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The Foundation’s Facebook page connects nearly 6,000 people in a virtual community from over 17 countries around the world to share common experiences and provide mutual support. The WED Foundation does not endorse or promote any products on the page, the views posted on this page are not those of the Foundation. Suggestions or opinions should not be a substitute for professional healthcare advice - please consult your doctor.  Join the community and the conversation!

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The Foundation is always looking for new ways to increase awareness and to connect with all ages.  A new channel for us, we hope to gain young and old followers to spread the word about webinar opportunities, support group meetings and all of the resources we offer to educate others about Willis-Ekbom disease.

Click here to follow us on Twitter.