Member Portal

How do I gain access to the Members Only portal? If you are a Foundation member, please login here. If you are not yet a Foundation member, please follow these steps:

  1. First, Click here to join the Foundation by paying an annual fee* of $35 (U.S. or Canada) or $45 for International. Membership activation takes 1-2 business days before you will gain access to the portal. 
  2. Second, click here to create a username and password. Once your membership payment has been processed (usually within 24-48 hours) then your online account will be activated giving you access to all of the resources in this Member Portal.

*If you cannot afford the cost of membership, please email us at info@rls.org or call (512) 366-9109 to request a scholarship.

Benefits of Membership

As a member, you will receive:

  1. NightWalkers, our quarterly print magazine covering research advances and treatments
  2. An RLS Medical Bulletin—the most comprehensive resource on RLS—to share with your healthcare provider
  3. Access to "Members Only" website section with NightWalkers archives, webinar archives and downloadable publications 
  4. A Medical Alert Card listing RLS-safe medications for your reference and to share with your healthcare provider
  5. A Membership Card with Special Accommodations for use when traveling
  6. Discount and early registration for RLS Foundation events
  7. The strength, knowledge and hope gained from working together with thousands of others to support important education, awareness, advocacy and research leading to better treatments and a cure

Foundation Reviews

"It was so comforting to find an organization that totally understand restless legs syndrome and the affect it can have on one's life. Sleep deprivation is serious. I've learned about side effects of medications used to treat the disease, that it is genetics, that there are things one can do from a nutritional and supplemental aspect to help. They have now established quality centers. The webinars are very educational. They've given me hope. This is such a stupid and silly disease. People have a very difficult time understanding it, if they have never been affected. This organization is awesome."

To read other reviews or submit a review on the Foundation, please click here.