Looking for Support and Connection

Hey I have hEDS and pots but I also had a blood clot 2 years ago and am limited for my treatment options. Always free for a chat! Xx

Hey! I have EDS and am going through problems with fainting, which may be associated with POTS, so I’d love to talk if you’d wanna! <3

Looks like we're really similar! How are you? X

Hi me too!

Hihi! Would be happy to chat any time :)

you’re not alone!! I’ve met some awesome people through groups and chats like this!

Was chronically injured first and then discovered I was chronically ill. Would be happy to talk to you bc I know how isolating it feels before you find a community. I promise you're not alone in this journey

Hi! I have undiagnosed hEDS. I've just in the past few months connected all the dots to get there, and my rhuem appointment is next month

Hi! I’m newly diagnosed with hEDS and suspect I have POTS but no diagnosis for that yet. Would love to talk!

We do be almost the same though. Friends?

Hello! I have been diagnosed with EDS for a couple years at this point, while I don't have POTS, ect, if you're ever interested in knowing my experience you can always shoot me a message!! 💕

I am newly diagnosed and would love to connect with others

Hi, we are quite similar

Hi I also have eds - hypermobility and I am currently being investigated for pots would love to chat

Hi! I have EDS and POTS as well. Feel free to message me if you wanna chat! I love that this app gives us an opportunity to support one another like this.