So...I have a genetic disorder called Ehlers-Danlos Syndrome, or EDS. I wanted to make this video because you, my lovely followers, deserve to know why I might go MIA for a few weeks occasionally. ;) So, yeah... This is why.
I also want to raise awareness for EDS, which often goes undiagnosed or misdiagnosed for years, like mine did. I am not a doctor, please do not take anything in this video as medical advice. Not everyone with EDS has all of the symptoms; some have more, some have less.
If you or a loved one has EDS, POTS, CFS, or another chronic illness, my heart goes out to you, and I would love to connect! Drop a comment!
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