Resources/

Below are a few helpful resources that I have used along my journey.

I want more information on EDS

My favorite sites to learn from are: The Ehlers Danlos Society Ehlers Danlos Support UK
I want to find a doctor that knows about EDS

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.
The Best Book About EDS

This has by far been my favorite resource: "Understanding Hypermobile Ehlers Danlos Syndrome and Hypermobility Spectrum Disorder" by Claire Smith