O TYM ODCINKU
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!
Język angielski
Stany Zjednoczone
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WYSZUKAJ MINIONE ODCINKI
Wyszukaj minione odcinki Chronically.m.e.
INNE ODCINKI W TYM PODCASCIE
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.
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…
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.
CFS affects so many, so Im back with Amy and Jessica to discuss our experiences with Chronic Fatigue Syndrome.
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 …
Zastrzeżenie: Podcast i grafika osadzone na tej stronie pochodzą z chronically.m.e , który jest własnością jego właściciela i nie jest powiązany ani wspierany przez Listen Notes, Inc.
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