Hello, I'm new to this forum. I'm going to the dysautonomia and MVP center in Birmingham, AL in a few weeks. I was diagnosed with dysautonomia - vasodepressor syndrome by my cardiologist in October 2012, but I didn't feel like he had a true understanding of the different types of dysautonomia, and therefore couldn't treat me accurately. I was just curious, for those of you who have been to the dysautonomia center in Birmingham, do they test for the different types of dysautonomia? Or is it just testing to see if you have it? After researching the different types online, I'm pretty sure I have hyperadrenergic POTS. Any input would be helpful Amanda