I Think I have EDS. What Happens Next? The Ehlers Danlos Series

You have been feeling sick for a very long time. Had many routine tests come back clear. Yet, you have … More

Go Fund Me: Morgan’s EDS Mobility Aids

Hello everyone, Some of you may or may not know that I am suffering from an incurable connective tissue disorder … More

Hello Guys, I am asking for kind donations of art materials from my Amazon wish list to make animal drawings … More

As it is coming up to my 2 year EDS diagnosis anniversary (if we can even call it that), I … More

Hey Guys, I was asked to be a contributor in an educational film to present to medical professionals by Troy … More

Hey Guys, As the sun is shining it is clear summer has started … but for those of you … More

Hola Amigos, When I started Brains & Bodies, I did not want to accept guest posts from practitioners, mainly because … More

It is hard enough for University students to balance their coursework and exams with their social life. So, when a … More

Hey, I am Morgan, a 27 years old, living with mental and chronic illnesses. My Health: Growing Up Unbeknown to … More