OT Media lies about vitamin C, cancer cures and nutritional medicine (plus other news)

[Guest guest]

http://www.naturalnews.com/024380.html

In headlines around the world, Vitamin C is once again under attack. The vitamin is extremely dangerous, researchers now say, because it might "interfere with the toxic effects of chemotherapy." These mainstream media articles, of course, are attempting to convince cancer patients to stop taking vitamins that support health and, instead, allow chemotherapy to poison their body's cells without any protection whatsoever for healthy cells.

The same brainwashing exercise was conducted in the South African news media

http://www.iol.co.za/index.php?set_id=1 & click_id=31 & art_id=nw20081001065312229C266868 & newslett=1 & em=177508a1a20081001ah

Henaney acknowledged that:

Chemotherapy drugs damage mitochondria in cancer cells."When mitochondria are damaged, they can send signals to the cell to die. And that's, we think, one of the ways that the chemotherapy drugs exert their beneficial effects. And vitamin C helps to preserve the health of the mitochondria," Heaney said.By protecting the mitochondria, vitamin C prevents chemotherapy agents from working to their full potential.

Okay, let's look at the "beneficial effects" of one of the chemotherapy drugs mentioned here, Pfizer's GLEEVEC (Imantinib Mesolyte).

http://www.rxlist.com/cgi/generic/gleevec_wcp.htm

First of all, it's a pregnancy category D drug, meaning it can cause fetal harm. In addition to causing fluid retention and edema, anemia, neutropeni and thrombocytopenie, severe congestive heart failure, hepatotoxicity, hemorrrhage, gastrointestinal perforation,dermatolobic toxicity (s- syndrome) this drug from hell will actually cause the cancers it is supposed to " destroy" (see below). Note: "the relevance of these findings in the rat carcinogenicity study for humans is NOT KNOWN", meaning humans brainwashed and conditioned to believe that this toxic concoction would actually save their life, are the real guinea pigs

Carcinogenesis, Mutagenesis, Impairment of Fertility

In the 2-year rat carcinogenicity study administration of imatinib at 15, 30 and 60 mg/kg/day resulted in a statistically significant reduction in the longevity of males at 60 mg/kg/day and females at ≥ 30 mg/kg/day. Target organs for neoplastic changes were the kidneys (renal tubule and renal pelvis), urinary bladder, urethra, preputial and clitoral gland, small intestine, parathyroid glands, adrenal glands and non-glandular stomach. Neoplastic lesions were not seen at: 30 mg/kg/day for the kidneys, urinary bladder, urethra, small intestine, parathyroid glands, adrenal glands and non-glandular stomach, and 15 mg/kg/day for the preputial and clitoral gland. The papilloma/carcinoma of the preputial/clitoral gland were noted at 30 and 60 mg/kg/day, representing approximately 0.5 to 4 or 0.3 to 2.4 times the human daily exposure (based on AUC) at 400 mg/day or 800 mg/day, respectively, and 0.4 to 3.0 times the daily exposure in children (based on AUC) at 340 mg/m2. The renal tubule adenoma/carcinoma, renal pelvis transitional cell neoplasms, the urinary bladder and urethra transitional cell papillomas, the small intestine adenocarcinomas, the parathyroid glands adenomas, the benign and malignant medullary tumors of the adrenal glands and the non-glandular stomach papillomas/carcinomas were noted at 60 mg/kg/day. The relevance of these findings in the rat carcinogenicity study for humans is not known.

Ingrid

[Guest guest]

http://www.naturalnews.com/024380.html

In headlines around the world, Vitamin C is once again under attack. The vitamin is extremely dangerous, researchers now say, because it might "interfere with the toxic effects of chemotherapy." These mainstream media articles, of course, are attempting to convince cancer patients to stop taking vitamins that support health and, instead, allow chemotherapy to poison their body's cells without any protection whatsoever for healthy cells.

The same brainwashing exercise was conducted in the South African news media

http://www.iol.co.za/index.php?set_id=1 & click_id=31 & art_id=nw20081001065312229C266868 & newslett=1 & em=177508a1a20081001ah

Henaney acknowledged that:

Chemotherapy drugs damage mitochondria in cancer cells."When mitochondria are damaged, they can send signals to the cell to die. And that's, we think, one of the ways that the chemotherapy drugs exert their beneficial effects. And vitamin C helps to preserve the health of the mitochondria," Heaney said.By protecting the mitochondria, vitamin C prevents chemotherapy agents from working to their full potential.

Okay, let's look at the "beneficial effects" of one of the chemotherapy drugs mentioned here, Pfizer's GLEEVEC (Imantinib Mesolyte).

http://www.rxlist.com/cgi/generic/gleevec_wcp.htm

First of all, it's a pregnancy category D drug, meaning it can cause fetal harm. In addition to causing fluid retention and edema, anemia, neutropeni and thrombocytopenie, severe congestive heart failure, hepatotoxicity, hemorrrhage, gastrointestinal perforation,dermatolobic toxicity (s- syndrome) this drug from hell will actually cause the cancers it is supposed to " destroy" (see below). Note: "the relevance of these findings in the rat carcinogenicity study for humans is NOT KNOWN", meaning humans brainwashed and conditioned to believe that this toxic concoction would actually save their life, are the real guinea pigs

Carcinogenesis, Mutagenesis, Impairment of Fertility

In the 2-year rat carcinogenicity study administration of imatinib at 15, 30 and 60 mg/kg/day resulted in a statistically significant reduction in the longevity of males at 60 mg/kg/day and females at ≥ 30 mg/kg/day. Target organs for neoplastic changes were the kidneys (renal tubule and renal pelvis), urinary bladder, urethra, preputial and clitoral gland, small intestine, parathyroid glands, adrenal glands and non-glandular stomach. Neoplastic lesions were not seen at: 30 mg/kg/day for the kidneys, urinary bladder, urethra, small intestine, parathyroid glands, adrenal glands and non-glandular stomach, and 15 mg/kg/day for the preputial and clitoral gland. The papilloma/carcinoma of the preputial/clitoral gland were noted at 30 and 60 mg/kg/day, representing approximately 0.5 to 4 or 0.3 to 2.4 times the human daily exposure (based on AUC) at 400 mg/day or 800 mg/day, respectively, and 0.4 to 3.0 times the daily exposure in children (based on AUC) at 340 mg/m2. The renal tubule adenoma/carcinoma, renal pelvis transitional cell neoplasms, the urinary bladder and urethra transitional cell papillomas, the small intestine adenocarcinomas, the parathyroid glands adenomas, the benign and malignant medullary tumors of the adrenal glands and the non-glandular stomach papillomas/carcinomas were noted at 60 mg/kg/day. The relevance of these findings in the rat carcinogenicity study for humans is not known.

Ingrid