Did others here get diagnosed with EDS after Covid? I've had Long Covid for almost 2 years now. And a few months ago, a dysautonomia doctor diagnosed me with EDS based on my symptoms and hypermobility (which also runs in my family). I'm struggling with a ton of pain (and also fatigue) and wondering if there are any modules for people like me that don't aggravate any LC issues. Really hoping for some relief because being in an overlap between LC and EDS really feels like no-mans land.

Posted by bikkigill at 2023-04-16 12:59:01 UTC