Resources/

My favorite sites to learn from are:

The Ehlers Danlos Society

Ehlers Danlos Support UK

If you suspect you or a loved one might have EDS, I have found it is very helpful to have a care team that understands the condition.

The Ehlers Danlos Society is a great resource for finding a provider near you that is knowledgable on the condition.

This has by far been my favorite resource:

"Understanding Hypermobile Ehlers Danlos Syndrome and Hypermobility Spectrum Disorder" by Claire Smith