24 Hours of EDS || a day in my life

Posted on May 13, 2017 by

276 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]

If you’ve enjoyed any of my videos, I’d love you to please subscribe to my channel 🙂

#edsawarenessmonth #thisismyEDS

Category: Illness, UncategorizedTags: , , , , , , , , , , , , , , , , , , , , , , , , , ,

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

Leave a Reply

Your email address will not be published. Required fields are marked *