That would be great! A bonus for me would be if the conference offered time slots for individuals wanting to book with a speaker/specialist for a private consult. Even if a firm diagnosis is not possible, I am hoping someone of expertise could give their opinion on whether or not I have EDS. I have symptoms of hydrocephalus and MCAS and was diagnosed with POTS 1 yr. ago.
Looking forward to the video. Thank-you Dr. Diana! 🙂