Thursday, February 16, 2012

restless legs and chronic pain

Written by

teero09

teero09

Fri, October 02, 2009

HAS ANYONE HERE EVER HAD TROUBLE WITH RESTLESS LEGS WITH THEIR CHRONIC PAIN?? LAST SUMMER I THOUGHT I WAS GOING TO GO CRAZY. I WOULD PUT OFF GOING TO BED. I FINALLY SAW A NEUROLOGISY WHO PUT ME ON REQUIP, HE HAD TO KEEP UPING THE DOES UNTIL IT TOOK CARE OF THE PROBLEM.  THATS SOME NEED TO KNOW INFORMATION!!!Laughing  HOPE IT HELPS  SOMEONE ELSE

10/ 4/09 11:23pm

Yes I have this problem as well. I can't sit anywhere for any period of time without getting up to move around. (I had some surgery lately and I was later told that my arms and feet were on the move even in the recovery room!) Sitting at a table having dinner my legs are constantly doing what my kids called "my dance". I have to keep apologizing for stepping on everyone elses' feet. I have taken Sinement and Mirapex. The Mirapex seems to be the most effective for me. Not that it stops "the dance" but at least it doesn't seem to bother ME as much- even though, unfortunately  it continues to drive those around me absolutely crazy! Sorry you have had to fight this fight! My thoughts are with you!

Sandy

Anonymous
teero56
10/ 5/09 1:28am

well i finally have mine under controll THANK THE LORD  their is a medicine called REQUIP  it is espeicially made for restless legs. tell your doctors that you have this problem and stop the dance. it is so horrible, not that we dont have anything else to deal with. Im a possitive person but this just about drove me crazy, and thats a short trip. also some vitamin E helps .  my neurologist is the one who started me on this but im sure any doctor could do this. Good luck everyone. Sealed

10/11/09 7:22pm

Thank you for the suggestion. I will ask my Doctor about this medication- REQUIP. I appreciate your response!

10/31/09 3:01pm

I have suffered for many years from restless legs.  About 6 years ago my primary doctor at the time also put me on Requip.  fter a few years I had to have it changed to Mirapex.  In 2007-2008 I was at the emergency room once a month due to an inability to sleep for three or more days.  I also have chronic pain and arthritis.  My pain doctor put me on dilaudid, small dose and I have not spoent any time in the past year at the emergency room due to this condition.  I hope people keep their primary and pain dr.s advized of what happens with them, they could receive better care from all. 

11/ 1/09 3:14pm

thank you for your comment,  restless legs is not a topic many people know about, you feel so alone because people dont understand it. they just say go to bed, they dont realize that you cant do that, your legs wont let you.

do you fall down alot too??? sometimes when my fibro and arthritus get bad at the same time i just fall alot. no one knows why. it just seems like im not picking up my feet or something. they just classify me as a high risk faller.

i just keep going though, pick myself up and keep going.  have a great day  and be blessedSealed

11/ 2/09 3:05am

My husband helped with the diagnosis of my restless legs.  I just thought it part of fibro and did not realize that I was actually kicking me in my sleep.  He happened to be with my while seeing my sleep specialist.  My doctor acted like my husband had just turned the lights on for me.  This was over 10 years ago.  I took several combinations of Parkinson's medications, and I currently take Mirapex.  There have been times when I had to walk the floors because I could not even sit and unfortunately we were at the home of friends.  I was so embarassed because I could not stay seated. It was then that my doctor advised me to up my dosage and take in day if I continued to have problems like that.  Thank goodness those have stopped. I am on just one tablet per day and it seems to be controlling the restless legs.  I have now started having something like seizures in my sleep where I violently move my arms and legs.  My husband observes and said that it starts from my face and moves down my body. My eyes roll all the way to the side and there are odd expressions on my face and my mouth twitches along with my eyes rolling back and forth. Then the violent movements of my arms and legs begin.  I have even tried pulling out his hair, but I don't seem to be aware of any of this. It is very scary to both of us.  I'm just tired of seeing doctors

and I'm afraid they may not believe my husband.  I've gotten afraid to try to sleep because I don't want this happening to me. Has anyone ever experienced anything like this?  I feel like I am some type of a freak, and I'm too embarassed to tell anyone that I know.

11/12/09 2:39am

yes, Iv'e had it for a few years but keep it under control by taking magnesium and Baclofen tablets.

11/12/09 7:53am

I was diagnosed with RLS during my third sleep study when the sleep specialists saw my legs moving all night.  While I was being treated for RSDS a few years ago my pain mgmt. doc was trying to wean me off of the duragesic patch that I was on for pain.

Whenever the drug was almost completely out of my system I was getting these wierd sensations, tingling in my feet and legs.  I would have to walk the floors to relieve it.  All the time I thought it was withdrawals from the meds and it was RLS.  Finally during a sleep study for my sleep apnea I was diagnosed with RLS and was given Mirapex for it.  I take it at night before I go to bed, but sometimes during the day especially late afternoon when I am sitting relaxing my legs act up so I get up and walk around the house.  I don't think the RSDS, med withdrawal or pain had anything to do with the RLS.  It's just something I developed and didn't know about it until the Duragesic I was on was out of my system and had stopped repressing the symptoms of the RLS.

 

I realize now that my Dad had this also.  Thinking back on how restless he was and how my Mom and stepmom complained how much he moved at night I'm sure he also had it but back then it wasn't known about.  I have read that it can run in families so now I know where I got it from.  It's one of those annoying diseases that can be controlled with medication.  So if your legs are always moving or you feel like you have to always move them, talk to your doctor there is something that can help you.  I am just glad it isn't painful since I already have Rheumatoid Arthritis.Smile

8/10/10 2:41am

My Mom has a Parkinson's like disease ... her legs are always bicycling when she's trying to sleep ... she tried the pills on www.homecure.com for that, and it's really helped!  First time a pill has helped that problem. 

 

They have great products ... we also use ColonQwik ... great for IBS sufferers. 

10/11/10 9:19am

Me and my sister both suffer from  RLS and have tryed several meds some seem to work a while but it never seems to last im tired of loosing sleep,Im sick of people not understanding,Im tired of having to sleep on the couch when i can sleep,Im sick of crying,Pepole think im  a spaz because how i ack or feel stupid because i just cant sleep and i make a lot of mistake and i mean really simple things become hard.I just want to lay down and die sometimes.Im so tired of some doctors pushing zanax on me because they think im just  stressed a lot well i am but not in that way and then i take a zanax and become very tired but then the RLS gets going and its bad because the zanax made me sleepey but the RLS wont let me then the battle is on .I have become very depressed when night time comes because im just getting to tired for the fight and people want to know why im such a air head well how do they think i feel not beeing able to add 2+2 sometimes because im so out of it because of the pain and lack of sleep.

10/12/10 11:17am

Donna - it's just like reading my life ... i believe in The Lord ... but i don't want to continue living like this ... it's a quality of life issue ... family is tired of my being a burden ... doctors tired of me ... call me the "puzzle" ... keep giving me pills that don't work ... wonder when they'll have a solution for xmrv or the murine leukemia (think all this is caused by mice) .... i will keep you in my prayers ... i know it's awful ... but it relieves me being able to talk to someone in the same boat ... awful ... i've had two certivical spine surgeries and my gallbladder removed ... they said it was all "referred pain"  ... they always ask me if i feel like commiting suicide ... i say no - but i do feel like a little dr-cide (doctor homicide) ... i wish the doctors felt our symptoms and pain ... they would believe us and work harder ... ice helps me ... can't take hot showers or baths or use heating blankets ... every breath hurts ...

 

prayers for you ... i'll keep you up on anything that works (i've been on every med there is) ... my Mom has periodic leg movement disorder ... they told her just to up her Klonopin dosage ... didn't help ... she did buy a bottle on www.homecure.com (their colon quik is incredible. for her plmd and they actually help her! 

 

i'm going to order their inflammation pills and will let you know

 

Kim

 

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