Tag: Wikipedia

Salvation is from the Jews…and maybe damnation too…

To: Roy Schoeman
Author of Salvation Is from the Jews

My dear Mr. Schoeman,

I am veraciously enjoying your book Salvation Is from the Jews. As happens so often with my Jewish brothers, I find myself so on the same wavelength with your edgy wordsmithing and even sometimes your risqué investigative style that I have to call the experience “spiritually immersive”! Not least owing to our common affinity for sound mysticism and according skepticism of so-called “Churchianity,” Augustino-Calvinist Puritanism and scholasto-Jesuitical sophism, just some of the anacondas strangling Western Christianity in too many quarters. Your Old-New Testament insight about the eldest sons and analogously Israel missing the blessing I find particularly insightful and cannot restrain myself from asking, Is it not at the very least postulable that this principle can apply today to the Roman “See of Peter”? (Some would argue that the Fourth Ecumenical Council at Chalcedon thinks the answer is positively yes.)

On the flip-side, my relish of what you say understandably served to augment my distaste for crucial truths you omit and thereby falsehoods you imply. I am willing to overlook the almost total eclipse of post-biblical Middle Eastern history—your Ashkenazim, your Antiochian Orthodox Christians, your Khazaria, and then in the West your Sephardim and your Rothschilds with their fractional reserve banking cartel with its death-grip on the so-called Renaissance plus “modern times”! I am no Anti-Semite/racist, no Holocaust denier/revisionist and I am fully satisfied that the Protocols of the Learned Elders of Zion is a forgery and that Council of Jamnia never necessarily went down as theorists describe it, and you basically do justice to the wrongness of Mesoretic and other such renderings as well, the contemporary prevalence of depraved esotericism among the astral/noetic rulers (“ascended masters”) of this present darkness and the patent inner workings of occult brotherhoods that masquerade as “charitable fraternities.” (Yet why you abstain from fingering “Catholic” occult equestrian orders and the Jesuits I can’t explain to my satisfaction.) Nay indeed, more than just not being a racist, I consider racial theory a sad and quintessentially unmanly cop-out in the case of Hitler (part-Jewish and one-time art aspirant in a [then as now] Jew-dominated arts community) and all his ilk! No truly spiritual or godly undertaking orders, countenances or even contemplates violence, malice or certainly any evil. But I am a “truther” first and last, all unanswered questions remain for me on the table, and there are questions that loom especially large for serious historical researchers that you leave conspicuously unmentioned.

I am here going to assume that you at any rate regard the “gentile” or ”goy” as at least nominally human, so I won’t even go into the fact that Communism killed between 85 and 100 million and counting to Nazism’s 11 million. Except to ask: At a conservative (but not neoconservative) estimate, how many Jews do you think Communism killed? (I am morally certain that Communism has killed more Jews—leave alone many times more humans!—than Nazism.) And even the suckling babe knows with the crispest clarity that Communism, which is more conspiracy than revolution, was a Jewish aristocrat’s brainchild (or rather Rothschild). We also certainly won’t mention Saul Alinsky, the modern Karl Marx, who holds as his ideological (noetic?) marionettes all our nation’s top leaders. Your otherwise wondrous exposé fails to edify inasmuch as it does not excavate the modern underpinnings of Communism and global banking.

No, we’d best leave that golden calf alone, but what I do want to address, for example, is your failure to name “Nazim,” Zionists and other nationalist types (be they sluggish in the head or thuggish in the heart) who have sharply influenced contemporary U.S. American culture and policy like Werner von Braun, Walt Disney, Ayn Rand and yea G. K. Chesterton.

Most disturbingly of all, while you do mention Hitler’s willingness to spare Jews for export, you fail to mention that, as even Wikipedia admits, “Palestine was the only location to which any Nazi relocation plan succeeded in producing significant results, by means of an agreement begun in 1933 between the Zionist Federation of Germany (die Zionistische Vereinigung für Deutschland) and the Nazi government, the Haavara Agreement” (ostensibly quoted from Dr. Anwar El-Shahawy’s book Allah and Space). In other words, the élite in all quarters do not adhere to the same ideological lines of division they feed the masses. I contend that Nazism, in its inner circles, is not about race and is about the same thinking that set Madame Blavatsky apart, who (until exposed as a charlatan) was more accepted by spiritualists than bloodline-obsessed Masons. It would be hard to overstate her direct influence on Hitler. And in conclusion, it is nearly impossible to exaggerate the extent to which we have been lied to concerning the relationship among socialisms, and particularly between Nazism and Zionsim.

I think your use of the “yeast in the dough” imagery is the reverse of Jesus’ and hence is theologically the most questionable thing in the book thus far, and I stop just short of calling it impious and a total sell-out of the Faith. Jesus was patently not describing the Jewish Race or Religion as the “yeast in the dough” (or salt of the earth or light of the world) but rather his followers as the yeast in the dough that is each nation, Jewish or “Goyish.” The Church is the New Israel. That is the focal point of all Christians. The Jews are become a footnote, albeit a fascinating footnote, and a mysterious tool in prophetic literature in which nothing is clear much less nationalistically applicable. But let’s stop beating around the bush: the Judaizer heresy is just that, a filthy, base and demonic heresy. If emphasizing the Jewish Law is a slap in the face to Christ, how much more emphasizing the Jewish bloodlines!

I take exception, however, to any condemnation of the preservation of Jewish culture within Christian communities. I want to retain my (majority) Irish heritage and saints in how I worship because it makes me the more fully part of the whole Church. I’m told that some “Russian” Orthodox Christians, being of Jewish descent, were let back into Israel and, subsequently, there are Jerusalem parishes that celebrate the Divine Liturgy in Hebrew. I rejoice for them. And yes, they have a special perspective on Jesus being of His same household, and I rejoice with them. I love every chance I get chewing the fat with Jews, however secular, Orthodox or even Hasidic. I love hanging out with Catholics and Protestants. I even sometimes can stand Hindus and even (maybe) Buddhists. Wiccans? Druids? Why not. Mormons? JWs? Seventh Day Adventists? Sure, though obviously we’re bordering on the contrived and probably artificially preserved. Scientology obviously is downright dark, but their members are equally people. And I believe I am a missionary to everyone and everyone is a missionary to me.

Though I am the staunchest localist you’re ever likely to meet, I can never. Ever. Ever condone nationalism, because it is mass-insanity. I’ve heard a lot of people go on and on about a lot of things. I know an insecure, vacuous rant from a true scholarly thesis (however well calculated the former’s buzzwords to play on the contrived sympathies of my nation’s telehypnotized positivist sanctimonious funk). Every culture that’s old (read decadent) enough never shuts the heck up about some haplessly worldly claim (again, better suited to theater than academia) to being “the most special” or to having bestowed upon the undeserving unwashed and unappreciative “leftovers of genésis” their most vital (sometimes even implying spiritual) flair—and the ones who brag the most tend to offer the least substantive value—so by and large my Jewish (and, God Almighty help us all, “Christian”) Zionist-leaning brethren should get real and get in line because the sun doesn’t rise and set on their hex* deity, certainly no less evil than any swastika or moon, which like the “Nazim,” they flamboyantly procure to cast, and are indeed casting, upon the whole earth.

I say, A hex on our accursed ignorance.

A final question: What if anything did the honest, common “Goys” and Jews (Christian and otherwise) of the earth—especially of the United States—ever do to deserve the endless shower of pseudogodliness that is modern Hebrew Nationalism?

I get that you’re a bit shy—a neurosis you’ve perhaps mistaken for contemplation, toward which your personality, once informed by the truth, could yet lend itself—as well as unconvinced—your at times mumbled reading of your own writing betrays it—but try to hear this: even despite your occasionally poor dynamics a lot of people hang on your words. My father does. Even as I embrace you as a brother, I, with my whole being, request a clarification, at your leisure, of the loose ends I’ve listed above. I ask you to consider writing a sequel if not errata.

Most sincerely,
John

________
* Even Wikipedia admits the hexagram has not been in circulation among the Israelites for a day over 2,400 years if that. Not even Solomon in his wildest apostasy used it, much less Great King David. Another disgrace, another lie to the Babel-high pile. As for me, I want no part in Israel’s self-inflicted curses.

0

All About DCA A Natural Holistic Cancer Cure

Dichloroacetic acid

From Wikipedia, the free encyclopedia
Dichloroacetic acid
Identifiers
CAS number 79-43-6  Yes
PubChem 6597
ChemSpider 10771217  Yes
UNII 9LSH52S3LQ  Yes
DrugBank DB08809
KEGG C11149  Yes
MeSH Dichloroacetate
ChEBI CHEBI:36386  Yes
ChEMBL CHEMBL13960  Yes
RTECS number AG6125000
Jmol-3D images Image 1
Properties
Molecular formula C2H2Cl2O2
Molar mass 128.94 g mol−1
Appearance Colorless liquid
Density 1.5634 g/cm3 (20 °C)
Melting point 9-11 °C, 282-284 K, 48-52 °F
Boiling point 194 °C, 467 K, 381 °F
Solubility in water miscible
Solubility miscible with ethanol, diethyl ether[1]
Acidity (pKa) 1.35[1]
Thermochemistry
Std enthalpy of
formation ΔfHo298		 -496.3 kJ·mol-1[1]
Hazards
MSDS MSDS (jtbaker)
R-phrases R35 R50
S-phrases (S1/2) S26 S45 S61
NFPA 704
NFPA 704.svg
1
3
0
Related compounds
Related chloroacetic acids Chloroacetic acid
Trichloroacetic acid
Related compounds Acetic acid
Difluoroacetic acid
Dibromoacetic acid
 Yes (verify) (what is: Yes/?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Dichloroacetic acid, often abbreviated DCA, is the chemical compound with formulaCHCl2COOH. It is an acid, an analogue of acetic acid, in which two of the three hydrogenatoms of the methyl group have been replaced by chlorine atoms. The salts and esters of dichloroacetic acid are called dichloroacetates. Salts of DCA have been studied as potential drugs because they inhibit the enzyme pyruvate dehydrogenase kinase.[citation needed]

Contents

[hide]

[edit]Chemistry and occurrence

The chemistry of dichloroacetic acid is typical for halogenated organic acids. It is a member of the chloroacetic acids family. The dichloroacetate ion is produced when the acid is mixed with water. As an acid with a pKa of 1.35,[1] pure dichloroacetic acid is verycorrosive and extremely destructive to tissues of the mucous membranes and upper respiratory tract.[2]

DCA does not occur in nature. It is a trace product of the chlorination of drinking water and is produced by the metabolism of various chlorine-containing drugs or chemicals.[3] DCA is typically prepared by the reduction of trichloroacetic acid.

[edit]Therapeutic use

Owing to the highly corrosive action of the acid, only the salts of dichloroacetic acid are used therapeutically, including its sodium and potassium salts, sodium dichloroacetate and potassium dichloroacetate.

[edit]Lactic acidosis

The dichloroacetate ion stimulates the activity of the enzyme pyruvate dehydrogenase by inhibiting the enzyme pyruvate dehydrogenase kinase.[4] Thus, it decreases lactateproduction by shifting the metabolism of pyruvate from fermentation towards oxidation in the mitochondria. This property has led to trials of DCA for the treatment of lactic acidosisin humans.[5][6][7][8]

A randomized controlled trial in children with congenital lactic acidosis found that while DCA was well tolerated, it was ineffective in improving clinical outcomes.[6] A separate trial of DCA in children with MELAS (a syndrome of inadequate mitochondrial function, leading to lactic acidosis) was halted early, as all 15 of the children receiving DCA experienced significant nerve toxicity without any evidence of benefit from the medication.[7] A randomized controlled trial of DCA in adults with lactic acidosis found that while DCA lowered blood lactate levels, it had no clinical benefit and did not improve hemodynamicsor survival.[8]

Thus, while early case reports and pre-clinical data suggested that DCA might be effective for lactic acidosis, subsequent controlled trials have found no clinical benefit of DCA in this setting. In addition, clinical trial subjects were incapable of continuing on DCA as a study medication owing to progressive toxicities.

[edit]Potential cancer applications

Cancer cells generally express increased glycolysis, because they rely on anaerobic respiration that occurs in the cytosol (lactic acid fermentation) rather than oxidative phosphorylation in the mitochondria for energy (the Warburg effect), as a result of hypoxia that exists in tumors and malfunctioning mitochondria.[9][10] Usually dangerously damaged cells kill themselves via apoptosis, a mechanism of self-destruction that involves mitochondria, but this mechanism fails in cancer cells.

A phase I study published in January 2007 by researchers at the University of Alberta, who had tested DCA on human[11] cancer cells grown in mice, found that DCA restored mitochondrial function, thus restoring apoptosis, allowing cancer cells to self-destruct and shrink the tumor.[12]

These results received extensive media attention, beginning with an article in New Scientist titled “Cheap, ‘safe’ drug kills most cancers”.[11] Subsequently, the American Cancer Society and other medical organizations have received a large volume of public interest and questions regarding DCA.[13] Clinical trials in humans with cancer have not been conducted in the USA and are not yet final in Canada, emphasizing the need for caution in interpreting the preliminary results.[13][14]

[edit]Results of phase II clinical trials

In in vitro studies, Evangelos Michelakis of University of Alberta found that in tissue samples from 49 patients, DCA caused depolarization of mitochondria in GBM tissue but not in healthy brain tissue.[15]

Five palliative patients with primary GBM were entered into a phase II trial. Three had not responded to several chemotherapies; two were newly diagnosed. After surgical removal of tumor mass, they were treated with DCA and chemotherapy.[15]

Of the five patients tested, one died after three months. The surviving four were followed for 15 months. Their Karnofsky scores were unchanged in two cases, and decreased by 10 points in two patients.[15]

DCA was associated with tumor regression and had a good safety profile. DCA side effects were minimal.[15]

Michelakis is proceeding with phase three human studies with private funding from philanthropic groups and individuals. DCA’s legal status as a discovery is public domain because it was made or discovered as far back as 1864[16] and has been used in the treatment of canine and human lactic acidosis, some who presented at the beginning of treatment with cancer.

[edit]Concerns about pre-trial use

Following its initial publication, The New Scientist later editorialized, “The drug may yet live up to its promise as an anti-cancer agent – clinical trials are expected to start soon. It may even spawn an entirely new class of anti-cancer drugs. For now, however, it remains experimental, never yet properly tested in a person with cancer. People who self-administer the drug are taking a very long shot and, unlikely as it may sound, could even make their health worse.”[17]

In 2010, it was found that for human colorectal tumours grown in mice, under hypoxic conditions, DCA decreased rather than increased apoptosis, resulting in enhanced growth of the tumours.[18] These findings suggest that at least in some cancer types DCA treatment could be detrimental to patient health, highlighting the need for further testing before it can be considered a safe and effective cancer treatment.[18]

[edit]Planned and ongoing clinical trials

DCA is non-patentable as a compound, though a patent has been filed for its use in cancer treatment.[19] Research by Evangelos Michelakis has received no support from the pharmaceutical industry.[20] Concerns have been raised that without strong intellectual property protection, the financial incentive for drug development is reduced, and therefore obtaining sufficient funds to conduct clinical trials presents difficulty.[11][13][14][21] However, other sources of funding exist; previous studies of DCA have been funded by government organizations such as the National Institutes of Health, the Food and Drug Administration, the Canadian Institutes of Health Researchand by private charities (e.g. the Muscular Dystrophy Association). Recognizing anticipated funding challenges, Michelakis’s lab took the unorthodox step of directly soliciting online donations to fund the research.[22] After 6 months, his lab had raised over $800,000, enough to fund a small Clinical Phase 2 study. Michelakis and Archer have applied for a patent on the use of DCA in the treatment of cancer.[19][23]

On 24 September 2007, the Department of Medicine of Alberta University reported that after the trial funding was secured, both the Alberta local ethics committee and Health Canada approved the first DCA clinical trial for cancer.[24] This initial trial was relatively small with enrollment of up to 50 patients. The trial was completed in August 2009.[25] In May 2010 the team published a press release[26]stating no conclusions could be drawn as a result of the trial. A paper describing the results was published[27] but not linked from the press release. Only five patients had been treated with the drug during the trial.

In May 2011, online reports[28] suggested that the Alberta group had released new data which the media “had not reported”. However, this appeared to be caused by confusion between dates (the previous update was May 2010[29]) and cancer charities moved quickly to counter these rumours,[30][31] which were subsequently covered in New Scientist magazine.[32]

The use of this compound as an anti-cancer agent has been patented.[33]

[edit]Side effects

Reports in the lay press after the 2007 University of Alberta announcement claim that dichloroacetate “has actually been used safely in humans for decades”,[34] DCA is generally well tolerated, even in children.[35] Short-term, infused, bolus doses of DCA at 50 mg/kg/day have been well tolerated.[36]

At sustained, higher doses(generally 25 mg/kg/day taken orally, or greater), there is increased risk of several reversible toxicities, especially peripheral neuropathy, neurotoxicity, and gait disturbance.[4][34]

Studies have also shown that it can be carcinogenic in male B6C3F1 mice at high doses.[37]

[edit]Neuropathy

A clinical trial where DCA was given to patients of MELAS (a form of genetically inherited lactic acidosis) at 25 mg/kg/day was ended prematurely due to excessive peripheral nerve toxicity.[38] Dichloroacetate can also have anxiolytic or sedative effects.[3]

Animal studies suggest that the neuropathy and neurotoxicity during chronic dichloroacetate treatment may be partly due to depletion of thiamine, and thiamine supplementation in rats reduced these effects.[39] However, more recent studies in humans suggest that peripheral neuropathy is a common side effect during chronic DCA treatment, even with coadministration of oral thiamine.[40][41] An additional study reported that 50 mg/kg/day DCA treatment resulted in unsteady gait and lethargy in two patients, with symptoms occurring after one month for one patient and two months for the second. Gait disturbance and consciousness were recovered with cessation of DCA, however sensory nerve action potentials did not recover in one month.[42]

It has been reported that animals and patients treated with DCA have elevated levels of delta-aminolevulinic acid (delta-ALA) in the urine. A study published in 2008 suggests that this product may be the cause of the neurotoxic side effect of DCA by blocking peripheralmyelin formation.[43]

[edit]Carcinogenicity

Long term use (three years or more) of high doses (> 77 mg/kg/day) of DCA has been shown to increase risk of liver cancer in mice.[37]Studies of the trichloroethylene (TCE) metabolites dichloroacetic acid (DCA), trichloroacetic acid (TCA), and chloral hydrate suggest that both DCA and TCA are involved in TCE-induced liver tumorigenesis and that many DCA effects are consistent with conditions that increase the risk of liver cancer in humans.[44] It should be noted here that the maximum recommended dose for cancer treatment is 20mg/kg/day (less than 1/3rd of the 77mg/kg/day shown to increase liver cancer risk in mice).

[edit]Self-medication

The promise of DCA as a cheap, effective and safe treatment for cancer generated a great deal of public interest. Many people turned to self-medication.[45][46]

Doctors warned of potential problems if people attempt to try DCA outside a controlled clinical trial. “If it starts going badly, who is following you before it gets out of control? By the time you realize your liver is failing, you’re in big trouble”, said Laura Shanner, Associate Professor of Health Ethics at the University of Alberta.[47]

[edit]References

  1. ^ a b c d Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). CRC Press.ISBN 1439855110.
  2. ^ J.T. Baker MSDS
  3. ^ a b Stacpoole P, Henderson G, Yan Z, James M (1998).“Clinical pharmacology and toxicology of dichloroacetate”.Environ Health Perspect 106 Suppl 4: 989–994.doi:10.2307/3434142 . JSTOR 3434142 . PMC 1533324.PMID 9703483.
  4. ^ a b Stacpoole PW (1989). “The pharmacology of dichloroacetate”. Metabolism 38 (11): 1124–1144.doi:10.1016/0026-0495(89)90051-6 . PMID 2554095.
  5. ^ Stacpoole P, Lorenz A, Thomas R, Harman E (1988). “Dichloroacetate in the treatment of lactic acidosis”. Ann Intern Med 108 (1): 58–63. PMID 3337517.
  6. ^ a b Stacpoole P, Kerr D, Barnes C, Bunch S, Carney P, Fennell E, Felitsyn N, Gilmore R, Greer M, Henderson G, Hutson A, Neiberger R, O’Brien R, Perkins L, Quisling R, Shroads A, Shuster J, Silverstein J, Theriaque D, Valenstein E (2006). “Controlled clinical trial of dichloroacetate for treatment of congenital lactic acidosis in children”. Pediatrics 117 (5): 1519–1531. doi:10.1542/peds.2005-1226 . PMID 16651305.
  7. ^ a b Kaufmann P, Engelstad K, Wei Y, Jhung S, Sano M, Shungu D, Millar W, Hong X, Gooch C, Mao X, Pascual J, Hirano M, Stacpoole P, DiMauro S, De Vivo D (2006). “Dichloroacetate causes toxic neuropathy in MELAS: a randomized, controlled clinical trial”. Neurology 66 (3): 324–330.doi:10.1212/01.wnl.0000196641.05913.27 .PMID 16476929.
  8. ^ a b Stacpoole P, Wright E, Baumgartner T, Bersin R, Buchalter S, Curry S, Duncan C, Harman E, Henderson G, Jenkinson S (1992). “A controlled clinical trial of dichloroacetate for treatment of lactic acidosis in adults. The Dichloroacetate-Lactic Acidosis Study Group”. N Engl J Med 327 (22): 1564–1569.doi:10.1056/NEJM199211263272204 . PMID 1435883.
  9. ^ Xu R, Pelicano H, Zhou Y, Carew J, Feng L, Bhalla K, Keating M, Huang P (2005). “Inhibition of glycolysis in cancer cells: a novel strategy to overcome drug resistance associated with mitochondrial respiratory defect and hypoxia”. Cancer Res 65(2): 613–21. PMID 15695406.
  10. ^ Kim JW, Dang CV (2006). “Cancer’s molecular sweet tooth and the Warburg effect” . Cancer Res. 66 (18): 8927–8930.doi:10.1158/0008-5472.CAN-06-1501 . PMID 16982728.
  11. ^ a b c “Cheap, ‘safe’ drug kills most cancers” . New Scientist. 2007-01-17. Retrieved 2007-01-17.
  12. ^ Bonnet, Sébastien; Archer, Stephen L.; Allalunis-Turner, Joan; Haromy, Alois; Beaulieu, Christian; Thompson, Richard; Lee, Christopher T.; Lopaschuk, Gary D. et al. (2007). “A Mitochondria-K+ Channel Axis Is Suppressed in Cancer and Its Normalization Promotes Apoptosis and Inhibits Cancer Growth”. Cancer Cell 11 (1): 37–51.doi:10.1016/j.ccr.2006.10.020 . PMID 17222789.
  13. ^ a b c “DCA: Cancer Breakthrough or Urban Legend?”  FromABC News, 5 February 2007. Accessed 15 February 2007.
  14. ^ a b “No Wonder Drug” , letter to New Scientist from Ralph Moss Lemont. Published February 3, 2007. Accessed 16 February 2007.
  15. ^ a b c d Michelakis, E. D.; Sutendra, G.; Dromparis, P.; Webster, L.; Haromy, A.; Niven, E.; Maguire, C.; Gammer, T. L. et al. (2010). “Metabolic Modulation of Glioblastoma with Dichloroacetate” . Sci Transl Med 2 (31): 31ra34–31ra34.doi:10.1126/scitranslmed.3000677 . PMID 20463368.
  16. ^ T. E. (Thomas Edward) Thorpe. A Dictionary of Applied Chemistry. Vol. 3. Page 9 of 189 at http://www.ebooksread.com/authors-eng/t-e-thomas-edward-thorpe/a-dictionary-of-applied-chemistry-volume-3-hci/page-9-a-dictionary-of-applied-chemistry-volume-3-hci.shtml
  17. ^ “Editorial: Gambling with your life” , New Scientist, 31 March 2007
  18. ^ a b Shahrzad, Siranoush; Lacombe, Kristen; Adamcic, Una; Minhas, Kanwal; Coomber, Brenda L. (November 2010). “Sodium dichloroacetate (DCA) reduces apoptosis in colorectal tumor hypoxia”. Cancer Letters 297 (1): 75–83.doi:10.1016/j.canlet.2010.04.027 . PMID 20537792.
  19. ^ a b “CTV.ca: Researchers launch website on new cancer research” . CTV News.
  20. ^ “CTV.ca: Small molecule offers hope for cancer treatment” . CTV News. Retrieved 21 April 2012.
  21. ^ “Small molecule offers big hope against cancer” , by Ryan Smith. From ExpressNews, a University of Alberta publication. Published January 16, 2007. Accessed 15 February 2007.
  22. ^ Official University of Alberta DCA Site
  23. ^ A Method of Treating Cancer Using Dichloroacetate , Application to the European Patent Office, 19 October 2006
  24. ^http://www.dca.med.ualberta.ca/Home/Updates/letter_092407.pdf , 24 September 2007
  25. ^ The Safety and Efficacy of DCA for the Treatment of Brain Cancer , ClinicalTrials.gov identifier: NCT00540176
  26. ^ Outlook 2008 , Tufts Center for the Study of Drug Development
  27. ^ Michelakis, ED; Sutendra, G; Dromparis, P; Webster, L; Haromy, A; Niven, E; Maguire, C; Gammer, TL et al. (2010). “Metabolic modulation of glioblastoma with dichloroacetate”.Science translational medicine 2 (31): 31ra34–31ra34.doi:10.1126/scitranslmed.3000677 . PMID 20463368.
  28. ^ The Cure for Cancer Has Been Found and is Purposely Being Ignored  – Technorati blog (accessed 16/05/2011)
  29. ^ DCA Research Team publishes results of Clinical Trials  – University of Alberta website
  30. ^ Potential cancer drug DCA tested in early trials  – Cancer Research UK science blog
  31. ^ @CR_UK tweet  – tweeted 16/05/11
  32. ^ Cancer drug resurfaces and threatens false optimism  – New Scientist, 16 May 2011
  33. ^ US 8071645 , Newell, M. Karen; Newell, Evan & Villalobos-Menuey, Elizabeth, “Systems and methods for treating human inflammatory and proliferative diseases and wounds, with fatty acid metabolism inhibitors and/or glycolytic inhibitors”
  34. ^ a b Picard, André (2007-01-17). “Long-used drug shows new promise for cancer” . Toronto: The Globe and Mail. Retrieved 2007-01-17.
  35. ^ Pearson H; Kurtz, TL; Han, Z; Langaee, T (2008). “Role of dichloroacetate in the treatment of genetic mitochondrial diseases”. Adv Drug Deliv Rev. 60 (13,14): 1478–1487.doi:10.1016/j.addr.2008.02.014 . PMID 18647626.
  36. ^ Agbenyega T, Planche T, Bedu-Addo G, Ansong D, Owusu-Ofori A, Bhattaram VA, Nagaraja NV, Shroads AL, Henderson GN, Hutson AD, Derendorf H, Krishna S, Stacpoole PW (2003). “Population kinetics, efficacy, and safety of dichloroacetate for lactic acidosis due to severe malaria in children”. J Clin Pharmacol. 43 (4): 386–396.doi:10.1177/0091270003251392 . PMID 12723459.
  37. ^ a b DeAngelo AB, Daniel FB, Stober JA, Olson GR (1991). “The carcinogenicity of dichloroacetic acid in the male B6C3F1 mouse”. Fundam Appl Toxicol. 16 (2): 337–347.doi:10.1016/0272-0590(91)90118-N . PMID 2055364.
  38. ^ Kaufmann P, Engelstad K, Wei Y et al. (2006). “Dichloroacetate causes toxic neuropathy in MELAS: a randomized, controlled clinical trial”. Neurology 66 (3): 324–330. doi:10.1212/01.wnl.0000196641.05913.27 .PMID 16476929.
  39. ^ Stacpoole P, Harwood H, Cameron D, Curry S, Samuelson D, Cornwell P, Sauberlich H (1990). “Chronic toxicity of dichloroacetate: possible relation to thiamine deficiency in rats”.Fundam Appl Toxicol 14 (2): 327–37. doi:10.1016/0272-0590(90)90212-3 . PMID 2318357.
  40. ^ Kurlemann G, Paetzke I, Moller H, Masur H, Schuierer G, Weglage J, Koch HG (1995). “Therapy of complex I deficiency: peripheral neuropathy during dichloroacetate therapy”. Eur J Pediatr 154 (11): 928–32. doi:10.1007/BF01957508 .PMID 8582409.
  41. ^ Spruijt L, Naviaux RK, McGowan KA, Nyhan WL, Sheean G, Haas RH, Barshop BA (2001). “Nerve conduction changes in patients with mitochondrial diseases treated with dichloroacetate”. Muscle Nerve 24 (7): 916–24.doi:10.1002/mus.1089 . PMID 11410919.
  42. ^ Oishi K, Yoshioka M, Ozawa R, Yamamoto T, Oya Y, Ogawa M, Kawai M (2003). “Dichloroacetate treatment for adult patients with mitochondrial disease”. Rinsho Shinkeigaku 43 (4): 154–61. PMID 12892050.
  43. ^ Felitsyn, N; McLeod, C; Shroads, AL; Stacpoole, PW; Notterpek, L (2008). “The heme precursor delta-aminolevulinate blocks peripheral myelin formation”. Journal of Neurochemistry 106 (5): 2068–2079. doi:10.1111/j.1471-4159.2008.05552.x . PMC 2574579. PMID 18665889.
  44. ^ Caldwell JC, Keshava N (September 2006). “Key issues in the modes of action and effects of trichloroethylene metabolites for liver and kidney tumorigenesis” . Environ. Health Perspect.114 (9): 1457–63. PMC 1570066. PMID 16966105.
  45. ^ Pearson, Helen (2007). “Cancer patients opt for unapproved drug”. Nature 446 (7135): 474–475. doi:10.1038/446474a .PMID 17392750.
  46. ^ Interview: Would you try an untested cancer drug? , New Scientist, August 15, 2007
  47. ^ Andrea Sands (March 18, 2007). “Experts caution against patients compiling own data on unapproved cancer drug” . Edmonton Journal.

[edit]External links

  • International Chemical Safety Card 0868
  • CTV.ca News Staff (16 January 2007). “Small molecule offers hope for cancer treatment” . CTV.ca Website (CTV television network). Retrieved 2007-01-31.
  • DCA Research Information Website  (University of Alberta)
  • Wait for Clinical Trials , New Scientist, 24 February 2007
  • Potential cancer drug DCA tested in early trials , by Cancer Research UK
  • Interviewing Drs. Akbar and Humaira Khan about DCA
  • Cancer Biology – Cramping Tumors  Economist, January 18, 2007
  • Official University of Alberta DCA (dichloroacetate) Website , The University of Alberta Discovery. March 15, 2007

  • Dichloroacetate Orders

    Telephone Orders: 1-347-535-4322 (New York area)
    We are VERY busy, if you get the answering machine leave your name and phone number, we will call you back.

    UPDATE we now have DCA in capsules
    333 mg per capsule, Click To Buy DCA

    dichloroacetate-cancer
    60 Day DCA Treatment Kit is now available in the DCA Store

    What’s New With Dichloroacetate?

    February 2012 Video added “Using a Scale to Measure DCA”
    August 31, 2011 Doctor Flavin, M.D. read his letter Doctor Flavin’s letter
    March 20, 2011 Read how one person beat cancer using DCA.
    May 12, 2010 Latest Positive DCA Clinical Trials and More! Visit the University of Alberta  (the university site is currently down, try this link to read about the doctor )

    Recent Medical Research at a Canadian University has confirmed that scientists do understand the cause of cancer. The dying off of old cells to be replaced by new cells is a normal part of our cellular lifecycle and keeps us well. It seems that in cancerous cells, our body has forgotten how to tell the aged cells how to die off and be replaced by healthy new cells. This process is governed by the mitochondria and is known as “cell death” or “apoptosis”. In a cancer cell, the mitochondria has lost the ability to direct the cell to die off – the sick cell becomes “immortal”, spreading and making the person increasingly unwell. Recent Medical trials using Pure DCA have proven this compound can reactivate the mitochondria restoring the cell’s original function of “apoptosis” enabling shrinkage in tumor size and mass. Testimonials have shown reversal in illness, remission, clean health tests, increased health and vitality. Favourable results (scientifically measurable) have been accomplished within days (less than a week) of starting treatment with Pure DCA.

    “Dr. Evangelos Michelakis, a professor at the U of A Department of Medicine, has shown that dichloroacetate (DCA) causes regression in several cancers, including lung, breast, and brain tumors.”

    Sodium dichloroacetate offered by PureDCA.com is more than 99% pure. It is made using a sophisticated synthesis process. No organic solvents are used during the production. WE SHIP DCA WORLDWIDE.

    We are working with Doctors around the world but also service individual orders for Pure DCA for those looking for an alternative cancer treatment. You do NOT need a prescription.

    We ship dichloroacetate internationally, with no exceptions. We are a reliable source of sodium dichloroacetate (Pure DCA). Buy sodium dichloroacetate.

    Below you can find a description of the main sections of this website.

    Pure DCA Store

    • Buy DCA Online or by Telephone
    • Pure DCA Powder is available in 3 sizes: 20 grams, 50 grams, and 100 grams
    • Pure DCA in Capsules (333mg)
    • Pure Powdered Thiamine (Vitamin B1)
    • Pure NAC Powder (N-Acetyle L-Cysteine)
    • Medicinal dosing scales also available

    Pure DCA Information
    The main facts about sodium dichloroacetate, pure DCA

    Questions
    Frequently Asked Questions

    Contact Us

    Dichloroacetate has been used in recent human trials and was found to shrink tumors. These trials were done by a university and their results have been published for anyone to read about the dichloroacetate cancer connection. The link to the universities dichloroacetate  study.

Related articles
3

The Peaceful Nuclear Explosions Treaty

Peaceful nuclear explosions
From Wikipedia, the free encyclopedia
Peaceful nuclear explosions (PNEs) are nuclear explosions conducted for non-military purposes, such as activities related to economic development including the creation of canals. During the 1960s and 1970s, both the United States and the Soviet Union conducted a number of PNEs.
Six of the explosions by the Soviet Union are considered to have been of an applied nature, not just tests.
Subsequently the United States and the Soviet Union halted their programs. Definitions and limits are covered in the Peaceful Nuclear Explosions Treaty of 1976. The Comprehensive Nuclear-Test-Ban Treaty of 1996 prohibits all nuclear explosions, regardless of whether they are for peaceful purposes or not.
Contents [hide]
1 The Peaceful Nuclear Explosions Treaty
2 United States: Operation Plowshare
3 Soviet Union: Nuclear Explosions for the National Economy
4 Other nations
5 Spaceflight Applications
6 See also
7 References
8 External links
[edit]The Peaceful Nuclear Explosions Treaty

In the PNE Treaty the signatories agreed: not to carry out any individual nuclear explosions having a yield exceeding 150 kilotons; not to carry out any group explosion (consisting of a number of individual explosions) having an aggregate yield exceeding 1,500 kilotons; and not to carry out any group explosion having an aggregate yield exceeding 150 kilotons unless the individual explosions in the group could be identified and measured by agreed verification procedures. The parties also reaffirmed their obligations to comply fully with the Limited Test Ban Treaty of 1963.
The parties reserve the right to carry out nuclear explosions for peaceful purposes in the territory of another country if requested to do so, but only in full compliance with the yield limitations and other provisions of the PNE Treaty and in accord with the Non-Proliferation Treaty.
Articles IV and V of the PNE Treaty set forth the agreed verification arrangements. In addition to the use of national technical means, the Treaty states that information and access to sites of explosions will be provided by each side, and includes a commitment not to interfere with verification means and procedures.
The protocol to the PNE Treaty sets forth the specific agreed arrangements for ensuring that no weapon-related benefits precluded by the Threshold Test Ban Treaty are derived by carrying out a nuclear explosion used for peaceful purposes, including provisions for use of the hydrodynamic yield measurement method, seismic monitoring and on-site inspection.
The agreed statement that accompanies the Treaty specifies that a “peaceful application” of an underground nuclear explosion would not include the developmental testing of any nuclear explosive.
[edit]United States: Operation Plowshare

One of the Chariot schemes involved chaining five thermonuclear devices to create the artificial harbor.
Operation Plowshare was the name of the U.S. program for the development of techniques to use nuclear explosives for peaceful purposes. The name was coined in 1961, taken from Micah 4:3 (“And he shall judge among the nations, and shall rebuke many people: and they shall beat their swords into plowshares, and their spears into pruning hooks: nation shall not lift up sword against nation, neither shall they learn war any more”). Twenty-eight nuclear blasts were detonated between 1961 and 1973.
One of the first U.S. proposals for peaceful nuclear explosions that came close to being carried out was Project Chariot, which would have used several hydrogen bombs to create an artificial harbor at Cape Thompson, Alaska. It was never carried out due to concerns for the native populations and the fact that there was little potential use for the harbor to justify its risk and expense. There was also talk of using nuclear explosions to excavate a second Panama Canal.[1]
The largest excavation experiment took place in 1962 at the Department of Energy’s Nevada Test Site. The Sedan nuclear test carried out as part of Operation Storax displaced 12 million tons of earth, creating the largest man-made crater in the world, generating a large nuclear fallout over Nevada and Utah. Three tests were conducted in order to stimulate natural gas production, but the effort was abandoned as impractical because of cost and radioactive contamination of the gas.[2][3]
There were many negative impacts from Project Plowshare’s 27 nuclear explosions. For example, the Gasbuggy site,[3] located 55 miles east of Farmington, New Mexico, still contains nuclear contamination from a single subsurface blast in 1967.[4] Other consequences included blighted land, relocated communities, tritium-contaminated water, radioactivity, and fallout from debris being hurled high into the atmosphere. These were ignored and downplayed until the program was terminated in 1977, due in large part to public opposition, after $770 million had been spent on the project.[5]
[edit]Soviet Union: Nuclear Explosions for the National Economy

The Soviet Union conducted a much more vigorous program of 239 nuclear tests, some with multiple devices, between 1965 and 1988 under the auspices of Program No. 6 and Program No. 7-Nuclear Explosions for the National Economy. Its aims and results were similar to those of the American effort, with the exception that many of the blasts were considered applications, not tests.[6] The best known of these in the West was the Chagan test in January 1965 as radioactivity from the Chagan test was detected over Japan by both the U.S. and Japan. The United States complained to the Soviets, but the matter was dropped.
In the 1970, the Soviet Union started the “Deep Seismic Sounding” Program, that included the use of peaceful nuclear explosions to create seismic deep profiles. Compared to the usage of conventional explosives or mechanical methods, nuclear explosions allow the collection of longer seismic profiles (up to several thousand kilometers).[7]
There are proponents for continuing the PNE programs in modern Russia. They (e.g. A. Koldobsky) state that the program already paid for itself and saved the USSR billions of rubles and can save even more if continued. They also allege that the PNE is the only feasible way to put out large fountains and fires on natural gas deposits and the safest and most economically viable way to destroy chemical weapons.
Their opponents (include the academician A.V. Yablokov) [8] state that all PNE technologies have non-nuclear alternatives and that many PNEs actually caused nuclear disasters.
Reports on the successful Soviet use of nuclear explosions in extinguishing out-of-control gas well fires were widely cited in United States policy discussions of options for stopping the Deepwater Horizon oil spill.[9][10]
[edit]Other nations

This unreferenced section requires citations to ensure verifiability.
Germany at one time considered manufacturing nuclear explosives for civil engineering purposes. In the early 1970s a feasibility study was conducted for a project to build a canal from the Mediterranean Sea to the Qattara Depression in the Western Desert of Egypt using nuclear demolition. This project proposed to use 213 devices, with yields of 1 to 1.5 megatons detonated at depths of 100 to 500 m, to build this canal for the purpose of producing hydroelectric power.
The Smiling Buddha, India’s first explosive nuclear device was described by the Indian Government as a peaceful nuclear explosion.
In Australia proposed blasting was put forward as a way of mining Iron Ore in the Pilbara [11]
[edit]Spaceflight Applications

Nuclear explosions have been studied as a possible method of spacecraft propulsion. The most well known example was Project Orion, which studied the possibility of a spacecraft propelled by the detonation of nuclear devices which it released behind itself.
Another application would be for deflecting or destroying celestial objects like comets, meteors, or asteroids on a collision course with Earth that have the potential for causing destruction.
[edit]See also

Project Gnome
[edit]References

^ “US Congressional Record pg. 25747, 1968-09-05”. Retrieved 2012-01-22.
^ U.S. Department of Energy, Office of Legacy Management: Rulison, Colorado, Site. Fact Sheet [1].
^ a b Peter Metzger (February 22, 1970). Project Gasbuggy And Catch-85*: *That’s krypton-85, one of the radioactive by-products of nuclear explosions that release natural gas Project Gasbuggy and Catch-85 “It’s 95 per cent safe? We worry about the other 5”. New York Times. p. SM14.
^ “DOE Environmental Management (EM) – Gas Buggy Site”. Em.doe.gov. Retrieved 2010-09-19.
^ Benjamin K. Sovacool (2011). Contesting the Future of Nuclear Power: A Critical Global Assessment of Atomic Energy, World Scientific, pp. 171-172.
^ Nordyke, M. D. (2000-09-01). The Soviet Program for Peaceful Uses of Nuclear Explosions. Lawrence Livermore National Laboratory. pp. 34–35. DOI:10.2172/793554. Report no.: UCRL-ID-124410 Rev 2. U. S. Department of Energy contract no.: W-7405-Eng48.
^ University of Wyoming: http://w3.uwyo.edu/~seismic/dss/
^ “А. В. ЯБЛОКОВ, “ЯДЕРНАЯ МИФОЛОГИЯ КОНЦА XX ВЕКА””. Biometrica.tomsk.ru. Retrieved 2011-08-13.
^ Broad, William J. (2010-06-02). “Nuclear Option on Gulf Oil Spill? No Way, U.S. Says”. New York Times. Retrieved 2010-06-18.
^ Astrasheuskaya, Nastassia; Judah, Ben; Selyukh, Alina (2010-07-02). “Special Report: Should BP nuke its leaking well?”. Reuters. Retrieved 2010-07-08.
^ Nuclear blasting proposed for Pilbara Iron Ore Project in Industrial Reviews and Mining Year Book, 1970 pp.255-259
[edit]External links

Peaceful Nuclear Explosions Comprehensive Nuclear-Test-Ban Treaty Organization Preparatory Commission
Video of the 104Kt Sedan PNE as part of Operation Plowshare.
Video of the Soviet Chagan PNE
Video of the Soviet Taiga PNE
On the Soviet nuclear program
On the Soviet program for peaceful uses of nuclear weapons, American Office of Scientific and Technical Information
United States Nuclear Tests, July 1945 through September 1992 (DOE/NV-209 [Rev.14]).
ARMS CONTROL AGREEMENTS,Federation of American Scientists
World Reaction to the Indian Nuclear Tests, Center for Nonproliferation Studies
Nuclear Files.org Treaty between the USA and USSR on underground nuclear explosions for peaceful purposes
Peter Kuran’s “Atomic Journeys” – documentary film includes tests of Peaceful nuclear Explosions.
[hide] v t e
Nuclear technology
Science
Chemistry Engineering Physics Atomic nucleus Fission Fusion Radiation ionizing
Fuel
Deuterium Fertile material Fissile Helium-3 Isotope separation Plutonium Thorium Tritium Uranium enriched depleted
Neutron
Activation Capture Cross-section Fast Fusion Generator Poison Radiation Reflector Temp Thermal
Reactors
Fission
reactors
by
primary
moderator
Water
Aqueous homogeneous reactor Boiling BWR ABWR Heavy CANDU PHWR SGHWR
Natural (NFR) Pressurized PWR VVER EPR Supercritical (SCWR)
Graphite
by coolant
Water
RBMK
Gas
Advanced gas-cooled (AGR) Magnox Pebble bed (PBMR)
UHTREX UNGG reactor Very high temperature (VHTR)
Molten Salt
FLiBe
Fuji MSR Liquid fluoride thorium reactor (LFTR)
Molten-Salt Reactor Experiment (MSRE)
Hydrocarbon
Organically moderated and cooled reactor
BeO
Aircraft Reactor Experiment (ARE)
None
(Fast)
Breeder (FBR) Integral (IFR) Liquid-metal-cooled (LMFR) SSTAR Traveling Wave (TWR)
Generation IV by coolant Gas (GFR) Lead (LFR) Sodium (SFR)
Fusion
reactors
by
confinement
Magnetic
Field-reversed configuration Levitated dipole Reversed field pinch Spheromak Stellarator Tokamak
Inertial
Bubble fusion (acoustic) Fusor electrostatic Laser-driven Magnetized target Z-pinch
Other
Dense plasma focus Migma Muon-catalyzed Polywell Pyroelectric
List of nuclear reactors
Power
Nuclear power plant By country Economics Fusion Isotope thermoelectric (RTG) Propulsion rocket Safety
Medicine
Imaging
by
radiation
Gamma camera
Scintigraphy Positron emission (PET) Single photon emission (SPECT)
X-ray
Projectional radiography Computed tomography
Therapy
Boron neutron capture (BNCT) Brachytherapy Proton Radiation Tomotherapy
Weapon
Topics
Arms race Delivery Design Explosion effects History Proliferation Testing underground Warfare Yield TNTe
Lists
Popular culture States Tests Treaties Weapon-free zones Weapons
Waste
Products
Actinide: (Reprocessed uranium Reactor-grade plutonium Minor actinide) Activation Fission LLFP
Disposal
Fuel cycle HLW LLW Repository Reprocessing Spent fuel pool cask Transmutation
Debate
Nuclear power debate Nuclear weapons debate Anti-nuclear movement Uranium mining debate Nuclear power phase-out

1

Adam Kokesh and Poker Face Came to Rochester NY

Adam Kokesh and Poker Face Came to Rochester NY Saturday night for Rock The Primary 2012 a Ron Paul event

Unedited Uncut! with Daniel J Leach and Adam Kokesh at McGinny’s Sports Pub .

If you live near Rochester, you did not want to be anyplace else but McGinnys Sports Pub on East River Road for Rock The Primary Party from 6pm-midnight. Guest speaker Adam Kokesh and liberty protest band Poker Face for a Rocking good time.   Poker Face Played at “Rock The Primary” for the first time.   While Adam Kokesh of Adam VS the Man gave a inspirational speech in support of freedom Liberty and Dr Ron Paul for the 2012 Presidential run.   April 21, 2012 Poker Face performing April 21, 2012 in Rochester, NY at McGinny’s Sports Pub
Angela RH Adam is a wonderful person. We had a great time Saturday. It was a lot of planning and hard work but very much worth it.
From Wikipedia, the free encyclopedia
Adam Kokesh

Adam Charles Kokesh (born February 1, 1982) is an American activist and talk radio host. Kokesh was a Corporal in the United States Marine Corps Reserve and is a veteran of the Iraq War. He is an outspoken opponent of the U.S. military intervention in Iraq and has received media attention related to anti-war protest activities. He is the son of Charles Kokesh, a Santa Fe venture capitalist, founder of a firm called Technology Funding and owner of the Santa Fe Horse Park.

Marine Corps service

Kokesh attended the Native American Preparatory School in San Ysidro, New Mexico. He enlisted in the United States Marine Corps in 1999. In 2004, he served in Fallujah. He was a liaison between the U.S. military and Iraqi civilians as a member of the 3rd Civil Affairs Group. He also worked a security checkpoint while in Iraq. He brought home a pistol from Iraq in 2004 in violation of military rules, which prevented his return for a second Iraq tour. Kokesh “had risen to the rank of sergeant after three-and-a-half years in the Reserves” and “was demoted to corporal and soon thereafter discharged honorably with a re-enlistment code that basically said, ‘you can’t re-enlist.'” Having experienced combat in Fallujah, Kokesh received the Combat Action Ribbon and the Navy Commendation Medal after his honorable discharge from active duty.

Poker Face has been dubbed the leading truth/freedom band in the Union. Through the use of various multi-media sources, this four piece band has made it their mission to expose the lies & scandals coming out the Union’s Capitol. With a sound that is unmistakably their own, Poker Face mixes a variety of styles & orchestrations to take you on a true musical journey.
Paul Topete and crew are forever experimenting with new directions. The two previous albums releases focused mainly on developing their works around the keyboard. For the 3rd disc, they have set aside the ivories and focused on a more guitar oriented sound. This has enabled them to create a vibe similar to the acoustic hard rock sound of Alice in Chains or Days of the New, while keeping their roots firmly planted in the melodic classic rock stylings of Boston & Pink Floyd.
The information contained within the Sex, Lies and Politiks album is an in-depth look into the conspiracies and cover-ups committed by a government that serves the agendas of money hungry elitists the control the world, hell bent on domination of the human race.SLP is followed by Made in America. Where the interactivity of the MIA-CD grows exponentially. There are hours of ForeFather and Americas history to investigate, and explore, Pictures of the band, and videos to watch. It is chuck full of eye and ear candy for the parent and the child to see and hear. We made learning about our history FUN!The journey of exposure continues with the driving tunes on the latest album: PEACE OR WAR. Poker Face has released this new musically-explosive CD October of 2009.
Who Was Recently Harassed By FBI – Poker Face The Band
Written by YIKES

by Yikes

Why? Listen At: http://www.TheAmericanVoice.com – Date: Tue. 4.6.10 – Time: 10:00 pm ET ~ 7:00 pm PT ~ Hosted by: John Clark ~ Is Protest ‘Rock’ Bad? ~ Be there or be Un-Aware! …        Why? Because patriotic groups play their music !!! The Hutaree 9. But ‘gangsta Rap’ Oh that’s OK?

Poker Face has been dubbed the leading truth/freedom band in the Union.  Through the use of various multi-media sources, this four piece band has made it their mission to expose the lies & scandals coming out the Union’s Capitol.  With a sound that is unmistakably their own, Poker Face mixes a variety of styles & orchestrations to take you on a true musical journey, while keeping their roots firmly planted in the melodic classic rock stylings of Boston & Pink Floyd.

The information contained within the Sex, Lies and Politiks album is an in-depth look into the conspiracies and cover-ups committed by a government that serves the agendas of money hungry elitists the control the world, hell bent on domination of the human race.

The journey of exposure continues with the driving tunes on the latest album: PEACE OR WAR. Poker Face has released this new musically-explosive CD January 2010.

http://www.pokerface.com/

Poker Face performing April 21, 2012 in Rochester, NY at MicGinny’s Sports Pub. For info go to this link http://www.digitalhda.com/ROCK-THE-PRIMARY.html

1

Create a website or blog at WordPress.com

Up ↑