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originally posted by: MystikMushroom
a reply to: cooperton
The Yamamoto study has been retracted.
I'm not saying this stuff isn't something to look into -- but let's be careful about citing sources that have been retracted due to poor scientific methods.
originally posted by: imd12c4funn
a reply to: MystikMushroom
So no reason to kill doctors if it's a non-issue and scientifically flawed.
2nd
originally posted by: MystikMushroom
a reply to: imd12c4funn
I'm not saying the entire substance is scientifically flawed, but I've been reading through cancer forums and I can't find anyone that's had any positive results from this stuff. I see a lot of hopeful people, and a lot of money being spent, but I haven't seen an overwhelming number of success stories.
What I am seeing is that this stuff is insanely cheap to make, and the dose is in the nanogram range. For that little amount of active ingredient, the stuff should be a lot cheaper.
From what I've read, it seems the probiotic route would be the cheapest and most effective way to go.
I'm a big fan of probiotics, they do all kinds of things -- and I think we're barley scratching the surface of their worth. But $150 an injection for a few nanograms of gcmaf? I'd rather eat some yogurt or take a good probiotic.
originally posted by: MerkabaTribeEntity
I study the endocannabinoid system, cannabinoid pharmacodynamics and the potential applications of phytocannabinoids in the treatment of various diseases, so the potential here has me tickled somewhat. I'm off to read some more on this,
The Gc-Protein has a sugar side chain consisting of three sugar molecules , namely N – acetyl galactosamine , galactose, and sialic acid a so-called “tri- saccharide” (= “triple sugar”). When sialic acid and galactose are removed from this tri- saccharide, N -acetyl- galactosamine remains as a single sugar moiety. For Gc-Protein modified in this manner a strong activating effect on macrophages has been described: this modified Gc-Protein is a “Macrophage-Activating Factor”, abbreviated as “MAF”. More specifically the partially de-glycosylated Gc protein -derived macrophage-activating molecule is called “Gc -MAF” ( Saharuddin et al. 2002 Kuchiike et al. , 2013 Kisker et al. 2003)
How is Nagalase thought to inactivate Gc-MAF?
The enzyme “Nagalase” completely eliminates the sugar side chain of the Gc protein: the thus-modified Gc protein can no longer be converted to Gc MAF, its immune-stimulatory effect is no longer available. In other words, the effect of Nagalase on Gc Protein prevents the formation Gc -MAF. Insofar, tumor-derived Nagalase may have immune-suppressive properties.
Artificially produced Gc-MAF for treating diseases
When the macrophage activating activity of Gc-MAF became known, research was conducted towards synthetic production of Gc MAF and its use as an immune-stimulating agent. The therapy with artificial GcMAF is thought to benefit from the fact that artificial GcMAF cannot be inactivated by Nagalase. Accordingly, methods have been developed for in vitro production of Gc-MAF which is then administered to patients ( Inui et al. , 2013, Thyer et al. 2013A , Uto 2012 , Yamamoto et al. 2008a , 2008b , 2008c ).
Some authors described (Fabris et al 2012; Pacini et al 2012) that the effect of Gc -MAF depends on the genetic variants of the vitamin D receptor, the so-called “VDR genotypes “. In particular, the VDR variants “Fok 1″ and “BSM1″ were explored. The best responding patients (“responders”) seem to have the genotype FF / bb, followed by Ff / Bb . The genotype Ff / BB seems to be “low” responders.
Right, I'm really having a hard time finding any positive first hand accounts from anyone using this stuff. It seems like the "theory" is more sound than the actual practice of using it. Just because something make sense on paper doesn't mean it always translates to real-world results.
originally posted by: ignorant_ape
i have a few questions for the thread :
1- the claim " nagalese is in vaccines " :
got evidence ???????????????????
i would like to see the data showing the nagalese content [ micrograms ] in each vaccine please
2 - the claim " autistic children have HIGH nagalese levels "
again got evidence ??????????????
i want nagalse [ mg / kilo body weight ] data for these autistic children
2b - if the above claim is true - has the counter hypothesis of :
" the physiology that leads to autisdm produces nagalese "
been investigated ?????????????
3 - the thread title and various sources cited link nagalese to both autism and cancer
3a - why dont adult cancer patients display autism symptoms too
3b - where is the peadiatric cancer corralation to autism diagnosis ?
4 at what level [ micrograms / kilo body weight ] does nagalese have a statisticsaly observable effect on physiology ?
thats enough for a starter - lets see what answers [ if any ] fall out the tree
Doctors found dead and/or went missing felt that nagalase was being introduced to the body through vaccines
originally posted by: ignorant_ape
a reply to: Boadicea
err NO
nice try - but i asked those 7 questions for a very specific reason...
if the " alternative doctors " who claim to be researching this had done ANY actually reasarch - they should have already published the answers to every one of my questions
Q 1 is so painfull it hurts
i am not a medical researcher - i am an engineer - its not my job to do this crap
so dont palm the task off on me...
- look to your " alternate medicine " heroes - and ask - what the hell are they actually doing...
originally posted by: Boadicea
So while doing more research on GcMAF treatment, I came across the website offering nagalase testing, with much (MUCH!) better explanation/description of exactly what GcMAF is than I have been able to offer:
The Gc-Protein has a sugar side chain consisting of three sugar molecules , namely N – acetyl galactosamine , galactose, and sialic acid a so-called “tri- saccharide” (= “triple sugar”). When sialic acid and galactose are removed from this tri- saccharide, N -acetyl- galactosamine remains as a single sugar moiety. For Gc-Protein modified in this manner a strong activating effect on macrophages has been described: this modified Gc-Protein is a “Macrophage-Activating Factor”, abbreviated as “MAF”. More specifically the partially de-glycosylated Gc protein -derived macrophage-activating molecule is called “Gc -MAF” ( Saharuddin et al. 2002 Kuchiike et al. , 2013 Kisker et al. 2003)
How is Nagalase thought to inactivate Gc-MAF?
The enzyme “Nagalase” completely eliminates the sugar side chain of the Gc protein: the thus-modified Gc protein can no longer be converted to Gc MAF, its immune-stimulatory effect is no longer available. In other words, the effect of Nagalase on Gc Protein prevents the formation Gc -MAF. Insofar, tumor-derived Nagalase may have immune-suppressive properties.
More interesting -- and worrisome -- is this:
Artificially produced Gc-MAF for treating diseases
When the macrophage activating activity of Gc-MAF became known, research was conducted towards synthetic production of Gc MAF and its use as an immune-stimulating agent. The therapy with artificial GcMAF is thought to benefit from the fact that artificial GcMAF cannot be inactivated by Nagalase. Accordingly, methods have been developed for in vitro production of Gc-MAF which is then administered to patients ( Inui et al. , 2013, Thyer et al. 2013A , Uto 2012 , Yamamoto et al. 2008a , 2008b , 2008c ).
So apparently my concerns about the safety of blood products was unfounded because at least some of the "GcMAF" being used to treat patients is being made in a lab. Shame on me for presuming too much.... and my apologies for not getting it right the first time. My only excuse is ignorance and that I'm learning about this as I go along too. I can't promise perfection (so sorry!) but I can promise as I learn better I will do better.
The concerns about safety and efficacy remain. If we're going to be injecting this stuff into people's bodies -- people who are already sick -- then we need to be damn sure it is both safe and effective. That requires research and peer-reviewed clinical studies. So now I wonder... are these GcMAF providers being shut down by authorities because more research is needed? Or because someone doesn't want the necessary research done? And how many of these artificial GcMAF providers are among those who don't want the necessary research done because there is no profit in it for them? After all, one can patent an artificial GcMAF and charge obscene amounts of money under our current medical patent system... they can't do that with the real thing. Nor can they make boatloads of cash off the natural probiotics and cannabinoids that would allow our bodies to heal itself as nature intended. Hmmmm...
Apparently, genetics play a role as well:
Some authors described (Fabris et al 2012; Pacini et al 2012) that the effect of Gc -MAF depends on the genetic variants of the vitamin D receptor, the so-called “VDR genotypes “. In particular, the VDR variants “Fok 1″ and “BSM1″ were explored. The best responding patients (“responders”) seem to have the genotype FF / bb, followed by Ff / Bb . The genotype Ff / BB seems to be “low” responders.
The article also lists several studies/published papers on GcMAF.
Stay away from anything synthetic.
The very first thing they inject infants with is a Synthetic Vitamin K shot.
originally posted by: MystikMushroom
I'm not saying this stuff isn't something to look into -- but let's be careful about citing sources that have been retracted due to poor scientific methods.
If this stuff was the miracle it's claimed -- I'm wondering why researchers aren't clamoring over one another to be the first to somehow prove it.