Together, we can continue to advance knowledge, research, awareness, education, and support for all those living with EDS, HSD, and related conditions everywhere around the world. The Ehlers-Danlos Society is working hard to produce more global events, translate materials into multiple languages, and is working to translate core content and printable materials. Making conferences and resources more accessible worldwide is a long-term goal.
Translation disclaimer:
The Ehlers-Danlos Society provides translations of content on this website for the accessibility of our users. These translations are generated by automated tools, third-party services or volunteers and may not always be accurate or complete.
We do not guarantee the accuracy, reliability, or suitability of the translations provided. Users are advised to use these translations as a general guide and not as medical advice.
The Ehlers-Danlos Society is not responsible for any inaccuracies, errors, or misunderstandings that may arise from the use of translated content. Users accept full responsibility for any consequences that may result from relying on translated information.
By using our website and accessing translated content, you agree to these terms and acknowledge that The Ehlers-Danlos Society is not liable for any damages or losses incurred as a result of using translated information.
