Instagram story viewer> @endonaturopath> Post
2 months ago
107
Posted On: August 26th 2026, 04:09 am
If you’ve been told you “just have POTS” and the plan is just salt, compression, exercise, and meds, this is for you…
Those tools can be genuinely life changing. I use them. I recommend them. And for many people they are exactly what’s needed.

But I want you to know that “blood pooling” is a description, not an explanation. In complex cases, the next step is asking why the body can’t regulate blood flow and volume, why preload is low, why brain blood flow can feel so unstable even when you’re doing the right things.

That’s where I start thinking about the whole picture, including gut and pelvic circulation, connective tissue, and whether there are mechanical or structural bottlenecks affecting return flow.

Comment READY if you’re ready to address your POTS, EDS, MCAS, and endometriosis holistically.

#posturalorthostatictachycardiasyndrome #hypermobileehlersdanlossyndrome #potssyndrome #dysautonomia #vascularcompressionsyndromes
Comments (107)
pattydolce7 11 days ago
lunnend8 14 days ago

lunnend8

Ready

maddieward326 14 days ago
jesposito a month ago

jesposito

Ready

kedis_kep a month ago

kedis_kep

Ready 🙌

sscarv5 2 months ago

sscarv5

Ready!!

karolinalipinski 2 months ago
anitaruttermakeupartist 2 months ago
macey_eloise 2 months ago

macey_eloise

How is blood pooling assessed?

macey_eloise 2 months ago

macey_eloise

How is the

macey_eloise 2 months ago
lisa.grigg1 2 months ago
apettyquarrel 2 months ago
valfleming7 2 months ago
jwoodvet 2 months ago

jwoodvet

great point. feel free to write your own review for JAMA, look forward to reading it when it comes out

Load More

More posts

back to up