24 Hours of EDS || a day in my life

Posted on May 13, 2017 by

174 Comments

Living with a chronic illness is a 24/7 job where you never get a day off. This video shows you a fairly typical day in my life. Ehlers Danlos Syndrome is different for everyone so I wanted to share with you what EDS is like for me. I want to show you a real day without the frills of nice clothes or make up which usually get put on for the camera, so excuse the puffy eyes. I walk the dog, make lunch, talk to about trip to see a dogs purpose, play with my boyfriends Niece & Nephew, get my blue badge in the post, sleep, attempt to get up and take a trip to the doctor. Plus trying to deal with my EDS, POTS & Migraine symptoms. Hope you like this video and let me know in the comments if you’d like to see more videos in this style.
[youtube https://www.youtube.com/watch?v=17mABwMnlW4]

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#edsawarenessmonth #thisismyEDS

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174 Comments on “24 Hours of EDS || a day in my life”

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