{"version":"1.0","type":"rich","provider_name":"Acast","provider_url":"https://acast.com","height":250,"width":700,"html":"<iframe src=\"https://embed.acast.com/$/5f5ecee581d7b1132d35e681/652153668e657c0011d30d99?\" frameBorder=\"0\" width=\"700\" height=\"250\"></iframe>","title":"Miranda Allen & Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) ","thumbnail_width":200,"thumbnail_height":200,"thumbnail_url":"https://open-images.acast.com/shows/5f5ecee581d7b1132d35e681/1696681387430-f94d1b0ea8046aeab1a2cfca2b023823.jpeg?height=200","description":"<p>Happy Tuesday! When I was passing through London, UK in July I was able to sit down and chat with <strong>Miranda Allen</strong> about her diagnosis of myalgic <strong>encephalomyelitis/chronic fatigue syndrome (ME/CFS)&nbsp; </strong></p><p> </p><p>In this episode, Miranda looks back with hindsight and explains where it’s possible her symptoms began, the years of not really knowing what was going on, how she got a diagnosis, what on earth ME even is, her day to day symptoms, how she manages them and her latest creative endeavours. </p><p> </p><p>Some of you might remember Miranda from a previous That’s So episode (<a href=\"https://open.spotify.com/episode/7hogpgBHpjdzwVIMSQeQhd?si=1fc30d3316ee4bd0\" rel=\"noopener noreferrer\" target=\"_blank\">That’s So: Unrest documentary</a>) but we didn’t get to chat too much about her story then, so I’m really excited to be able to bring you this episode with a lot more information today! </p><p> </p><p>Watch Miranda on Penn &amp; Teller: <a href=\"https://www.youtube.com/watch?v=CfGGIQbsrrE\" rel=\"noopener noreferrer\" target=\"_blank\">youtube.com/watch?v=CfGGIQbsrrE</a>&nbsp; </p><p> </p><p>EeZeeGo website: <a href=\"https://www.eezeego.co.uk\" rel=\"noopener noreferrer\" target=\"_blank\">https://www.eezeego.co.uk</a> </p><p> </p><p>Symptom tracking app Visible: <a href=\"https://www.makevisible.com/\" rel=\"noopener noreferrer\" target=\"_blank\">www.makevisible.com</a> </p><p> </p><p>And don’t forget to connect over on <a href=\"https://www.instagram.com/thatssochronic\" rel=\"noopener noreferrer\" target=\"_blank\">IG</a> and <a href=\"https://www.tiktok.com/@thatssochronic\" rel=\"noopener noreferrer\" target=\"_blank\">Tiktok</a>, I’m <a href=\"https://www.instagram.com/thatssochronic\" rel=\"noopener noreferrer\" target=\"_blank\">@thatssochronic</a>&nbsp; </p><p> </p><p><a href=\"https://www.instagram.com/thatssochronic\" rel=\"noopener noreferrer\" target=\"_blank\">@thatssochronic</a> | <a href=\"https://www.instagram.com/jessssbrien\" rel=\"noopener noreferrer\" target=\"_blank\">@jessssbrien</a> | #thatssochronic </p><p> </p><p>Free monthly newsletter: <a href=\"http://thatssochronic.substack.com\" rel=\"noopener noreferrer\" target=\"_blank\">thatssochronic.substack.com</a> </p><p> </p><p>Application form to share your story: <a href=\"https://forms.gle/csebLkwfwAjiLApK9\" rel=\"noopener noreferrer\" target=\"_blank\">https://forms.gle/csebLkwfwAjiLApK9</a>&nbsp; </p><p> </p><p>Disclaimer: Here at That's So Chronic we are sharing personal stories and are not advocating any type of treatment, therapy, procedure or intervention. Everyone is unique so please seek professional medical advice before making any decisions for yourself or for others. </p><p><br></p><p><br></p>","author_name":"Jess Brien"}