Hi! I certainly see more sensitivities in the patients we see at POTS Care, but I can’t say that about “EDS” per se — only POTS patients with EDS (or joint hypermobility). Does that make sense?
We are digging deep for the answers to your questions and looking forward to releasing what we’ve learned. We have a blood study going on right now in fact! It is not too late, if you or anyone you know is interested in participating! Just email Research@GeneticDZ.com and they’ll get you fixed up! 🙂