Hi people!
I’ve accidentally stumbled across this site, so quickly signed up. Hoping to communicate with people with similar experiences and issues.
Not sure how active the form is so I’ll have a look around and see.
kind regards 😘
Hi people!
I’ve accidentally stumbled across this site, so quickly signed up. Hoping to communicate with people with similar experiences and issues.
Not sure how active the form is so I’ll have a look around and see.
kind regards 😘
Welcome to the EDS forum.We can be a bit sleepy but we are hear and will respond with helpful tips and understanding if we can.
Have you recently been diagnosed with EDS or are you unsure if you could have it and need advice about what to do next?
Or are you just looking for a herd of zebras to join up with?😆😆😆
Whatever the reason we are here for you , and do have a look at the Ehlers Danlos Syndrome UK for the best round up of information on this condition which also has self help tips and an online magazine.
Take care , Bee