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 patient quality of life may be improved with LDN
MS patient quality of life may be improved with LDN
MS-UK - http://www.ms-uk.org/
Re: MS patient quality of life may be improved with LDN
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
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
Re: MS patient quality of life may be improved with LDN
It was awful for me, didn't help and made me feel worse. I posted in the LDN side effects thread.
Re: MS patient quality of life may be improved with LDN
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.
- 1eye
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Re: MS patient quality of life may be improved with LDN
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://creativedestructionofmedicine.com/?p=3
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://creativedestructionofmedicine.com/?p=3
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Not a doctor.
"I'm still here, how 'bout that? I may have lost my lunchbox, but I'm still here." John Cowan Hartford (December 30, 1937 – June 4, 2001)
Not a doctor.
"I'm still here, how 'bout that? I may have lost my lunchbox, but I'm still here." John Cowan Hartford (December 30, 1937 – June 4, 2001)
- savouryourlife
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Re: MS patient quality of life may be improved with LDN
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!
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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