Tag: #edsawarenessmonth

24 Hours of EDS || a day in my life

Posted on May 13, 2017 by Chronically Jenni

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… Continue Reading “24 Hours of EDS || a day in my life”

Category: Illness, UncategorizedTags: #edsawarenessmonth, #thisismyeds, 24 hours, a dogs purpose, blue badge, chronic fatigue, chronic illness, chronic migraine, chronic pain, day, day in the life, disability, disabled, dog, eds, eds awareness month, ehlers-danlos, ehlers-danlos syndrome, headache, life, living, migraine, postural orthostatic tachycardia syndrome, pots, video, vlog, youtube

Living With Ehlers Danlos Syndrome #EDSAwarenessMonth

Posted on May 5, 2017 by Chronically Jenni

333 Comments

Happy May Everyone! You know what that means? It’s EDS Awareness Month! I was diagnosed with Ehlers Danlos Syndrome last February and it’s been a long battle ever since. I started off by fighting the comorbities that come with EDS, for me that’s POTS… Continue Reading “Living With Ehlers Danlos Syndrome #EDSAwarenessMonth”

Category: Illness, UncategorizedTags: #edsawarenessmonth, awareness, blog, chronic fatigue, chronic illness, chronic pain, collaboration, eds, eds awareness month, ehlers-danlos, ehlers-danlos syndrome, living with, living with eds, may, month, project, spoonie, video, vlog, youtube, zebra, zebras

#EDSAwarenessMonth Project

Posted on April 20, 2017 by Chronically Jenni

Chronically Jenni

Tag: #edsawarenessmonth

24 Hours of EDS || a day in my life

Living With Ehlers Danlos Syndrome #EDSAwarenessMonth

#EDSAwarenessMonth Project

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