10 EDS Myths Debunked! 

Are there any other common myths you also hear about EDS? 🦓 Thanks for watching! Xxx

Thank You for sharing this info!! I started fainting daily at age 8 as a child. I also had an entire list of additional symptoms, as well as being very clumsy… always bruised, had joint dislocations multiple times a year, as well as many fractures from being “clumsy”… I was always doing my party tricks with my flexibility… I was diagnosed with Dysautonomia, POTS, NCS, MVP, and Cardiologist noted Hypermobility at age 11…. My Cardiologist passed away when I was in my 20’s. It’s been hard to find Good Doctors that truly understand all this. Most Doctors now will treat my other Diagnosed illnesses but totally dismiss H-EDS (bc previous doc only made a note of Hypermobility & not EDS) I recently had an appt Genetics doctors that finally diagnosed H-EDS along with my other issues. But, still being dismissed by my regular doctors as just a flexibility thing and not the reason why I have so many dislocations/injuries & pain.

Very cool video about EDS hun. Done great research here. Well done, love the animations and editing💗💗💖💖

So informative! I had no idea babe ❤️

Like your video, it’s very interesting and educational . Sending you big hugs 🤗😻💕💕

Please talk about the allergies and flare up meds. I am recently diagnosed and have terrible allergies and sensitivities, but my MD didn't mention this as connected. Thank you for this!