RE: Report your findings about LDN on remedy findings

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http://www.remedyfind.com/ is the site.

From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of Aletha WittmannSent: Sunday, August 21, 2005 1:55 PMlow dose naltrexone Subject: Re: [low dose naltrexone] Report your findings about LDN

Hi Everyone,I noticed that we have so many wonderful results from LDN from chatters on our site and not very many of them are posted in Remidyfind.com. When I talk to people regarding LDN I usually send them to that site first, but I don't feel it is currently representing what we are experiencing. If we have over 1400 people on our chat site, I would think we would have more than 200 stories reported on Remidyfind.comThanks everyoneAletha [low dose naltrexone] Re: One Year ago--To tell your doc or not about LDN> CJ> Congratulations on stopping your progression with LDN, glad you could> join this happy club :-)>> Everybody needs to respect everyone's choice about telling their doc> about LDN, I remember that paralyzing dependence I had on my docs> before LDN, because there was no hope except what they could offer.> And even with LDN, there is always that unknown future when you might> need their help again.>> All I can do is report my experience with telling my docs, for those> who are pondering this. My TX neuro back in 2004 said No when I asked> for LDN, so I got it elsewhere, then converted him to an LDN scripter> when I went back in 4 weeks no longer using my cane and so much> better. Since then I have told my story to 2 GP's who wrote scripts.> I went back to my WA neuro a few weeks ago, I was happy to find that> she has been hearing LDN stories, and has no problem writing the> script, and this is at a major Seattle MS center. So this is a major> way we can keep chipping away and spread clinical experience with> LDN, so docs won't be afraid of it.>> The other way is research. Please contribute if you can!> http://ldninfo.org/research_funding.htm>> SammyJo>>>>>>>>