Guest guest Posted July 9, 2004 Report Share Posted July 9, 2004 Hello wonderful people, I dont post a lot on here, which i should do but i have a question to ask all you wonderful people; Are charities in anyway funded by by drug companies? You know, drug companies who make MS Drugs? My friend Sam has been banned from the MS Society so many times talking about LDN & it's plus sides. But as i've read through his postings & emails, the MS Society aren't backing trials or are bothered in talking about a drug, which is shrappnel compared to the present MS Drugs. Why could this be? Its sunny here but bloody cold for July. Dan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 9, 2004 Report Share Posted July 9, 2004 Dan, Unfortunately we have to battle not only this rotten disease but a multitude of organizations that are making money off it. It's sad when we can't even trust the NMSS, which is suppposed to exist for our benefit. When it seems that they don't even want to listen to us it makes you wonder. Do they really want to find a cure or are they happy making tons of money, while saying they are searching for one? Chris -------------- Original message -------------- Hello wonderful people,I dont post a lot on here, which i should do but i have a question to ask all you wonderful people; Are charities in anyway funded by by drug companies? You know, drug companies who make MS Drugs? My friend Sam has been banned from the MS Society so many times talking about LDN & it's plus sides. But as i've read through his postings & emails, the MS Society aren't backing trials or are bothered in talking about a drug, which is shrappnel compared to the present MS Drugs. Why could this be?Its sunny here but bloody cold for July.Dan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 9, 2004 Report Share Posted July 9, 2004 This seems like a horrible state of affairs to be in. I used to post on the MS Society web site but now- cos i've wiped their address from my Favorites list i'll- please- write more on here as i'm taking the drug next month. i've so many emails stating what you state but my underlining thought is- is this legal? Surely a charity cant get funding from drug companies or can they? Much appreciated Chris. Dan > Dan, Unfortunately we have to battle not only this rotten disease but a multitude of organizations that are making money off it. It's sad when we can't even trust the NMSS, which is suppposed to exist for our benefit. When it seems that they don't even want to listen to us it makes you wonder. Do they really want to find a cure or are they happy making tons of money, while saying they are searching for one? Chris > > -------------- Original message -------------- > Hello wonderful people, > > I dont post a lot on here, which i should do but i have a question > to ask all you wonderful people; > > Are charities in anyway funded by by drug companies? You know, drug > companies who make MS Drugs? My friend Sam has been banned from the > MS Society so many times talking about LDN & it's plus sides. But as > i've read through his postings & emails, the MS Society aren't > backing trials or are bothered in talking about a drug, which is > shrappnel compared to the present MS Drugs. Why could this be? > > Its sunny here but bloody cold for July. > > Dan > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 10, 2004 Report Share Posted July 10, 2004 DAN, I WOULD HAVE THOUGHT THAT THE MS SOCIETY WOULD HAVE BEEN THRILLED TO HEAR THAT SO MANY PEOPLE WITH MS FELT THEY WERE BENEFITTING FROM LDN. THEIR REACTION WAS QUITE THE OPPOSITE. IF THEY WON'T LISTEN TO US HOW CAN THEY CLAIM TO REPRESENT US AND OUR INTERESTS? CHRIS -------------- Original message -------------- This seems like a horrible state of affairs to be in. I used to post on the MS Society web site but now- cos i've wiped their address from my Favorites list i'll- please- write more on here as i'm taking the drug next month.i've so many emails stating what you state but my underlining thought is- is this legal? Surely a charity cant get funding from drug companies or can they?Much appreciated Chris.Dan> Dan, Unfortunately we have to battle not only this rotten disease but a multitude of organizations that are making money off it. It's sad when we can't even trust the NMSS, which is suppposed to exist for our benefit. When it seems that they don't even want to listen to us it makes you wonder. Do they really want to find a cure or are they happy making tons of money, while saying they are searching for one? Chris> > -------------- Original message -------------- > Hello wonderful people,> > I dont post a lot on here, which i should do but i have a question > to ask all you wonderful people; > > Are charities in anyway funded by by drug companies? You know, drug > companies who make MS Drugs? My friend Sam has been banned from the > MS Society so many times talking about LDN & it's plus sides. But as > i've read through his postings & emails, the MS Society aren't > backing trials or are bothered in talking about a drug, which is > shrappnel compared to the present MS Drugs. Why could this be?> > Its sunny here but bloody cold for July.> > Dan> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 10, 2004 Report Share Posted July 10, 2004 The NMSS is paid off dearly by the CRAB drug companies. The are slandering themselves for money, which they are more interested in than helping people with MS. They crate lots of highly paying jobs, especially for the big wigs (give them a haircut, perhaps with over sized scissors, capable of removing heard.) Perhaps the alquida have a good solution for them! B. DAN, I WOULD HAVE THOUGHT THAT THE MS SOCIETY WOULD HAVE BEEN THRILLED TO HEAR THAT SO MANY PEOPLE WITH MS FELT THEY WERE BENEFITTING FROM LDN. THEIR REACTION WAS QUITE THE OPPOSITE. IF THEY WON'T LISTEN TO US HOW CAN THEY CLAIM TO REPRESENT US AND OUR INTERESTS? CHRIS -------------- Original message -------------- This seems like a horrible state of affairs to be in. I used to post on the MS Society web site but now- cos i've wiped their address from my Favorites list i'll- please- write more on here as i'm taking the drug next month.i've so many emails stating what you state but my underlining thought is- is this legal? Surely a charity cant get funding from drug companies or can they?Much appreciated Chris.Dan Quote Link to comment Share on other sites More sharing options...
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