 2026 Easterseals Di... Please engage with the video on the Easterseals channel - there are prizes for several different winning categories! Likes, comments, and shares of the YouTube video of Strangely Optimistic all contribute. Thank you! Oh, and if you watch the video and spot Nina's homage to me, comment on it and tag me! :) How to Support the Awareness Campaign: From April 4–13, the public can support the film’s mission by watching, liking, and commenting on the official Easterseals YouTube and Facebook posts. These engagement metrics directly contribute to the "Best Awareness Campaign" award, elevating the conversation around Long COVID on a global stage. Thank you so much! And thanks for listening to and supporting A Friend for the Long Haul!Also mentioned in this episode: Dr. Wes Ely's Reverse Long Covid Trial: https://www.reversinglongcovid.org/Beth's "Rest is Medicine" shirt is by Dr. Julia Moore Vogel, and you can see her craftiness on her Instagram account: / pineapple_sewing If you'd like to support A Friend for the Long Haul, you can do so by: Subscribing to this YouTube channel!Following on Instagram: / afriendforthelonghaul Substack: https://f4lh.substack.com/TikTok: / afriendforthelonghaul Send me something helpful from my Amazon Wishlist: https://www.amazon.com/registries/gl/...Buy your everyday goods through my Amazon Storefront: https://a.co/d/05Dr2htOLike and share when an episode moves you! Thanks so much! I am a one-woman disabled by LC team!
SummaryLong Covid, Mental Health, and Finding a Therapist Who Gets It: A Conversation with Olivia Belknap
Mar 3101:08:43Tap to summarizeWelcome back to A Friend for the Long Haul - A Long Covid Podcast! I have wanted to have Olivia Belknap on this podcast for a long time, and I'm so glad we finally made it happen! Even though I was terribly late and embarrassed lol - Olivia was so kind and gracious!Olivia is a marriage and family therapist in California working with neurodivergent, chronically ill, COVID-conscious, and queer folks...basically all our favorite people. She's also a long hauler herself, which means this conversation is honest, specific, and zero percent "have you tried going outside more?"We talk about what it actually means to find a therapist who understands long COVID and chronic illness, and what it costs your nervous system just to get through a single day. We talk about why the therapeutic relationship matters more than any modality, more than EMDR, more than IFS, and why compartmentalizing your COVID consciousness in a session that's supposed to feel safe defeats the whole purpose.We also get into the messier stuff: the overlap of neurodivergence and chronic illness, interoception and why so many of us are simultaneously dissociated and hyperaware, the boom and bust burnout cycle, complex pandemic trauma, and the very specific exhaustion of being a chronically ill therapist who conducts sessions from the couch during a POTS flare while helping other people regulate their nervous systems.Olivia is also doing really important work to educate other clinicians because she doesn't think you should have to spend your session time teaching your therapist what long COVID is. That is not what you're there for.Topics covered:COVID-informed and COVID-conscious therapyLong COVID and mental healthFinding a therapist who understands chronic illness and disabilityThe overlap of neurodivergence and long COVIDInteroception, alexithymia, and body disconnectionComplex pandemic trauma and ongoing relational traumaPacing, burnout, and nervous system regulation for chronically ill peopleDynamic disability and how symptoms present in therapyBarriers to accessing therapy as a chronically ill personEMDR, IFS, and trauma-informed care for long haulersThe COVID-conscious therapist directoryPOTS, MCAS, ME/CFS, and neurodivergent-affirming careMentioned in this episode:Olivia Belknap: @oliviabelknaptherapy on Instagram | oliviabelknaptherapy.comBeyond Fatigue and Brain Fog: Help for Today's Cognitive and Health Issues: presentation through the Chicago School of Psychology with Olivia Belknap, Erin Batali, and Kate McNultyThe COVID-Conscious Therapist DirectoryDisability Visibility by Alice WongInternal Family Systems (IFS) | EMDR📞 The Long Haul Line: 720-432-9368 - You can leave a message or text this number anytime - leaving questions, messages, or guest suggestions📧 Email: afriendforthelonghaul@gmail.com📬 Substack: f4lh.substack.comA Friend for the Long Haul is a low budget/high love production made by a disabled woman. If it means something to you, share it with someone whose earballs need it.If you'd like to help me keep the podcast going, you can:get your Amazon staples through my Storefrontgrab me something I could use from my Amazon Wish ListPurchase some long covid gear through my online store, where I sell tshirts, mugs, bags, etcCheck out my long covid stickers for sale
Transcribe →We All Need a Witness: A Conversation with the COVID Long Haulers Podcast
Mar 2300:56:30Tap to summarizeWelcome to season 4, episode 3 of A Friend for the Long Haul - A Long Covid Podcast! What was supposed to be a quick 10-to-15-minute chat turned into three hours. I am not sorry.CW: We do discuss topics such as medical trauma and gaslighting, the Faces of Covid Victims project, and the fear that wells up when folks in your support group don’t post for a while.I got to sit down with Emerson and Jessie from the COVID Long Haulers Podcast and at the end, I announced that I’m adopting them. We talked for so long that what you're hearing is just my portion of the conversation, and it still clocked in at an about an hour. That tracks.We talked about how both of our podcasts started: out of desperation, out of Discord servers, out of needing to find even one other person who understood what it felt like when plain water dehydrates you, or when your symptoms are so bizarre and so new that you don't have words for them yet. We talked about what it costs to do this work when you're homebound, bedbound, or running on borrowed spoons. And we talked about something that I think about a lot, which is what it actually means to be witnessed. Not fixed or reassured or told be positive. Just truly seen by someone who says: that sounds really hard.We clearly didn't want this conversation to end. I hope you feel the same way while listening to it.This is a Long COVID Awareness Month episode about grief, gallows humor, knitted activist vests, and the community that keeps showing up when everyone else kind of backs into the bushes like Homer Simpson.Topics covered:Long COVID community and patient-led advocacyIsolation, online support, and the limits of our abled friends and familyMedical gaslighting Grief, mortality, and bearing witnessPrivilege and representation in patient storytellingDysautonomia, POTS, MCAS, ME/CFS, and medication sensitivityCommunity-sourced treatment knowledge (we talk about meds that have and have not worked for us - always consult your doctor before trying anything new!)Co-hosting a podcast while chronically illRELEVANT LINKS:As a Linguist, I want to find the words to measure chronic illness by M. Corvi in The Sick TImesCovid Long Haulers Podcast Support Discord📞 The Long Haul Line: 720-432-9368, call or text anytime 📧 Email: afriendforthelonghaul@gmail.com📬 Substack: f4lh.substack.comA Friend for the Long Haul is a low budget/high love production made by a disabled one-woman operation. If it means something to you, share it with someone whose earballs need it. You can support this podcast by buying long covid merch from my shop, buying your goods via my Amazon Storefront, or sending helpful stuff from my Amazon wishlist.
Transcribe →The Friends Who Show Up: Love Letters to the Long Covid Community
Mar 2000:38:41Tap to summarizeWhat does it really mean to be supported when you're living with Long Covid? In this special community episode, I share stories submitted by long haulers, caregivers, and allies...real voices answering questions about isolation, chosen family, and the kind of help that actually helps.Contributors include Dr. Julia Moore Vogel, pacing buddy extraordinaire Katrina Dreamer, Nina Storey, Katherine Fox, and members of the Covid Long Haulers podcast Discord, (Thank you to Emerson, Jessie, Mika, Vic, Kai, Robyn, Joyce, Jojo, and more) along with a handful of anonymous long haulers who remind us that sometimes the people who understand us most are the ones whose legs we've never seen.This episode explores what it looks like when community shows up: friends attending doctor's appointments to combat medical gaslighting, online friends building their own Covid-conscious community across Switzerland, a rental cat named Katja who has thoughts about pacing, and two little boys - Ellis and Holden - who became besties on PlayStation because their moms both have Long Covid and, as Ellis put it, "we understand each other."Contributors also talk about what people get wrong when they try to help, and what "let me know if you need anything" actually sounds like to someone who's already been fighting for their life for years.This is an episode about what we've built together. Not in spite of this illness, but because of it.Topics covered include:Long COVID community and chosen familyIsolation and online support for long haulersWhat caregivers and loved ones get wrong about supportCovid-conscious community buildingPeer support, pacing buddies, and mutual aidChildren of long haulers finding connectionLong Covid Awareness Month 2026Mentioned or featured in this episode:The Covid Long Haulers Podcast (Emerson & Jessie)Dr. Julia Moore VogelNina Storey (singer-songwriter & long hauler)Katrina Dreamer (my pacing buddy, ep. 1, season 2 & season 3)Lissy Donovan (long hauler and business owner, ep. 9, season 3)@alecbradburyfnp, @_jemma_bella, @dougieslifewithmecfs📞 The Long Haul Line: 720-432-9368! Call or text to share a story, suggest a guest, or just say hi!📧 Email: afriendforthelonghaul@gmail.com📬 Substack: f4lh.substack.comI'm also on Instagram.A Friend for the Long Haul is a low budget/high love production made by a disabled one-woman operation. If it means something to you, share it with someone whose earballs need it. Thank you!
Transcribe →How Covid Long Haulers Build Community - A Conversation with Kathleen Banks
Mar 1701:03:57Tap to summarizeSeason 4 of A Friend for the Long Haul - A Long Covid Podcast is here! We're starting where it all begins: with each other.CW: in this episode, we do discuss depression, medical trauma, suicidal ideation, and suicide. In this first episode of the new season, I sit down with Kathleen Banks, a health systems researcher and Long Covid patient, for a conversation about something none of us planned for: finding our biggest cheerleaders and chosen family in our pockets.We talk about "pocket friends," - what Kathleen calls the people living in your phone who already know how you feel, who you can reach out to when a symptom scares you at 2am and, who don't need an explanation if you have to cancel a FaceTime. We explore how so many of us arrived on social media not necessarily looking for friends, but for validation, and found so much in each other. We also get into the real cost of being sick in America. It's not just co-pays and premiums, but the fancy expensive bandages you need because of MCAS, and the $77 supplements that you go without because you have to pay your phone bill so you don't lose access to your lifelines. We also discuss community care: what it looks like when you can just send someone money, no questions asked, because you know what it is to need it, or when strangers send your kids more birthday gifts than their grandparents do.Kathleen also shares her work training public health researchers in trauma-informed methods for interviewing Long Covid patients and why she used episodes of this very podcast to supplement her work. We talk about disability justice, the particular grief of Long Covid Awareness Month, and what it means to still be here, building something remarkable out of what's left.Oh, and somewhere in the middle of that, we talk about moss. I'm girl moss, not a girl boss.This is the first episode of my Long Covid Awareness Week series. Season 4 is about community - the ways we've been discarded, and about what we've built for each other anyway. We're still here because of us. My call for listener feedback on community was so well-heeded that this "episode" is being split into several parts that will all be released this week. More information about Kathleen, my beloved wife:Kathleen Banks is a health systems researcher with expertise on patient-physician relationships; systems thinking; patient advocacy; and dignity in healthcare. She specializes in the translation of evidence, high-level policies, and systems decisions at the point of care. Ms. Banks has worked with policymakers and officials from the grassroots to the global level, and uses that experience to bridge understanding on how to design and implement effective programs and policies .Ms. Banks is currently finishing her Doctor of Public Health degree at Boston University School of Public Health. Her research focuses on access to patient-centered healthcare for people living with Long COVID. Ms. Banks has been a member of the Patient-Led Research Collaborative since 2024.You can listen to the Long Covid Theme Songs Playlist on Spotify. It's full of songs from people who have joined me on the podcast. Each song represents some aspects of that guest's long covid experience. You can find me on Instagram, TikTok, and on my Substack, called Haulin' Ass.A Friend for the Long Haul is produced by a disabled Long Covid patient. Support community care through my Bonfire shop or my Amazon wishlist, or make purchases for your everyday items through my Amazon Storefront.
Transcribe →
It Comes in Waves: Weaving Art and Long Covid Stories with Heather Schulte of Stitching the Situation
Dec 1000:38:41Tap to summarizeWelcome to Season 3, Episode 13 of A Friend for the Long Haul - A Long Covid Podcast! In this episode, I got to connect with Heather Schulte. Heather is the powerhouse behind Stitching the Situation. From her website: "Stitching the Situation is a continuation of artist Heather Schulte’s textile work, Situation Report, a daily cross-stitch documentation of the coronavirus case and death counts in the U.S. from Jan 20-June 25. The Situation Report panels began as the artist’s way to record cases in the US, and translate them visually with stitch. "We discuss a unique art exhibition called "It Comes in Waves," centered around the impacts of COVID-19. Set in The People's Building, an art gallery located on the east side of Aurora, Colorado, Heather took me on a tour of the displayed art pieces, which include drawings, dye sublimation prints, and masks. The exhibition, organized by Heather, features a mix of personal stories and collective experiences related to living with Long Covid. Special attention is given to the ‘Stitching the Situation’ project, which involves community participation in cross-stitching data and personal stories onto cloth. The discussion also highlights the incorporation of art from incarcerated individuals, collaborations with other artists, and the logistical challenges of managing such a significant project. I'm absolutely thrilled that this podcast is included in the exhibit. I called my portion "A Life Redacted," and it is made up of excerpts of episodes with words redacted from the transcripts. It Comes in Waves illustrates the power of art in documenting and processing collective trauma. Heather, you are amazing, thank you for all the work you do!You can find Heather on Instagram at https://www.instagram.com/stitchingthesituation/ and https://www.instagram.com/heatherdschulte/Press for It Comes in Waves includesThis feature from Visit DenverA review from DARIA Art MagazineOne woman’s method for coping with COVID turned into a 5-year art project, now on display in AuroraArt Show It Comes in Waves Brings Long COVID Stories to LightFrom Denver Westword: Running through December 30, It Comes in Waves invites viewers to consider what happens when a crisis slips from public view but its consequences remain. Supported by an INSITE Fund grant from RedLine Contemporary Art Center, the project builds on artist Schulte’s ongoing initiative Stitching the Situation, a national effort to document the human toll of COVID-19 through collective textile work.
Transcribe →