Here is an excerpt from Nelly Furtado’s sister’s book:
I will not become part of the New World [Order] they are planning, they will inevitably bring the world population down, but they won’t get me. I am wolf not a sheep with my eyes wide shut…
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104 thoughts on “Nelly Furtado is Paranoid About Depopulation”
@Dr. Fishman the health authority is blocking fecal transplants in BC. Feces is pretty much free so that’s an unacceptable treatment. My brother says he has to drive to Portland to get the treatment.
That’s the way it is Goyim. It’s medicine for profit. Feces doesn’t make a profit for the Pharmaceutical companies even though it is the obvious cure for bowel problems.
@nellyfurtado Selenium costs pennies a day. Try eating Brazil nuts instead of selenium supplements.
Cystic Fibrosis ( Mucoviscidosis )
Primarily a Selenium Deficiency Disease; plus essential fatty acids and copper.
Let’s Play Doctor
J. D. Wallach, DVM, ND and Ma Lan, MD, MS
Copyright 1989 – Double Happiness Publishing Co., Bonita, Ca.
Cystic Fibrosis is the “crime” of the century second only to diabetes ( and that is only because diabetes affects millions and CF “only affects thousands each year” ) in that it is preventable, 100% curable in the early stages and can be far better managed in chronic cases than it is currently managed by “orthodox” medicine. Cystic fibrosis is an important fatal disease of humans. CF was originally thought to be limited to white populations of central European origin: today, CF has been diagnosed in all the peoples of the earth.
CF is thought to be genetically transmitted by the “orthodox” pediatricians, yet “they” have failed to prove their theory despite multimillions of dollars spent in research. Classically, the diagnosis is made when any two of four criteria are present, yet most “orthodox” pediatricians will not diagnose CF without a positive “sweat test” ( elevated level of sodium, chloride and potassium in the sweat – greater than 65 mEq.L.)
The “sweat test” has been elevated by dogma to “the diagnostic test” for CF yet there are at least 17 known diseases and syndromes that can give a positive sweat test leading at least one group of investigators to refer to CF as a syndrome rather than a disease.
Initially described in 1933, CF was first thought to be the result of a vitamin A deficiency in children dying with celiac disease. In 1938 the term “cystic fibrosis” was coined because the pathologist mistakenly thought the changes in the pancreas were true cysts ( fluid filled spaces lined with normal tissue ). It is well known today that the “cysts” of CF are, in fact, a dilation of the pancreatic functional unit ( acini ) with atrophy ( shrinking ) of the lining tissue. In 1952, the fact that congenital CF occurred in a significant in a significant number of CF patients was established. The foundation of the genetic theory of CF transmission is based on the frequent congenital appearance and two very poor papers, one published in 1913, which claimed that two children with diarrhea had an “inborn error in fat metabolism” and one in 1965 that did an epidemiological study of a group of 232 Australian families with CF – despite six sets of twins, the study failed to shed clear light on the proposed genetic theory. These papers were so poor they would not get past the letter opener at any “orthodox” medical journal today. We have spent an inordinate amount of time on CF because this syndrome again demonstrates very clearly that if any medical specialty will be eliminated by discovery, that discovery will never be given to the public by the “orthodox” doctors !!!
In 1978, the first universally accepted diagnosis of CF in a laboratory animal was made by one of us ( Dr. Joel Wallach ). The diagnosis was based on characteristic CF changes in the pancreas and liver in baby monkeys and were confirmed by CF experts from Johns Hopkins School of Medicine, Emory University and the University of Chicago !! Experts from NIH and the CF Foundation were overjoyed – that is until they learned that one of us ( Wallach ) could reproduce the CF changes with acongenital selenium deficiency in almost any animal species. With this revelation, Wallach was fired with 24 hours notice and “black-balled” from research ( to show you how ruthless they are, Wallach was fired ten days after his wife died of cancer ).
It has been learned recently that the positive “sweat test” is the result of an essential fatty acid deficiency that causes a secondary deficiency of “prostaglandin” ( very short lived hormones ) that control the sodium, chlorides and potassium levels of the sweat !!! Remember the talk by the distinguished anthropologist, Dr. Johnathon Leaky, SR. who said, the more facts you have, the better the truth you have.
The prevention of CF has been accomplished in pet, farm and laboratory animals by the veterinary profession by assuring adequate levels of selenium and essential fatty acid nutrients to the preconception, pregnant and nursing mother. This is not as easy as it sounds because of malabsorption problems ( i.e. celiac diseases and Crohn’s Disease ) in a percentage of women !!! All things being normal a supplementation of 200 mcg selenium per day and 5 grams of flaxseed oil twice a day would be adequate to prevent CF.
Treatment of CF is very basic – treat the infant as early as possible with selenium IM at 10 – 25 mcg per day. Plant derived colloidal minerals may be used orally thereafter (Selenium Picolinate). Provide 5 grams of flaxseed oil orally twice daily. Most importantly YOU MUST DETERMINE IF THE INFANT IS ALLERGIC TO WHEAT, COW’S MILK OR SOY!!! If you do not correct the malabsorption problem, treatment will only be minimally effective. In the case of older CF patients, IV essential fatty acids and IM selenium provide excellent management leading to a normal life expectancy of 75 years !!!
Compare this approach to the heart and lung transplant offered by the “orthodox” pediatricians !!! If the proper treatment is carried out, the “typical CF lung disease” will not develop. The lungs of CF patients are normal at birth and only develop bronchiectasis after chronic essential fatty acid and copper deficiencies have taken their toll ( Copper Picolinate ). Don’t forget the base nutritional supplementation here!
We went to China in 1988 to study Keshan Disease, a known selenium deficiency disease of Chinese children. We studied 1,700 autopsies and found 595 cases or 35% had pancreatic CF ( Remember CF is supposed to be a “genetic disease of children of middle European extract” – to justify this finding the proponents of the genetic theory will no doubt claim that a very virile English missionary impregnated 125,00 Chinese girls and unfortunately, he was “carrying the gene for CF”.)
She still doesn’t know what to do Fishman.
@nellyfurtado oy vey! Stop eating dead foods like chicken and fish. Eat raw foods. JUICE. eat foods rich in selenium like brazil nuts. eat foods rich in copper like cashew nuts. take essential oils. take supplements. filter your water. GET SERIOUS about your health.
Shalom
Dr. F
75 years? A normal lifespan? But she keeps eating toblerone and getting thick mucus in her lungs from the milk. She has to eat it now that she endorses the product. She ate a giant stick of it.
No wheat. No dairy. No soy? Tough to do when your on the road singing. She lacks motivation Fishman. She needs to look inside a chicken farm to truly understand the depravity. Or see how close we are to fishing out the ocean.
Gluten is difficult to escape. It’s in everything even women’s make up. Women who use make-up on a daily basis are absorbing almost 5lb of chemicals a year into the body through the skin.
Especially Rockefeller’s cancer center. The Rockefeller-controlled Sloan-Kettering Cancer Center in New York, the world’s leading cancer mausoleum, which originated as the toy of a mad doctor exiled from South Carolina to New York because of his insane experiments
How could you pray for her to be sick? Don’t you care?
I don’t want to know. I had a girl. I had a life. Now I have nothing. My girlfriend was upset that I liked her music. I never told her that I knew her from Catholic school.
“Turn Off The Light” song by NELLY FURTADO: It’s getting so lonely inside this bed Don’t know if I should lick my wounds or say woe is me instea…
Release date. Canada, August 14, 2001
She was singing about being in the hospital with Cystic Fibrosis. After all the rounds of anti-biotics killed all the good bacteria in her gut she developed a mental illness. Iatrogenic. Doctor induced disease.
@fabulous I pray for her to get better. I prayed for her when i was a kid watching her kneeling to the virgin mary statue. I still pray for her. That’s the troof and nothing but the truth. so don’t give me no guilt trip.
@Dr. Fishman the health authority is blocking fecal transplants in BC. Feces is pretty much free so that’s an unacceptable treatment. My brother says he has to drive to Portland to get the treatment.
That’s the way it is Goyim. It’s medicine for profit. Feces doesn’t make a profit for the Pharmaceutical companies even though it is the obvious cure for bowel problems.
@nellyfurtado Selenium costs pennies a day. Try eating Brazil nuts instead of selenium supplements.
Cystic Fibrosis ( Mucoviscidosis )
Primarily a Selenium Deficiency Disease; plus essential fatty acids and copper.
Let’s Play Doctor
J. D. Wallach, DVM, ND and Ma Lan, MD, MS
Copyright 1989 – Double Happiness Publishing Co., Bonita, Ca.
Cystic Fibrosis is the “crime” of the century second only to diabetes ( and that is only because diabetes affects millions and CF “only affects thousands each year” ) in that it is preventable, 100% curable in the early stages and can be far better managed in chronic cases than it is currently managed by “orthodox” medicine. Cystic fibrosis is an important fatal disease of humans. CF was originally thought to be limited to white populations of central European origin: today, CF has been diagnosed in all the peoples of the earth.
CF is thought to be genetically transmitted by the “orthodox” pediatricians, yet “they” have failed to prove their theory despite multimillions of dollars spent in research. Classically, the diagnosis is made when any two of four criteria are present, yet most “orthodox” pediatricians will not diagnose CF without a positive “sweat test” ( elevated level of sodium, chloride and potassium in the sweat – greater than 65 mEq.L.)
The “sweat test” has been elevated by dogma to “the diagnostic test” for CF yet there are at least 17 known diseases and syndromes that can give a positive sweat test leading at least one group of investigators to refer to CF as a syndrome rather than a disease.
Initially described in 1933, CF was first thought to be the result of a vitamin A deficiency in children dying with celiac disease. In 1938 the term “cystic fibrosis” was coined because the pathologist mistakenly thought the changes in the pancreas were true cysts ( fluid filled spaces lined with normal tissue ). It is well known today that the “cysts” of CF are, in fact, a dilation of the pancreatic functional unit ( acini ) with atrophy ( shrinking ) of the lining tissue. In 1952, the fact that congenital CF occurred in a significant in a significant number of CF patients was established. The foundation of the genetic theory of CF transmission is based on the frequent congenital appearance and two very poor papers, one published in 1913, which claimed that two children with diarrhea had an “inborn error in fat metabolism” and one in 1965 that did an epidemiological study of a group of 232 Australian families with CF – despite six sets of twins, the study failed to shed clear light on the proposed genetic theory. These papers were so poor they would not get past the letter opener at any “orthodox” medical journal today. We have spent an inordinate amount of time on CF because this syndrome again demonstrates very clearly that if any medical specialty will be eliminated by discovery, that discovery will never be given to the public by the “orthodox” doctors !!!
In 1978, the first universally accepted diagnosis of CF in a laboratory animal was made by one of us ( Dr. Joel Wallach ). The diagnosis was based on characteristic CF changes in the pancreas and liver in baby monkeys and were confirmed by CF experts from Johns Hopkins School of Medicine, Emory University and the University of Chicago !! Experts from NIH and the CF Foundation were overjoyed – that is until they learned that one of us ( Wallach ) could reproduce the CF changes with acongenital selenium deficiency in almost any animal species. With this revelation, Wallach was fired with 24 hours notice and “black-balled” from research ( to show you how ruthless they are, Wallach was fired ten days after his wife died of cancer ).
It has been learned recently that the positive “sweat test” is the result of an essential fatty acid deficiency that causes a secondary deficiency of “prostaglandin” ( very short lived hormones ) that control the sodium, chlorides and potassium levels of the sweat !!! Remember the talk by the distinguished anthropologist, Dr. Johnathon Leaky, SR. who said, the more facts you have, the better the truth you have.
The prevention of CF has been accomplished in pet, farm and laboratory animals by the veterinary profession by assuring adequate levels of selenium and essential fatty acid nutrients to the preconception, pregnant and nursing mother. This is not as easy as it sounds because of malabsorption problems ( i.e. celiac diseases and Crohn’s Disease ) in a percentage of women !!! All things being normal a supplementation of 200 mcg selenium per day and 5 grams of flaxseed oil twice a day would be adequate to prevent CF.
Treatment of CF is very basic – treat the infant as early as possible with selenium IM at 10 – 25 mcg per day. Plant derived colloidal minerals may be used orally thereafter (Selenium Picolinate). Provide 5 grams of flaxseed oil orally twice daily. Most importantly YOU MUST DETERMINE IF THE INFANT IS ALLERGIC TO WHEAT, COW’S MILK OR SOY!!! If you do not correct the malabsorption problem, treatment will only be minimally effective. In the case of older CF patients, IV essential fatty acids and IM selenium provide excellent management leading to a normal life expectancy of 75 years !!!
Compare this approach to the heart and lung transplant offered by the “orthodox” pediatricians !!! If the proper treatment is carried out, the “typical CF lung disease” will not develop. The lungs of CF patients are normal at birth and only develop bronchiectasis after chronic essential fatty acid and copper deficiencies have taken their toll ( Copper Picolinate ). Don’t forget the base nutritional supplementation here!
We went to China in 1988 to study Keshan Disease, a known selenium deficiency disease of Chinese children. We studied 1,700 autopsies and found 595 cases or 35% had pancreatic CF ( Remember CF is supposed to be a “genetic disease of children of middle European extract” – to justify this finding the proponents of the genetic theory will no doubt claim that a very virile English missionary impregnated 125,00 Chinese girls and unfortunately, he was “carrying the gene for CF”.)
She still doesn’t know what to do Fishman.
@nellyfurtado oy vey! Stop eating dead foods like chicken and fish. Eat raw foods. JUICE. eat foods rich in selenium like brazil nuts. eat foods rich in copper like cashew nuts. take essential oils. take supplements. filter your water. GET SERIOUS about your health.
Shalom
Dr. F
75 years? A normal lifespan? But she keeps eating toblerone and getting thick mucus in her lungs from the milk. She has to eat it now that she endorses the product. She ate a giant stick of it.
No wheat. No dairy. No soy? Tough to do when your on the road singing. She lacks motivation Fishman. She needs to look inside a chicken farm to truly understand the depravity. Or see how close we are to fishing out the ocean.
Gluten is difficult to escape. It’s in everything even women’s make up. Women who use make-up on a daily basis are absorbing almost 5lb of chemicals a year into the body through the skin.
I can’t wait to see this evil city get nuked:
[img]https://www.conspirazzi.com/wp-content/uploads/2013/02/bucket-list-rockefeller.jpg[/img]
Especially Rockefeller’s cancer center. The Rockefeller-controlled Sloan-Kettering Cancer Center in New York, the world’s leading cancer mausoleum, which originated as the toy of a mad doctor exiled from South Carolina to New York because of his insane experiments
How could you pray for her to be sick? Don’t you care?
I don’t want to know. I had a girl. I had a life. Now I have nothing. My girlfriend was upset that I liked her music. I never told her that I knew her from Catholic school.
“Turn Off The Light” song by NELLY FURTADO: It’s getting so lonely inside this bed Don’t know if I should lick my wounds or say woe is me instea…
Release date. Canada, August 14, 2001
She was singing about being in the hospital with Cystic Fibrosis. After all the rounds of anti-biotics killed all the good bacteria in her gut she developed a mental illness. Iatrogenic. Doctor induced disease.
@fabulous I pray for her to get better. I prayed for her when i was a kid watching her kneeling to the virgin mary statue. I still pray for her. That’s the troof and nothing but the truth. so don’t give me no guilt trip.
Don’t you feel better telling the truth?