Tuesday, May 31, 2016

The Best Kept Secret for Healing

By Gretchen DuBeau
Alliance for Natural Health USA

How my difficult personal journey became a career
dedicated to protecting your natural health options,
and why the tide is turning in our favor

In a Nutshell

Many people have undiagnosed or misdiagnosed illnesses and conditions that profoundly affect their daily lives. Most conventional medical professionals treat such illnesses with powerful drugs, even though these medicines do nothing to change the underlying problem—assuming the physicians can identify the actual cause.

We have the tools and the knowledge to experience optimal health. By utilizing integrative medicine and Mother Nature, we can all eliminate the root causes of disease, allowing the body to heal itself. Three tools are of paramount importance: being treated by integrative doctors and practitioners; experiencing truly individualized medicine; and taking carefully chosen nutritional supplements.

Unfortunately, each of these tools are being threatened by the government’s cozy relationship with the pharmaceutical industry and the conventional medical establishment.

I’ve always believed that obstacles are opportunities in disguise, and the growth and learning derived from the most difficult of journeys are some of life’s greatest gifts. Perhaps that’s why, when my health utterly deteriorated at the age of 31, illness didn’t turn into devastation.

You know the old story: put a frog into a pot of boiling water, and it jumps right out, but put it in a pot of cool water and then turn on the heat, and the frog will complacently let itself be boiled alive. That was me. I’ve always been so good at keeping all the proverbial balls in the air—always finding the reserves necessary to get things done—that I didn’t even realize that my body was completely falling apart.

I was at an OB checkup after the birth of my daughter when my midwife asked me whether I was feeling tired. I had to think about it. Being a new mom was supposed to be exhausting, wasn’t it? But yes, I told her, I suppose I was a bit more tired than usual. She ran routine blood work and called me several days later to tell me that I had hypothyroidism and needed to see an endocrinologist.

“Hypo-what?” I said.

Hypothyroidism, or underactive thyroid, is a disorder of the endocrine system in which the thyroid gland does not produce enough thyroid hormone. I saw my first endocrinologist the following week. He ran some tests and confirmed that not only was I hypothyroid, but he had never seen such a high test result. The higher your levels of TSH, or thyroid-stimulating hormone, the worse your thyroid is performing; most good endocrinologists would agree that optimal TSH is somewhere between 1 and 2. My TSH was 174! He was surprised that with such a progressed disease, I was still able to walk.

By the time the results were in, fatigue had started to overwhelm me. I was the consummate “health nut,” so this hit me especially hard. I was given synthetic thyroid replacement hormone, but I was still exhausted. I started sleeping fourteen hours every night and taking three-hour naps in the afternoon. And the depression! And the nausea! I felt sick all over, all the time. Life was lived in tiny increments, windows of barely tolerable activity until the times when I could sleep. I would think, “It’s noon. In another half-hour I can have a 45-minute nap,” or “4 p.m.! Only four more hours till bedtime!”

With the synthetic thyroid treatment, my TSH levels came back into normal range. I saw a series of conventional doctors (including a total of five different endocrinologists), and each one of them said my test results were perfectly normal, so I was fine. But I was so far from fine that I couldn’t even articulate or identify the extent of my dysfunction.

Sadly, my daughter’s first couple of years are a blur, something I will forever lament. But she was also my inspiration. I dug in my heels, and with all my resolve I started to ask questions—starting with “Why?” Why did I become hypothyroid when I was such a health nut and so young? And why are all of these doctors telling me that a piece of paper says I am fine, so it must be so, even though I feel like death?

A Major About-Face

None of these questions, as you might imagine, were popular with my doctors, who couldn’t answer any of them. So I fired them. And I resolved to become my own advocate. I knew that my reality starkly contrasted with the one being trumpeted by the “trusted white coat,” and even though I was functioning at half-mast, I put my faith in myself, and moved on.

I began to read everything I could about hypothyroidism, and I discovered there are a lot of opinions about it—its causes, its complications, its cures. And I noticed that the writers who explored these issues, and grappled with the very questions I had raised, were integrative physicians. These are medical doctors who elect to receive advanced training in natural therapies, and they are most interested in addressing the root cause of disease rather than simply treating symptoms, as much of conventional medicine does—a crucial distinction. Let me explain.

A 1985 landmark report on nutrition in medical schools by the National Academy of Sciences found that on average, future physicians received only twenty-one hours of nutrition instruction over four years; two decades later, they receive even fewer hours. And their education focuses mainly on diagnosing disease states and then treating those disease states with conventional drugs. For example, I was diagnosed with hypothyroidism, and my conventional doctors—every single one—sought to treat me with drugs.

While integrative physicians also utilize drugs when necessary, they first utilize natural therapies—food and dietary supplements, for example—that don’t carry the negative side effects that drugs do. And they first seek to use these natural therapies to bring the body back into homeostasis so that it can heal itself—eliminating the underlying illness—rather than treating and managing the symptoms of chronic disease. Integrative physicians strive for optimal health in their patients. They don’t ask whether or not a patient has a disease, but whether or not a patient is healthy.

So here I was, now 32 years old and feeling 90. And I had stumbled onto this entirely different way of treating patients, of “doing” medicine. I had no idea how complicated my case was, or that it would take several years and an immutable commitment if I wanted my life back. I saw the best integrative physicians in the country, and I learned a great deal.

It turned out that I wasn’t just hypothyroid. I had Hashimoto’s, a disease of the immune system that manifests as thyroid dysfunction. I also had a severely impaired ability to detoxify the environmental pollutants we encounter on a daily basis, such as benzene in paint, exhaust from cars, and glyphosate on genetically engineered tofu, because of personal genetic polymorphisms or defects. Genetic polymorphisms are natural variations in a gene, DNA sequence, or chromosome—they’re responsible for differing characteristics in individuals of the same population or species.

Think of your body as a bathtub, slowly being filled with environmental contaminants—the pesticides on your tomatoes, the parabens in your face cream, and the BPA in your plastic lunch container. If your “bathtub drain” is clear, then while the toxins may do some damage on their way out, they will nevertheless exit your body. If the drain is clogged—because of an ill-functioning system caused by genetic mutations, stress, too many exposures, a poor diet, or other lifestyle factors—your “tub” will overflow, making every fresh chemical exposure a new assault, and causing dysfunction in all the connected major body systems.

My gut was so inflamed and damaged from the build-up of toxins and opportunistic gut infections that I was unable to absorb nutrients from my food. I was malnourished, which was like pouring gasoline on my raging internal fire. All of my defenses were beyond spent, and this led to a series of additional viral and bacterial infections, imbalances in my major hormonal systems, and finally, full-blown autoimmune disease.

This was such a crucial first step—identifying each of the health obstacles I needed to overcome, and understanding their root causes. While the process was overwhelming, it was also empowering to finally have a road map and competent doctors to help me along the way with practical advice.

Full disclosure: it was really, really hard. I had so many infections that I can’t remember them all; certainly Lyme disease was the worst. I read dozens and dozens of books, and took hundreds of dietary supplements. I had so many nutrient IVs that I lost count. Sometimes I had to get more than thirty vials of blood taken at once to monitor all of the nutrient levels and biological factors at play. But I slowly came back to life, and I have come through it all not a different person, but more myself than I ever was or could have been otherwise, so I don’t regret it. And I have learned through this process how important access to every piece of my own medical puzzle was to regaining health and vitality.

Not My Story Alone

Why should you care? I think you and I share the same health challenges. Perhaps mine manifested in a severe way. But maybe not any more severe than yours or those of your loved ones. It could have gone in a different direction for me. I could have just taken the thyroid drugs and managed to get through my life without identifying and eliminating the root causes and truly healing. Some days would have been better than others, severe fatigue and digestive issues, naps on the weekends, short attention span, heartburn, depression, maybe some day all of this leading to cancer—an all-too-common trajectory for many Americans.

My story sounds dramatic only because I made it that way. I bloody refused to accept things the way they were—neither my condition nor the answers I had been given. But sadly, poor health is the outcome for too many of us. Maybe it’s not Hashimoto’s for you or your best friend. Maybe it’s another autoimmune disease, like lupus or rheumatoid arthritis. According to the American Autoimmune Related Diseases Association, 50 million Americans suffer from autoimmune disease, more than heart disease and cancer combined.

Or maybe your health decline is just beginning. It’s nothing that you can even articulate, and certainly not something your doctor would find on a lab report. You just don’t feel well anymore, or you are tired, or you get heartburn sometimes. None of this is normal! The body talks to us for a reason. And if ignored—or “patched over” by eliminating symptoms with prescription drugs, such as acid blockers—the body will just speak louder and louder, until you listen.

If I hadn’t listened to my body’s cries, I’d have two more autoimmune diseases by now. If I hadn’t identified autoimmunity as one of my major players, I never would have reversed it. And I did, by the way, despite being told by conventional doctors that this was impossible. My antibodies—all evidence of Hashimoto’s—have been gone for years. Maybe for some of you, it’s cancer, or Parkinson’s. But it doesn’t have to be this way.

And that’s the great news—the best-kept secret of all: We have the tools and the knowledge to experience optimal health. By utilizing integrative medicine and Mother Nature, we can all eliminate the root causes of disease, allowing the body to heal itself.

Learning this changed my life, not only because I am stronger and healthier physically than I have ever been in my life, but because one of the opportunities ingrained in this most difficult of journeys also led to a deeply satisfying career change. Today, I am the executive and legal director of the Alliance for Natural Health USA—a nonprofit organization that goes head-to-head with the conventional medical paradigm. We’re politically active, and we’re not afraid to take on the pharmaceutical companies eager to sell one-size-fits-all pills as well as the biotech companies making synthetically manufactured food for the masses.

We are engaged in a number of important campaigns: fighting the use of genetically modified organisms and toxic herbicides in our food; maintaining access to honestly healthy foods like real milk and grass-fed beef; protecting the integrity of organic standards; upholding citizens’ rights to vaccine choice; and advocating for the best healthcare possible for America’s citizens. ANH-USA is dedicated to promoting natural and sustainable health—and, in particular, consumer freedom of choice in healthcare—through good science and good law.

As I struggled to regain my health, three tools became of primary importance, and these are the three primary focuses of our organization as well: integrative doctors and practitioners; truly individualized medicine; and carefully chosen nutritional supplements.

The problem is, each of these vital tools is threatened. The medical establishment targets integrative doctors, so many Americans do not have access to the practitioner of their choice. The US Food and Drug Administration (FDA) is trying to pass regulations to restrict access to compounded, individualized medicines and preparations. And the pharmaceutical industry is doing everything it can to crush its chief competition—nutritional supplements—by getting its friends in government (the FDA in particular) to do its dirty work.

Let’s look at each of the three in greater depth:

The Practitioners of Your Choice

What does it mean to have access to the doctor or healthcare practitioner of your choice? And why isn’t it a given?

Integrative physicians are targeted simply because their approaches are different. In many states, anonymous complaints are sufficient—which means an insurance company can anonymously lodge a complaint against a doctor who, for example, uses expensive lab testing to measure nutrient deficiencies or toxicity levels. That physician then has to spend hundreds of thousands of dollars defending his or her (demonstrably superior) patient care, without ever learning that the complaint began simply because an insurance company didn’t want to pay for it!

Many conventional physicians don’t understand integrative medicine—even though an integrative physician is just an MD who has had extra training. Some are hostile to the idea of natural treatment modalities; others simply don’t like the competition. State medical boards, run by conventional doctors, single out those practicing really cutting-edge medicine and label it “outside the standard of care”—meaning that another doctor in a similar situation would likely have done something different. The “standard of care” is a legal standard—and it might be true that other doctors would have treated the patient differently, but only because most of conventional medicine is thirty years behind the latest advances in science.

At ANH-USA, we work to protect your access to the healthcare practitioners of your choice. We educate the public, and work with state legislatures and state medical boards to modify monopolistic laws and create better practice protections for integrative doctors. Most importantly, our network of half a million grassroots activists lobby their own legislators to make natural healthcare in their state open and accessible to everyone.

Any list of the greatest integrative physicians of America would include Jonathan V. Wright, MD, founder of the Tahoma Clinic in Washington state. He is a pioneer who has developed innovative and successful natural therapies utilizing food, supplements, and lifestyle changes for a host of maladies that conventional medicine cannot cure. His style of medicine represents our future. Unfortunately, the state’s Medical Quality Assurance Commission (MQAC) is notorious for treating integrative physicians more harshly than their conventional counterparts, and MQAC has attacked and harassed Dr. Wright at every opportunity, often with trivial charges. As a result of our public relations outreach and research demonstrating their abuse of the process, MQAC is currently being investigated by the Washington State Auditor’s Office.

Find an integrative practitioner in your area.

Individualized Medicine

Compounding is a method of preparing drug or nutrient ingredients that are individualized for a patient’s specific needs.

Compounding allows prescribers to create medications that are the exact strength, dosage, and ingredient mix best suited to treat an individual patient, customizing medical treatment depending on the patient’s allergies, age, medical background, and even flavor and delivery preferences.

Common examples include nutrient IVs to support malnourished patients unable to cleave nutrients from food; hormone preparations such as Estriol, the natural and bioidentical estrogen replacement therapy millions of women rely on; individually dosed testosterone for sensitive patients; and time-release thyroid.

Unfortunately, the pharmaceutical industry lobbied Congress to pass the Drug Quality and Security Act, which gave the FDA increased authority over compounding pharmacies, and the agency responded by trying to regulate estriol, other hormones, and hundreds of other vital compounded medications out of existence. ANH-USA is working with a huge coalition of interested organizations, physicians, and individuals. We are using regulatory, legislative, and legal action to protect individualized medicine and hold the FDA accountable to the American public. And we’re making progress—the House Appropriations Committee recently scolded the FDA for implementing the law “in a manner inconsistent with its legislative intent.” This isn’t the first time that members of Congress have made it clear that the FDA is going too far in its compounding regulations.

Dietary Supplements

We are a country of malnourished individuals. Industrial agricultural practices have raped the soil of her nutrients, which translates to lower levels in our food. As one researcher put it, “You’d have to eat ten servings of spinach to get the same level of minerals from just one serving about fifty years ago.” On top of that, as a nation, our dietary habits are extremely poor, and we often reach for processed and fast food. Even those of us with impeccable diets sometimes have impaired abilities to digest food and make use of what nutrients are still there.

Our bodies simply require abundant nutrients to function optimally, reverse disease, and heal from within. Nutritional supplements fill the void when diets are insufficient and, more importantly, provide huge amounts of nourishment that no diet could ever supply when disease has created extreme imbalances.

Here’s the problem: supplements, and everything they represent—a natural, integrative approach to health not reliant on patented “blockbuster” drugs—threaten the medical establishment, which is pulling the strings. The FDA, the pharmaceutical industry, and a handful of rogue politicians are trying to regulate supplements out of existence. Their goal? A pre-market approval system akin to the FDA drug approval process, even though Congress, in passing the Dietary Supplement Health and Education Act of 1994, said supplements should be regulated as food, not drugs.

The truth is, supplements are already highly regulated, by both the FDA and the Federal Trade Commission, and they must adhere to strict current good manufacturing practices to ensure the safety of the products consumers buy. In this case, the current system actually works: supplements have a sterling track record of safety. One is actually more likely to get killed by lightning than to die from taking dietary supplements.

ANH-USA is working directly with lawmakers to ensure continued access to supplements. With the help of our network of citizen activists, we’ve successfully thwarted numerous attempts to sweep supplements off your store shelves. We even forced the FDA to rewrite its guidance on how new supplements are treated—which kept over 29,000 different safe and effective supplements available to the consumers who need them so desperately.

A Powerful Future

What I think is the most important and inspiring aspect of our work is not simply that we are changing the conventional medical paradigm—and we are. It’s not just that we’re protecting natural healthcare for millions of Americans—though we are. It’s that this organization is nothing more than a group of 500,000 individuals who care enough to get involved. Together we are making such an important difference. Won’t you join us? Learn more about our grassroots movement at ANH-USA.org.

Originally published in The Optimist magazine.

from The Alliance for Natural Health http://ift.tt/1O26drN via Aloe for Health




from http://ift.tt/1Pgle9q

The Best Kept Secret for Healing

By Gretchen DuBeau
Alliance for Natural Health USA

How my difficult personal journey became a career
dedicated to protecting your natural health options,
and why the tide is turning in our favor

In a Nutshell

Many people have undiagnosed or misdiagnosed illnesses and conditions that profoundly affect their daily lives. Most conventional medical professionals treat such illnesses with powerful drugs, even though these medicines do nothing to change the underlying problem—assuming the physicians can identify the actual cause.

We have the tools and the knowledge to experience optimal health. By utilizing integrative medicine and Mother Nature, we can all eliminate the root causes of disease, allowing the body to heal itself. Three tools are of paramount importance: being treated by integrative doctors and practitioners; experiencing truly individualized medicine; and taking carefully chosen nutritional supplements.

Unfortunately, each of these tools are being threatened by the government’s cozy relationship with the pharmaceutical industry and the conventional medical establishment.

I’ve always believed that obstacles are opportunities in disguise, and the growth and learning derived from the most difficult of journeys are some of life’s greatest gifts. Perhaps that’s why, when my health utterly deteriorated at the age of 31, illness didn’t turn into devastation.

You know the old story: put a frog into a pot of boiling water, and it jumps right out, but put it in a pot of cool water and then turn on the heat, and the frog will complacently let itself be boiled alive. That was me. I’ve always been so good at keeping all the proverbial balls in the air—always finding the reserves necessary to get things done—that I didn’t even realize that my body was completely falling apart.

I was at an OB checkup after the birth of my daughter when my midwife asked me whether I was feeling tired. I had to think about it. Being a new mom was supposed to be exhausting, wasn’t it? But yes, I told her, I suppose I was a bit more tired than usual. She ran routine blood work and called me several days later to tell me that I had hypothyroidism and needed to see an endocrinologist.

“Hypo-what?” I said.

Hypothyroidism, or underactive thyroid, is a disorder of the endocrine system in which the thyroid gland does not produce enough thyroid hormone. I saw my first endocrinologist the following week. He ran some tests and confirmed that not only was I hypothyroid, but he had never seen such a high test result. The higher your levels of TSH, or thyroid-stimulating hormone, the worse your thyroid is performing; most good endocrinologists would agree that optimal TSH is somewhere between 1 and 2. My TSH was 174! He was surprised that with such a progressed disease, I was still able to walk.

By the time the results were in, fatigue had started to overwhelm me. I was the consummate “health nut,” so this hit me especially hard. I was given synthetic thyroid replacement hormone, but I was still exhausted. I started sleeping fourteen hours every night and taking three-hour naps in the afternoon. And the depression! And the nausea! I felt sick all over, all the time. Life was lived in tiny increments, windows of barely tolerable activity until the times when I could sleep. I would think, “It’s noon. In another half-hour I can have a 45-minute nap,” or “4 p.m.! Only four more hours till bedtime!”

With the synthetic thyroid treatment, my TSH levels came back into normal range. I saw a series of conventional doctors (including a total of five different endocrinologists), and each one of them said my test results were perfectly normal, so I was fine. But I was so far from fine that I couldn’t even articulate or identify the extent of my dysfunction.

Sadly, my daughter’s first couple of years are a blur, something I will forever lament. But she was also my inspiration. I dug in my heels, and with all my resolve I started to ask questions—starting with “Why?” Why did I become hypothyroid when I was such a health nut and so young? And why are all of these doctors telling me that a piece of paper says I am fine, so it must be so, even though I feel like death?

A Major About-Face

None of these questions, as you might imagine, were popular with my doctors, who couldn’t answer any of them. So I fired them. And I resolved to become my own advocate. I knew that my reality starkly contrasted with the one being trumpeted by the “trusted white coat,” and even though I was functioning at half-mast, I put my faith in myself, and moved on.

I began to read everything I could about hypothyroidism, and I discovered there are a lot of opinions about it—its causes, its complications, its cures. And I noticed that the writers who explored these issues, and grappled with the very questions I had raised, were integrative physicians. These are medical doctors who elect to receive advanced training in natural therapies, and they are most interested in addressing the root cause of disease rather than simply treating symptoms, as much of conventional medicine does—a crucial distinction. Let me explain.

A 1985 landmark report on nutrition in medical schools by the National Academy of Sciences found that on average, future physicians received only twenty-one hours of nutrition instruction over four years; two decades later, they receive even fewer hours. And their education focuses mainly on diagnosing disease states and then treating those disease states with conventional drugs. For example, I was diagnosed with hypothyroidism, and my conventional doctors—every single one—sought to treat me with drugs.

While integrative physicians also utilize drugs when necessary, they first utilize natural therapies—food and dietary supplements, for example—that don’t carry the negative side effects that drugs do. And they first seek to use these natural therapies to bring the body back into homeostasis so that it can heal itself—eliminating the underlying illness—rather than treating and managing the symptoms of chronic disease. Integrative physicians strive for optimal health in their patients. They don’t ask whether or not a patient has a disease, but whether or not a patient is healthy.

So here I was, now 32 years old and feeling 90. And I had stumbled onto this entirely different way of treating patients, of “doing” medicine. I had no idea how complicated my case was, or that it would take several years and an immutable commitment if I wanted my life back. I saw the best integrative physicians in the country, and I learned a great deal.

It turned out that I wasn’t just hypothyroid. I had Hashimoto’s, a disease of the immune system that manifests as thyroid dysfunction. I also had a severely impaired ability to detoxify the environmental pollutants we encounter on a daily basis, such as benzene in paint, exhaust from cars, and glyphosate on genetically engineered tofu, because of personal genetic polymorphisms or defects. Genetic polymorphisms are natural variations in a gene, DNA sequence, or chromosome—they’re responsible for differing characteristics in individuals of the same population or species.

Think of your body as a bathtub, slowly being filled with environmental contaminants—the pesticides on your tomatoes, the parabens in your face cream, and the BPA in your plastic lunch container. If your “bathtub drain” is clear, then while the toxins may do some damage on their way out, they will nevertheless exit your body. If the drain is clogged—because of an ill-functioning system caused by genetic mutations, stress, too many exposures, a poor diet, or other lifestyle factors—your “tub” will overflow, making every fresh chemical exposure a new assault, and causing dysfunction in all the connected major body systems.

My gut was so inflamed and damaged from the build-up of toxins and opportunistic gut infections that I was unable to absorb nutrients from my food. I was malnourished, which was like pouring gasoline on my raging internal fire. All of my defenses were beyond spent, and this led to a series of additional viral and bacterial infections, imbalances in my major hormonal systems, and finally, full-blown autoimmune disease.

This was such a crucial first step—identifying each of the health obstacles I needed to overcome, and understanding their root causes. While the process was overwhelming, it was also empowering to finally have a road map and competent doctors to help me along the way with practical advice.

Full disclosure: it was really, really hard. I had so many infections that I can’t remember them all; certainly Lyme disease was the worst. I read dozens and dozens of books, and took hundreds of dietary supplements. I had so many nutrient IVs that I lost count. Sometimes I had to get more than thirty vials of blood taken at once to monitor all of the nutrient levels and biological factors at play. But I slowly came back to life, and I have come through it all not a different person, but more myself than I ever was or could have been otherwise, so I don’t regret it. And I have learned through this process how important access to every piece of my own medical puzzle was to regaining health and vitality.

Not My Story Alone

Why should you care? I think you and I share the same health challenges. Perhaps mine manifested in a severe way. But maybe not any more severe than yours or those of your loved ones. It could have gone in a different direction for me. I could have just taken the thyroid drugs and managed to get through my life without identifying and eliminating the root causes and truly healing. Some days would have been better than others, severe fatigue and digestive issues, naps on the weekends, short attention span, heartburn, depression, maybe some day all of this leading to cancer—an all-too-common trajectory for many Americans.

My story sounds dramatic only because I made it that way. I bloody refused to accept things the way they were—neither my condition nor the answers I had been given. But sadly, poor health is the outcome for too many of us. Maybe it’s not Hashimoto’s for you or your best friend. Maybe it’s another autoimmune disease, like lupus or rheumatoid arthritis. According to the American Autoimmune Related Diseases Association, 50 million Americans suffer from autoimmune disease, more than heart disease and cancer combined.

Or maybe your health decline is just beginning. It’s nothing that you can even articulate, and certainly not something your doctor would find on a lab report. You just don’t feel well anymore, or you are tired, or you get heartburn sometimes. None of this is normal! The body talks to us for a reason. And if ignored—or “patched over” by eliminating symptoms with prescription drugs, such as acid blockers—the body will just speak louder and louder, until you listen.

If I hadn’t listened to my body’s cries, I’d have two more autoimmune diseases by now. If I hadn’t identified autoimmunity as one of my major players, I never would have reversed it. And I did, by the way, despite being told by conventional doctors that this was impossible. My antibodies—all evidence of Hashimoto’s—have been gone for years. Maybe for some of you, it’s cancer, or Parkinson’s. But it doesn’t have to be this way.

And that’s the great news—the best-kept secret of all: We have the tools and the knowledge to experience optimal health. By utilizing integrative medicine and Mother Nature, we can all eliminate the root causes of disease, allowing the body to heal itself.

Learning this changed my life, not only because I am stronger and healthier physically than I have ever been in my life, but because one of the opportunities ingrained in this most difficult of journeys also led to a deeply satisfying career change. Today, I am the executive and legal director of the Alliance for Natural Health USA—a nonprofit organization that goes head-to-head with the conventional medical paradigm. We’re politically active, and we’re not afraid to take on the pharmaceutical companies eager to sell one-size-fits-all pills as well as the biotech companies making synthetically manufactured food for the masses.

We are engaged in a number of important campaigns: fighting the use of genetically modified organisms and toxic herbicides in our food; maintaining access to honestly healthy foods like real milk and grass-fed beef; protecting the integrity of organic standards; upholding citizens’ rights to vaccine choice; and advocating for the best healthcare possible for America’s citizens. ANH-USA is dedicated to promoting natural and sustainable health—and, in particular, consumer freedom of choice in healthcare—through good science and good law.

As I struggled to regain my health, three tools became of primary importance, and these are the three primary focuses of our organization as well: integrative doctors and practitioners; truly individualized medicine; and carefully chosen nutritional supplements.

The problem is, each of these vital tools is threatened. The medical establishment targets integrative doctors, so many Americans do not have access to the practitioner of their choice. The US Food and Drug Administration (FDA) is trying to pass regulations to restrict access to compounded, individualized medicines and preparations. And the pharmaceutical industry is doing everything it can to crush its chief competition—nutritional supplements—by getting its friends in government (the FDA in particular) to do its dirty work.

Let’s look at each of the three in greater depth:

The Practitioners of Your Choice

What does it mean to have access to the doctor or healthcare practitioner of your choice? And why isn’t it a given?

Integrative physicians are targeted simply because their approaches are different. In many states, anonymous complaints are sufficient—which means an insurance company can anonymously lodge a complaint against a doctor who, for example, uses expensive lab testing to measure nutrient deficiencies or toxicity levels. That physician then has to spend hundreds of thousands of dollars defending his or her (demonstrably superior) patient care, without ever learning that the complaint began simply because an insurance company didn’t want to pay for it!

Many conventional physicians don’t understand integrative medicine—even though an integrative physician is just an MD who has had extra training. Some are hostile to the idea of natural treatment modalities; others simply don’t like the competition. State medical boards, run by conventional doctors, single out those practicing really cutting-edge medicine and label it “outside the standard of care”—meaning that another doctor in a similar situation would likely have done something different. The “standard of care” is a legal standard—and it might be true that other doctors would have treated the patient differently, but only because most of conventional medicine is thirty years behind the latest advances in science.

At ANH-USA, we work to protect your access to the healthcare practitioners of your choice. We educate the public, and work with state legislatures and state medical boards to modify monopolistic laws and create better practice protections for integrative doctors. Most importantly, our network of half a million grassroots activists lobby their own legislators to make natural healthcare in their state open and accessible to everyone.

Any list of the greatest integrative physicians of America would include Jonathan V. Wright, MD, founder of the Tahoma Clinic in Washington state. He is a pioneer who has developed innovative and successful natural therapies utilizing food, supplements, and lifestyle changes for a host of maladies that conventional medicine cannot cure. His style of medicine represents our future. Unfortunately, the state’s Medical Quality Assurance Commission (MQAC) is notorious for treating integrative physicians more harshly than their conventional counterparts, and MQAC has attacked and harassed Dr. Wright at every opportunity, often with trivial charges. As a result of our public relations outreach and research demonstrating their abuse of the process, MQAC is currently being investigated by the Washington State Auditor’s Office.

Find an integrative practitioner in your area.

Individualized Medicine

Compounding is a method of preparing drug or nutrient ingredients that are individualized for a patient’s specific needs.

Compounding allows prescribers to create medications that are the exact strength, dosage, and ingredient mix best suited to treat an individual patient, customizing medical treatment depending on the patient’s allergies, age, medical background, and even flavor and delivery preferences.

Common examples include nutrient IVs to support malnourished patients unable to cleave nutrients from food; hormone preparations such as Estriol, the natural and bioidentical estrogen replacement therapy millions of women rely on; individually dosed testosterone for sensitive patients; and time-release thyroid.

Unfortunately, the pharmaceutical industry lobbied Congress to pass the Drug Quality and Security Act, which gave the FDA increased authority over compounding pharmacies, and the agency responded by trying to regulate estriol, other hormones, and hundreds of other vital compounded medications out of existence. ANH-USA is working with a huge coalition of interested organizations, physicians, and individuals. We are using regulatory, legislative, and legal action to protect individualized medicine and hold the FDA accountable to the American public. And we’re making progress—the House Appropriations Committee recently scolded the FDA for implementing the law “in a manner inconsistent with its legislative intent.” This isn’t the first time that members of Congress have made it clear that the FDA is going too far in its compounding regulations.

Dietary Supplements

We are a country of malnourished individuals. Industrial agricultural practices have raped the soil of her nutrients, which translates to lower levels in our food. As one researcher put it, “You’d have to eat ten servings of spinach to get the same level of minerals from just one serving about fifty years ago.” On top of that, as a nation, our dietary habits are extremely poor, and we often reach for processed and fast food. Even those of us with impeccable diets sometimes have impaired abilities to digest food and make use of what nutrients are still there.

Our bodies simply require abundant nutrients to function optimally, reverse disease, and heal from within. Nutritional supplements fill the void when diets are insufficient and, more importantly, provide huge amounts of nourishment that no diet could ever supply when disease has created extreme imbalances.

Here’s the problem: supplements, and everything they represent—a natural, integrative approach to health not reliant on patented “blockbuster” drugs—threaten the medical establishment, which is pulling the strings. The FDA, the pharmaceutical industry, and a handful of rogue politicians are trying to regulate supplements out of existence. Their goal? A pre-market approval system akin to the FDA drug approval process, even though Congress, in passing the Dietary Supplement Health and Education Act of 1994, said supplements should be regulated as food, not drugs.

The truth is, supplements are already highly regulated, by both the FDA and the Federal Trade Commission, and they must adhere to strict current good manufacturing practices to ensure the safety of the products consumers buy. In this case, the current system actually works: supplements have a sterling track record of safety. One is actually more likely to get killed by lightning than to die from taking dietary supplements.

ANH-USA is working directly with lawmakers to ensure continued access to supplements. With the help of our network of citizen activists, we’ve successfully thwarted numerous attempts to sweep supplements off your store shelves. We even forced the FDA to rewrite its guidance on how new supplements are treated—which kept over 29,000 different safe and effective supplements available to the consumers who need them so desperately.

A Powerful Future

What I think is the most important and inspiring aspect of our work is not simply that we are changing the conventional medical paradigm—and we are. It’s not just that we’re protecting natural healthcare for millions of Americans—though we are. It’s that this organization is nothing more than a group of 500,000 individuals who care enough to get involved. Together we are making such an important difference. Won’t you join us? Learn more about our grassroots movement at ANH-USA.org.

Originally published in The Optimist magazine.



from The Alliance for Natural Health http://ift.tt/1O26drN via Aloe for Health
from Tumblr http://ift.tt/1TVjF0Y

Gluten in Your Thyroid Drug?

What will drug makers think up next?

A major drugmaker may be adding a new ingredient to their thyroid medication that will make many patients sicker. What is behind this ignorant or thoughtless move? Two Action Alerts!

Hypothyroid patients, take note: your medicine might now include gluten as an ingredient. A representative from Pfizer has said that the source of the starch in Cytomel cannot be verified and could come from corn, potato, or wheat.

Pfizer does not seem to know or care that this is not just a problem for those with general gluten sensitivity or, worse, Chrohn’s Disease. It may also make thyroid conditions worse, even much worse, totally defeating the purpose of the drug in the first place.

Cytomel contains the T3 thyroid hormone, one of five hormones produced by the thyroid (the others are T1, T2, T4, and calcitonin). Most thyroid medications for hypothyroid patients (those who cannot produce enough thyroid hormone) contain the T4 hormone, which the body is supposed to convert into T3. But not everyone can convert T4 and must take the T3 hormone instead. Since Cytomel is the only mass-marketed T3 medication, if it is tainted with gluten, many patients (even if they understand the problem) will have nowhere to turn—especially if compounded T3 is eliminated, which is exactly what the FDA and drug companies seem to want. More on this below.

Why is gluten a problem, particularly for hypothyroid patients? The cause of hypothyroidism for 90% of people is Hashimoto’s disease, where the body’s own immune system attacks the thyroid. Many patients are unaware that they have Hashimoto’s, however, because conventional doctors don’t test for it. Why? Because there is no drug to treat it, thus they don’t think it can be treated. They too don’t “get it.” With proper nutrition and a strict gluten-free diet, as well as addressing underlying causes such as toxic exposures, it can be completely reversed. We have seen this because an ANH-USA staffer had Hashimoto’s disease and was able to cure it with this approach. (See our companion article in this issue.)

Doctors are finding that those with Hashimoto’s disease benefit greatly from a gluten-free diet, likely because gluten triggers the autoimmunity that is the root cause of their hypothyroidism. If a hypothyroid patient with Hashimoto’s takes a pill that contains gluten, the autoimmunity that flares up as a result could cause systemic inflammation and additional problems with autoimmunity.

That this critically important connection is lost on pharmaceutical companies making thyroid medications is not that surprising, but no less concerning for patients who will become sick taking these drugs. This is one more instance of the conventional medical paradigm focusing on treating symptoms while taking no interest in the root cause of disease. We hate to say this, but curing patients once and for all is not profitable medicine.

There are, of course, alternatives to pharmaceutical drugs for treating hypothyroidism. Compounding pharmacies can make customized, natural medicines that give hypothyroid patients the hormones they need. Unfortunately, as we’ve been reporting for some months, the FDA has been passing draconian regulations on the compounding industry, severely limiting the natural medicines they can produce. We’ve seen natural medicines rejected from the Bulk Drug list, and delivery systems such as time-release medicines nominated to the “Difficult to Compound” list (not to mention the bioidentical hormones such as estriol and progesterone that have also been targeted for extinction so that drug companies can have a monopoly). We’ve also recently reported that new FDA guidances are making it even harder for traditional compounding pharmacies to do business—and without compounding pharmacies, there can be no compounded thyroid medicine.

These restrictions make the inclusion of gluten in thyroid drugs even more concerning. If the FDA eliminates access to compounded thyroid medicines, the only alternative will be the gluten-containing drug. We believe that this is by design. The goal of the FDA’s war on natural medicine is to eliminate competition for drugs—even if those drugs will make people sicker.

Action Alert! Tell the FDA to maintain access to compounded thyroid treatments and other natural medicines. Please send your message immediately.

 Take-Action

Action Alert! Write to Pfizer and tell them to remove gluten from their thyroid medication. Please send your message immediately.

Take-Action

from The Alliance for Natural Health http://ift.tt/1TUnUJ0 via Aloe for Health




from http://ift.tt/1XbZ0IT

Action Alert: Remove Gluten From Thyroid Medication

Related article: Gluten in Your Thyroid Drug?

Trouble Taking Action? Click here.

.errordiv { padding:10px; margin:10px; border: 1px solid #555555;color: #000000;background-color: #f8f8f8; text-align:center; width:500px; }
var ai_iframe_width_iframe2921 = 0; var ai_iframe_height_iframe2921 = 0;var aiIsIe8=false;var aiReadyCallbacks = ( typeof aiReadyCallbacks != ‘undefined’ && aiReadyCallbacks instanceof Array ) ? aiReadyCallbacks : [];var onloadFirediframe2921 = false; function aiShowIframe() { jQuery(“#iframe2921”).css(“visibility”, “visible”);} function aiShowIframeId(id_iframe) { jQuery(id_iframe).css(“visibility”, “visible”);} function aiResizeIframeHeight(height) { aiResizeIframeHeight(height,iframe2921); } function aiResizeIframeHeightId(height,width,id) {aiResizeIframeHeightById(id,height);} http://ift.tt/1WMKWEVvar ifrm_iframe2921 = document.getElementById(“iframe2921”);
var hiddenTabsDoneiframe2921 = false;
function resizeCallbackiframe2921() {}

from The Alliance for Natural Health http://ift.tt/1TUo56X via Aloe for Health




from http://ift.tt/1XbYIBV

Gluten in Your Thyroid Drug?

What will drug makers think up next?

A major drugmaker may be adding a new ingredient to their thyroid medication that will make many patients sicker. What is behind this ignorant or thoughtless move? Two Action Alerts!

Hypothyroid patients, take note: your medicine might now include gluten as an ingredient. A representative from Pfizer has said that the source of the starch in Cytomel cannot be verified and could come from corn, potato, or wheat.

Pfizer does not seem to know or care that this is not just a problem for those with general gluten sensitivity or, worse, Chrohn’s Disease. It may also make thyroid conditions worse, even much worse, totally defeating the purpose of the drug in the first place.

Cytomel contains the T3 thyroid hormone, one of five hormones produced by the thyroid (the others are T1, T2, T4, and calcitonin). Most thyroid medications for hypothyroid patients (those who cannot produce enough thyroid hormone) contain the T4 hormone, which the body is supposed to convert into T3. But not everyone can convert T4 and must take the T3 hormone instead. Since Cytomel is the only mass-marketed T3 medication, if it is tainted with gluten, many patients (even if they understand the problem) will have nowhere to turn—especially if compounded T3 is eliminated, which is exactly what the FDA and drug companies seem to want. More on this below.

Why is gluten a problem, particularly for hypothyroid patients? The cause of hypothyroidism for 90% of people is Hashimoto’s disease, where the body’s own immune system attacks the thyroid. Many patients are unaware that they have Hashimoto’s, however, because conventional doctors don’t test for it. Why? Because there is no drug to treat it, thus they don’t think it can be treated. They too don’t “get it.” With proper nutrition and a strict gluten-free diet, as well as addressing underlying causes such as toxic exposures, it can be completely reversed. We have seen this because an ANH-USA staffer had Hashimoto’s disease and was able to cure it with this approach. (See our companion article in this issue.)

Doctors are finding that those with Hashimoto’s disease benefit greatly from a gluten-free diet, likely because gluten triggers the autoimmunity that is the root cause of their hypothyroidism. If a hypothyroid patient with Hashimoto’s takes a pill that contains gluten, the autoimmunity that flares up as a result could cause systemic inflammation and additional problems with autoimmunity.

That this critically important connection is lost on pharmaceutical companies making thyroid medications is not that surprising, but no less concerning for patients who will become sick taking these drugs. This is one more instance of the conventional medical paradigm focusing on treating symptoms while taking no interest in the root cause of disease. We hate to say this, but curing patients once and for all is not profitable medicine.

There are, of course, alternatives to pharmaceutical drugs for treating hypothyroidism. Compounding pharmacies can make customized, natural medicines that give hypothyroid patients the hormones they need. Unfortunately, as we’ve been reporting for some months, the FDA has been passing draconian regulations on the compounding industry, severely limiting the natural medicines they can produce. We’ve seen natural medicines rejected from the Bulk Drug list, and delivery systems such as time-release medicines nominated to the “Difficult to Compound” list (not to mention the bioidentical hormones such as estriol and progesterone that have also been targeted for extinction so that drug companies can have a monopoly). We’ve also recently reported that new FDA guidances are making it even harder for traditional compounding pharmacies to do business—and without compounding pharmacies, there can be no compounded thyroid medicine.

These restrictions make the inclusion of gluten in thyroid drugs even more concerning. If the FDA eliminates access to compounded thyroid medicines, the only alternative will be the gluten-containing drug. We believe that this is by design. The goal of the FDA’s war on natural medicine is to eliminate competition for drugs—even if those drugs will make people sicker.

Action Alert! Tell the FDA to maintain access to compounded thyroid treatments and other natural medicines. Please send your message immediately.

 Take-Action

Action Alert! Write to Pfizer and tell them to remove gluten from their thyroid medication. Please send your message immediately.

Take-Action



from The Alliance for Natural Health http://ift.tt/1TUnUJ0 via Aloe for Health
from Tumblr http://ift.tt/1TV9NEh

Action Alert: Remove Gluten From Thyroid Medication

Related article: Gluten in Your Thyroid Drug?

Trouble Taking Action? Click here.



from The Alliance for Natural Health http://ift.tt/1TUo56X via Aloe for Health
from Tumblr http://ift.tt/1P11D7M

Thursday, May 26, 2016

Action Alert: Reform the FDA!

Related article: Systemic Corruption at FDA

Trouble Taking Action? Click here.

.errordiv { padding:10px; margin:10px; border: 1px solid #555555;color: #000000;background-color: #f8f8f8; text-align:center; width:500px; }
var ai_iframe_width_iframe283 = 0; var ai_iframe_height_iframe283 = 0;var aiIsIe8=false;var aiReadyCallbacks = ( typeof aiReadyCallbacks != ‘undefined’ && aiReadyCallbacks instanceof Array ) ? aiReadyCallbacks : [];var onloadFirediframe283 = false; function aiShowIframe() { jQuery(“#iframe283”).css(“visibility”, “visible”);} function aiShowIframeId(id_iframe) { jQuery(id_iframe).css(“visibility”, “visible”);} function aiResizeIframeHeight(height) { aiResizeIframeHeight(height,iframe283); } function aiResizeIframeHeightId(height,width,id) {aiResizeIframeHeightById(id,height);} http://ift.tt/1OPuhbTvar ifrm_iframe283 = document.getElementById(“iframe283”);
var hiddenTabsDoneiframe283 = false;
function resizeCallbackiframe283() {}

from The Alliance for Natural Health http://ift.tt/1XzGXKR via Aloe for Health




from http://ift.tt/1P0vDpL

Action Alert: Tell the USDA to Ban Meat Glue!

Related article: Glue in Your Meat?

Trouble Taking Action? Click here.

.errordiv { padding:10px; margin:10px; border: 1px solid #555555;color: #000000;background-color: #f8f8f8; text-align:center; width:500px; }
var ai_iframe_width_iframe2926 = 0; var ai_iframe_height_iframe2926 = 0;var aiIsIe8=false;var aiReadyCallbacks = ( typeof aiReadyCallbacks != ‘undefined’ && aiReadyCallbacks instanceof Array ) ? aiReadyCallbacks : [];var onloadFirediframe2926 = false; function aiShowIframe() { jQuery(“#iframe2926”).css(“visibility”, “visible”);} function aiShowIframeId(id_iframe) { jQuery(id_iframe).css(“visibility”, “visible”);} function aiResizeIframeHeight(height) { aiResizeIframeHeight(height,iframe2926); } function aiResizeIframeHeightId(height,width,id) {aiResizeIframeHeightById(id,height);} http://ift.tt/20GEEVJvar ifrm_iframe2926 = document.getElementById(“iframe2926”);
var hiddenTabsDoneiframe2926 = false;
function resizeCallbackiframe2926() {}

from The Alliance for Natural Health http://ift.tt/1TDoSMD via Aloe for Health




from http://ift.tt/1TGNOjl

Action Alert: Reform the FDA!

Related article: Systemic Corruption at FDA

Trouble Taking Action? Click here.



from The Alliance for Natural Health http://ift.tt/1XzGXKR via Aloe for Health
from Tumblr http://ift.tt/1Vk5i7r

Action Alert: Tell the USDA to Ban Meat Glue!

Related article: Glue in Your Meat?

Trouble Taking Action? Click here.



from The Alliance for Natural Health http://ift.tt/1TDoSMD via Aloe for Health
from Tumblr http://ift.tt/1qLLcGq

Tuesday, May 24, 2016

Estriol, Thyroid, and Other Natural Medicines Face a New Threat

If the pharmacy has been put out of business, it can’t prepare your medication, right? Action Alert!

Last week we told you about the recent guidance from the FDA that ignores directives from Congress and continues to ban office use by doctors of prepared medications such as injectable vitamin B12—while carving out a potentially lucrative exemption for hospital pharmacies.

Unfortunately, the bad news doesn’t stop there. The FDA has released another guidance on yet another seemingly technical matter that would put traditional compounding pharmacies in even greater jeopardy.

The Drug Quality and Security Act of 2013 (DQSA) separated pharmacies that make customized medicines at a doctor’s direction for individual patients into two categories:

  • “traditional” compounding pharmacies (regulated under section 503A of the Food, Drug, and Cosmetic Act), and
  • “outsourcing” compounding pharmacies (regulated under section 503B of the same law).

Among the main differences between these two pharmacies are that outsourcing pharmacies can engage in office use compounding (making medicines for doctors to keep on-hand in their offices), can ship medicines interstate without restriction (traditional pharmacies can only ship 5% of total orders out-of-state, unless the state enters into a memorandum of understanding), and can only compound substances from a preapproved list from the FDA. It is already clear that the FDA intends this medications list to be very short indeed. Because outsourcing facilities can compound for office use and ship interstate, they are well-placed to capture a large portion of the market—even if they can only compound from a shorter list of ingredients.

In a nutshell, the new guidance says that a pharmacy cannot register as both a traditional and an outsourcing facility. The stated rationale is that outsourcing facilities must follow stringent current good manufacturing practices (cGMPs) while traditional pharmacies do not—and if one facility has both a 503A and a 503B operation, it will be “difficult to ensure that all of the products were made under the correct standards.”

It will be evident that this purported justification is a complete sham. Where would the difficulty be in having one division of a facility compound drugs under one set of rules, and having another division of the same facility compound medicines under a different set of rules? Such an arbitrary ruling further strengthens our contention that this is part of a larger campaign by the FDA to eliminate traditional pharmacies altogether, since they compete with the pharmaceutical industry, which pays the FDA’s bills.

The FDA’s real goal with this guidance, and many other restrictions on the industry, is to get all traditional facilities to register as outsourcing facilities, since what can be compounded at outsourcing facilities is completely at the FDA’s whim and can be very narrowly defined. This will likely eliminate many traditional compounding pharmacies altogether, and leave only the largest companies open for business—and those can be expected to be owned by Big Pharma.

Thus far, the FDA has been accomplishing its goal of eliminating compounding by making it impossible for traditional pharmacies to stay in business by restricting what medicines they can make and how much they can ship out of state, and by eliminating office use.

Before this new ruling, one possible way to continue to make the medicines that integrative doctors and countless patients rely upon was to register as both a 503B and a 503A pharmacy. But with this guidance, the FDA has now eliminated that possibility—another nail in the coffin for traditional pharmacies.

The FDA clearly does not feel responsible to the public. If it did, it might take heed of Congress’s repeated warnings that the agency is going too far in its implementation of DQSA, a bill Congress intended as a tool to regulate—not abolish!—compounding pharmacies.

Action Alert! Write to the FDA and urge them to amend this guidance and preserve consumer access to natural medicines by allowing 503A facilities to register also as 503B facilities. Please send your message immediately.

Take-Action

Additional Action Alert! If you haven’t already, write to your representative in the House and urge him or her to support the FY 2017 appropriations language that would withhold funding from the FDA until the agency states how it will allow “office use” of compounded medicines to continue, and how the overall compounding of supplements and medications will move forward and at reasonable prices. Please send your message immediately.

Take-Action

from The Alliance for Natural Health http://ift.tt/1TxCKmn via Aloe for Health




from http://ift.tt/1TvKV7S

FDA Reverses Its Folate Ban

Some good news to report!

Thanks to the sustained advocacy of ANH-USA members and our allies, a serious threat to folate availability has been reversed. Unfortunately, other problems with new nutrition facts rules remain unaddressed.

In 2014, we told you that the FDA was proposing a backdoor ban on natural folate in dietary supplements. The word “folate” would be banned from Supplement Fact labels—only the term “folic acid” would be allowed. Since it would be fraudulent for the supplement to list synthetic folic acid among its ingredients but to use natural folate instead, it would become illegal to use folate in dietary supplements. Very sneaky.

Never mind that a substantial minority of Americans are physically unable to process synthetic folic acid into folate—as we’ve pointed out before, many individuals have a genetic defect that prevents them from producing the enzymes necessary to convert synthetic folic acid into the active form of the B vitamin our bodies need. This includes up to 44% of North American Caucasians and over 50% of Italians, and over 90% of patients who are predisposed to diseases such as cancer, heart disease, and autism. The human body needs folate to thrive and even survive. Many citizens would thus be dependent on expensive folate drugs prescribed by a doctor.

ANH-USA submitted joint comments with the Weston Price Foundation and the Organic Consumers of America in response to the FDA’s proposal. We pointed out the illegality (not to mention the absurdity) of the agency’s proposal on folate, and discussed our concerns over the agency’s reevaluation of Reference Daily Intakes (RDI) for vitamins and minerals—the amount of a nutrient considered sufficient to meet the minimum requirements of most individuals in every demographic.

In a response to comments published in advance of the final rule, which was just released, the FDA seems to have relented on its folate ban. Specifically, in response to a comment pointing to the danger of not allowing “folate” on Supplement Facts labels, the FDA stated that “the final rule requires the use of the term ‘folate’ on Supplement Facts labels….”

This is a major victory for public health. Banning natural folate in supplements would have put significant portions of the population in jeopardy and caused great harm, so it is good that the FDA listened to reason.

Unfortunately, the agency has stubbornly kept its pitifully low RDI proposals for vital nutrients intact. As we pointed out in our initial comments, current knowledge concerning appropriate dosage levels of vitamins and minerals in relation to different population groups means that few practicing clinical nutritionists would agree with the RDIs proposed by the FDA. Instead of reflecting optimal intakes, the proposed RDIs reflect only minimum, or insufficient, intakes. Considering the large percentages of Americans who are deficient in key nutrients, the FDA’s stance on this issue is likely to make a bad problem even worse.

For example, the FDA will be lowering the RDI for vitamin B12 from 6 mcg. per day to 2.4 mcg. per day—meaning that a 5,000-mcg.-per-day B12 product will have to be labeled as 208,333% of the daily value. This will mislead consumers into thinking such a level is too high or dangerous, despite a total lack of evidence of potential harm to the vast majority of people.

Nonetheless, the reversal of the folate ban is a real victory for natural health—one that will save countless lives.

Other articles in this week’s Pulse of Natural Health:

Estriol, Thyroid, and Other Natural Medicines Face a New Threat

FDA Backs Down on Censoring Food Label

Anti-Supplement Amendment Coming

from The Alliance for Natural Health http://ift.tt/1WMKIh4 via Aloe for Health




from http://ift.tt/1TvKHxH

FDA Backs Down on Censoring Food Label

Yet only recently the agency held that KIND snack bars couldn’t claim to be healthy because they contained too much fat. Never mind that the fats in question are the good fats we need.

Last year the FDA sent a warning letter to KIND Healthy Snacks, telling them their products were advertised as being “healthy” without meeting the federal definition of “healthy”—that is, they must have no more than one gram of saturated fat per serving—whereas the KIND bars cited by the FDA contain anywhere between one and five grams of saturated fat. Even if saturated fat actually were bad for your heart, which scientists have now refuted, this wouldn’t exactly be an artery-clogging amount. Now, under pressure from us and others, the FDA is reversing its decision. The agency reportedly informed KIND that it could return to using the term “healthy” on its products.

So far so good. But the agency says it is allowing KIND to market its products as “healthy” only to express the company’s corporate philosophy, not as a nutrient claim! So does the FDA think that fat—and in particular, saturated fat—is always unhealthy, or not? And what does it mean to “express your philosophy” without making a health claim? This is bureaucratic doublespeak.

As we’ve seen with the woefully outdated advice given by the Dietary Guidelines Advisory Committee, the government is incapable of using the most recent science to advise Americans on nutrition. Last year we told you about the FDA’s proposal to declare that a diet of 10% added sugar was “healthy.” This week the agency made it official—by July 2018, Nutrition Facts labels must include a line for “added sugars.” The FDA is saying that the average American on a 2000-calorie-per-day diet can have 50 grams of added sugars in addition to any sugars that are naturally present in the food. (Actually, because it’s a recommended daily value, they’re saying American should have 50 grams of added sugar each day.)

Why is the FDA giving Americans such poor nutrition advice? It could be because of scientific incompetence. A congressional audit of the agency rated its science competence “extremely poor.”

More likely it is the influence of big companies. The FDA simply does not want consumers to have access to information about food and supplements, since they are competition for the pharmaceutical drugs whose manufacturers pay the agency’s bills. If the FDA—or the Federal Trade Commission, which we believe works in cahoots with the FDA on this issue—can keep gagging natural food producers, it will help Big Pharma maintain its monopoly over healthcare and prevention.

Other articles in this week’s Pulse of Natural Health:

Estriol, Thyroid, and Other Natural Medicines Face a New Threat

FDA Reverses Its Folate Ban

Anti-Supplement Amendment Coming

from The Alliance for Natural Health http://ift.tt/1TxCV0K via Aloe for Health




from http://ift.tt/1TvKt9H

Action Alert: Save Traditional Pharmacies!

Related article: Estriol, Thyroid, and Other Natural Medicines Face a New Threat

Trouble Taking Action? Click here.

.errordiv { padding:10px; margin:10px; border: 1px solid #555555;color: #000000;background-color: #f8f8f8; text-align:center; width:500px; }
var ai_iframe_width_iframe2921 = 0; var ai_iframe_height_iframe2921 = 0;var aiIsIe8=false;var aiReadyCallbacks = ( typeof aiReadyCallbacks != ‘undefined’ && aiReadyCallbacks instanceof Array ) ? aiReadyCallbacks : [];var onloadFirediframe2921 = false; function aiShowIframe() { jQuery(“#iframe2921”).css(“visibility”, “visible”);} function aiShowIframeId(id_iframe) { jQuery(id_iframe).css(“visibility”, “visible”);} function aiResizeIframeHeight(height) { aiResizeIframeHeight(height,iframe2921); } function aiResizeIframeHeightId(height,width,id) {aiResizeIframeHeightById(id,height);} http://ift.tt/1WMKWEVvar ifrm_iframe2921 = document.getElementById(“iframe2921”);
var hiddenTabsDoneiframe2921 = false;
function resizeCallbackiframe2921() {}

from The Alliance for Natural Health http://ift.tt/1TxCp2N via Aloe for Health




from http://ift.tt/1TvKt9K

Estriol, Thyroid, and Other Natural Medicines Face a New Threat

If the pharmacy has been put out of business, it can’t prepare your medication, right? Action Alert!

Last week we told you about the recent guidance from the FDA that ignores directives from Congress and continues to ban office use by doctors of prepared medications such as injectable vitamin B12—while carving out a potentially lucrative exemption for hospital pharmacies.

Unfortunately, the bad news doesn’t stop there. The FDA has released another guidance on yet another seemingly technical matter that would put traditional compounding pharmacies in even greater jeopardy.

The Drug Quality and Security Act of 2013 (DQSA) separated pharmacies that make customized medicines at a doctor’s direction for individual patients into two categories:

  • “traditional” compounding pharmacies (regulated under section 503A of the Food, Drug, and Cosmetic Act), and
  • “outsourcing” compounding pharmacies (regulated under section 503B of the same law).

Among the main differences between these two pharmacies are that outsourcing pharmacies can engage in office use compounding (making medicines for doctors to keep on-hand in their offices), can ship medicines interstate without restriction (traditional pharmacies can only ship 5% of total orders out-of-state, unless the state enters into a memorandum of understanding), and can only compound substances from a preapproved list from the FDA. It is already clear that the FDA intends this medications list to be very short indeed. Because outsourcing facilities can compound for office use and ship interstate, they are well-placed to capture a large portion of the market—even if they can only compound from a shorter list of ingredients.

In a nutshell, the new guidance says that a pharmacy cannot register as both a traditional and an outsourcing facility. The stated rationale is that outsourcing facilities must follow stringent current good manufacturing practices (cGMPs) while traditional pharmacies do not—and if one facility has both a 503A and a 503B operation, it will be “difficult to ensure that all of the products were made under the correct standards.”

It will be evident that this purported justification is a complete sham. Where would the difficulty be in having one division of a facility compound drugs under one set of rules, and having another division of the same facility compound medicines under a different set of rules? Such an arbitrary ruling further strengthens our contention that this is part of a larger campaign by the FDA to eliminate traditional pharmacies altogether, since they compete with the pharmaceutical industry, which pays the FDA’s bills.

The FDA’s real goal with this guidance, and many other restrictions on the industry, is to get all traditional facilities to register as outsourcing facilities, since what can be compounded at outsourcing facilities is completely at the FDA’s whim and can be very narrowly defined. This will likely eliminate many traditional compounding pharmacies altogether, and leave only the largest companies open for business—and those can be expected to be owned by Big Pharma.

Thus far, the FDA has been accomplishing its goal of eliminating compounding by making it impossible for traditional pharmacies to stay in business by restricting what medicines they can make and how much they can ship out of state, and by eliminating office use.

Before this new ruling, one possible way to continue to make the medicines that integrative doctors and countless patients rely upon was to register as both a 503B and a 503A pharmacy. But with this guidance, the FDA has now eliminated that possibility—another nail in the coffin for traditional pharmacies.

The FDA clearly does not feel responsible to the public. If it did, it might take heed of Congress’s repeated warnings that the agency is going too far in its implementation of DQSA, a bill Congress intended as a tool to regulate—not abolish!—compounding pharmacies.

Action Alert! Write to the FDA and urge them to amend this guidance and preserve consumer access to natural medicines by allowing 503A facilities to register also as 503B facilities. Please send your message immediately.

Take-Action

Additional Action Alert! If you haven’t already, write to your representative in the House and urge him or her to support the FY 2017 appropriations language that would withhold funding from the FDA until the agency states how it will allow “office use” of compounded medicines to continue, and how the overall compounding of supplements and medications will move forward and at reasonable prices. Please send your message immediately.

Take-Action



from The Alliance for Natural Health http://ift.tt/1TxCKmn via Aloe for Health
from Tumblr http://ift.tt/25eW4fm

FDA Reverses Its Folate Ban

Some good news to report!

Thanks to the sustained advocacy of ANH-USA members and our allies, a serious threat to folate availability has been reversed. Unfortunately, other problems with new nutrition facts rules remain unaddressed.

In 2014, we told you that the FDA was proposing a backdoor ban on natural folate in dietary supplements. The word “folate” would be banned from Supplement Fact labels—only the term “folic acid” would be allowed. Since it would be fraudulent for the supplement to list synthetic folic acid among its ingredients but to use natural folate instead, it would become illegal to use folate in dietary supplements. Very sneaky.

Never mind that a substantial minority of Americans are physically unable to process synthetic folic acid into folate—as we’ve pointed out before, many individuals have a genetic defect that prevents them from producing the enzymes necessary to convert synthetic folic acid into the active form of the B vitamin our bodies need. This includes up to 44% of North American Caucasians and over 50% of Italians, and over 90% of patients who are predisposed to diseases such as cancer, heart disease, and autism. The human body needs folate to thrive and even survive. Many citizens would thus be dependent on expensive folate drugs prescribed by a doctor.

ANH-USA submitted joint comments with the Weston Price Foundation and the Organic Consumers of America in response to the FDA’s proposal. We pointed out the illegality (not to mention the absurdity) of the agency’s proposal on folate, and discussed our concerns over the agency’s reevaluation of Reference Daily Intakes (RDI) for vitamins and minerals—the amount of a nutrient considered sufficient to meet the minimum requirements of most individuals in every demographic.

In a response to comments published in advance of the final rule, which was just released, the FDA seems to have relented on its folate ban. Specifically, in response to a comment pointing to the danger of not allowing “folate” on Supplement Facts labels, the FDA stated that “the final rule requires the use of the term ‘folate’ on Supplement Facts labels….”

This is a major victory for public health. Banning natural folate in supplements would have put significant portions of the population in jeopardy and caused great harm, so it is good that the FDA listened to reason.

Unfortunately, the agency has stubbornly kept its pitifully low RDI proposals for vital nutrients intact. As we pointed out in our initial comments, current knowledge concerning appropriate dosage levels of vitamins and minerals in relation to different population groups means that few practicing clinical nutritionists would agree with the RDIs proposed by the FDA. Instead of reflecting optimal intakes, the proposed RDIs reflect only minimum, or insufficient, intakes. Considering the large percentages of Americans who are deficient in key nutrients, the FDA’s stance on this issue is likely to make a bad problem even worse.

For example, the FDA will be lowering the RDI for vitamin B12 from 6 mcg. per day to 2.4 mcg. per day—meaning that a 5,000-mcg.-per-day B12 product will have to be labeled as 208,333% of the daily value. This will mislead consumers into thinking such a level is too high or dangerous, despite a total lack of evidence of potential harm to the vast majority of people.

Nonetheless, the reversal of the folate ban is a real victory for natural health—one that will save countless lives.

Other articles in this week’s Pulse of Natural Health:

Estriol, Thyroid, and Other Natural Medicines Face a New Threat

FDA Backs Down on Censoring Food Label

Anti-Supplement Amendment Coming



from The Alliance for Natural Health http://ift.tt/1WMKIh4 via Aloe for Health
from Tumblr http://ift.tt/1s7QCwz

FDA Backs Down on Censoring Food Label

Yet only recently the agency held that KIND snack bars couldn’t claim to be healthy because they contained too much fat. Never mind that the fats in question are the good fats we need.

Last year the FDA sent a warning letter to KIND Healthy Snacks, telling them their products were advertised as being “healthy” without meeting the federal definition of “healthy”—that is, they must have no more than one gram of saturated fat per serving—whereas the KIND bars cited by the FDA contain anywhere between one and five grams of saturated fat. Even if saturated fat actually were bad for your heart, which scientists have now refuted, this wouldn’t exactly be an artery-clogging amount. Now, under pressure from us and others, the FDA is reversing its decision. The agency reportedly informed KIND that it could return to using the term “healthy” on its products.

So far so good. But the agency says it is allowing KIND to market its products as “healthy” only to express the company’s corporate philosophy, not as a nutrient claim! So does the FDA think that fat—and in particular, saturated fat—is always unhealthy, or not? And what does it mean to “express your philosophy” without making a health claim? This is bureaucratic doublespeak.

As we’ve seen with the woefully outdated advice given by the Dietary Guidelines Advisory Committee, the government is incapable of using the most recent science to advise Americans on nutrition. Last year we told you about the FDA’s proposal to declare that a diet of 10% added sugar was “healthy.” This week the agency made it official—by July 2018, Nutrition Facts labels must include a line for “added sugars.” The FDA is saying that the average American on a 2000-calorie-per-day diet can have 50 grams of added sugars in addition to any sugars that are naturally present in the food. (Actually, because it’s a recommended daily value, they’re saying American should have 50 grams of added sugar each day.)

Why is the FDA giving Americans such poor nutrition advice? It could be because of scientific incompetence. A congressional audit of the agency rated its science competence “extremely poor.”

More likely it is the influence of big companies. The FDA simply does not want consumers to have access to information about food and supplements, since they are competition for the pharmaceutical drugs whose manufacturers pay the agency’s bills. If the FDA—or the Federal Trade Commission, which we believe works in cahoots with the FDA on this issue—can keep gagging natural food producers, it will help Big Pharma maintain its monopoly over healthcare and prevention.

Other articles in this week’s Pulse of Natural Health:

Estriol, Thyroid, and Other Natural Medicines Face a New Threat

FDA Reverses Its Folate Ban

Anti-Supplement Amendment Coming



from The Alliance for Natural Health http://ift.tt/1TxCV0K via Aloe for Health
from Tumblr http://ift.tt/25eVJcy

Action Alert: Save Traditional Pharmacies!

Related article: Estriol, Thyroid, and Other Natural Medicines Face a New Threat

Trouble Taking Action? Click here.



from The Alliance for Natural Health http://ift.tt/1TxCp2N via Aloe for Health
from Tumblr http://ift.tt/1s7QmxA

Anti-Supplement Amendment Coming

With your help, we can defeat it once again. Action Alert!

Last week we told you about an anti-supplement amendment that we think will be attached to a must-pass bill to fund the military in fiscal year 2017. We also believe this amendment will be introduced to the full Senate this week, so it is crucial to reach out to your senators and urge them to oppose this legislation.

To recap, the amendment, offered by Sen. Richard Blumenthal (D-CT), would subject supplements sold on military bases to third-party review for “recognized public standards of identity, purity, strength, and composition, and adherence to related process standards.”

As we’ve argued before, this law is completely unnecessary. Supplement companies by law must already hold to current good manufacturing practices (cGMPs), which require that their products be processed in a consistent manner and meet explicit quality standards. Second, supplement companies will likely be expected to pay huge sums for this review. Only the biggest companies—many of them owned by Big Pharma—will be able to comply. Yet another government-created monopoly will be handed over to big drug companies.

Of particular concern is the amendment’s language mandating “adherence to related process standards.” This language is extremely vague and could subject supplements sold on military bases to duplicative or otherwise unnecessary red tape—which would likely result in our servicemen and women losing access to high-quality supplements.

More importantly, passing this amendment makes it easier to apply such standards to all dietary supplements.

Action Alert! Write to your senators and urge them to oppose Sen. Blumenthal’s anti-supplement amendment and preserve our access to quality dietary supplements! Please send your message immediately.

Take-Action

Other articles in this week’s Pulse of Natural Health:
FDA Continues to Threaten Your Estriol, Thyroid, and Other Natural Medicines

FDA Reverses Its Folate Ban

FDA Backs Down on Censoring Food Label

from The Alliance for Natural Health http://ift.tt/20wHgFM via Aloe for Health




from http://ift.tt/1TvvQ6b

Anti-Supplement Amendment Coming

With your help, we can defeat it once again. Action Alert!

Last week we told you about an anti-supplement amendment that we think will be attached to a must-pass bill to fund the military in fiscal year 2017. We also believe this amendment will be introduced to the full Senate this week, so it is crucial to reach out to your senators and urge them to oppose this legislation.

To recap, the amendment, offered by Sen. Richard Blumenthal (D-CT), would subject supplements sold on military bases to third-party review for “recognized public standards of identity, purity, strength, and composition, and adherence to related process standards.”

As we’ve argued before, this law is completely unnecessary. Supplement companies by law must already hold to current good manufacturing practices (cGMPs), which require that their products be processed in a consistent manner and meet explicit quality standards. Second, supplement companies will likely be expected to pay huge sums for this review. Only the biggest companies—many of them owned by Big Pharma—will be able to comply. Yet another government-created monopoly will be handed over to big drug companies.

Of particular concern is the amendment’s language mandating “adherence to related process standards.” This language is extremely vague and could subject supplements sold on military bases to duplicative or otherwise unnecessary red tape—which would likely result in our servicemen and women losing access to high-quality supplements.

More importantly, passing this amendment makes it easier to apply such standards to all dietary supplements.

Action Alert! Write to your senators and urge them to oppose Sen. Blumenthal’s anti-supplement amendment and preserve our access to quality dietary supplements! Please send your message immediately.

Take-Action

Other articles in this week’s Pulse of Natural Health:
FDA Continues to Threaten Your Estriol, Thyroid, and Other Natural Medicines

FDA Reverses Its Folate Ban

FDA Backs Down on Censoring Food Label



from The Alliance for Natural Health http://ift.tt/20wHgFM via Aloe for Health
from Tumblr http://ift.tt/1TBWJ5q