I originally thought I had hypermobility like my Mom, but it made since when the Geneticist told me bc of my POTS and MVP and the way my skin is and bruises I had Classical. Makes sense, so I figured they just misdiagnosed my mother. It just worries me that I could still have Vascular although both Geneticist told both my mother & I that I shouldn’t worry we have too many other symptoms that it couldn’t be vascular — and they wouldn’t even offer to do the testing.
I don’t know my type yet, but I hope the check me for the vascular form. There are a lot of overlapping symptoms and it is possible to have more than one type. I hope you still see a cardiologist for monitoring. All of us EDSers have a risk of vascular rupture.