Guest guest Posted June 16, 2004 Report Share Posted June 16, 2004 Hi,I thought you might like this page I found on the Multiple Sclerosis Society website. Go to the address below:http://www.mssociety.org.uk/go.rm?id=12383 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2004 Report Share Posted June 16, 2004 Reg, thankyou for posting this link to the webpage of the MS Society in UK on LDN. Although there are some untruths, or lack of correct information on their part, the main point is, ITS OUT THERE. A big step forward. Any one with MS will make up their own mind and look into it by performing an internet search on LDN, research and come to their own conclusion and informed decision to try it or not. Goodness knows we are definitely not satisfied with what is already available and will always search for more answers. Then this (LDN awareness) becomes bigger and bigger across the world, petition signing etc. It will snowball. It's a far better article on LDN than the NMSS of America put out not long ago and caused outrage amoungst us all, don't you agree? Once again, thanks for sharing. Friday Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2004 Report Share Posted June 16, 2004 It has brought ldn to the forefront as you say, however I think they are calling Dr.Lawrence a poor health care proffesional as he prescribes without an office visit,right? I assume the retired Dr. is Dr.Lawrence, but even if it isn't so what? According to DrBahari allmost anyone can benefit from using ldn. Now if this is true, and I for one don't doubt it, then a lot of diseases that we now face would fade into obscurity, if everyone took one 3.0mg pill a night. I think that in an effort to discredit ldn. they will go to any extreme. We do have the internet on our side though, and a very large majority of ldn. user's will fight to the last man(or woman)to defend ldn. How many would be that stong of a defender for Rebif? or Novantrone? or any other injectable drug? The U.K. seems to be farther ahead of us in a lot of areas when it comes to being open minded, Reg. -------Original Message------- From: low dose naltrexone Date: 06/16/04 12:42:21 low dose naltrexone Subject: [low dose naltrexone] Re: Multiple Sclerosis Society webpage... Reg, thankyou for posting this link to the webpage of the MS Society in UK on LDN. Although there are some untruths, or lack of correct information on their part, the main point is, ITS OUT THERE. A big step forward. ____________________________________________________ IncrediMail - Email has finally evolved - Click Here Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 7, 2004 Report Share Posted August 7, 2004 Hi Everyone, Sorry if that other address didn't work for the LDN MS society webpage. Try this one- http://www.mssociety.org.uk/research/research_explained/ldn.html Regards Audrey --- mumpuss@... wrote: --------------------------------- Hi, I thought you might like this page I found on the Multiple Sclerosis Society website. Go to the address below: http://www.mssociety.org.uk/go.rm?id=12383 Quote Link to comment Share on other sites More sharing options...
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