There is help!

[kare43]

Yes, Chicabel, you’re not alone. I’d say first join the RLS Foundation, find them on the web. They’ll send a packet of very helpful info including a thorough and well done pamphlet for health care providers. But sounds like you need a visit to one of the major medical centers where there are doctors who are very familiar with our disease. ( and it IS a disease with ICDM category for billing!) I live in Michigan so closest Center for me is Mayo in Minnesota. As I think about it that info may be on line. Check the RLS site. Blessings to you!