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15 Things which Thyroid Patients should teach their Doctors

Screen Shot 2015-08-07 at 4.28.31 PMMany thyroid patients will tell you they have, or have had, doctors they love! I, Janie, have had many of them.

But it doesn’t take away from the fact that those in a medical profession have been sorely lacking for decades about correct knowledge on how to diagnose and treat hypothyroidism or Hashimotos, besides have inappropriate familiarity about all the issues related to being hypothyroid. Even their knowledge on how to correctly read labwork has been lazy.

Because of that poverty of correct knowledge, patients were forced to take the bull by the horns and figure things out for themselves! Stop the Thyroid Madness, the flagship of “patient experiences and wisdom”, represents all that wisdom!

Here are 15 things that any thyroid patient not only has to learn, but needs to teach any medical practitioner the best way they know how:

1) My fatigue and weight gain is not simply because I need to exercise more and eat less.

Granted, we know that exercise and how we eat is important! But being undiagnosed hypothyroid, or poorly treated due to Synthroid or any other T4-only medication, or being held to the TSH, keeps many of us with a low metabolism. The latter results in very easy weight gain, or the failure to do the kind of exercise which would help us!

2) Depression is strongly related to continued hypothyroidism!

We know there can be a variety of reasons for depression, but for most thyroid patients, our depression is a sure sign that we are either undiagnosed due to the lousy TSH lab test, or undertreated due to being on only one of five thyroid hormones like T4-only, or being held hostage to the TSH, a pituitary hormone.

3) The TSH lab test has been a failure for too many years.  

Yes, though a seriously low TSH can detect if we have hypopituitary, for most of us, we’ve had a “normal” TSH yet obvious hypothyroid symptoms. Additionally, when we are optimally treated on Natural Desiccated Thyroid, T4/T3 or T3-only, our TSH lab test is always below range without one hint of bone loss or heart problems. We want to go by the free T3 and free T4, plus symptom removal and a good heartrate and blood pressure instead. //www.stopthethyroidmadness.com/tsh-why-its-useless

4) To figure out if I have Hashimotos,  BOTH antibodies labs need to be tested, not just one. 

To detect if we have the autoimmune version of thyroid problems, patients saw right away that one antibody could be high, but the other one not.  So we need both the anti-peroxidase AND the anti-thyroglobulin lab tests. And by the way, many Hashi’s patients soar on Natural Desiccated Thyroid if they raise it correctly. See #5.

5) Natural Desiccated Thyroid (NDT) has been changing patient lives for years now, just as it did for decades before Synthroid hit the market. 

Though some patients do better on T4-only meds than others…at first..there is simply too many reported experiences by patients for 15+ years that it’s not the way to go. And those same reports show that being on the five hormones that NDT gives makes much more sense.  Even adding synthetic T3 to synthetic T4 has produced better results.

6) I can’t wait six weeks before having a raise!

Thyroid patients found out the hard way that if they stay on a starting dose of NDT (which is usually one grain) longer than a few weeks, the feedback loop causes hypothyroidism to come back with a vengeance in some way or another. So we raise every two weeks and start slowing those raises in the two grain area or close to three to start finding our optimal dose. //www.stopthethyroidmadness.com/natural-thyroid-101

7) My lab results are not about being in the “normal” range.

This was a huge discovery by informed thyroid patients as they kept observing each others lab results for years: it’s about “where” the lab result falls that tells the story…not just because it falls in a suspicious “normal” range based on the testing participants the lab facility chose. //www.stopthethyroidmadness.com/lab-values

8) If I react poorly to NDT, it’s not because NDT isn’t right for me. 

Patients who have had problems with NDT found out that there are five correctible reasons for most of them:  a) being kept on lower doses far too long b) not raising high enough because of being held to the TSH range c) having low iron d) having a cortisol problem 5) having Lyme. This page explains: //www.stopthethyroidmadness.com/ndt-doesnt-work-for-me

9) Yes, there really is such a thing as adrenal fatigue/adrenal insufficiency/hypocortisolism.

Easily more than 50% of thyroid patients end up with a cortisol problem, either due to being undiagnosed for years thanks to the use of the faulty TSH lab test, or being put on only one of five thyroid hormones–T4. And to learn more about it, one of your doctor’s own colleagues has written a brilliant chapter as to biologically why we get low cortisol, found in the Stop the Thyroid Madness II book, chapter 15. And this:  //www.stopthethyroidmadness.com/adrenal-info

10) Saliva testing for cortisol is far more accurate than blood testing

Saliva is said to be testing one’s cellular levels of cortisol, plus it does so at four key times during a 24-hour period, which is important to know. And patients found that the results (from reputable companies) fit their symptoms! Whereas blood cortisol testing is measuring both bound and unbound cortisol, and most of the time does NOT fit the symptoms, showing high cortisol when we are really low, or vice versa. //www.stopthethyroidmadness.com/adrenal-info

11) If some or most of my saliva cortisol results are low, there are safe and effective ways to treat it. 

The adrenal area is one which thyroid patients took great time and care to learn, based on what we read from experts, plus our repeated experiences and wisdom. This is where our doctor, need to be open-minded enough to learn from Stop the Thyroid Madness, both on the website and in the revised STTM book, chapters 5 and 6.

12) If I have acid reflux or stomach problems, it’s usually due to low stomach acid caused by our hypothyroid state, not the need for Prilosec (Omeprazole). And some of us need to be off gluten, especially if we have Hashimotos.

i.e. what we need is to restore a better level of acid in our stomachs, which our hypothyroid state lowers–the latter which causes problems in absorbing vitamins and minerals. That’s why we need to put lemon juice or apple cider vinegar in the liquids we use to swallow our meds and supplements. And a large body of us with Hashimotos need to be off gluten.

13) I’m not stupid just because I didn’t go to medical school, plus I live in my own body. So I need you to see us as a team. 

Because of what Stop the Thyroid Madness gives me, both the website and the books, it’s important to me that you see us as a team–BOTH my knowledge and your own.

14) No, thyroid cancer is not the easy cancer.

Thyroid cancer patients hate their cancer as much as anyone does…plus it’s worrisome, surgery nor RAI is not a picnic, and recurrence is on our minds. //www.stopthethyroidmadness.com/2015/01/31/thyroid-cancer-easy-cancer-thyroid-cancer-patients-appalled/

15) My thyroid labwork should be done before I take my thyroid meds for the day. 

Patients discovered that the T3 is NDT will peak about two hours after meds are taken, then a slow fall. If patients are on T3-only, it’s a 4-hour peak. We want to measure what still lingers in us, not the peak or rise.

What else do you think our doctors need to learn?

JanieSignature SEIZE THE WISDOM

* Join the STTM Facebook page for daily information, tips and inspiration!
* Get your STTM books here and become INFORMED: //www.laughinggrapepublishing.com You can also consider buying them for your favorite doctor (and perhaps get reimbursed when you check out of his or her office after a visit.)

THYROID CANCER IS AN EASY CANCER?? Patients are appalled!

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“May your choices reflect your hopes, not your fears.” ~ Nelson Mandela

It’s not uncommon when perusing the internet to see the word “easy” associated with “thyroid cancer”, or described as “the best kind of cancer to get”… as if of all cancers, this one is somehow less difficult, less arduous, a walk in the park or a piece of cake cancer.

Nor is it uncommon for thyroid cancer patients to be told something in a similar vein by their doctors. And of course, many of those doctors will use the “one little pill” pronouncement about the treatment afterwards. Easy-peasy, lemon squeezy!!

So where is the truth? Do you have reason to be nervous about your surgery? About your cancer? Is it that easy? What will your life be like after surgery?

One side of the story

Many thyroid cancer patients do report that all went well in many ways. They caught it early enough. It didn’t spread to their lymph nodes. Some didn’t even have to use pain medications after their surgery. If some did, it was short-lived. Others moved over to Tylenol after going home. Or ice packs. Drains were removed smoothly. Recovery went smoothly. Energy returned in several weeks. And they report that the cancer remained gone.

But here’s the other side of the story which completely dispels the myth that thyroid cancer is easy or the “best” cancer to get.

1) No matter where the cancer is, the emotional reaction is the same.

Many a thyroid cancer patient will tell you about their fears, depression, aloneness or anxiety when they were told. Or the denial, anguish, anger and stress they feel. Or the numbness. Or the fears of it returning. Or the unknown.

2) No surgery is fun, and that includes thyroid removal

Who wants to endure the pre-op or the aftereffects of surgery. No matter if some do better than others, it’s not fun to be in a hospital, be put to sleep, the waking up, the drains, the recovery, the discomfort, the time away, and the cost.

3) Many thyroid cancer patients have to endure RAI treatment after surgery and the side effects

RAI stands for Radioactive Iodine Ablation, also called I-131, given in either in liquid or capsule form. Since the thyroid easily absorbs iodine, and the radiation is strong, it serves to destroy any remaining tissue or cells that might still have thyroid cancer in them.

And side effects are far from pleasant and can include isolation, stomach problems, heart palps, neck tenderness, all over achiness, changes in taste, salivary inflammation and parotitis, facial or neck redness or “sunburns”, peeling skin, fatigue, fogginess, nausea, dry eyes, irregular period or other reported problems.

Then comes the reported risks that can come later in life due to having RAI, which include “bladder, breast, central nervous system, colon and rectum, digestive tract, stomach, pancreas, kidney (and renal pelvis), lung, or melanoma of skin”. Keep in mind this is about “risk” rather than a definite outcome, but it’s not fun to consider.

You can read of one patient’s opinion and experience with RAI titled Why have million of patients been treated with RAI?

4) The fear of recurrence always lingers!

Life-long monitoring is a sure bet when one has had thyroid cancer. The itchy reminder that it “could” come back never goes away when one has to have neck examinations, certain thyroid blood tests or neck ultrasounds.

5) The “one little pill” mantra of easiness is foolhardy

That one little pill is a reference to T4-only, aka thyroxine or levothyroxine, also commonly known as Synthroid or other brand names. And reported patient experiences for all too many reveal continual problems, sooner or later.  Equally as silly, that one little pill leads to the use of many other pills to treat the symptoms of continued hypothyroidism that many report finding themselves with while on the T4-only, one little pill. Those include statins, anti-depressants, anti-anxiety or pain meds, to name a few.

The conclusion?

You are not alone. Thyroid patients know that thyroid cancer is not as “easy” as they make it sound, nor is it the “better” cancer!  We are with you! Join the group below for camaraderie, wisdom and support!

This page was brilliantly updated July, 2015 to reflect even better information. Enjoy!

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The Case of the Missing Thyroid Nodules

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Have you ever had thyroid nodules? Read the real life testimony of thyroid and Hashimoto’s patient Cheryl and how she single-handedly removed her nodules with iodine and selenium…even though she has Hashimoto’s disease!  ~Janie, hypothyroid patient and site creator

Remember: this is just Cheryl’s remarkable experience and information. Each person reading this has to decide for themselves or in working with their doctor.

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My first thyroid ultrasound came as I was fighting for proper thyroid care.

The new doctor I had just recently hired had decided that my thyroid looked “spongy.” I knew that an ultrasound was a step up on the ladder that would eventually lead to a diagnosis and therefore treatment.

Within three days after the ultrasound study, my doctor called me and stated she was referring me to an endocrinologist. Multiple nodules covered my thyroid and several were going to need a biopsy. It would be much later before I found out how many nodules I had and exactly what shape my thyroid was in.

To say that those words, nodules and biopsy, scared me would be an understatement.

Never the less, I did what so many of us do when confronted with a health issue. I hit the Internet. First, I looked up the words “Thyroid nodules.” What exactly did that mean? Was it a nice way of saying I had cancer? Thyroid nodules, according to Mayo Clinic, are “solid or fluid-filled lumps that form within your thyroid.” The article went on to state that most are benign (over 95%) and not serious. That was not enough of a definition. I wanted, needed, and felt I deserved more information.

The next site, The American Thyroid Association page (which is good with this info but lousy with other parts), said virtually the same thing, only adding that it was an abnormal growth of thyroid cells on the thyroid gland. I kept perusing the internet, reading anything and everything I could find on thyroid nodules including the size at which a nodule becomes clinically significant (1cm and over) and needs a biopsy. I also found that not all nodules are solid abnormal growths but that some are the result of tissue breakdown. Those are the fluid-filled cysts and can occur due to Hashimoto’s.

Once I was satisfied with the information I gathered on the how and why of nodules- I made it my next mission to find out about biopsies of these “abnormal growths.”

The biopsy, and was I going to die?

What I learned was that Fine Needle Aspiration is the preferred method to biopsy a clinically significant thyroid nodule, and the doctor usually performs it right in the office. The endocrinologist inserts a hollow needle into the “lump” and extracts a sample of cells for analysis. It is a safe and relatively painless procedure.

The biopsy went flawlessly, as they always do, and my results came back: The lumps, numbering 21, (with only two being significant), were classified as being hyperplastic (adnomatoid) nodules. Being benign, they mostly contained follicular cells, Hurthle cells, and some foamy macrophages. When I asked about treating my thyroid, the nodules, and medication, I got the usual answer. “We aren’t doing anything. We are going to watch and wait.” I left that endocrinologist’s office with a sense of defeat. I was for sure I was going to die and no one in the world was going to help me.

The fighter in me did not stay down for long.

I was not going to “watch and wait.” “Not this girl,” I thought. It was obvious to me that my thyroid was floundering and needed help! By the time I got home from the follow up visit, about an hour and half away, I once again hit the World Wide Web to educate myself on the pathology findings. The next phase of my journey for true thyroid care began.

In the days immediately following my biopsy results, my primary care physician finally agreed to test my Free T3, Free T4, and both antibodies tests. When the results of those tests came back, they clearly proved my suspicions. My thyroid was down for the count. It was then that my doctor agreed to medication and natural desiccated thyroid was my choice (T4/T3 can work well, too). She started me off small with one 60 mg pill a day (…which is meant to be raised until we are optimal. How we raise is also in Chapter 2 of the updated revision STTM I book).

But, I did not stop there.

I had nodules that the field of medicine had completely disregarded. I started reading on how to treat an under medicated thyroid. I read about what nutrients and supplements the thyroid had to have for proper functioning. I started digging into benign tumors and how to treat them as well. I, then, packaged that information into a regimen of supplements made easy by online ordering.

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My regimen to begin with consisted of a working NDT (From Janie: this can also be T4 and T3) and selenium. I started the selenium first because I understood that it was critical to the thyroid. So vital, in fact, that the body will take selenium from the brain for thyroid use. It was determined from the lab/biopsy results that I had Hashimoto’s and I had heard that people with Hashi’s should not take iodine. Through my research, though, I began to understand that those with Hashi’s could take iodine but do need the selenium to protect the delicate thyroid. So, I started my selenium (400 micrograms a day). I began taking it a full two weeks before my iodine. I did not want to have a Hashi’s flare from taking iodine and knew the selenium would need a while to build up completely in my system.

Iodine supplementation was next

I had visited several sites regarding the use of iodine to cure cancers and tumors. I had joined an iodine group and absorbed Stephanie Buist’s information. I visited Breast Cancer Choices.org and found a ton of helpful information there as well. I educated myself on the many uses of iodine and the vital role it plays in the human body. I learned that as important as selenium was to the thyroid, iodine was just as important. It is the main ingredient in all thyroid hormones.

I was cautious with the iodine. I worked on building up a tolerance. I started with one drop of J.Crow’s Lugol’s 2% iodine solution a day for one week. I then “upped” the dose to 2 drops (6mg) a day for a week. And so on and so forth until I exhibited “hyper” symptoms at which time I dropped back down to the next lower dose. My body was set at 33 milligrams of iodine a day. I was going to heal my thyroid or die trying.

(From Janie: going low and slow is a good idea with iodine. It starts a detox of what we have too much of in our bodies: bromide, chloride, fluoride, etc. This is true for all but especially true if you have Hashimoto’s.)

What happened next has left many, including my physician, declaring a miracle.

Three months after the initial ultrasound, my doctor ordered a repeat. The results left her scratching her head and claiming divine intervention. In three months, I had lost 14 smaller clinically insignificant nodules. Fourteen nodules on my thyroid just disappeared. When I asked her, “How does that happen?” her response was “I don’t know – God.” I smirked but I knew it was the iodine and selenium I had religiously been taking.

As an experiment, and to confirm to myself what I already knew, I did come off the iodine and selenium, for a while, to see what would transpire. I told no one what I was doing, as I wanted to see it for myself, without influence or interference. For four months, I took no iodine or selenium- only the Armour. The following ultrasound showed a new nodule. That was proof enough for me. I went back on the iodine and selenium and continued to take my Armour, which, my doctor had upped to 2.5 grains a day.

Now, three years later, I am nearly “lump” free.

I no longer have any clinically significant nodules. In fact, I only have three nodules and the ultrasound reports shows that they are shrinking as well.

However, that is not all. For the first time since my fight for thyroid care began, my thyroid itself is no longer swollen and is in “acceptable normal limits,” meaning it is a “normal” size. While I know my thyroid will need consistent life-long care, as I do have Hashimoto’s, I no longer feel like I am a slave to my supplements or that my thyroid is more of a burden than a blessing. The fight for my thyroid, as long and as arduous as it has been, has been worth it. The “the Siamese sisters of the thyroid,” what I now call selenium and iodine, have given me my thyroid, and consequently, my life back. The ultrasounds alone prove it.

Cheryl

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Read more about selenium. Here’s good information about iodine.

Keep track of any US-made desiccated thyroid products. There were three that were rightly recalled in 2020, for example.

Do you experience hyper-like symptoms when you try to raise a working desiccated thyroid or T3 in your treatment in order to get optimal? That can point to an adrenal issue. Read here.

Have you raised a working desiccated thyroid or T3 and still feel hypothyroid? Read here.

And this is your patient-to-patient book, below, with Hashimoto’s. Order here.

Actress Sofia Vergara doing thyroid patients no favor by representing Synthroid!

Sofia Vergara

A new campaign has started called “Follow the Script” and you will see the smiling face of Emmy-nominated actress Sofia Vergara next to the proclamation: ‘YOUR THYROID CAN AFFECT THE WAY YOU LOOK, FEEL & SOUND.

Oh sure…it looks all well and good. We want everyone to be aware of the problems of hypothyroidism! And we’re glad if Sofia Vergara feels she is doing well enough for the moment to let herself be paid to do this ad.

But…the Follow the Script campaign is for promotion of Synthroid — a T4-only medication, which represents only one of five thyroid hormones. The campaign is sponsored by AbbVie, a “new, independent biopharmaceutical company composed of Abbott’s former proprietary pharmaceutical business” i.e the company is the result of a January 2013 division of Abbott Labs, the pharmaceutical company which makes Synthroid.

Says Sofia Vergara: “In 2000, I was diagnosed with thyroid cancer and had to have my thyroid removed. As a result, I have a hypothyroid condition and need to take medicine to treat it.” She continues: “In my career, I’m known to ad lib and go off-script but not when it comes to my health. I make sure to ‘Follow the Script’ so I get exactly what my doctor prescribed. This is so important to me, because you can’t enjoy what you have without your health.”

And this is where you hear a booming THUD.

As reported by a huge and growing body of patients in groups all over the internet and across the world, T4-only medications just like Synthroid have done nothing more than keep them sick and sicker in their own degree and kind with their hypothyroidism…sooner or later. In addition, all too many T4-only patients find themselves falling into adrenal fatigue, low iron, low B12, low Vitamin D, immune dysfunction, weight gain, rising blood pressure or cholesterol, reactivated Epstein Barr Virus and more…all due to the inadequate treatment of their hypothyroidism with T4-only meds like Synthroid!

i.e. this is NOT about “whatever works for you”– the watered-down, walk-the-fence message that fails to tell the truth about what T4-only medications has done to millions, besides exposing many more newly-diagnosed thyroid patients to the problems that befall so many while on T4-only. It’s about promoting a product that has left all too many with compromised lives and declining health as compared to the life-changing results from the use of T3-only or even better, natural desiccated thyroid. It’s natural desiccated thyroid which gives you everything your own thyroid would be – T4, T3, T2, T1 and calcitonin. And it’s changed lives!

Informed and intelligent thyroid patients worldwide who know the ugly truth about Synthroid are not going to be the least impressed with celebrities who think it’s hunky dory to make money promoting an inadequate medication which has only served to compromise their lives in their own degree and kind…sooner or later…and which will do the same for many others, guaranteed. 

P.S. Read Chapter 1 in the revised STTM book about the history concerning T4-only medications.

VITAMIN D AND MAGNESIUM GO TOGETHER

A common scenario with hypothyroid patients who have been on T4-only medications is finding themselves with low levels of many nutrients, including Vitamin D. Why? It appears that continued hypothyroidism lowers stomach acid, and that in turn hinders nutrient absorption like Vit. D, iron, B12 and more.

And it turns out that once you get your Vitamin D levels back up, it’s also crucial to have enough magnesium for your body to utilize Vitamin D effectively. Says the Vitamin D Council, magnesium helps your body activate vitamin D into a form your body can use, as well as helps maintain your calcium levels. They state that you may need more magnesium supplementation that is normally recommended, such as between 500 and 700 mg a day. Dr. Mercola feels that 80% of you aren’t optimal in magnesium.

So it may be wise to get your magnesium levels checked and keep them optimal. Foods higher in magnesium include green leafy veggies like spinach, avocados, dried coriander, cocoa powder (hooray!!) pumpkin seeds, almonds, sesame and sunflower seeds.

THERE’S A NEW DESICCATED THYROID OUT – WESTHROID-P

The makers of Naturethroid, RLC Labs, have reinvented their tried and true Westhroid version of natural desiccated thyroid into “Westhroid-P”, calling it “the purest treatment for hypothyroidism” with only three listed inactive ingredients: Inulin (a natural fiber with natural sweetness), Medium Chain Triglycerides, and Lactose Monohydrate (which is inherent in the NDT). It’s also stated to be gluten free.  Looks promising. We’ll see how it work for patients, because it’s patient experiences, not opinions, which rule! 🙂

Warning!! STTM is about bat-guano crazy conspiracy theorists…and more Thyroid Tidbits!

ANNOUNCINGACELLA’S NP THYROID IS ON BACKORDER  

It’s a back-handed compliment. i.e. Acella‘s brand of Natural Desiccated Thyroid has been in great demand! But…success can equal problems, because they weren’t keeping up…or that’s how we understand it. So when you go back to get a refill, the pharmacist may try to put you another brand if they are already out. So hang tight. Acella states that they will be back into better production by the end of April.

DO YOU REALLY NEED COMPOUNDED DESICCATED THYROID?

Progressive doctors have been having a love-affair with compounded medications for several years. And for some medications, as well as for patients who are sensitive or allergic to certain fillers, it makes complete sense! (Compounded means that the pharmacist “combines, mixes, or alters ingredients in response to a prescription to create a medication tailored to the medical needs of an individual patient”).

But…most thyroid patients are discovering that they really do NOT need compounded NDT and that is especially true for “slow release” compounded NDT.  First, compounded NDT is far more expensive than the prescription brands. Second, the T4 in desiccated thyroid is your “natural slow release” of T3 throughout your day. So it makes financial sense to go with the prescription brands if you have no sensitivities or problems with fillers. And even if you go with compounded….you don’t need slow-release!

YES, THE STTM WEBSITE HAS BEEN UPDATED, plus more pages!

In case you didn’t notice, there’s a new look to STTM. Part of it is because we needed STTM to be far more user-friendly on your cell phones. I think you’ll like what you see. You’ll also find links at the TOP of each page instead of to the left.

There are also new pages from the last several weeks: one on parathyroid issues, especially hyperparathyroidism (i.e. if you have high calcium levels, you need to read this page); another is an issues related to hypo landing page showing you several conditions which can outright be related to your hypothyroidism and you may not even realize it (like fibromyalgia); another about problems that can occur if you overeat high oxalate foods (as happened to ME!); how hypothyroid patients can have low stomach acid and its consequences (like acid reflux and poor absorption issues)….and you can always keep up with What’s New on STTM.

ALL THE BUZZ ABOUT MTHFR

If you haven’t heard about it, you probably will. Because lots of thyroid patients are finding themselves with a defect in a particular gene called the MTHFR, which is the acronym for “methylenetetrahydrofolate reductase” gene (methyl-ene-tetra-hydro-folate-re-duc-tase). This gene is supposed to make the MTHFR enzyme. But if there’s a defect, the enzyme doesn’t work right and you can be left with a multitude of health issues (or see them in your ancestors) including heart disease (and high homocysteine levels), breast cancer, other cancers, addictions, miscarriages, chemical sensitivities, IBS, strokes and so much more. Those with this defect can also find themselves with high levels of mercury, or iron, or other toxins. Go here to read what it’s all about.

BERBERINE. INSULIN RESISTANCE, and THYROID CANCER

Since it’s pretty obvious to me that I have insulin resistance (i.e. it takes twice as much insulin to do the job, which means more fat storage), I was pretty excited when I learned about Berberine. It’s a natural alkaloid salt found in a variety of different plants and it’s stated to make your insulin more effective, thus your blood sugar levels can come down. I notice that some folks are using it in place of Metformin, as well, and reporting better glucose levels. It’s supposedly been used for centuries in Ayurvedic and Chinese medicine.

***But there’s another interesting possibility about Berberine: studies have shown it to be effective in reducing thyroid cancer cells, here. Talk to your doctor about it before assuming you can use it for cancer in lieu of other treatments, please.

AND ABOUT THE TITLE OF THIS BLOG POST...

Bet ya didn’t know that STTM is bat-guano crazy, did ya?? lol. This misinformed comment was found as a comment of a random blog post, and tells me that some still don’t get that this isn’t about conspiracy or theory. This is about patients worldwide who have either found that T4-only meds weren’t doing the job in their own degree and kind, or….patients were getting bit in the behind years later thanks to the inadequacy of thyroxine. Even worse, doctor who have been diagnosing or treating by the TSH pituitary hormone were leaving patients sick!

So what you have on STTM is more than ten years of GOOD patient experiences, the good and the bad. LEARN from it, and expect to take it into your doctor’s office to help them catch up with us!

STTM BOOK IS COMING SOON IN SPANISH  

First there was English, then came Swedish, then came German….and later, you’ll see Spanish! I’ll announce it when it’s out. I also plan on updating a few parts of the current revised STTM English book by Fall–just some corrections here or there. For example, the current one states that the percent saturation should be 25 – 45% for women, but we know that most women, when optimal, fall somewhere around 35% and definitely not 25%. So I’ll correct that, because somehow, it didn’t get in Addendum C of the current revised edition! Get your book here…and consider two or three, because your shipping rate is much better. Give the extras to a friend or loved one.