November is World Scholarships Month and the perfect time to announce our 2021 Event Scholarships! Thanks to the generosity of donors, The Ehlers-Danlos Society will be providing a number of scholarships in 2021. Scholarship applicants can apply for either the Virtual Summer Conference 2021 or for the series of five individual one-day meetings, part
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We cherish the opportunities our in-person events give us: meeting so many of you and enabling people living with the Ehlers-Danlos syndromes and hypermobility spectrum disorders a chance to connect with others sharing similar experiences, yet this year has shown us how much we can accomplish virtually – and how many more people impacted by these conditions
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Hello, my lovelies! My name is Lori, I’m 19, and I’m the founder of and writer at the blog ‘From Bud to Bloom’. It is all about my journey towards self-love and self-fulfillment as someone with chronic illness and mental health problems – I also happen to battle with hEDS, PoTS, ME, scoliosis and hip
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Finding appropriate healthcare has been a nightmare. Not only do doctors not know about EDS in order to diagnose the disease, they know even less about how to treat the symptoms. My daughter was hospitalized and later diagnosed at the beginning of the opioid crisis (2017). Because of the new rules they “could not treat
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