ÜBER DIESE EPISODE
Michelle (@mybodyliberation on instagram) and I chat about the diagnosis experience, namely trying to get one. Michelle lives with endometriosis which statistically takes 6-10 years to diagnose! For a lot of us this time is stressful, confusing, invalidating and isolating so let's talk about it!
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VERGANGENE FOLGEN SUCHEN
Vorhandene Folgen von Chronically.m.e durchsuchen.
WEITERE EPISODEN IN DIESEM PODCAST
Whats it like living with CFS and Fibro? Leslie (@phelpsie1989 on Instagram) and I dive into our experiences of managing symptoms, medical gaslighting, self-advocating, staying positive and gluten intolerance/celiac disease. Thanx for listening to chronically.m.e Id love to hear from you. Whether i…
Symptoms, incompetence of healthcare, positivtiy and representation weve got it all. Join Leslie and I for part two as we dive further into the chronically ill experience.
CFS? What's that? Chronic Fatigue Syndrome or ME is a debilertating illness that causes immense fatigue along with a lot of other symptoms and diverse experiences. Which is why Ive enlisted the help so some friends to share their experiences with CFS/ME. All answering the same questions Iman, Anna …
CFS affects so many, so Im back with Amy and Jessica to discuss our experiences with Chronic Fatigue Syndrome.
Get excitied for this teaser trailer where I introduce myself and the podcast! I also briefly explain my diagnoses. Theres so many topics i wanna dive into and so much to talk about, Id love to hear your suggestions.
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Vielen Dank, dass Sie uns helfen, die Podcast-Datenbank auf dem neuesten Stand zu halten.
