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Never knew there were so many people with RLS. Luckily or unluckily I have

another, well two heritary disorders and received a booklet entitled " Brain

Connections " . In there was the address for RLS Foundation. Have been

having problems for years, since 30's. At that time was diagnosed as

nocturnal myoclonus, which I still have but then progrossed to this other

horrible creepy-crawly feeling. Walked all night, no sleep, only making

everything else worse. Luckily my doctor knew what I had!! Happy day, or

not, depending on how you look at it. My mother has had it forever, my

grandmother, uncles and my sister is developing. No physician, but mine,

had ever paid any attention to their symptoms. Gave brochure to my mother

who took to her physician, we are both now on Sinemet. After first pill,

sleep! How wonderful.

I have been on Sinemet now for 9 months and how great it is. I know if I

have forgotten to take a dose, my legs start creeping and then jumping.

It was wonderful to find out I wasn't crazy and not imagining it. Just

getting over flu so this is first post since I subscribed over a week ago.

I have a LOT of emails to go through.

AGain, it is very nice to know we are not alone. One last thing, I did

find, as I believe others did, that ephedrine or pseudoephedrine as is now

on markets, in antihistamines aggravates condition. Am not supposed to be

taking anyway but sometimes just have to because of sinus problems. Does

not occur so far while on Sinemet.

Again, glad to be on board and know there are others out there. NOW, how

to educate physicians!!!

Ginger

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