Restless Legs Syndrome (RLS) Discussion Board

You have my permission to use rlsbecat, Ruby.

I'm saying yes to the pain question.

However, I've had it this way all my life and have found that it's in our family's genetic code.

Love y'all for helping with this.

No!

WOW, Thanks again. Not happy about the answers of NO, but glad to know the truth.

Again, to all, numbers and responses are going to be helpful for us all.

Thanks you tons.

Keep on voting, Please.

Hugs and the moon to all
Lynne

HI Corrie, and to all;

Thanks to all that are responding, IT ALL HELPS. I hope many more answer, we need numbers, no matter the answers.

This is awesome, please suggest to everyone please, to answer these.

Hugs and Thanks again.

This is the second part of the poll. I am limiting it to just a yes or no answer and anyone may answer.

The question is: Do you feel you are receiving the best treatment or enough treatment?

No comments please, this is just for research.

I hope I did this all right, it's been a while...:), so ...

This is a poll for specific information about those people with EKD or RLS, who suffer with pain as a symptom or part of your symptoms.

Poll will end on June 15th, 2011. Thank you in advance for your help!

If I did this wrong please just post the answer, cause I don't see the poll, hmm. LOL ...

Hey Sug glad to see you around.
So sorry to hear that it has gotten worse.

I have thought for a long time that (I have pain, as well) sees any kind of rise in my system as stress. Whether it means I'm happy and looking forward to something or really ill or upset. It's all stress. Or seems to be for ...

NEPH! Brother, so awesome to see your name here and a couple of post. My heart beeps with you about the discovery to your key of NON RLS living. Yahoo and blessing abound. Yeah, I'm happy to hear that is still just working gangbusters for you.

Love to see new pictures, I'll send you my new or use ...

Thank you for the link. Thank you Doety!

Roger and yes, our own Miss Rubyslippers, did great by us all.

As, they always do.

Dakota, Hi and welcome.
Never heard of the setting for RLS, however, the vet verison and the people version were at one time very different.
Dakota, that is awesome that it is working for you. I hope that was not a test for you, but a aid in healing. I will pray with you on that one.
Love success ...

The largest "takers" from the pharma companies....is the US government.

Pharma companies did not go back into time and find some sap from my family to slip the gene into action. It's just apart of my family genetics.

Betty I sure hope your treatment keeps on chugging along. It's been a while ...

Hi BB,

Yes, I have many friends that say that the CPap and BiPap are helping them sleep. I think I might be on one myself someday, but have more hope than fear about that.

I wish I had some great answer for you about the RLS and Sleep deprivation issue. I have 2 out of 7 days that I sleep almost ...

Note on the uses of certain vitamins.

!. Vitamin E should be started very slowly. The smallest dose use to be 50IUs, don't just start at any dose, as this vitamin starts working on muscle first. Your largest muscle is the heart.
Your blood pressure will change as you take Vitamin E, so take it ...

Thanks Corrie, same to you. I hope that all is near control or manageable.

I know my body is truly paying for not sleeping and the chronic pain....not normal to all..... is really changing my life in ways I had no idea about.

I hope like you, for all of us, that progression is just out of the ...