The content on this website is for educational purposes only and should not be used as a substitute for medical advice. Please consult with your healthcare provider prior to initiating any of these treatments. The use of this website does not imply nor establish any type of doctor-client relationship.

Updated 1-23-2020

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©2019 by Wetzel's EDS Life.  Some images and videos may be from other sources, I do not claim ownership of them. If the owners of the different types of media wish for me to take them down, please email me at edslife2019@gmail.com with the specifics information and I will be happy to do so. It is my hope that posting pictures from multiple sites and sources will help spread awareness.

Have a questions or want to report something? Send me an email at edslife2019@gmail.com
Social Groups and Community

Talking to others who have the same condition can sometimes be the best therapy. Facebook, Snapchat, and Twitter can be great platforms to do this from. But they are highly censored, and they are incorporated. Wetzel's EDS Life in a non-profit website. You can freely talk about conditions and ask questions that you may have. All we ask is that you keep them clean, and be respectful to others. No discussion of politics, religion or vaccination points of view. We have several Forums on different aspects of Ehlers Danlos and related conditions. Click the button to the right to check them out!


Here at Wetzel's EDS, we try to help those with questions find the answers or the resources to find those answers. If you have a question, write and submit it and I will get back to you as soon as I can. This service is not meant to diagnose, treat, or cure any illness. This should be done by a licensed physician, Please sign up at the bottom of the page to get regular emails about the latest in medical news, EDS, POTS, MCAS and medical treatments.Thank you for your patronage.