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Author Topic: Restless legs  (Read 2117 times)
Kforsythe
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« on: June 08, 2015, 05:35:04 PM »

I have restless legs right before dialysis, during dialysis and when I try to sleep.  It is so frustrating. This is new since I started dialysis.   What I hate about this disease is that people who don't have it think they have the answers.  I have been laying quietly for the past thirty minutes and my legs started to bother so I said something to my husband. His answer ' I think it is in your head because it is only when you are laying down'.  Argggg.  He almost did not keep his head. I know there are people with bigger problems.  I know I am blessed to be alive, but I don't want this either.   I am usually pretty positive, bu this disease has taken so much from me.  I don't feel positive today. Especially when I am told something is just in my head. Thanks for listening.  Thought it better to rant on here than cry for an hour. Reading these boards help me feel not so alone
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Kim
Polycystic kidney disease
Home hemo since May 2014
Lis
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« Reply #1 on: June 08, 2015, 07:12:52 PM »

 There is nothing that makes me see red more than when someone suggests it's all in our head.   >:(  I too have RLS, and its always worse at night. Which is typical.  I also get it when I sit too long.  I wanted to take calcium-magnesium supplements but my kidney doctor vetoed it, said the magnesium could become toxic to me. Someone else I know recommends quinine water/soda but not sure if okay. And just yesterday, someone on my FB kidney group recommended an ointment made by Hyland's Homeopathy meds and swears it works. I might try it but I we should cheek with our nephs first.  RLS is really annoying o deal with and causes sleep issues. 

PKD diagnosed 3 years ago
About to have fistula put in
GFR of 13
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Lis
Diagnosed with PKD 2013
Stage 5 ESRD, GFR of 7
Fistula created July 2015
Angioplasty on fistula Jan 2016
Transposition on fistula April 2016
Started training for home hemodialysis July 2016
Started home hemodialysis August 2016
Had five donors try but didn't pass
On waiting list at UCSF
PrimeTimer
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« Reply #2 on: June 08, 2015, 07:34:01 PM »

Don't know if this will help you folks that have kidney disease and doing dialysis but, I often use a rolled up bed pillow or big bath towel (something somewhat firm and rolled up like a tootsie roll) and place it just under my knees or under the upper parts of my calves when my legs act up at night. Sometimes a heating pad or heated rice bag helps, too. I couldn't imagine having to sit still for 3-4 hours and on-top of that, getting hit with RLS in the chair. I feel for you guys!
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Husband had ESRD with Type I Diabetes -Insulin Dependent.
I was his care-partner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
After more than 150 days of being hospitalized with complications from Diabetes, my beloved husband's heart stopped and he passed away 06-08-21. He was only 63.
dialysisuser82
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« Reply #3 on: June 17, 2015, 07:40:29 AM »


Some patients have worst RLS during dialysis!  I've seen some who could only stand up during the whole treatment.

I have to take clonazepam (Klonopin) to treat the RLS for over 20 years.  It does work.

                         ~ Great works are performed not by strength, but by perseverance.  ~Samuel Johnson
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Jean
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« Reply #4 on: June 20, 2015, 05:47:38 PM »

Wal Mart has a product called Leg Cramps. It works for RLS too and really fast. My neph approved it, and I keep it very handy. It's worth a try.
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One day at a time, thats all I can do.
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