LDN Survey Form

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

LDN Survey Form

Postby Loma » Fri Jan 14, 2005 3:53 am

Hi All,

As far as I am aware there have been only 137 people who have
responded to the survey set up by The LDN Research Trust. Hundreds
of people worldwide take LDN, so why is there so few of you filling
out the form? The Trustees have put a lot of time and effort into
trying to get LDN into trial and responses like this make their work
even harder. Now,we would ALL like to see LDN available for
everyone, so why has there been a terrible response to the survey.
Maybe those of us who are taking LDN and getting benefit from it are
sitting back on our laurels saying "I`m alright, I`m on LDN so I`ll
leave the work to others". Well we should all be caring and trying
to get LDN into trial for those who aren`t as fortunate as us in
getting LDN from their doctor. Not only that we should be thinking
about future generations, our kids for example, should they succumb
to this horrid illness their best hope is LDN.

Please, please visit www.ldnresearchtrust.org and take time to fill
in the form. Let`s help this cause in anyway we can.

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Postby flora68 » Fri Jan 14, 2005 8:36 am

Last edited by flora68 on Wed Feb 09, 2005 3:28 pm, edited 1 time in total.
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Postby Loma » Fri Jan 14, 2005 8:49 am


If people are interested in LDN they`ll have been on many message boards and read about it, therefore they should have heard of The LDN Research Trust, it has been well publised. Sammy got 267 people to respond to her survey, so where are they now? I am not digging at anyone, I just want to jar peoples minds who have forgotten about the form. So please visit www.ldnresearchtrust.org and fill in the form. These people are taking no pay for all the work they are doing, so the least we can do, as LDN users is help them in anyway we can. If not for yourself, for your kids, My father has MS, his cousin has MS, I have MS and I have serious worries about my daughter having it too.

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