This week we talked to Dr. Sadie Whittaker, the Chief Scientific Officer of Solve ME/CFS Initiative- a nonprofit whose mission is to find a cure for & end Myalgic encephalomyelitis/chronic fatigue syndrome. The developments …
We round out our Parosmia Series with Gemma who experiences parosmia and it's equally evil twin: phantosmia. For those who don't know, phantosmia is an olfactory hallucination that makes you smell things that aren't there. F…
Chrissi Kelly is the founder of AbScent, a UK-based charity that is dedicated to providing support and trusted information to those affected by anosmia and other smell disorders. After her own struggles with smell loss, she …
Compared to Brooke's episode on Tuesday, this episode is a great example of "same virus, different stories." In the second episode of our Parosmia Series, we talk to Marilyn who had some of the weirdest and worst symptoms of…
We're kicking off Season 2 with a series about parosmia, perhaps the most odd and startling long-hauler symptom to date. Parosmia is dysfunctional smell detection characterized by the inability of the brain to correctly iden…
Fatigued Podcast was born out of two friends getting Covid and sharing their experiences. Listen to learn more about this project, who they've interviewed, how it's helped, and where it's going from here. Full episodes and…
Caroline and Raymond (and an awkward little-sounding voice) say goodbye to Season One. Our cohosts give updates on their personal Covid stories, tell us about what's coming up in Season Two (launching March 9th, 2021), and …
Last March Maria spent nineteen days in the hospital with COVID-induced double pneumonia. Can you even imagine? From the CPAP machine to rash and bed rest, she experienced the full gamut. We are so lucky she lived to tell th…