Ehlers Danlos Syndrome Commonly Asked Questions
What is it like having Ehlers-Danlos? -Jacey
Having EDS is having constant joint pain. Waking up in the morning and knowing I am hurting more than everyone else. It's an invisible disease. -Lexie
What is the hardest part of having EDS? -Jacey
The hardest part is knowing it's an invisible disease. -Lexie
What are some life changes you've had to make? -Jacey
I do a lot of things different. Im not able to do certain exercises while strengthening for my sport. I have to use certain aids in order to reduce joint pain.
Remember that time you sprained your ankle?
Imagine living your life with that pain, every hour, every day.