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Healthy food can make you ill?
The Times of India ^ | 22 Oct., 2008. | The Associated News of India (ANI)

Posted on 10/21/2008 9:07:33 PM PDT by MyTwoCopperCoins

Healthy food can make an individual more susceptible to diseases, according to a new controversial book.

In the book titled, 'Trick and Treat: How Healthy Eating Is Making Us Ill,' author Barry Groves claims that healthy eating can sometimes fail to keep an individual hale and hearty.

"Most people are eating in a way that is unnatural to us as a species," the Telegraph quoted Barry, who holds a doctorate in nutritional science, as saying.

"We're a carnivorous species - our gut is identical to that of a big cat. Yet we're encouraged to eat foods that have been padded out with modified starch and vegetable oils, and complex carbohydrates such as bread, pasta and rice, which have all been labelled healthy - but not the fatty meat that our body actually recognises," he added.

He said that's the reason why we don't know when to stop eating.

"Try to eat too much fat - cheese, say - and your body will quickly tell you when it has had enough. But when you eat processed, 'low fat'' food, your body never gets the message it has had enough, so doesn't tell the mind it is full," he said.

Previous studies on rabbits have shown that eating saturated fat would lead to heart disease. This is because, Barry says, the rabbits were fed unnatural diet.

"The first, in 1950, showed that if rabbits were fed a cholesterol-rich diet, it would fur up their arteries.

"Yet, rabbits are only designed to eat plant life, which has no cholesterol. The clogged arteries were caused by feeding them an unnatural diet. It could have been an allergic response.

Taking about the other tenets of a healthy life - five portions of fruit and veg, wholegrain cereals, soya milk, low-fat yogurts, he said, "Vegetables are not the problem but there's no biological or chemical reason to eat them. Liver, for example, has all the minerals and vitamins we need," he added.

"But fruit? The natural sugar it contains - fructose - is much more dangerous than simple glucose or table sugar. It has been linked to the rise in obesity," he added.

He also revealed that wheat collects bacteria and dirt as it grows, and is impossible to clean. Then stored in silos, it is a haven for mice and rats, so it gets sprayed with insecticides. Put a wheat flower under the microscope and you'll see traces of rat faeces," he said.

Soy milk is made with unfermented soya beans - "highly dangerous," claims Barry. As for yogurts made with skimmed milk, they "lack conjugated linoleic acid, which prevents cancer".

For healthy eating he advised, "eat purer foods, and ones that are more natural to us as a species. Cut down on bread and eat more fish, eggs, butter - any animal protein, anything that used to move around, that wasn't stuck in the ground. Liver, kidneys, snails - even insects will do."


TOPICS: Culture/Society; News/Current Events
KEYWORDS: cholesterol; fat; food; health
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To: TypeZoNegative

Extensive exercise routine

...and then you give the *diet* credit.


101 posted on 10/22/2008 3:32:53 PM PDT by Gondring (Paul Revere would have been flamed as a naysayer troll and told to go back to Boston.)
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To: Rennes Templar
The exception does not prove the rule!

Obviously, you fail to understand that expression.

Ever heard of "Proving Grounds" or the like? It means that you're testing the rule...the exception tests the rule and shows that it isn't a rule.

102 posted on 10/22/2008 4:13:26 PM PDT by Gondring (Paul Revere would have been flamed as a naysayer troll and told to go back to Boston.)
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To: Gondring

“Good for you! Dead animal flesh is to be buried, not eaten. I prefer them thrashing about when I chomp, too.”

Yep, I tried to eat an oyster and even though I’d blinded the critter with lemon juice he crawled right back up with all his buddies. But it too late, I’d already tossed their shells so those poor blind oysters, having no where to live anymore had to give it up.


103 posted on 10/22/2008 4:55:16 PM PDT by count-your-change (You don't have be brilliant, not being stupid is enough.)
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To: kruss3

o.k.


104 posted on 10/22/2008 11:54:08 PM PDT by count-your-change (You don't have be brilliant, not being stupid is enough.)
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To: count-your-change
Metformin Can Kill You. News and Information for Medical Professionals This article originally posted February 12, 2008 and appeared in Issue 403 Accord Study Stops Intensive Diabetes Management Due To Increase in Deaths Treating to normal blood sugars may cause an increase in death. The National Heart, Lung, and Blood Institute (NHLBI) of the National Institutes of Health has stopped one treatment within a large, ongoing North American clinical trial of diabetes and cardiovascular disease 18 months early due to safety concerns after review of available data, although the study will continue. In this trial of adults with type 2 diabetes at especially high risk for heart attack and stroke, the medical strategy to intensively lower blood glucose (sugar) below current recommendations increased the risk of death compared with a less-intensive standard treatment strategy. Study participants receiving intensive blood glucose lowering treatment will now receive the less-intensive standard treatment. The ACCORD (Action to Control Cardiovascular Risk in Diabetes) study enrolled 10,251 participants. Of these, 257 in the intensive treatment group have died, compared with 203 within the standard treatment group. This is a difference of 54 deaths, or 3 per 1,000 participants each year, over an average of almost four years of treatment. The death rates in both groups were lower than seen in similar populations in other studies. A thorough review of the data shows that the medical treatment strategy of intensively reducing blood sugar below current clinical guidelines causes harm in these especially high-risk patients with type 2 diabetes, said Elizabeth G. Nabel, M.D., director, NHLBI. Though we have stopped this part of the trial, we will continue to care for these participants, who now will receive the less-intensive standard treatment. In addition, we will continue to monitor the health of all participants, seek the underlying causes for this finding, and carry on with other important research within ACCORD. In stopping this part of the trial, Nabel accepted the recommendation of the 10-member Data and Safety Monitoring Board (DSMB)� an independent advisory group of experts in diabetes, cardiovascular disease, epidemiology, patient care, biostatistics, medical ethics, and clinical trial design that has been monitoring ACCORD since it began. A specific charge of any DSMB is to monitor participant safety. ACCORD participants will continue to receive blood sugar treatment from their study clinicians until the planned trial conclusion in June 2009. Those participants in the intensive treatment group will now be treated to the same A1C goals as those already in the standard treatment group. The intensive treatment group had a target blood sugar goal, measured by hemoglobin A1C, of less than 6 percent. This is similar to blood sugar levels in adults without diabetes. The standard treatment group aimed for a target similar to what is achieved, on average, by those with diabetes in the United States (A1C of 7 to 7.9 percent) and lower than at study entry. The ACCORD findings are important, but will not change therapy for most patients with type 2 diabetes. Few patients with high cardiovascular risk like those studied in ACCORD are treated to blood sugar levels as low as those tested in this study, said Judith Fradkin, M.D., director, Division of Diabetes, Endocrinology, and Metabolic Diseases at the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK). People with diabetes should never adjust their treatment plan or goals without consulting their health care providers. In ACCORD, intensive treatment group participants achieved, on average, A1C values lower than standard treatment group participants. Half of the participants in the intensive treatment group achieved an A1C of less than 6.4 percent, and half of the participants in the standard treatment group achieved an A1C of less than 7.5 percent. The average blood sugar levels for both groups were lower than when they entered the study. The ACCORD trial was designed to determine whether intensively lowering blood sugar would reduce the risk of cardiovascular events such as heart attack, stroke, or death from cardiovascular disease, specifically in people with type 2 diabetes who are at particularly high risk for a cardiovascular event. Prior studies suggested that reducing blood sugar to levels found in non-diabetic adults may reduce the rate of cardiovascular diseases among those with diabetes. However, a randomized clinical trial was needed to determine whether that hypothesis is accurate. ACCORD is an important study intended to find new answers to help people with type 2 diabetes reduce their high risk of heart disease, said Denise G. Simons-Morton, M.D., Ph.D., NHLBI project officer for ACCORD and a member of the ACCORD steering committee. Hypotheses about treatments to prevent cardiovascular disease in people with type 2 diabetes need to be tested in clinical trials such as ACCORD. The ACCORD results, along with results from other studies, will contribute to determining what the treatment goals should be in patients with various characteristics. Conducted at 77 sites nationwide and in Canada, the trial includes adults between the ages of 40 and 82 at enrollment who, in addition to type 2 diabetes, also have two or more other risk factors for heart disease or had been diagnosed with heart disease before entering the study. Thus, participants were included in the ACCORD trial because they were at especially high risk,� more risk than is associated with diabetes alone �for having a heart attack, stroke, or of dying from cardiovascular disease. Participants, who on average had diabetes for 10 years at enrollment, were randomly assigned to either standard (5,123 participants) or intensive (5,128) blood sugar treatment goals. They were also enrolled in one of two other ACCORD randomized clinical trials examining effects of treatments for blood pressure or blood lipids; those study components will continue. Participants had been followed for 2 years to 7 years at the time the intensive blood sugar control treatment was stopped. These results from ACCORD do not apply to patients with type 1 (juvenile) diabetes, according to Fradkin. It is also unclear whether the results apply to patients with recently diagnosed type 2 diabetes or those whose cardiovascular risk is lower than the participants studied in ACCORD. Extensive analyses by ACCORD researchers have not determined a specific cause for the increased deaths among the intensive treatment group. Based on analyses conducted to date, there is no evidence that any medication or combination of medications is responsible. Most participants in the intensive treatment group achieved their lower blood sugar goals with combinations of Food and Drug Administration-approved diabetes medications. For both the intensive and standard treatment groups, study clinicians could use all major classes of diabetes medications available: metformin, thiazolidinediones (TZDs, primarily rosiglitazone), insulins, sulfonylureas, exanatide, and acarbose. Because of the recent concerns with rosiglitazone, our extensive analysis included a specific review to determine whether there was any link between this particular medication and the increased deaths. We found no link, said William T. Friedewald, M.D., ACCORD Steering Committee Chair and Clinical Professor of Medicine and Public Health at Columbia University.
105 posted on 10/23/2008 7:49:54 AM PDT by kruss3 (Kruss3@gmail.com)
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To: kruss3

Thank you for the information. What I see as the gist of the article is that intensive efforts to lower blood sugar in patients with other serious conditions or risks may increase the number of deaths in this group.
Further the article points out that the intensive treatment was lower blood sugar levels “below” current recommendations. Why this would be done in high risk patients isn’t stated but it seems rather curious.
Having a dead patient with a “good” blood sugar level doesn’t seem a successful outcome to me, but then I’m no physician.


106 posted on 10/23/2008 8:47:01 AM PDT by count-your-change (You don't have be brilliant, not being stupid is enough.)
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To: count-your-change

My first fasting glucose was over 400. I had blurred vision, diabetic retinopathy, and significant nerve damage.

I was able to restore my fasting glucose numbers to almost normal ranges without losing weight, exercise or massively changing my diet (THREE YEARS AGO).

I have since calibrated the total restoration process and now my HbA1c and lipids are normal. BP is 105 over 65.

I take NO MEDICATIONS.

ken in houston
832-655-6520


107 posted on 10/23/2008 9:16:33 AM PDT by kruss3 (Kruss3@gmail.com)
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To: kruss3

Interesting! How did you do it? If I may ask.


108 posted on 10/23/2008 9:20:12 AM PDT by count-your-change (You don't have be brilliant, not being stupid is enough.)
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To: count-your-change

I have an agenda to build a diabetes mentoring organization
to help rid the world of diabetes. The organizational structure would be faith based and similar to other 12 step processes.

ken in houston
832-655-6520


109 posted on 10/23/2008 9:33:50 AM PDT by kruss3 (Kruss3@gmail.com)
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To: Gondring

LMAO! I’m sorry, but what you said was funny.

Unlike many vegans, I don’t take myself too seriously and I’m always up for a joke that offends the masses.

Re: exercise:

But yeah, back when I exercised this frequently and ate meat, I lost weight too, but I didn’t lose as much weight as I did when I went vegan. Now, I’ve gone vegan and there’s barely any fat on me.


110 posted on 10/23/2008 10:53:15 PM PDT by TypeZoNegative (Pro life & Vegan because I respect all life, Republican because our enemies don't respect ours.)
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To: BruceysMom
You eat that with the incredible shape your body is in???

Heh! Nothing incredible in my shape. I wear all black. Hides the gut I get from overindulging the McD's from time to time.
BTW, in a single sitting at McD's, the items consumed by me alone are:
2 Big Macs
1 Double Quarter pounder with cheese only pickles, cheese and ketchup
1 supersized fries
1 supersized coke

This is usually before starting a 12-hour shift.

I have what I call a, "Tiger's Metabolism."
I eat a hugh meal every 12-hours.
111 posted on 10/24/2008 4:37:59 AM PDT by RandallFlagg (Satisfaction was my sin)
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To: Gondring

The rule is, primate eating patterns are herbivorous. The exceptions are, a few species that have omnivorous patterns. The fact is, humans are closer to primates in anatomy.

The fallcy is in the article,” We’re a carnivorous species - our gut is identical to that of a big cat.”. The trap is, freepers who buy into that argument to justify carnivorous patterns in humans.


112 posted on 10/24/2008 1:04:49 PM PDT by Rennes Templar (If the election were today, Obama would win.........in Europe.)
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