Guest guest Posted August 17, 2003 Report Share Posted August 17, 2003 Reading Maries post on clinical testing of LDN just makes me so sad. It's so unbelievably sad that the government (or whoever) won't conduct the testing on this drug that is doing so many people so good. I do want to ask though, that if someone did do the studies, why would there be no patent? is it because naltrexone and revia (i believe that's the right non-generic name) are already marketed drugs? I even told my neuro that I didn't see testing coming b/c no one stands to make $$ and he basically agreed. Kinda surprised me, but he did! It's just sad... Very sad. Even in the case of an online friend of mine who could possibly benefit from it, she prefers to stick with the "proven" treatments. Just think if she'd go out on the limb and take LDN and feel so much better? She's young too, maybe 36. Think of how her quality of life could possibly stay the same? I'm so anxious for my LDN and since I think the way I do, it's hard for me to understand how people can read all the great things and still have to wonder. I'm very open-minded and if I read all your posts on all the good results, that's all I need. Of course, I have investigated the side effects, but honestly, most of my information has come from you guys!! For that I'm so thankful. I'm thankful for the internet and all of the endless possibilities of learning & research there are out here. And, the wonderful people who you can meet and share with. I sometimes think to myself, geez, if I had no internet, I'd never know about LDN, and probably neither would 99% of you guys! Imagine it. Sorry, I'm rambling here. Just thinking outloud. Kathy PS congrats on your LDN!!! I can't wait to hear your results soon :-) Quote Link to comment Share on other sites More sharing options...
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