I second that! Barb is a bundle of knowledge! Can you tell us why YOU think you have EDS? Perhaps we can brain storm with you. Do you have POTS/dysautonomia? I know of one man who has EDS but who didn’t really appear hypermobile. Dr. McDonell (in the states) asked him to put his foot on his forehead,and she looked for hypermobility in other ways. My skin is stretchy in certain places only. That seems pretty common. I know of one family of 5 – 4 of whom are hypermobile and have the EDS diagnosis. The fifth one is not hypermobile — but get this. She develops POTS/dysautonomia just like her other 4 siblings! What is up with that? There is more to this than we understand, certainly! Meanwhile, please share your symptoms/signs with us and we’ll see what we can do! 😉