Virginia Wilson pins it down it down to a t when she gives an excellent and concise overview of RLS and how it affects it's victims. She and the doctors who wrote with her also give hope to the millions of those afflicted with what I call the scourge of my life, RLS.

The book is a good source of info and places to get help. As a health care professional I felt the book was a good source for medical professionals and laymen.
 

This is a must read for RLS sufferers and their family. I have been suffering from RLS and its "cousins" for at least 23 years. For the most part, doctors have never taken me seriously.

This book says it all. It describes the syndromes, the reactions of friends, family, and the medical community (we are imagining it all), and offers some help and comfort. The latter in knowing what we knew all along: we have a real ailment that is making our lives miserable! Pressure your doctors to look into this disease.

Change doctors if you must until you find someone who listens. It was infuriating for me to learn that Dr. Daniel Picchietti, a noted expert in the field referenced in this book, has been working at Carle Clinic, where I have been a patient for 17 years, and no one ever told me about him or refered me to him.

I have an appointment now. Thank you so much, Virginia! [Footnote: I did see Dr. Picchietti and found relief. Daily doses of Mirapex have been a great help. For once I am being taken seriously and treated that way. Get help, fellow RLS sufferers.]

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