Tag Archive: vEDS

Earl sits at a desk looking into the camera wearing a suit, shirt, and tie.

The day will come when all medical professionals know about vEDS

I’m 66 years old and have vascular Ehlers-Danlos syndrome. Anyone familiar with this EDS type understands how blessed I am as the median life expectancy is 48 years. My vEDS life began 22 years ago, although I didn’t know it at the time. On Christmas Eve in 1996 I began having abdominal pain around 6:00pm.
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Which type do I have? Doctors don’t always agree

By Caleb H. In January of 2000, when I was 2-years-old I came down with an illness which, contrary to EDS, most of the world has enough familiarity with to despise: the unfortunately common, unpleasant, but benign wintertime stomach flu. And common, unpleasant, but benign is how it should have gone. But, ironically, this common
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Vascular EDS does not stop me from living life

By Lynley W. Hi, I’m Lynley, and I have vascular Ehlers-Danlos syndrome. I was born club-footed; my feet were almost completely turned around. Doctors told my parents that I would be in a wheelchair for all of my life. I am happy to say I am not in a wheelchair! I’ve had multiple surgeries and
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VASCULAR EDS: MAKING EACH DAY COUNT

For however long God gives me on this earth; I would like to make each day count. If I educate just one person a day or even a week, when my time here is over, my family will be able to say she made a difference in at least one person’s life.
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STANDING MY GROUND

So I fight on like the EDS Warrior that I am. And I will continue to fight and push on until I’m called home! 
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To Shine Forth, Head Held High

by Matt Smith Since being diagnosed back in 2013 with vascular Ehlers-Danlos syndrome, there has been a constant internal conflict of whether or not being diagnosed with a life-threatening, rare, genetic, incurable condition, is a good thing or a bad thing. The fear and anxiety caused by the knowledge that you have this condition that
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