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I have belonged to the RLS foundation since 1994. There is a $25 fee for

a year and you get a news letter every quarter. The letter was called

Night . This month I received a new letter called We Move a

larger, more informative letter than the past it seems like they got

their act together. I found I get a lot more info from this group

because they are the ones who have the symptoms and have tried most

every medication and know what works and what don't. The doctors can

only tell you what they know and that's very much not until they do a

lot more research. My suggestion stay with this group you will learn a

lot more from people who know.

Rodney 65 NEPA

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