MS patient quality of life may be improved with LDN

A board to discuss Low Dose Naltrexone (LDN) as a treatment for Multiple Sclerosis

MS patient quality of life may be improved with LDN

Postby MSUK » Fri Aug 29, 2014 2:02 am

Multiple sclerosis patient quality of life may be improved with low dose naltrexone

Low dose naltrexone (LDN) may be on its way to becoming a new therapeutic agent for multiple sclerosis. Evidence for its efficacy in attenuating multiple sclerosis symptoms is scarce, but results of a phase 3 clinical trial, “A Randomized Placebo-Controlled, Crossover-Design Study of the Effects of Low Dose Naltrexone,” suggest that LDN enhances the mental health quality of life of patients with multiple sclerosis..... Read More - http://www.ms-uk.org/LDN
MS-UK - http://www.ms-uk.org/
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Re: MS patient quality of life may be improved with LDN

Postby dlynn » Fri Aug 29, 2014 6:32 am

I believe that ldn should be offered also, to ms patients by their neuros. or GPs. This has been nothing short of a
miracle for me. No side effects other than two nights of restless sleep at the start. I have an occasional bad few days,
but I now have more energy and stamina than the injectables could ever provide for me.
Thanks for the link MSUK
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Re: MS patient quality of life may be improved with LDN

Postby misslux » Fri Aug 29, 2014 4:36 pm

It was awful for me, didn't help and made me feel worse. I posted in the LDN side effects thread.
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Re: MS patient quality of life may be improved with LDN

Postby Kronk » Mon Sep 01, 2014 8:21 am

I haven't noticed anything good or bad. May as well be a vitamin. But i stick with it because of user reports like dlynn and the fact it is cheap.
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Re: MS patient quality of life may be improved with LDN

Postby 1eye » Wed Sep 10, 2014 6:36 am

It's all a matter of trust, isn't it?

Just as you trusted your spouse when you took your wedding vows, you have to be able to trust your doctor, don't you?

So what are we going to do with all those doctors who said LDN and CCSVI were both "nonsense"? Fortunately I've fired all of those who told me that. I have a new GP and a new neurologist. But now, I think I have to ask them too. I may have to fire them too.

Is there going to be a big doctor shortage? Or will some of them step up, and admit they were wrong, for their patients' sake (not just their income's)?

http://www.youtube.com/watch_popup?v=r13uYs7jglg

http://creativedestructionofmedicine.com/?p=3

http://www.ted.com/talks/eric_topol_the ... f_medicine
"Try - Just A Little Bit Harder" - Janis Joplin
CCSVI procedure Albany Aug 2010
'MS' is over - if you want it
Patients sans/without patience
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Re: MS patient quality of life may be improved with LDN

Postby savouryourlife » Thu Sep 18, 2014 7:46 pm

I am gladI read your post. Just started LDN's and I am restless at night. So look forward toeing on it longer as hopeful restlessness will calm down and I will get some sleep. Took some magnesium tonight and now will take melatonin

Btw am also allergic to chocolate!
Feb 18, 2010 Eco-Doppler Vaughan, MRV Frankfurt, left INT Jugular valve problem x2, RRMS since 1996, Angioplasty in Frankfurt March 10/10<div>Inclined bed therapy - 09/09/10</div>
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