does rls symptoms affect your arms
does rls symptoms affect your arms
not sure if i have rls, but certain i do, although so far it only affects me about once a month. my question is can a person have the same symptoms in their arms as well as their legs?
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Cary, the search function here isn't the greatest, but there are lots of past posts on arms - yes many people have it in arms and all over the body.
Here's a recent post: http://www.restlesslegs.org/phpBB2/viewtopic.php?t=1006
Ann
Here's a recent post: http://www.restlesslegs.org/phpBB2/viewtopic.php?t=1006
Ann
I have RLS in my arms. I've had it in my legs since grade school (I'mnow 38). I was an adult before it made its way to my arms. I think my arms are more frustrating than my legs. For my legs I can simply stand up, for my arms doing handstands isn't real convenient, not that I haven't done them though. My dr. said it makes sense because RLS just gets worse as you get older. I don't look forward to old age!!
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I have severe RLS - it is in my hips - especially my right hip, both feet, lets, and my lower back - right side -and my left arm. NOT arms, just the left one. I am always stretching and rubbing it at night. Thought it was carpal tunnel but tests were negative. When the doc held my hand down - nothing, but after 2 or 3 minutes it got antsy.
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I too have severe RLS in my legs, hips, arms and shoulders as well as my feet, especially on my left side. Sometimes I feel like I could swing the arms and legs involuntarily and whack someone up against their head. I feel out of control when I have this sensation and pain. I am a very active person so it doesn't come from just sitting around all day, it is a daily occurrence with me.
Donna
Donna
Donna
yes..restless leg of the arm
I have the creeepy crawly kind of restless leg. usually the legs but it can go up first calves then to thighs...real bad when it goes to the groin...(nothing to move to relieve the sensation...I keep trying to urninate). sometimes but rarely the arms and sometimes the wrists ( but that may be more of my ganglion problem, which seems to randomly goes up and down).
So to answer your question...yes, arms can be involved, more rare than legs but can happen in the arms.....looking into some arm compression sleeves since the compression stockings helps with the legs.... still looking for cure to the groin problem....experimenting with very tight long leg girdles...so far seems to help.
So to answer your question...yes, arms can be involved, more rare than legs but can happen in the arms.....looking into some arm compression sleeves since the compression stockings helps with the legs.... still looking for cure to the groin problem....experimenting with very tight long leg girdles...so far seems to help.
Ain't nuthin like an RLS Attack that hits you from all directions!! Hips to toes and shoulders to fingers ... gotta luv it ... not!!
Yup, RLS surely can be felt in the arms ... you might want to check out the thread under the New To RLS Topic called "New Members and Current Members Please Help" http://beta.restlesslegs.org/phpBB2/viewtopic.php?t=192 where a lot of our members (and i hope a lot more add to it sometime soon!!) have listed out their symptoms and cocktails as well as other ailments they are dealing with.
I hate it when my arms join in on the action ... it's THE MOST frustrating of all frustrations when you want to chop off all four major limbs simply due to not knowing "where to put them". Those attacks are thankfully pretty rare now that i've learnt more about RLS and "listen" to my body but when they do hit, can cause a pretty good attack of anxiety as well.
As for the side-topic of RLS getting worse ... i've had it since i was born ... and it's definitely worse now than when i was a child ... and is becoming increasingly harder to stay on one cocktail that actually works for an extended period of time before either augmentation sets in OR side-effects set in (e.g. 2 week chronic kidney infections). I'm not game to looking into the crystal ball to find out if mine will get worse still ... i'm happy enough to take things one day at a time and enjoy each day that I don't have any symptoms.
Yup, RLS surely can be felt in the arms ... you might want to check out the thread under the New To RLS Topic called "New Members and Current Members Please Help" http://beta.restlesslegs.org/phpBB2/viewtopic.php?t=192 where a lot of our members (and i hope a lot more add to it sometime soon!!) have listed out their symptoms and cocktails as well as other ailments they are dealing with.
I hate it when my arms join in on the action ... it's THE MOST frustrating of all frustrations when you want to chop off all four major limbs simply due to not knowing "where to put them". Those attacks are thankfully pretty rare now that i've learnt more about RLS and "listen" to my body but when they do hit, can cause a pretty good attack of anxiety as well.
As for the side-topic of RLS getting worse ... i've had it since i was born ... and it's definitely worse now than when i was a child ... and is becoming increasingly harder to stay on one cocktail that actually works for an extended period of time before either augmentation sets in OR side-effects set in (e.g. 2 week chronic kidney infections). I'm not game to looking into the crystal ball to find out if mine will get worse still ... i'm happy enough to take things one day at a time and enjoy each day that I don't have any symptoms.
Nadia
My philosophy is simply this: Life is too short to be diplomatic. Your friends should not care what you do, or say; and for those who are not your friends ... their loss!!!
My philosophy is simply this: Life is too short to be diplomatic. Your friends should not care what you do, or say; and for those who are not your friends ... their loss!!!
Hi there Nan
Hi there Nan,
Glad to see you.
Yes, RLS is a whole body issue. My arms are different than my legs. I had somewhat gotten use to my legs and the pain.......the normal of this stuff.
My arms are new in the last two years and are sometimes hard to deal with. While on vacation this summer I knew they were tired and worn out. You know that I've carried my purse far too long and why do I need all this in my purse anyway! On one special evening we were all dressed up and I wore a sleeveless dress.......I got this twitch in my arm that everyone could see. In fact they couldn't take their eyes off it......LOL it's was maddening but I just had to laugh. Showered, Dressed Up, hair and makeup and all.........My arm got the attention. I did, I had to laugh, it's the only thing that made it manageable that night.
I know, I'm only 41 and this side of severe.......what does the future bring? Like everyone else I try to keep up hope.......there are some days it's harder than others.....
I'm so glad we have each other here. It's make a world of difference to me.
Hugs to you all.
Glad to see you.
Yes, RLS is a whole body issue. My arms are different than my legs. I had somewhat gotten use to my legs and the pain.......the normal of this stuff.
My arms are new in the last two years and are sometimes hard to deal with. While on vacation this summer I knew they were tired and worn out. You know that I've carried my purse far too long and why do I need all this in my purse anyway! On one special evening we were all dressed up and I wore a sleeveless dress.......I got this twitch in my arm that everyone could see. In fact they couldn't take their eyes off it......LOL it's was maddening but I just had to laugh. Showered, Dressed Up, hair and makeup and all.........My arm got the attention. I did, I had to laugh, it's the only thing that made it manageable that night.
I know, I'm only 41 and this side of severe.......what does the future bring? Like everyone else I try to keep up hope.......there are some days it's harder than others.....
I'm so glad we have each other here. It's make a world of difference to me.
Hugs to you all.
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Becat and other members,
I don't think we must think of the future too often. It's unbearable. I don't believe in a cure, but do in better meds/therapies. But when? I want them NOW!
Until that time I guess we will have drug holidays all the time, changing our meds etc. Another reason for trying not to look forwards.
Anyway, have a nice day!
Corrie
I don't think we must think of the future too often. It's unbearable. I don't believe in a cure, but do in better meds/therapies. But when? I want them NOW!
Until that time I guess we will have drug holidays all the time, changing our meds etc. Another reason for trying not to look forwards.
Anyway, have a nice day!
Corrie