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Just got back from the doctor, and its official. I have Ehlers-Danlos syndrome.
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To add to your last point, it definitely takes a huge weight off of your shoulders when you have a clearer picture of what's going on in your body.
I'm not sure if you were diagnosed with the vascular type of EDS (vEDS), but regardless, don't overlook the continued advances of EDS research and treatment methods. As long as you're mindful with what you have and keep a positive mindset, that's really the best you can do.
EDS doesn't define you, but maybe vk bandomen do =P.
ᕦ(ò_óˇ) ˢᵗᵃʸ ˢᵗʳᵒⁿᵍᵎ
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