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Aaron is 33 and was diagnosed a year and a half ago with vascular Ehlers Danlos Syndrome (vEDS). He tells us his story of diagnosis and events that he has experienced so far. He also tells us about his father’s story with vEDS, which was undiagnosed when he passed away two years ago.
This interview was done in person over the weekend that the vEDS collaborative met in Seattle.
To make a donation to the vEDS Collaborative, https://app.mobilecause.com/vf/vEDS
If you have vEDS, or have or lost a family member with vEDS, and want to be on this podcast, reach out! translucentone.blog/contact-me
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سلب مسئولیت: پادکست و آثار هنری تعبیه شده در این صفحه متعلق به Katie Wright است که متعلق به صاحب آن است و به Listen Notes، Inc وابسته یا تایید نشده است.
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