All Posts Tagged With: "fatigue"

Urgent Plea from Linda

Linda’s comment:  please write letters to the below listed people ASAP….this is a serious health matter for everyone in the USA .  I had the meters removed from my home as it was causing my heart to race and skip beats, fatigue, severe headaches and not sleeping. 
PLEASE  help us to stop this ….
Regards,
Linda
Complaint regarding Smart meters Letter to the commissioners VERY IMPORTANT. THIS MATTERS
To: Cindy dB <auraconnection@hotmail.com>

Hello

Please write a letter to Arizona corporations commissions with email addresses below
enter e-Docket Number: E-OOOOOC-11-0328

email this to below is all the commissioners of Arizona regarding a complaint on the Smart meters and how you want it ban from the State of Arizona and all the health problems it’s causing, example headaches, insomnia, a number of heart problems and all the ill side effects people are having. Do this ASAP! They will be voting very soon on this issues on an op out program or like California it’s mandatory in most areas for smart meter instillation. Tell them to forward it to the Docket number
IF you know anyone in Arizona sent this around on your email list.
Also in AZ they need to write a letter in the complaint department to APS AND SRP Power companies as well. This really does matter.
Thank you

Cindy

Commissioner Paul Newman: Newman-web@azcc.gov

Commissioner Brenda Burns: Burns-web@azcc.gov

Commissioner Gary Pierce: Pierce-web@azcc.gov

Commissioner Bob Stump: Stump-web@azcc.gov

Postural orthostatic tachycardia & Lyme

Linda’s comment:  Ok so some may respond to antibiotics, where does the tatigue, joint pain and cognitive dysfunction come from….While IDSA says there is no such thing as chronic Lyme or post treatment LD, this very report speaks of them…..

Link: http://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=21305487&retmode=ref&cmd=prlinks

Excerpt:

Conclusions: In an appropriate clinical setting,
evaluation for POTS in patients suffering from post LD syndrome may lead to
early recognition and treatment, with subsequent improvement in symptoms of
orthostatic intolerance. (Cardiol J 2011; 18, 1: 63-66).

A Day In The Life Of Chronic Illness

 

Linda’s comments:  This was written by a Lyme friend of mine….it is beautiful and speaks volumns…  Please read the rest of her poems in the Poem section….Thank you Laura this is beautiful….

Excerpt:

 

I know that there’ll be a better day

When the clouds break and the sun shines my way

When all my troubles are kept at bay…

But that day is not today

 

I know that better times are ahead

When I will feel like getting out of bed

When my body wont weigh so heavy like lead…

But for now those are just words to be said

 

I know there will be a better time

When I wont spend my life living on a dime

And every moment I’ll be feeling fine…

But of “better days” I have seen no sign

 

I know that there are battles to be won

Like a stroll on the beach in the bright hot sun

Or going shopping with my daughters and having some fun…

But of victories I have not seen a single one

 

But still I keep pressing on each day

Hoping a cure will come my way

And all that happened in my adversity….

Will one day be just a sad memeory

 

So here’s to “better days” ahead

For all of us whose lives are led

By the hope that all the dreams that be…

WILL ONE DAY BE REALITY!

By: Laura Moore

 

Heart problems in Lyme disease

Link: http://www.ncbi.nlm.nih.gov/pubmed/21305487

Excerpt:

Results: Five patients (all women), aged 22-44 years, were identified 
for inclusion in this study. These patients developed symptoms of 
fatigue, cognitive dysfunction, orthostatic palpitations and either near 
syncope or frank syncope. The debilitating nature of these symptoms had 
resulted in lost of the employment or inability to attend school. Three 
patients were also suffering from migraine, two from anxiety and 
depression and one from hypertension. All patients demonstrated a good 
response to the employed treatment. Four of the five were able to engage 
in their activities of daily living and either resumed employment or 
returned to school.

Conclusions: In an appropriate clinical setting, evaluation for POTS in 
patients suffering from post LD syndrome may lead to early recognition 
and treatment, with subsequent improvement in symptoms of orthostatic 
intolerance. (Cardiol J 2011; 18, 1: 63-66).

Can Progesterone Cream Work?

Since I like topical Progesterone, I thought this rather balanced review might be interesting to all. 

Garry F. Gordon MD,DO,MD(H) 
President, Gordon Research Institute 
www.gordonresearch.com 

Excerpt:

Can Progesterone Cream Work? 

By ROBERT J. DAVIS 
Special to THE WALL STREET JOURNAL 
August 30, 2005; Page D5 

Concerns about the safety of hormone-replacement therapy have prompted many women to seek alternatives. One option, “natural” progesterone cream sold over the counter, is gaining in popularity among women looking for relief from symptoms of menopause or PMS. While some doctors recommend the creams, many others question their effectiveness and worry that unsupervised use could pose long-term risks. 
Most of the creams contain progesterone derived from soybeans or Mexican yams. In contrast, the most commonly prescribed hormone-replacement medications, which are taken orally, contain synthetic progesterone, known as progestin. Because progesterone in creams comes from plants and is structurally identical to the human hormone, it is often called “natural.” But like progestin, it is synthesized in a lab. 
The creams, which are sold in health-food stores and over the Internet, are classified by the Food and Drug Administration as cosmetics, not drugs. Therefore, manufacturers aren’t permitted to claim their products can treat or prevent conditions. But some do anyway. Most, however, make vague promises to promote “healthy hormone balance” or “balance and harmony within the female body.” 

The leading proponent of natural progesterone, the late physician John Lee, argued that in premenopausal women, too much estrogen relative to progesterone can lead to weight gain, bloating, irritability, fatigue, uterine fibroids, endometriosis and lumpy and tender breasts. Correcting the imbalance with progesterone cream, he said, can alleviate such problems. Likewise, he claimed creams reduce symptoms associated with menopause, such as hot flashes, mood swings, memory loss and decreased bone density. 

Clinical presentation of childhood neuroborreliosis

Excerpt:

89 cases of neuroborreliosis were reported; in 66 cases diagnosis was confirmed. Facial weakness was one of the presenting symptoms in 47 cases (71%) and the only symptom in nine children (14%). The five complaints most frequently reported were: malaise, headache, fatigue, fever and neck pain. 52 children (79%) had one or more objective neurological signs at presentation, of which facial nerve palsy, other cranial nerve abnormalities and meningeal signs were most frequent. 14 patients (21%), however, had no neurological signs at physical examination. In these patients, the number of subjective complaints was higher, and the time interval to diagnosis was longer compared with those with objective neurological abnormalities.

Conclusions

In this study, 79% of paediatric neuroborreliosis patients presented with neurological signs, most often facial nerve palsy. 21% presented in an atypical way without neurological signs. A thorough neurological examination is essential once neuroborreliosis is considered in children. Even in the absence of neurological signs, neuroborreliosis may be suspected in children with typical antecedents and multiple symptoms. Cerebrospinal fluid investigations are then required to confirm the diagnosis.

Anti-neural antibody reactivity in patients with Lyme

Full article: http://www.aldf.com/pdf/Armins_Published_paper_in_Brain.pdf

Excerpt:

Some Lyme disease patients report debilitating chronic symptoms of pain, fatigue, and cognitive deficits despite recommended courses of antibiotic treatment. The mechanisms responsible for these symptoms, collectively referred to as post-Lyme disease syndrome (PLS) or chronic Lyme disease, remain unclear. We investigated the presence of immune system abnormalities in PLS by assessing the levels of antibodies to neural proteins in patients and controls. Serum samples from PLS patients, post-Lyme disease healthy individuals, patients with systemic lupus erythematosus, and normal healthy individuals were analyzed for anti-neural antibodies by immunoblotting and immunohistochemistry. Anti-neural antibody reactivity was found to be significantly higher in the PLS group than in the post-Lyme healthy (p<0.01) and normal healthy (p<0.01) groups. The observed heightened antibody reactivity in PLS patients could not be attributed solely to the presence of cross-reactive anti-borrelia antibodies, as the borrelial seronegative patients also exhibited elevated anti-neural antibody levels. Immunohistochemical analysis of PLS serum antibody activity demonstrated binding to cells in the central and peripheral nervous systems. The results provide evidence for the existence of a differential immune system response in PLS, offering new clues about the etiopathogenesis of the disease that may prove useful in devising more effective treatment strategies. Copyright 2010 Elsevier Inc. All rights reserved.

Suspected Needle Stick Transmission of Bartonella vinsonii

Full article: http://onlinelibrary.wiley.com/doi/10.1111/j.1939-1676.2010.0563.x/abstract

Excerpt:

Suspected Needle Stick Transmission of Bartonella vinsonii

subspecies berkhoffii to a Veterinarian

  1. A.M. Oliveira1,
  2. R.G. Maggi1,
  3. C.W. Woods2,
  4. E.B. Breitschwerdt1

Article first published online: 2 AUG 2010

DOI: 10.1111/j.1939-1676.2010.0563.x

Court grants Lyme disease autopsy

Full article: http://www.smh.com.au/nsw/court-grants-lyme-disease-autopsy-20100719-10hyx.html

Excerpt:

A SYDNEY woman has been awarded a Supreme Court injunction to have her dead husband tested for a disease the Health Department says does not exist in Australia.

Mualla Akinci’s husband, Karl McManus, died last Wednesday – three years after he was bitten by a tick she says carried Lyme disease, a bacterial infection which, if left untreated, can cause profound neurological damage.

Mr McManus, 43, from Turramurra, was bitten on the left side of his chest during filming for the television show Home and Away in bushland in Waratah Park, northern Sydney. Within six weeks he lost mobility in one of the fingers on his left hand. That quickly spread to paralysis in his left arm and across to his right arm.

Mr McManus was diagnosed with multifocal neuropathy after testing negative for Lyme disease, but Ms Akinci, a pharmacist, insisted he be tested again at clinics in the US and Germany. Both tests returned positive for Lyme disease.

She argues that Australian tests are inadequate because pathologists looks for antibodies in the blood, rather than for proteins in specific bacteria within tissue.

”Lyme doesn’t usually live in the blood. It lives in tissues unless someone’s system is flushed with it so it stands to reason that every test will come back negative,” Ms Akinci said.

The Health Department maintains that no case has been transmitted in Australia and the organisms that cause it – three species of the genus borrelia – are not carried here by wildlife, livestock or their parasites.

The NSW Health Minister, Carmel Tebbutt, said in May there was not enough evidence to support the existence of ticks carrying the borrelia organism.

”Until there is solid evidence to indicate that locally acquired Lyme disease is a significant public health matter in Australia, specific measures to educate the general public or clinicians are difficult to justify,” she said.

From: Dr. Rashid A. Buttar, Chairman of ABCMT

This doctor from The Institute for Functional Medicine will raise consciousness about the need for LIFELONG DETOXIFICATION in order to deal with Lead, Mercury, Cadmium, etc. just like Mark Hyman has been doing on PBS with his video specials. This Voice America will reach many who have suffered with fibromyalgia and fatigue etc.

Fortunately, the public will start to learn that this is a lifetime program, as once you take some chelation you have only removed the readily accessible stores of lead etc. Since lead is in bones, the program must deal with slow bone turnover, usually 15 years, if you are to deal with the total body lead toxicity, not just the initial removal of readily accessible lead stores in soft tissues. It makes you feel much better, but the lifetime program is where you really change the outcomes since all causes of morbidity and mortality are documented to relate to how low you keep your lead levels throughout life.

Garry F. Gordon MD,DO,MD(H)
President, Gordon Research Institute
www.gordonresearch.com

____________

Dear Dr. Gordon,

We wanted to send this quick email to announce Dr. John Cline’s New Radio Show on Voice America. Every Friday at 3PM Pacific Time on the VoiceAmerica.com Health & Wellness Channel Beginning April 9, 2010. The new show is entitled ‘Detoxify for Life’.

For more information, please view the following PDFs:
http://www.DrButtar.com/files/DrClineVoiceAmericaShow.pdf
http://www.DrButtar.com/files/BusinessExaminerDrCline.pdf

#2: http://www.huffingtonpost.com/dr-mark-hyman/mercury-how-to-get-this-l_b_469358.html

February 20, 2010

Mark Hyman, MD

Practicing physician and pioneer in functional medicine
Posted: February 20, 2010 07:17 AM

Mercury: How To Get This Lethal Poison Out Of Your Body

If you are heavy, it could be making you sick and tired and age prematurely. And I don’t mean heavy with fat. I mean heavy with heavy metals — like mercury!

Unfortunately, toxic mercury problems are common. Along with polar bears, beluga whales, ducks, otters, panthers, and all river fish as well as most large ocean fish, we humans are poisoning ourselves with mercury at ever increasing rates.

There’s no doubt about it, mercury is the most alarming, disease-causing source of environmental toxicity that I see daily in my practice. Many of patients have toxic levels of mercury — and they’re not alone. I personally suffered from mercury toxicity and chronic fatigue syndrome –which I cured myself from, in part by getting rid of the mercury in my body. So I know about this first hand.

I became toxic because I polluted myself by growing up on tuna fish sandwiches, eating sushi, living in Beijing, which heats all its homes with coal — the major source of environmental mercury load — and having a mouthful of amalgam (a.k.a. mercury) fillings.
All of these exposures, combined with genes that prevent me from effectively detoxifying metals in my body, led to a slow and significant poisoning of my cells and mitochondria. And the effects were obvious …
I felt weak, tired, and couldn’t think. I had muscle pain and twitches, insomnia, digestive problems, food allergies, depression, and anxiety. And it was only by discovering high levels of mercury in my hair and urine — and slowly detoxifying myself — that I was able to get better.

I have seen this over and over in my patients, too. From chronic fatigue and fibromyalgia, to depression, anxiety, obesity, dementia, Parkinson’s disease, cancer, heart failure, and heart disease, the message is clear …We are being poisoned!

This is such an important public health and personal issue for so many people that I’m going to use this blog and next week’s blog to fully explain the extent of mercury issues and give you a comprehensive plan for reducing your exposure and healing from mercury toxicity. I’ll show you the science behind mercury toxicity, share some stories about my patients who have suffered, and talk about the way we need to deal with this major health problem.

First, I’d like to share with you what I learned at one of the most important international conferences on mercury yet to be held. It was called “The Impact of Mercury on Human Health and the Environment” and was presented at Tulane University School of Public Health and Tropical Medicine in New Orleans.

There, a unique international group of policymakers, environmental scientists, toxicologists, biochemists, journalists, academic physicians, practicing pediatricians, neurologists, and dentists gathered.

We were there to make sense of the environmental impact, toxicology, basic science, public policy and health implications of one the least studied and perhaps greatest potential threats to our long-term health — mercury. And I want to share some of what I learned at that conference with you.

Mercury Levels Are on the Rise
Barry Kohl, Ph.D. is an adjunct professor in the department of Earth and Environmental Sciences at Tulane University. At the conference he provided a unique overview of the impact of industrialization on environmental mercury levels through a description of the levels of mercury in the ice core extracted from the pristine Freemont Glacier in Wyoming.
There were small peaks in mercury concentration in the ice core from the 1815 Tambora volcanic eruption in Indonesia, the 1850-84 gold rush in California where mercury was used for smelting, the eruption in 1883 of the Sumatran volcano Krakatau 10,000 miles away, and the more recent Mount St. Helens eruption in 1980.

Overall, the changes in environmental mercury levels have been dramatic. Over the past 100 years, there has been a 30-fold increase in mercury deposition, 70 percent of which is from human sources. In fact, there was an exponential peak in mercury occurring in the last 40 years due to major industrialization. Much of this mercury comes from coal-fired industrial plants and from chlor-alkali plants that use mercury in the process of making chlorine used in plastics, pesticides, PVC pipes, and more.

One note of hope was the reduction in industrial mercury emissions from 220 million pounds to 120 million pounds a year over the last 10 years. But that’s small consolation when we’re talking about a substance that is toxic in parts per million, not in millions of pounds.

And the more mercury we are exposed to, the more we are likely we are to be toxic.

Risk Increases with Dose
Harvey Clewell from the ENVIRON Health Sciences Institute, Ruston, Louisiana, reviewed the epidemiologic studies from the Seychelles and Faroe islands. He showed that your risk of toxicity increases with higher doses of mercury.

Now, there are different types of mercury. Nearly all human exposures to one type, methylmercury, come from fish.

In the Seychelle Islands, there seemed be little effect on kids from mercury; however their fish consumption was predominately from low-risk small reef fish that don’t contain much mercury.

On the other hand, in the Faroe Islands people eat whale blubber, which contains high levels of mercury — over three parts per million. There, high levels of mercury were found in umbilical cord blood and correlated with reduced performance in neurologic testing in 917 mother-infant pairs.

The health effects from methyl mercury upon infants and children depend on the dose. Severe symptoms start with exposure to doses of 100 mcg/kg/day, mild symptoms with more than 10 mcg/kg/day, and sub-clinical symptoms with less than 1 mcg/kg/day. These symptoms include late development in walking and talking and decreased performance on neurological tests.

Dr. Clewell also reviewed the limitations of various forms of testing for mercury.
Methylmercury (also called organic mercury) is found predominately in red blood cells, which is what doctors check when they do a blood test for mercury. But unless you’ve been eating fish with mercury recently, you won’t see your total body level of mercury.
Plus, mercury is lipophilic, meaning that it concentrates in fatty tissues, especially in the brain, which is made mostly of fat. That means that blood levels aren’t an accurate measurement of total body burden of mercury.

Inorganic mercury from dental fillings (amalgams) is found in plasma but is rapidly cleared and stored in your tissues. Inorganic mercury is also converted from methylmercury by the body and is the main form of mercury in brain, which can lead to dementia, autism, ADHD and more.

All of these are reasons you need to get comprehensive testing done to assess you total mercury load. I will review the test you need in a moment, but first I want to talk about how mercury gets in your body and what it does to your body and brain.

Health Effects of Mercury
We get mercury in our bodies from many different sources including mercury vapors in ambient air, ingesting it via drinking water, fish, dental amalgams, vaccines, occupational exposures, home exposures including fluorescent light bulbs, thermostats, batteries, red tattoo dye, skin-lightening creams, over-the-counter products such as contact lens fluid and neosynephrine, and more.

You absorb about 80 percent of inhaled mercury vapor and nearly 100 percent of the mercury in fish through your gut.

Once this mercury is in your body it is then primarily distributed in the kidneys and brain and can be readily transferred to the fetus via the placenta.

The only way it can get out of your body is via urine, feces, expired air, and breast milk. The major reason it is toxic to human biology is because mercury has the ability to bind to sulfur-containing molecules in the body (found in nearly every enzyme and in the mitochondria), as well as other chemical binding sites in the cells.

We’ve learned a lot about how this mercury effects us and our children from reported exposures to mercury over the last 100 years. These include epidemics such as the Minimata Bay exposures in Japan, acrodynia or pink disease in children from calomel (HgCl) used in teething powder, “mad hatter syndrome” or erethism, and methylmercury fungicide grain seed exposures in Iraq and Pakistan.

The symptoms and diseases these exposures have caused are varied and mimic many other conditions. Nervous system toxicity can cause erethism (“mad hatter syndrome” as mentioned above) with symptoms of shyness; laughing, crying, and dramatic mood swings for no apparent reason; nervousness, insomnia, memory problems, and the inability to concentrate.

Other neurologic symptoms may include encephalopathy (non-specific brain malfunction), nerve damage, Parkinsonian symptoms, tremor, ataxia (loss of balance), impaired hearing, tunnel vision, dysarthria (slurred speech), headache, fatigue, impaired sexual function, and depression.

Kidney toxicity leads to proteinura (protein in the urine) and acute renal failure.
Gastrointestinal symptoms include nausea, vomiting, diarrhea, and colitis.
Skin toxicity causes allergic dermatitis, chelitis (cracked corners of the mouth), gingivitis (gum disease), stomatitis (sores in the mucous membranes of the mouth) and excessive salivation.

Clearly, mercury toxicity is VERY serious business!

Dentistry and Mercury
One of the more controversial sources of mercury toxicity is dental fillings. Silver dental fillings, or amalgams, contain inorganic mercury. Mercury exposure from amalgams is estimated to be between 3 to 17 micrograms per day from chewing, brushing, grinding, and even slow corrosion.

Questions have arisen about whether or not this amount is toxic … I am going to clear up the confusion here.

A recent study in the Journal of the American Medical Association found no significant neurologic or behavioral changes in children who had mercury amalgam (silver) fillings, compared to kids who had composite (white) fillings placed. But there were significant problems with that study …

First, the duration of the study was short and the effects subtle. Second, they failed to emphasize the significance of the fact that the kids who had the silver fillings had much higher levels of mercury in their urine than the kids with white fillings.

This is one of the most important details of that study, because it proves that mercury fillings in your mouth release mercury vapor that is absorbed into your body, ending up in your urine. It is deposited in your organs, including your brain, where it accumulates over time.

Whether your fillings are new or old, the mercury in them is constantly absorbed into your body. And even if you stop being exposed to that mercury, it sticks around. It takes up to 18 years for the body to clear half of the dose of mercury from the body. Once mercury is in the body it comes out only VERY slowly.

In fact, people with amalgam fillings have significantly elevated blood mercury levels, three to five times more mercury in the urine, and two to twelve times more mercury in their tissues than those without amalgam fillings.

However blood and urine mercury levels don’t necessarily relate to the mercury load in your body tissues or severity of clinical symptoms.

Research on sheep and monkeys with dental amalgams has shown that blood mercury levels remained low — even though their tissue mercury levels were raised.

Urine mercury levels aren’t much better as an indicator of your total mercury load. They mainly reflect the cumulative dose of inorganic mercury in the kidneys and there exists only a very weak correlation with levels in other target tissues.

Another speaker at the conference, Mike Robichaux, a practicing dentist, reviewed his experience with removal of amalgams fillings. He showed a remarkable video of mercury vapor being released from a 25-year-old tooth. You can watch it on the website of the International Academy of Oral Medicine and Toxicology.

But other dentists aren’t so concerned. In fact, the American Dental Association still says it is safe to use mercury or silver fillings. That’s something I’ve always wondered about, since the Environmental Protection Agency (EPA) considers old mercury fillings that have been removed from the body toxic waste that has to be disposed as such.

Let me put this another way. It’s apparently all right to put mercury fillings in your mouth — but not to throw them out in the garbage!

The danger of amalgam fillings has been confirmed by research from around the world.
At the conference, Anders Lindvall, M.D., from the Foundation for Metal Biology in Sweden, reported his work on the health effects of dental amalgams and presented a review of the controversial literature on dental amalgams and human health.

Many of his patients reported a symptom complex consistent with chronic fatigue syndrome that they believed were related to dental amalgams. So in 1990, Dr. Lindvall began a study at Uppsala University Hospital in Sweden to diagnose and treat 796 patients with suspected amalgam-related illness and to develop and evaluate diagnostic tools to assess toxicity from dental amalgams. (i)

Besides conventional measures of quality of life and symptoms, unique laboratory assessments were used to determine the presence and immunological toxicity of metals.
One was PIXE, an accelerator-based test on single blood cells that assesses intracellular levels of trace elements, which showed that, in lymphocytes (white blood cells), mercury is found in the nucleus, particularly in places where zinc is low.

The other was MELISA, a test of lymphocyte reactivity to metal compounds. Information about the MELISA test is available at www.melisa.org. (ii)

Dr. Lindvall’s patients were treated with antioxidants (B complex vitamins, vitamins C and E, and selenium); infections and jaw dysfunction were addressed; and selective removal of any incompatible dental material was performed using low-emission amalgam removal techniques and bio-compatible materials to replace the amalgams.

The cost of these procedures was covered by national health insurance.

Laboratory follow up at one year showed over 70 percent of patients reported significant improvement in symptoms after amalgam removal!

Unfortunately, this study had some problems too …

The clinic was closed after the study was published, so there was no further access allowed to the records, which contained over 1,000 untreated patients who could have served as a control group. And since 1999, amalgam dental restorations in Sweden are no longer covered by insurance.

But Dr. Lindvall’s study still suggests that silver amalgams can cause health problems — and that removing the fillings can help relieve these problems.

And other studies have had similar effects.

Research has found that patients with chronic fatigue and autoimmune thyroiditis show improvement in their health status after their amalgam fillings are replaced with composites. (iii)

In another study, 71 percent of people with autoimmune diseases, including multiple sclerosis, improved after amalgam removal. Low-dose exposure to inorganic mercury may be a contributing factor in the development of autoimmune diseases. (iv)

Animal and lab studies suggest that exposure to metallic mercury may cause nerve cell damage and promote the production the plaques found in the brains of Alzheimer’s patients. (v)

Plus, we know that mercury levels in the human placenta correlate with the number of maternal amalgam fillings — and a substantial amount of mercury from amalgams reaches the fetus.

Worse, mercury from dental amalgams in pregnant women may also contribute to development of autism in their children. In one study, mothers of 94 autistic children had statistically more amalgam fillings during pregnancy than 49 mothers of healthy kids. (vi)
In contrast to their higher mercury exposure during pregnancy, these autistic children had reduced mercury levels in their first haircut (mercury exposure can be measured in human hair). This may reflect a reduced capacity to excrete mercury from their body, which in turn may lead to elevated brain mercury levels.

And approximately 20 percent of the general public may experience sub-clinical central nervous system and/or kidney function impairment due to amalgam fillings.
When taken collectively, the research forces us to question the safety of dental amalgams. In my view, there is no doubt about it … they are a danger.

But before you start yanking out your fillings, there is something else to consider …

Genetic Variations in the Ability to Detoxify
Some of us are very good at detoxifying mercury and other toxins, while some of us store toxins like a toxic waste dump. Genetic variations (called polymorphisms) make some people more prone to metal toxicity.

One gene in particular is very important because it’s related to the body’s production of glutathione, our most powerful detoxifier and antioxidant. Your body can only excrete mercury when it’s bound with glutathione.

The polymorphism of the gene that controls the enzyme glutathione-S-transferase (GSST) prevents excretion of mercury. That is the gene problem I have that led to my mercury toxicity. When that happens, the mercury stays in tissues and does damage. Plus, mercury also binds to key enzymes that help us produce glutathione — in effect helping itself accumulate in our bodies.

Research also shows that people suffering from symptoms like fatigue, irritability, mood disorders, poor concentration, headaches, and insomnia due to their amalgam fillings are more likely than their peers to have the apolipoprotein E 4 (ApoE 4) gene. (vii)
ApoE 4 is known as the “Alzheimer’s gene.” It also promotes heart disease. ApoE 4 reduces detoxifying activity. This means that people with this gene can’t get rid of mercury from their brains, contributing to its toxic effects on this organ.

I know this all sounds very depressing. And it is. But the good news is that there are things you can do to reduce your exposure — and identify if you have toxic levels of mercury. So let me sum up what we learned in this week’s blog and offer some suggestions for reducing your exposure.

10 Truths and Tips about Mercury Toxicity
1. Industrial exposure to mercury is significant and mostly comes from coal burning (220 million pounds a year) and chlor-alkali plants.
2. The main ways that humans are exposed to mercury are from contaminated fish and dental amalgams or silver fillings.
3. Mercury can affect nearly all your organs, especially the brain, heart, kidneys, and gut.
4. Many chronic diseases may be caused or worsened by mercury, including neurologic disease, ADHD, autism, heart disease, autoimmune diseases, and more.
5. Some of us are genetically better adapted to detoxify mercury than others, leading to variable effects within the population.
6. You should reduce your exposure by avoiding large ocean fish (like tuna, swordfish, shark, and tilefish) and river fish. Eat only small wild fish. If it fits in your pan, it is probably okay.
7. Blood tests are relatively worthless for analyzing mercury toxicity, unless you have had a significant recent exposure or eat a lot of sushi or tuna.
8. Hair tests only check for mercury from fish, not from fillings so they only give you a partial picture.
9. The only way to find out your total body load of mercury is to take a medication with sulfur molecules that binds to the mercury like fly paper. This is called DMSA or DMPS.
This test should ONLY be done by a trained physician and involves taking one dose of this medicine, followed by a 6- or 24-hour urine collection to see how much comes out. (In my opinion, the most reliable testing is done by www.doctorsdata.com).
10. If you are toxic and sick, you may consider addressing your dental health by seeing a biological dentist who can safely help you deal with mercury in your mouth.
Going to see a conventional dentist who drills out your fillings without any precautions or protection can lead to serious health consequences. I strongly advise against it. However, amalgam filling removal CAN be done safely and effectively done by a dentist trained in the correct techniques.

That’s all for this week. Next week, I’ll give you more advice on how to safely eliminate the mercury in your body if you find you are toxic. Finding out if you are poisoned by mercury, limiting your exposures, and getting the mercury out of your body is absolutely critical if you want to achieve lifelong vibrant health.

If you would like to read more of the extensive research on the biologic effects of mercury and toxins on human health, please link to this extensive online bibliography. If you have any doubt about the evidence of harm across a broad range of health conditions of mercury, you must do your homework and review the research yourself.

To your good health,
Mark Hyman, M.D.

References
(i) Lindh U. Removal of dental amalgam and other metal alloys supported by antioxidant therapy alleviates symptoms and improves quality of life in patients with amalgam-associated ill health. Neuroendocrinology Letters 2002; 23(5/6):459-482.
(ii) Stejskal V. Metal-specific lymphocytes: biomarkers of sensitivity in man. Neuroendocrinology Letters 1999;20:289-298.
(iii) Sterzl I., et al. Mercury and nickel allergy: Risk factors in fatigue and autoimmunity. Neuroendocrinology Letters. 1999; 20: 221-228.
(iv) Prochazkova, J., et al. The beneficial effect of amalgam replacement on health in patients with autoimmunity. Neuroendocrinology Letters. 2004; 25(3): 211-218.
(v) Stejskal, J. and Stejskal, V. The role of metals in autoimmunity and the link to neuroendocrinology. Neuroendocrinology Letters. 1999; 20: 351-364.
(vi) Holmes, A.S., et al. Reduced levels of mercury in first baby haircuts of autistic children. International Journal of Toxicology. 2003. 22(4): 277-285.
(vii) Wojcik, D.P. et al. Mercury toxicity presenting as chronic fatigue, memory impairment, and depression: Diagnosis, treatment, susceptibility, and outcomes in a New Zealand practice setting (1994-2006). 2006. Neuroendocrinology Letters. 27(4): 415-423.