Hugh Cox

In this episode we’re going to talk to Hugh Cox, a member of the Vascular Ehlers-Danlos Syndrome community diagnosed just in 2022. He was first misdiagnosed with a clotting disorder.
Find more information, including support groups and webinars, about VEDS, Marfan, and Loeys-Dietz, at thevedsmovement.org (thevedsmovement...) , loeysdietz.org (loeysdietz.org) , and marfan.org (marfan.org) . You can also find information and resources through the John Ritter Foundation, johnritterfoundation.org (johnritterfoun...)
Links to resources, events, and research opportunities:
VEDS Collaborative Research Study: Email [e-mail] (mailto:[e-mail])
Marfan Foundation/The VEDS Movement/Loeys-Dietz Syndrome Foundation Events:
marfan.org/cal...
Join a Walk for Victory:
marfan.org/walk/
Help and Resource Center
marfan.org/ask
loeysdietz.org...
thevedsmovemen...
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Disclaimer
The views, information and opinions in the podcast are solely those of the individuals involved and the information presented does not constitute medical or other professional advice or services. Any opinions I express in this podcast are my own, and not of my employer.
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[@SandrinaN]

Thank you for sharing your story.