Willy wrote:
The whole tenor of this discussion has been to imply that the NMSS somehow should have something to say about the story.
Oh, for heaven's sake. Nobody "implied" anything. I asked a simple question out of pure curiosity. That is not an implication of anything.
Remember, many researchers are simply individual MS doctors who treat patients and do research and clinical trials for MS and MS drugs on the side! Of course there could possibly (I say possibly) be a connection, backlash, and/or a possible conflict of interest, etc. for the NMSS! My former neuro was doing many clinical trials sponsored by pharmaceutical companies (he had about 5 of them going at the same time) and getting paid for them, of course, as he should be. BUT.....It IS possible for a doctor who is in "tight quarters" with a pharmaceutical company to feel a little "pressured" from the pharmaceutical company (like the article mentions), if he's then asked to do a clinical trial that is NOT related to a pharmaceutical company. Nobody can say that "might" not happen. And then this WOULD relate and/or reflect on the NMSS because they
also provide grants to those same doctors!
UNLESS, does the NMSS have a policy that if an MS doctor is already doing a clinical trial sponsored and paid for by a pharmaceutical company that that neuro can NOT apply for grant funds from the NMSS to do another trial?
I tried to get my neuro to apply for grant funds from the NMSS, but with him doing so many pharmaceutical sponsored trials, it put him in a difficult spot, shall we say, but I don't think that "difficult spot" came from or was caused by the NMSS - which leaves me "wondering" if the pressure wasn't coming from the pharma company (which AGAIN relates it directly back to Harry's article). And if that's true, then how many MS drugs that are currently NOT being marketed and "pushed" by pharma companies for MS ARE being ignored due to this involvement and/or possible pressure (if the article proves correct) from the pharma companies? And if so, then maybe the NMSS is NOT getting totally unbiased research back from the "field"! Maybe there IS a policy such as that with the NMSS [i.e. that you can't receive grant funds from the NMSS if you are receiving funds from a pharmaceutical company for one of their clinical trials? I will only say that I doubt that there is, because the NMSS encouraged me to get an MS neuro - whom as I mentioned, most of them do pharmaceutical clinical trials on the side - to get involved (Coetzee said the word "engaged") in outside research, also.]
NOW do you see why I was wondering? My FIRST question after reading that article (which was posted on an MS forum - so I figured I wasn't the only one who was making a connection between it and MS) was "hmmmmm.....I wonder if that same sort of "pressure" from pharmaceutical companies is being applied to the MS doctors who are "partnered" with them for MS clinical trials. And if so, then I wonder if the NMSS will address this possible problem? It was NOT that far of a reach. And if I thought that, many other people will, also. I know I'm not THAT nuts, you guys!
Don't tell me nobody knew this?
Like Harry mentioned earlier, you just never know.......money talks.
Remember, MS researchers are also simply "doctors", who treat patients. My next regular neuro appointment is with the Vandy "researchers".
Deb