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TV personality Dr. “Drew” Pinsky is SORELY misinformed about desiccated thyroid!

YOU GOT IT WRONG DR. DREW!Note: though this STTM blog post will be mentioning a US presidential candidate, we will NOT approve comments that make political comments in any form.  We DO invite you to comment about the problem of medical professionals like Dr. Drew Pinsky being completely ignorant about the efficacy of Natural Desiccated Thyroid! SPEAK YOUR MIND!!

Recently, Dr. David Andrew “Drew” Pinsky (also known in the media as Dr. Drew) while being interviewed on KABC’s “McIntyre in the Morning,” made a ridiculously misinformed comment about the fact that Presidential candidate Hillary Clinton is on natural desiccated thyroid to treat her thyroid condition.1

The Washington Times stated that Dr. Drew and another doctor came to some “startling conclusions“ and were “gravely concerned“. The Times quoted Dr. Drew as saying

“Both of us concluded that if we were providing the care that she was receiving, we’d be ashamed to show up in a doctor’s lounge. We’d be laughed out,” he added. “She’s receiving sort-of 1950-level care by our evaluation.”

The article narrowed it down with this quote from Dr. Drew:

“She also has hypothyroidism, and she’d been treated for hypothyroidism with something called Armour Thyroid, which is very unconventional and something that we used to use back in the ‘60s,” Dr. Drew said. “And by the way, wow, Armour Thyroid sometimes has some weird side effects.”

Here are SIX REASONS Dr. Pinsky is exactly the kind of doctor that informed thyroid patients report avoiding like the plague

1) To the contrary to what Dr. Drew stated, this so-called “unnconventional” medication from “back in the 60’s” was being used on thyroid patients starting in the 1890s…and was clearly successful for six DECADES as the primary treatment for hypothyroidism, and as medical reports reveal.

2) This so-called “unconventional medication” was only substituted with Synthroid starting in the 1960’s (which is synthetic and only ONE of FIVE thyroid hormones) because money-eyed Knoll Pharmaceuticals promoted it as a way to make moola….and doctors stupidly fell for it. See Chapter 1 and 2 in the revised STTM book for verified history about the introduction of Synthroid followed by the successful use of NDT for decades.

3) The “conventional medication” of using only one of five thyroid hormones (aka Synthroid, Levoxyl, Levothyroxine, etc) has caused a multitude of problems for thyroid patients for over 50 years, as they have reported. The body does NOT force us to live for a storage hormone alone. Read //www.stopthethyroidmadness.com/t4-only-meds-dont-work  i.e. the use of Synthroid, Levoxyl and Levothyroxine has been the treatment producing “grave concerns” for too many patients. 

4) Natural Desiccated Thyroid has changed lives ten-fold, report patients who started back on it around the turn of the 21st century! The results have been clearly superior to T4-only for all-too-many thyroid patients. Read //www.stopthethyroidmadness.com/natural-thyroid-101

5) Any “weird side effects” from Natural Desiccated Thyroid has explainable and correctible reasons for most of us, ranging from misinformed doctors using the lousy TSH lab test to dose by, to keeping patients on low doses far too long, to the fact that NDT will reveal either inadequate iron levels or cortisol issue (the latter two which by the way, Dr. Drew, are due to the lousy and inadequate treatment with T4-only for most). Study this: //www.stopthethyroidmadness.com/ndt-doesnt-work-for-me

6) As far as Dr. Drew’s comment about being laughed out of the doctors lounge….that is exactly why informed patients are disgusted with, have so little respect for, feel immense frustration by, and run as fast as they can from doctors who would do that.  

All of YOU are the reason we are yelling “Stop the Thyroid Madness!”

Thyroid patients worldwide are sick and tired of the robotic way medical practitioners worship the TSH lab test, the complete and biased ignorance many have about Natural Desiccated Thyroid or even T3 in one’s treatment, the blindness to obvious clinical symptoms of a poor treatment with T4, and the failure to understand how a healthy thyroid works and why!

It’s NOT about a “conventional” storage hormone alone any more than it’s simply about a pituitary hormone!

To Doctors: LISTEN TO THYROID PATIENTS! OPEN YOUR MINDS!

We are not brainless little peons who walk into your offices: we do live in our own bodies and thus have some wisdom about what works and what does NOT; we DO know that our lives have changed thanks to Natural Desiccated Thyroid and going by the free T3 and free T4, NOT the TSH. //www.stopthethyroidmadness.com/things-we-have-learned

To Thyroid Patients: WANT TO TELL DR. DREW HE’S WRONG ABOUT NDT??

Go here: https://www.facebook.com/drdrew/ Also share this link to this blog post: //www.stopthethyroidmadness.com/2016/08/18/tv-personality-dr-drew-pinsky-sorely-misinformed-desiccated-thyroid/

 JanieSignature SEIZE THE WISDOM

 

 

 

 

 

REMINDER: Note: though this STTM blog post mentions a US presidential candidate, we will NOT approve comments that make political comments in any form.  We DO invite you to comment about the problem of medical professionals like Dr. Pinsky being completely ignorant about the efficacy of Natural Desiccated Thyroid! Speak your mind!!

  1. http://www.washingtontimes.com/news/2016/aug/18/dr-drew-pinsky-gravely-concerned-about-hillary-cli/

STTM graphic HEY DR. DREW....

Janie: The High Copper Detox Queen

Even though this Stop the Thyroid Madness blog, website and the books pertain to thyroid patients and their issues, it’s been observed that many thyroid patients have also found themselves with high copper, whether from low zinc due to illness, the MTHFR or other methyl mutations, chronic high stress, mold exposure (which can tank zinc), high estrogen, the use of a copper IUD, or other causes.

I am one who found myself with high copper. 

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My story

Looking back, I’m fairly certain my high copper was manifesting itself in Fall of 2014 by suddenly developing very weird iron labs. My serum iron plummeted from 103 down to 55 in just one week of high physical activity. Huh?? I’d get it back up, then down it would fall.

Turns out that high heavy metals can mess with your iron levels–others might see low ferritin with high iron. I also started to notice movement headaches in the Fall of 2014, and I’m not a headache person, so that was new. In October of 2014, I did hair testing and though copper was midrange, It should not have even been mid-range, but I didn’t understand the significance.

In early 2015, I was seeing my hair come out in clumps, yet I had gotten my iron back up once again. Finally in March of 2015, I was noticing I had ruminating negative thoughts--not at all like me!! What the heck was this about??

How my labs revealed a copper problem

First, the clue that a problem was brewing was shown in October 2014, but I didn’t understand the significance. i.e. it was the metals hair testing, called an HTMA, showing Copper was going up at 23 (11-37). This is the one I ordered and did: https://www.directlabs.com/sttm/OrderTests.aspx

By April of 2015, my symptoms were so horrible in my BRAIN that I did serum testing of copper and zinc. And there it was: high copper, relatively low serum zinc–they have a see-saw relationship! Another important test is hair testing, also  since not everyone is lucky with blood testing as I was. Finally, a good indication is high calcium, which I had and is called the calcium shell, but didn’t know the connection to high copper!

Additionally, a Calcium result was SUPER high 1840 (300-1200) which correlates to rising copper. It’s called a Calcium Shell, meaning a high tissue level that that forms to protect against stress. That should have screamed at me, but I wasn’t informed.

Here are my lab results in April 2015.

Copper, Serum: 1.36 mcg/mL (.75 – 1.45) HIGH
Zinc, Serum: .81 mcg/mL (.66 – 1.10) LOW (And if only I had done the RBC zinc!!)
Ratio: 1.68 (should be .7 – 1.0) TOO HIGH
Ceruloplasmin: 40.5 mg/dL (16 – 45) (this is the protein that binds and carries copper around)

Bound Cu: 121.5, Unbound Cu: 14.5 (optimal unbound Cu: 5-15)
% Unbound Cu: 10.7% (optimal 5-15%)

*** Note that I did serum copper and zinc–some will say it needs to be plasma, but serum confirmed it anyway as did my symptoms. Others recommend Copper RBC and Zinc RBC, and I would now do the RBC zinc, not the serum.

What caused my high copper

I’m fairly certain it was because 2014 was a year of constant and unrelenting high stress, both good and bad. I was editor of the STTM II book, plus had many other things going on in my life–good things, but chronic and stressful. And turns out that chronic high stress can deplete your zinc, which in turn can cause copper to rise.

Additionally, I was recovering from mold inhalation, which left me quite sick the year before. Not only is mold stated to lower zinc, but my immune system was in high gear battling it, and that can also tank nutrients like zinc. (You will see later in this article that only in 2017 did I discover my RBC zinc was BELOW range)

On top of the stress/mold zinc fact, I was eating a huge amount daily of stevia-sweetened dark chocolate daily as my way of self-comforting myself through the unrelenting stress. And chocolate is high copper! I was unknowingly feeding my internal levels of copper that were destined to climb in the face of my low zinc. 

Additionally, I found out later the next year via hair testing that I had low levels of both manganese and chromium—another inducement of rising copper.  Some literature states that deficient levels of B-vitamins and vitamin C can also promote rising copper levels—I had both deficiencies but didn’t know it at the time.

How I started the detox

This is where there is all sorts of strong opinions in groups, so I had to do careful reading make a decision for myself.

  1. The most important step I took is to get off of all high copper foods. That especially included all the stevia dark chocolate I had been consuming to self-treat stress. Bad mistake when zinc was so low. (I initially left this step off when I created this page, and shouldn’t have. It’s the most most important step!)
  2. I got on Manganese and Molybdenum (not even knowing I was low in both, as I found out later). Manganese is stated to help remove copper, especially from the liver. Molybdenum is stated to bind to copper and greatly facilitates its excretion.
  3. I also got on B-vitamins, especially b6 and zinc to start detoxing. But I had to learn the hard way that the b’s heightened the speed of my detoxing (and fatigue misery) and I had to take MUCH lower amounts. I may be a fast metabolizer.
  4. Some will say take no zinc whatsoever, but my experience is that low levels were fine.
  5. I was also taking curcumin and astaxanthin for inflammation
  6. To support my liver and kidneys (the detoxing glands), I used Milk Thistle (but use iron with it–it can lower iron levels) plus Dandelion Root, plus Swanson’s Kidney glandular. P.S.  I also detoxed a second time starting June, 2016)

My detoxing experience

I started detoxing in late April 2015, and it ended on its own by October 2015. And frankly for ME (though it may not be this bad for you), it was absolutely miserable with fatigue and weakness. I was completely exhausted the entire time in an extreme way–much worse than I read in others.

BUT, I later figured out that for whatever reason, I wasn’t breaking down carbs well to give me energy to endure the detox. And the latter was due to the fact that my pancreas wasn’t releasing enough of the enzyme called amylase which breaks down starches and carbs for energy! My situation was probably rare.  

But one thing did help back then before I knew about my low-amylase caused low energy: CoQ10! I got on 1500 mg liquid Ubiquinol daily. That did help! Because all the stress I was going through at the time also caused super high Succinate, Fumarate, Malate and a-ketoglutarate in my urine as revealed by an Organic Acids Test (OAT)–implying I had an energy metabolism disorder.

Ironically, though my body stopped detoxing on its own as I neared six months, and though my serum zinc levels were fabulous now, my serum copper was still a little too high. But I redid hair testing, and things were good enough there in my mind i.e. 16 (11 – 37). That was far better than the previous mid-range of 23—and which I have no doubt got MUCH higher before I caught it all (In hindsite, I found out my  probably should have detoxed more. That came in 2016) 

Did the high copper affect my emotions and brain?

It sure did. I had movement headaches in late 2014 before I ever knew about my rising copper i.e. if I bent down to pick up something, there it was. Right before I started to detox the first time in April 2015, and when my copper had to be sky high, I noticed I had ruminating fearful negative thoughts. My brain must have been loaded with copper by then, as copper is a known neurotoxin. The second time around in 2016, and as I was entering the third month of detoxing, I noticed depression was creeping in, irritability, impatience. I can imagine that the latter is related to the copper moving around to be released.

Did the high copper and especially the detox effect my thyroid?

Yup. It sent my reverse T3 (RT3) up, which is probably due to the inflammation levels it pushed up. I had to be on mostly T3 instead of the natural desiccated thyroid (NDT) I had been on.

Was I able to keep my copper levels down after detoxing?

Unfortunately, no. There was evidence that it went back up. Because in the Spring of 2016, I was seeing more hair loss than normal again, yet my iron was great. No, I didn’t have the movement headaches or the ruminating negative thoughts like I did the year before, but the hair loss was a sign. Then at the beginning of June 2016, my body started detoxing copper again! I wasn’t trying to do so–it happened from taking phospholipids, known to help heal the mitochondria (of which I had a problem as revealed by the Organic Acids Test and symptoms–not everyone does). But it turns out that phospholipids induce detoxing! So here I was, once again detoxing copper with the exact same symptoms I had in 2015–copper-colored stools, adrenal stress, fatigue. It all lasted nearly 6 months again. The two phospholipids were NT Factor and Body Bio–one in the morning and one in the evening. Some just use NT Factor.

Then it happened again in 2017, but luckily only a month. And you know what started the detox this time? Trying out 10 mg of lithium instead of 5. I was using low dose lithium to help get B12 to my cells better.

And then, again in April 2018–very strongly as revealed by the stools and fatigue. But this time, I was prepared, and taking many adrenal-calming supplements helped a lot in that area. I also went back up on my ubiquinol.

Why the continual copper detoxing? One clue is the excessively high amount I had–some literature says it can take a few years to get it all out. That seems true to my experience.

What did 2017 reveal about my zinc?

All through 2015 and 2016, I was always doing serum zinc labs. In April of 2015, when I first understood I had a serious Copper problem, it was LOW:  .81 (.7-1.10). I got it towards the top of the range by the end of 2015, and did so in 2016 and worked to maintain that. 

But in the Fall 2017, I did an RBC zinc instead of serum: BELOW RANGE. RBC stands for red blood cells. Seeing BELOW range threw me against the wall in shock: I may have had below range RBC zinc ALL this time. No wonder I had a copper problem!! I was already on 30 mg zinc, and I went to 80mg zinc. THAT is one way we can all control our levels of zinc–keep it up!

What about the MTHFR mutation in all this?

Since the MTHFR mutation can contribute to high heavy metals, there is a question if my single 1298 heterozygous mutation may have contributed, or my other methyl mutations like COMT.  I’ve seen that happen to others. So just in case, I stay on folate plus other B vitamins. 

What are surprises I had during the entire high copper journey?

My biggest one was finding out that not only did I have high copper, I also had high lead (though not as high as the copper). Both were revealed by the hair testing I did in 2014…and both came down after those six months of detoxing in 2015 as also revealed by another hair test.

The second surprise was discovering that copper detoxing (or high copper) can cause SIBO, Small Intestinal Bacterial Overgrowth. Have never had gut problems in my life, then found myself with SIBO that I had to treat. (Turns out SIBO can happen due to a poor release of bile from the gallbladder!) The third surprise was that I started to detox again in 2016 by accident!

And the final surprise?? Finding out why this may have all happened in the first place. My RBC zinc was BELOW range in 2017, that means it had to have been horridly low by 2014—-all due to my immune system in high gear in 2013 due to mold poisoning. Immune systems need a lot of nutrients to be effective.

Copper-color stools when detoxing–really??

Absolutely! It happened when I detoxed for six months in 2015 (and went away once my body stopped), happened exactly again when I started to detox in 2016, and happened in 2017 and 2018 for shorter, but still challenging, detoxes.

If I could change/improve anything about my high copper experience, as well as detoxing, what would that be?

  1. I find the biggest emphasis should be on supporting your natural detox organs like the liver, kidneys and skin. If you do a sauna to sweat out the metals, it’s the skin helping you. But I tended to support my liver (Milk Thistle for one) and kidneys (Swanson Kidney Extract twice a day) during the second round of detox. Why? Because I tend to naturally detox with the elimination organs!
  2. I find it quite important to take key antioxidants when detoxing like Astaxanthin, Grape Seed Extract, Vit. C and E, etc. I didn’t get into that well enough the first time around and regret it, so I did much better using them the second time around.
  3. It’s going to be quite important to find out if you have the MTHFR mutation causing high heavy metals and treat it. I don’t think this was my cause, but it would be for you, especially if you have the 677 MTHFR mutation. 
  4. With what I know now, I would be on high amounts of CoQ10 (ubiquinol, not ubiquinone) while detoxing to support my mitochondria. I did that for the second detox and felt a little better. But you may not have the energy metabolism issues I had as discovered via the Organic Acids Test. I also discovered via a stool test that I have an intermediate level of carbs in my stool–a carbohydrate metabolism disorder. I don’t uptake carbs well for energy! No wonder I was so exhausted with detoxing!
  5. I should have been on glutathione…a master antioxidant in your body. It was used up by all this detoxing and exposure to toxins, and I didn’t even find THAT out until January of 2019. UGH. I used infusions to get it up. No wonder I noticed myself aging quicker!

Did detoxing effect my adrenals in any way?

Boy did it. Detoxing heavy metals can be a huge stress on one’s adrenals! Now understand that I did NOT have an adrenal issue before I started detoxing. So at the beginning of detoxing, I didn’t even think about it. But as it continued, it became clear that my cortisol was shooting high. I started to have sleep issues through the night. I felt shaky in the morning (adrenal excess can go with high cortisol just as it can with low). And around dinner time later in my detoxing, I had the internal buzzing feeling that can go with a cortisol issue.

The second six month detox I went through brought on high cortisol again–sleep issues, morning adrenaline and shakiness, evening same. What was effective for me was to take Holy Basil in the morning, again in the late afternoon if I noticed symptoms, and before bed. A side note: during the second detox, and after 4-5 weeks of my mitochondrial treatment with high-dose CoQ10 and B-vitamins, and my cortisol issue mostly went away. I also learned to take supportive adrenal supplements like Taurine, GABA, holy basil, ashwagandha, rhodiola….etc. 

Want to know if your adrenals are being affected? You can order your own saliva cortisol test here. 

Other bits of info

  1. Once I start detoxing, my body is simply going to continue it on its own no matter what. I must be a super detoxer.
  2. If there is excess fatigue with detoxing, look at your mitochondrial function via an Organic Acid Test (OAT). I am thinking my mito were functioning less than optimal before my 2015 detox, and the detox plus the SIBO plus a yeast infection from hell….ruined my mito. I took a very high dose of CoQ10, and added in NADH, along with the other supplements that the OAT told me about. 
  3. I got a lot of good information from these websites: http://www.drlwilson.com/articles/copper_toxicity_syndrome.htm and http://www.coppertoxic.com/
  4. Use your best judgment after reading several sources. Be wise within any copper groups, as you will have to sift through strong opinion vs valid information and decide what fits you.
  5. This is the hair testing I have used twice, also called HTMA, and I will use it again to keep track of where my metals are: https://www.directlabs.com/sttm/OrderTests.aspx (3rd test down)
  6. Testing via blood should always be copper, RBC zinc and ceruloplasmin at the least (ceruloplasmin is the major copper-carrying protein). If ceruloplasmin is quite low or below range, might want to explore Wilson’s disease.
  7. It’s rare, but there are some who might have Wilson’s disease, which is an autosomal recessive inherited disorder. It causes accumulation of copper in major organs like your liver (failure to filter it out), brain, and more. www.wilsonsdisease.org/  That was not my cause, but you should read about it, just in case. 
  8. About zinc and how it can be depleted: http://drlwilson.com/Articles/ZINC.htm
  9. TEST YOUR RBC zinc!!
  10. About ceruloplasmin: http://www.clinchem.org/content/51/8/1558.full
  11. Since high levels of copper is usually in the unavailable unbound form, you might see problems with yeast/candida.
  12. Also going hand-in-hand with high copper is high calcium, called the “calcium shell”. With that high calcium can be lack of emotion/apathy.
  13. High copper can also cause excess fears or anxieties. Detoxing may create some of the same. That happened to me. Could also be related to the adrenal stress it all causes.
  14. You will see ceruloplasmin mentioned on key copper websites–the major copper-carrying protein. Some will state that the lower it is, the quicker copper will build up in your liver and brain. Janie had high ceruloplasmin and still an obvious brain buildup! Just to show that there can be exceptions to the rule, it seems.
  15. If you want to work with a doctor, find one who is open-minded about hair testing aka HTMA. But you may be lucky and the blood testing shows the problem anyway along with symptoms. Want to order your own HTMA?? You can! Go to the following page, scroll down and click on the DIRECT LABS icon, and the hair test is the 3rd one down: www.stopthethyroidmadness.com/recommended-labwork
  16. Copper IUD’s have caused many women problems with rising copper levels! That can especially be true if you have the MTHFR mutation or even high stress. 
  17. It’s stated that vegetarians have a high risk of becoming copper toxic.
  18. Foods high in copper include chocolate (darn it), avocados (darn it again) molasses, liver, oysters, shrimp, mushrooms, sesame or sunflower seeds, cashews, etc. A more comprehensive list is here.

PLEASE WORK WITH AN INFORMED DOCTOR IF YOU CAN FIND ONE.

If you found yourself with high copper, let us know your story by commenting below!

UPDATE FROM JANIE, late NOVEMBER 2016

Here is what I got down to in Sept. 2015 when I suddenly stopped detoxing following 5 1/2 months:

COPPER: 1400 (810-1990) (I was 1571 after detoxing two months)
ZINC: 1.09 (.66 – 1.10)
RATIO: 1.0 (you want it to be .7 – 1.0)

And here is where I am in late November 2016, after 5 1/2 months of detoxing high copper once again

COPPER: 1400 (810-1990)
ZINC: 130 ug/dL (60-130)
RATIO: 1.0 (you want it to be .7 – 1.0)

You can see they are nearly identical, each after detoxing 5 1/2 months. Zinc was a different measurement above, but at top of the range, just as last year.

And, with both detoxes:

1) High inflammation
2) High RT3, needing T3-only
3) Massive easy fatigue (I think both detoxes heavily messed with my mitochondria–the powerhouse of energy

Why test RBC levels of certain minerals? Because it’s measuring the intracellular levels in your body, which is even more important than serum levels. What can mess up your cellular levels? Toxic levels of other metals, for one. Those minerals which can have the RBC tested include Zinc, Copper, Potassium, Vanadium, Chromium, Manganese, Potassium, Selenium and Magnesium. The other metals need more then RBC, such as hair testing, i.e. they can be good with RBC, but high in hair. More good info here.

UPDATE FROM JANIE, late NOVEMBER 2018

Looking back, I have figured out that the stress of copper detoxing over the past few years may have contributed to gallbladder problems. The clues? The first one was having SIBO after my first detox in 2015–it’s strongly related to your gallbladder and bile levels. The second? I don’t break down fats well at all anymore. And there are other TMI clues that you can see by researching “symptoms of a sluggish gallbladder”. I have some; not all. But it’s very obvious. So I’m now taking Cholacol by Standard Process to help break down fats and which provides more bile. There are also things to be done to support a sluggish gallbladder, which you can also do an internet search for.

ADDITIONAL READING:

  1. This is a great read about what high copper can do to you: https://healdove.com/alternative-medicine/Hypercupremia-High-Copper And also note in the latter article that high copper can mess with your Glutamate/GABA balance, i.e. resulting in high glutamate levels in your brain (causing inflammation), plus in some, impaired speech, aggressive behavior, intense irritability, anxiety, inflammation of the gastrointestinal tract (GIT), and eventually neuronal destruction.
  2. Great website on the copper issue: https://coppertoxic.com/

 

Read what this Eye Doctor Observed in His T4-only Treated Patients!

Matt Dixon ODThe following Guest Blog Post has been written Matt Dixon, OD who currently practices optometry in Perry, Georgia.

And not only did Dr. Dixon find himself with hypothyroidism, he made quite an interesting observation: 90% of his patients currently taking levothyroxine still have symptoms!

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So how did an optometrist (eye doctor) become passionate and obsessive about spreading the news about what Janie calls the “Madness”?

My personal journey

I don’t quite fit the typical patient profile for a hypothyroid patient.  I’m not female, no weight issues. I’ve always been very active. Yet when the symptoms started, I was clueless about where they came from or that they all could even be related. 

All eye docs are trained to recognize thyroid eye disease, but truthfully, we focus on end-stage symptoms of Grave’s disease and the ophthalmopathy that often comes with it.  And the typical optometrist does not encounter this very often.  I had no clue that in my own practice, hypothyroidism was one of the most common conditions I see. 

I suppose my first symptoms were body aches and pains.  I had always experienced annoying back issues and I presumed that deterioration was setting in as I became older (40’s).  I’ve also always been cold-natured. And by 2010, I noticed that I was struggling to make it through the work day. So by the end of the day, I was exhausted.  In fact, I was no longer exercising, but found myself buried on the couch as soon as I came home, not getting up until I forced myself to climb into bed.  Once I made it to bed, I couldn’t fall asleep and became addicted to Ambien.  When the alarm clock woke me up the next morning, my wife had to literally pull me out of bed.  If I ever forced myself to jog, I felt as if I was carrying a 25 lb. backpack.  I also began to struggle with unexplainable stress and anxiety.  

But what finally prompted me to seek answers was in fact eye-related.  I was driving my kids home one night and the road in front of me actually moved suddenly from left to right.  I hit the brakes and feared for our safety!  My 17 year old son took the wheel and we made it home.

The madness for me began

My physician at the time is a well-liked internist in my community.  I made an appointment for a checkup complete with blood work.  I had some issues that I was concerned about, but neither the assistant nor doctor reviewed my symptoms. 

I went back in a week and promptly received a prescription for Synthroid for hypothyroidism.  With little discussion about the disease, I headed to the pharmacy. After a couple of weeks I began to improve.  But I wanted to know more.  I found the vast list of hypothyroid symptoms online and could not believe how many I was experiencing.  I read enough to know that elimination of symptoms was the best way to dose the medication and focusing on TSH only would lead to under-treatment. 

More importantly, if my doctor did not know any of my symptoms, how could he know when I was adequately treated?  It was time for a new doctor.

Why do MD’s undertreat hypothyroidism?

My new doctor, unlike the previous one mentioned above, did review my symptoms and pledged to increase Synthroid until my TSH was reduced to around 1.  I made sure they were paying attention to how I was feeling.  Yes, I improved tremendously and found my happy place on brand name Synthroid.  But I did move over to natural desiccated thyroid (NDT) and was even happier. As I adjusted to the new medication and found the correct dosage, I was able to get through the day with full energy and better mental focus.  Most days I am symptom free.

In my area, I have yet to find more than a handful of docs who use NDT with any frequency.  In my patient population, I rarely encounter a patient on NDT unless I have coached them to find a way to get the prescription.  (Optometrists are licensed to prescribe oral medications but only for eye conditions) 

Synthroid is the number one prescribed drug in America!

This is no accident and it will not be easy to battle the industry that achieved this coveted ranking.  Doctors clearly have been trained to use synthetic T4-only meds as the treatment of choice, having been convinced that it is highly effective.  Trying to change this at the medical school level will likely never happen.  Attempts to enlighten physicians who are convinced that levothyroxine treatment and normalizing TSH levels is the best care will rarely lead to change.  In fact, general practitioners and internal medicine docs will continue to get it wrong as long as endocrinologists and the American Thyroid Association (ATA) promote Synthroid religiously.  Those who have seen the light, thanks to educators like Janie Bowthrope, will laugh (then cry) when they read the preview from the ATA’s published pocket guidelines http://eguideline.guidelinecentral.com/i/521958-ata-hypothyroidism-pocket-card How could these smart folks be so misinformed and allow patients to suffer?

What can one eye doctor do?

I’ve decided to review residual symptoms with every patient who comes into my office taking any form of hypothyroid medication.  The majority of them have never reviewed such a list!  Occasionally, a patient will not circle a “single symptom”, but more often patients will have “several” symptoms.  I offer a 3-page summary of how hypothyroidism can be properly treated and, of course, I have them google STTM.  After counseling over 100 of these patients (with only one complaint), many have returned to say thank you.  Sadly, most patients get the push back from their MD and will remain on T4-only meds.  I’ve also learned that if a physician has not studied the use of natural desiccated thyroid and is only committed to normalizing TSH, even the patients who convert to NDT may still suffer due to ineffective dosing.

I treat many patients with dry eye syndrome, which is very common and sometimes costly to treat.  I am convinced that treating dry eye syndrome in a patient who is undertreated for hypothyroidism is like trying to change a flat tire on a car that is still moving.  Every eye doctor should take an interest in this disease even if for this reason alone!

What can a patient do?

Refuse to tolerate inadequate treatments.  Be passionate about your own health.  Recognize that very good doctors with good intentions have been misinformed and may be facing tremendous pressure in our rapidly changing healthcare system.  They do not quickly change deeply held beliefs when it comes to recommended treatments.

Study Janie’s recommendations.  Make an effort to help your physician understand.   //www.stopthethyroidmadness.com/doctors-need-to-rethink/  When seeking a new doctor, nurse practitioner, physician’s assistant or osteopath, ask questions before you make an appointment.  And do not assume that a board-certified endocrinologist is any more enlightened about this disease.

Final thoughts

My best analogy in attempting to drive home the importance of optimal treatment of hypothyroidism in my patients is to show them their vision as it would appear through a half-strength pair of glasses.  I ask them if they would be happy to see like this.  I ask them how quickly they would find a new eye doctor who prescribes full-strength glasses.  They get it.  I’m passionate about this disease and the patients who are literally suffering and feel uninvited to shout “I feel like crap!” to a doctor who won’t listen.  Together, we will make a difference.

Matt Dixon, OD

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Dr. Dixon has practiced in Perry and Warner Robins, GA for over 25 years.  He provides comprehensive eye care and frequently counsels patients regarding wellness.  He has written numerous articles on eye disease and the business of optometry.

He is married to Jenna and has 3 children and 2 dogs.  He is an aspiring songwriter and has recorded 2 albums.  Thanks to NDT, he is quickly becoming a CrossFit addict.  www.drmattdixon.com

A Speculative Account of the Effects of Iodine Supplementation at Different Doses

Screen Shot 2016-01-08 at 10.14.42 AMThe following Guest Blog Post was written by Malcolm Maclean, MD of the United Arab Emirates. Dr. Maclean serves as a Trustee and Medical Advisor for TPA (Thyroid Patient Advocacy) UK.

Dr. Maclean makes strong speculative proposals in this article as to why there are differing bodily experiences in the use of iodine and the doses used.

Take the time to read the below slowly and carefully–good points to consider!

NOTE: if you are receiving email notice of this blog post, a reply to the email goes nowhere. Instead, you need to click on the title of the blog post, which will take you directly to the STTM blog, and there you can comment.

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The value of iodine

Most folk in the Thyroid Community understand the requirement for Iodine because the body uses it to synthesize thyroid hormone.

But a variety of cells require iodine for optimum function, as well (e.g. breast, ovaries, pancreas and prostate). So Iodine is important for the body quite apart from supplying the thyroid gland with Iodine. This view is not widely held in the mainstream.

Further, several scientific reports point to widespread iodine deficiency, particularly in the UK and parts of Russia, pointing to the value of Iodine supplementation, at least in some cases.

Yet a problem and a challenge

The capacity of Fluoride and possibly Estrogen Dominance to aggravate dysfunctional Iodine metabolism argue for close attention. Because for those who choose to supplement with Iodine (and there is a strong case for this to prevent breast cancer, plus those diagnosed with Hashimoto’s Disease, see below), the response to such supplementation (based on reported experience of those contributing to Iodine Forums) appears to vary according to:

  1. the baseline Iodine status
  2. the state of the adrenal glands (operating at full strength or in a state of “adrenal insufficiency”?)
  3. whether Companion Nutrients are simultaneously supplemented.
  4. the chosen dose of Iodine
  5. how it is taken (via skin/orally)
  6. the size of the dose
  7. how quickly dosage is introduced

Important Point: For those in the Thyroid Community who have been diagnosed as having Hashimoto’s Disease, Iodine has a reputation for exacerbating Hashimoto’s Disease. However, Iodine may be tolerated provided that the “Companion Nutrients”, referred to above, are in place.

Why are Companion Nutrients important?

Arguably, the adverse effects attributed to Iodine, when used in the situation of Hashimoto’s Disease, are caused by the Iodine-induced, unbalanced and exaggerated activity of the activity of an important and powerful thyroid enzyme: Thyroid Peroxidase, thereby a creating Oxidative Stress and the potential for thyroid cell damage. The Companion Nutrients are designed to support the body’s antioxidant System. Companion Nutrients are used here to prevent damage arising from the unopposed action of Thyroid Peroxidase, as and when Iodine is introduced to the Thyroid Gland, especially in the situation of an inadequate anti-oxidant System.

The purpose of this article

The purpose of this text is to examine the variable experience of those who have reported the effect of supplementing with Iodine and to attempt to explain those experiences according to how the body responds in different metabolic situations. Therefore the purpose is not to influence the reader in any direction (as regards Iodine usage) but to perhaps enable a speculative view of what might happen if/as and when, Iodine is supplemented and why.

I believe that no one should adopt Iodine supplementation without a good deal of reading around the subject, e.g on the STTM and TPAUK websites.

I apologize for the length of this contribution. However, it deals with the complex issue of Iodine effects and it is tricky to give a brief interpretation of this little-understood, but important area, especially for those whose metabolism is out of whack because of the toxic effects of mercury, which has the capacity to damage adrenal, thyroid and methylation function (at least).

So, this text has also been written for those with suspected toxicity (e.g. from dental amalgam) in the hope that the text might explain and emphasize components of the Shade Protocol (designed for the elimination of mercury), which might be ignored by those who, unwisely, are too hasty to get better. 

The right dose of Iodine

I don’t think anyone fully understands what “the right” dose of Iodine is.

If your adrenals are out of whack, Iodine is liable to cause you to crash.

Nor is there agreement on what may be the further results of Iodine supplementation, especially at higher doses.

Some people assert that if you start supplementing with Iodine, two different effects may result, depending on what dose you start at:

Low Dose

Effect: Up-regulation of thyroid synthesis, especially for those who are Iodine deficient (many people are Iodine deficient, so that makes sense). However, if your adrenal function is down, the cells cannot handle the increased levels of stimulation (via thyroid hormone) without a correspondingly elevated level of cortisol.

It is known that thyroid hormone and cortisol work together. Hence, in the situation of adrenal insufficiency (possibly Mercury-induced in the first place, for some) there is the potential for an adrenal failure-induced “Crash” (= feeling dreadful +/- palpitations =”Thyroid toxicity”). So in these two situations… (a] adequate, vs  b]  inadequate adrenal function…taking Iodine may make you feel better or worse

High dose

Effect: Some people report benefit from the introduction of Iodine at a high initial dosage (going against the principle of starting low, increasing slow). This appears not to make sense.

The theory of taking high doses of Iodine

One theory involves acknowledging that Iodine may function as an antioxidant (that Iodine has antioxidant properties, is accepted, although, perhaps not widely so).  The theory goes: Iodine exerts its antioxidant properties but only noticeably at higher doses.

Further, so the theory goes, that antioxidant effect at higher doses tends to overcome the blockage of adrenal function that is creating impaired adrenal function in the first place. Meaning: Low cortisol synthesis and low cortisol levels, because of Mercury blocking cortisol Synthesis by exerting stress on the anti-oxidant system (Iodine usage here, supporting the anti-oxidant system and opposing Mercury).

That too makes a certain amount of sense, because Mercury is known to be able to block cortisol synthesis by acting as an oxidant and exerting stress on the anti-oxidant system.

Speculatively, once your Iodine dosage has (according to this scenario) restored adrenal function by opposing Mercury effects, any further increase may start to be counter-productive (meaning onset of Iodine overdose).

Speculatively, according to dosage therefore, these situations may result sequentially:

1. Baseline: Iodine deficiency in the diet.

Sub-optimal thyroid function with, perhaps, symptoms of Hypothyroidism.

2. Addition of Iodine at low dosage

a) Improves you if adrenal function is adequate
b) Crashes you if you have adrenal insufficiency

3. Addition of Iodine at high dosage

a) Bypasses the “Crash” effects
b) Remits the oxidative stress which is causing the (Mercury-induced) adrenal Insufficiency (with knock-on low Cortisol levels), enables the adrenals to restore Cortisol synthesis:

Result?  Feeling better

4. Supra-Optimal Iodine Dosage

Meaning: even higher dosage than that necessary to restore adrenal function and Cortisol levels:

Speculatively: Iodine Toxicity

Result: You start to feel down again.

Speculative summary of Iodine effects according to dosage

Starting at a “Low” baseline level (Iodine Deficient status) and from there, increasing daily dosage: Feels down-> Take more Iodine-> Feels better->Increase Iodine dosage. More iodine-> Feels worse-> Increase Iodine dosage. More Iodine->Feels better-> Increase Iodine dosage even further: feels worse

This is all theory and is provided for the benefit of those who speculate about what effects Iodine may have.

In preparing the description of this speculative scenario, I am indebted to the contribution (of a lawyer) to an Iodine Forum, who wrote interestingly on this topic as follows:

“Okay. This all-theoretical, mind you, but based on my experience, I think my theory may be correct. At lower doses of iodine, many of the symptoms labeled as bromide detox are identical to adrenal fatigue symptoms: air hunger, low blood sugar, weight gain, headaches, dizziness, fatigue, insomnia, anxiety, palpitations, etc. Another coincidence: the very things that Brownstein etc. recommend for bromide detox are actually things used to alleviate adrenal fatigue: Vitamin C, salt… This may explain many of the symptoms of detox at lower doses. It’s actually adrenal fatigue. Now, iodine can also act as an antioxidant, but only when the body uses excess iodine to make a lipid called delta-iodolactone. But the body will not make this unless it is such a high dose of iodine that the body feels confident that it has enough iodine for its basic needs, so it can use the excess iodine to make this antioxidant lipid. This antioxidant is like 300x more powerful than Vitamin C. I think that you have to take upwards of 100mg of iodine or higher for the body to make this. Because when I take 25mg, I have horrible detox symptoms, but when I take 100mg of iodine I feel normal. I think that at 100mg and up, the body makes delta-iodolactone, and this [is an] antioxidant . It’s the only thing that can account for the fact that people, who can’t take 25mgs without getting sick, can take 150mg without a problem. And there have been about 10 of us who have found this to be true”

The only difference between the lawyer’s interpretation of Iodine effect (at high dosage) and my interpretation:

My interpretation is that at high Iodine dosage, that strong antioxidant effect kicks in, thereby enabling Iodine to resurrect the adrenals (and thus cortisol levels) by opposing the strong oxidant and toxic effects of Mercury. The evidence for this speculation?  At high concentration, iodine appears to tighten up the mitochondrial membrane, thereby preventing leakage of cytochrome C from the mitochondria, across the mitochondrial membrane into the cytosol (cytoplasm).

Result? Less  in the cytosol diminishes oxidative processes in the cytosol.

Result? Less risk of the negative consequences of oxidative stress.

Result? Restoration of the important enzymes which have been suppressed by oxidative stress.

Result? Recovery of 17-Hydroxylase, 5′ Deiodinase, and Methionine Synthase, thereby contributing to the recovery of adrenal, thyroid and Methylation function respectively.

There are those, including myself, who attribute their thyroid & adrenal failure to Mercury toxicity (from dental amalgam). Importantly, this interpretation of Iodine effects draws attention to and emphasizes the importance of supplements described in the Shade Protocol (designed for the elimination of Mercury) and also described as the “Companion Nutrients” in “Iodine Context”.

To summarize: Iodine supplementation is a tricky area. Extensive reading prior to any usage is advised. Adrenal function should be good and the Companion Nutrients should be in place as supplements before embarking. Potential effects of Iodine at different doses have been speculatively described. Getting the right dose is especially tricky and there appears to be no way of knowing what is the right dose without just trying and seeing. Few would argue against a daily dosage of Iodine: one milligram per day, properly supported, as described above.

Further, importantly, this text is not a recommendation to start taking Iodine at massive doses, despite the fact that some report benefit from this approach. The reason for such caution is, as usual, that our metabolisms are all different.

Dr. Malcolm Maclean

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** Our “metabolism” as thyroid patients is an important topic. And Janie A. Bowthorpe, M.Ed. is one of several who were asked to speak on this important topic. Register for the METABOLISM SUMMIT which starts February 1st right on your computer. Go here to register: https://tinyurl.com/jp9yx78

** Read the #1 thyroid information anywhere via the revised STTM book and the new STTM II book–the latter totally written by practitioners. //www.laughinggrapepublishing.com

 

 

Read the mind-shattering realization by thyroid patients about what T4-only did to their hearts!

Screen Shot 2014-06-16 at 9.54.22 PMWhen my mother was in her 60’s, she had to have a heart procedure. It was scary. And at the time, I found it all very odd. There is no reported history in any of my ancestors of heart problems! Where did this anomaly come from?

It was only years later than I knew: her 30 odd years of T4-only use, which in her case was Synthroid. Not only did being on T4-only cause a daily need to nap, she was also totally dependent on antidepressants (which in turn made her emotionally flat) and she always had a weight problem. And, it caused high cholesterol and heart issues!

Today, patients realize that connection between their T4-use and heart-related problems. Here is what thyroid patient Carla sent me as one of many examples of a relationship between heart problems and being either hypothyroid or on a poor treatment with T4:

I had been on Synthroid for 12 1/2 years when I began to see certain problems coming along and getting worse. For one, my heartrate seemed to be rising. There were even times I literally felt like it was going to jump out of chest. Then there were chest pains. I just knew I was going to be one of those female heart attack statistics. I went to my family doctor, an Endocrinologist and a cardiologist. Hated driving in traffic to get to the cardiologist. But I got a fancy diagnosis of Supraventricular tachycardia (SVT) and worried myself to death.  Beta blockers were on the menu.

Fast forward, I found Stop the Thyroid Madness and then the FTPO forums, and convinced my doctor to start me on Natural Desiccated Thyroid and let me raise it to find the right amount for me. She was super worried about my heart in using NDT. I wasn’t because I had read how others had safely used it, and I followed my raises carefully. And I was right. My heartrate became normal! Normal!! I luckily didn’t have adrenal fatigue. 

I think back about all those years on Synthroid and realized that I had been seeing other problems almost from the beginning! I had depression. I had low iron. Minerals low. And I had doctors who dismissed me. And of course, I was a TSH disaster. TSH was normal; I was not. Year after year. Then I progress into heart problems? The makers of T4-only should be ashamed. 

And there are plenty of studies underscoring a connection between being hypothyroidism and heart issues:

  1. This abstract of the study underscores honestly that “restoration of normal thyroid function most often reverses the abnormal cardiovascular hemodynamics.” Cardiovascular involvement in General Medical Conditions: Thyroid Disease and the Heart
  2. This study outright admits that “Long-term levothyroxine treatment in young adults with congenital hypothyroidism is associated with impaired diastolic function and exercise capacity and increased intima-media thickness”  Long-Term Cardiovascular Effects of Levothyroxine Therapy in Young Adults with Congenital Hypothyroidism from The Journal Clinical Endocrinolgy Metabolism,
  3. This study states that “subclinical hypothyroidism is associated with impaired left ventricular diastolic function at rest, systolic dysfunction on effort, and enhanced risk for atherosclerosis and myocardial infarction.” Whoa. And continued hypothyroidism is what all-too-many thyroid patients report from being on T4-only Effects of Subclinical Thyroid Dysfunction on the Heart from Annals of Internal Medicine
  4. This one has always blown us away. It’s called Low-T3 Syndrome; A Strong Prognostic Predictor of Death in Patients With Heart Disease and underscores why the thyroid hormone T3 is so very important for one’s heart. Natural Desiccated Thyroid, just like a healthy thyroid, provides direct T3!

And there are many, many, many more studies showing the connection between heart problems and hypothyroidism. And eventually, we might see these studies catch up even better about the connection between T4-only and heart problems. The body is not meant to live for one of five thyroid hormones alone.

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Do you have a success story to share about how having T3 in your treatment reversed your heart problems. Use the STTM Contact form to let Janie know you want to send YOUR story and we’ll include it here!

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* Read more about T3 and your heart health!

* Did you know that those who had their thyroid removed due to cancer CAN be on NDT?

* Have reactivated Epstein Barr Virus? Janie has an ebook you can order to read about it.

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* OOPS!! Erfa Thyroid NDT has caused a return of hypo symptoms in many patients!! Something is very wrong!