RLS: I’ve had RLS for years and it is I... - Restless Legs Syn...

Restless Legs Syndrome

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RLS

pdpurdy54 profile image
11 Replies

I’ve had RLS for years and it is I would say it is drug induced 90% of the time. I also have a movement disorder that has miraculously been helped with a new drug called Ingrezza. I was told not to take the mirapex. Well... forget it! I still get RLS bad when I take a muscle relaxer or anything to help me sleep. So I need it!!! But sometimes (most of the time) the RLS is so bad I have to walk or jump around and shake my arms... pathetic right?

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pdpurdy54
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11 Replies
Allyp69 profile image
Allyp69

My RLS started iny 20s when pregnant so wasn't taking any medication. But my mother had it.Not convinced about the connection with drugs for me.....

LotteM profile image
LotteM

Somewhat similar for me. My RLS started in my 20s, spontaneously and not during pregnancy. Although it played up much later during oregnancy and menopause. I take no drugs other than for RLS.

Quite a few drugs are indeed likely to induce RLS, such as antidepressants and antihistamines. See for a long list and info rlshelp.org treatment page.

Noddedoffagain profile image
Noddedoffagain

I have had it since my early teens and I was never given any drugs to help. In fact nobody took it seriously. My father suffered and sadly one of my children too. I have only been taking drugs for the past 15 years to get some relief from this dire affliction. It has definitely got worse as I have got older. For my family it is definitely not drug induced.

junior19 profile image
junior19

I get it worse when on certain meds. It seems to be worse when the meds are wearing off. My meds are painkillers and benzos.

grandmahelen1 profile image
grandmahelen1

My rls started early in my life. No one knew what it was. My dad when I was a young child used to rub my legs until I went to sleep. In my late 50's it started to really be a problem and the neurontin I was taking was increased to 2400 mg. That worked for a while, then I saw a neurologist and he put me on 1 mg of mirapex at bedtime. Wonderful, could finally sleep without tearing up the bed. I can see why folks sleep in separate rooms. After a while I started getting problems during the day, added a morning pill. Well in 5 years I'm up to 4x a day and 4 mg. Its working now but for how long I don't know. I definiately know if I vorget pill. I can't sit still. I also have essential tremor and periodic limb movement discorder. I'm going to be moving so I'm getting a new neurolgist and I want an answer about whether I'm showing signs of parkinsons. My PCP says yes I do, my neurologist says I don't and I see subtle indications that I do.

rsears57 profile image
rsears57

Not pathetic, pretty typical of rls

Nope, not pathetic at all. I find myself doing the same things when my RLS is bad. I also find myself stretching the affected limbs to the point of them hurting in protest, telling me that they can’t be stretched any further. I am also not nice to my limbs when massaging them and have bruises and red marks to show for it.

TEAH35 profile image
TEAH35

I've had RLS since childhood (now 65) never took any drug until diagnosed 15 yrs ago. Have been RLS free ever since.

Graham3196 profile image
Graham3196 in reply toTEAH35

What drugs are you taking?

Fleur29 profile image
Fleur29 in reply toTEAH35

I see this is an older post, but I'm also interested in which drugs you took.

tweedy66 profile image
tweedy66

I've been getting symptoms in my arms lately.....also in bed shaking arms, rubbing legs.....what a mess !!

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