ALCAT and All That

???????????????????????????????The dog days of August are upon us in Minnesota. Define “dog days” you say? To me they are days of heat and humidity when all you want to do is lay around panting like a dog. defines it as “the sultry part of summer, supposed to occur during the period that Sirius, the dog star, rises at the same time as the sun; now often reckoned to be July 3-August 11. Also they say it is “a period marked by lethargy, inactivity or indolence”.

Food sensitivity?

As with many of us who have autoimmune issues I have looked at the possibility that I have food allergies or food sensitivities but I was never interested enough to try an elimination diet nor to spend the big bucks and have a blood test done. I did eliminate gluten entirely about three years ago and other than the accidental bits of gliadin protein that have managed to sneak in to my daily diet I have remained gluten free.

Sadly, as my SU is quick to point out, removing gluten from my diet has not been the magic bullet I was hoping it would be. I still have bloating. I still have bouts of diarrhea. I had a bout with eczema and I still have the occasional migraine headache. I have not “gotten over” my autoimmune issues and I still need thyroid medication (now taking 75 mcg of T3).


I have never been able to put my finger on the cause of my issues. I can tell you that I have, at one time or another, blamed almost everything that goes in my mouth.

I did give up gluten because I realized that every time we went on holiday, where I ate with abandon, every gluten containing item I was offered, I came home and got sick. Twice I developed a nasty rash on my lower right back that at first burned then oozed and itched, then scabbed over and looked distinctly like dermatitis herpetiformis. Once I got shingles within a month of our holiday. That was the year I had a light bulb moment. Gluten and getting sick were related and I eliminated gluten and anything that might contain the gliadin protein. I can report I have never again had that rash on my back nor shingles, so if nothing else that is an improvement.

Okay, so gluten was eliminated but problems still existed and as I said I blamed many things. I, at one time or another, thought coffee was the culprit, then tea, then dairy. I did realize, correctly as it turns out, turmeric was an issue but I also blamed coconut, citric acid and other herbs. With all these suspicions, and really no proof, I did consider a food allergy test.

Along came ALCAT

My doctor, Kim Lane, had been telling me about a food sensitivity test (IgA not IgE testing) she had done and what a difference it made for her. It came with a hefty price tag (almost $1200) that made my jaw drop but then again can we put a price tag on our health? Not really, and $1200 wouldn’t even pay for one hour much less one day spent in a hospital because you are now in dire need of medical intervention. I mulled it over for months. I talked to my spouse about it and my friends. I still didn’t do it.

A year later the defining moment arrived. I got my 23andMe results back and with my 17 mutations out of 58 polymorphisms I decided that I really needed to know if there were foods, herbs, drugs that were negatively impacting my health. Unlike many people I do not believe that we have to settle for whatever our genes have elected for us, we can take control of our health (quoting Dr. Mercola). The ALCAT that Dr. Lane was recommending seemed like the best thing I could pursue.

What does ALCAT stand for?

ALCAT (antigen leukocyte cellular antibody test) does not test IgE immune responses to food and chemicals but according to their literature it is “a highly sensitive, objective test of assessing which foods, chemicals and herbs you may be intolerant or sensitive to.  Food sensitivity/intolerances affect over 80% of the population while less than 5% of us actually have an IgE or ‘true’ food allergy.

I will not go into every detail regarding the test as anyone can “Google” that and find out. I will explain the details I find interesting. They take 5-6 vials of blood and test a lengthy list of items including 200 foods, 50 functional foods and medicinal herbs, 20 food additives and colorings, and 10 molds and antibotics and medications. A phlebotomist is sent to your home to make the blood draw and that is included in your test price. My phlebotomist was a retired nurse and while she seemed a bit confused about what was expected of her she was very proficient at drawing what seemed like endless vials of blood and sending them off.

When your results are back you have a consultation with your provider, in my case, Dr. Kim Lane. She went over the results and discussed the best way to go about working with my new found knowledge. A really interesting comment she made was the nutritionist was amazed at my test results and generally speaking they discussed how clean my diet must be to have very little that I am sensitive to. Huh?

I had no severe reactions to anything in the food and herb category, nothing. I had a moderate reaction to three things, strawberries, rhubarb and tilapia. My list of mild intolerance was longer and included two things I was having every day, turmeric and apples. Other things were not daily items but I did use them frequently, cumin, pork, beef, asparagus and red/green lettuce (grew that this year in my garden).

I did have a severe reaction  in the “chemicals and molds category” to one drug, Ibuprofen. And there was a severe reaction to a mold, trichoderma. I am not sure of the implication of the severe reaction to trichoderma but I avoid ibuprofen like the plague. I recently took one because I had a terrible case of conjunctivitis but that was the first one I had taken in a year or more. Now I had proof that it was not good for me and I was correct to avoid it.

What is prescribed?

According to an ALCAT site everything falls in to various categories. There is a red column. Those items falling in to the red category are avoided altogether for 6 months and then possibly can be added back on a rotation basis. The orange column items are not eaten for 3-6 months and then rotated back into your diet. The yellow column contains things that should be avoided for 3 months but might be okay to eat once a week. Green means you can eat and enjoy but they firmly believe everything should be rotated even if in the green category.

Since I had no severe reactions (no food items in the red column) my prescription is to remove the items that I am moderately intolerant to for six months, so no rhubarb, no strawberries and no tilapia. (At first, I exclaimed “Who even eats tilapia anymore?” One should never get too smug. Dr. Mercola’s supplement of krill is in a fish gelatin casing. What is that fish gelatin made of? Tilapia. Why is that important to me? I needed to replace my fish oil because it is in a beef gelatin capsule. I went to ready to order the krill until I saw the label. TILAPIA!)

Under the “mild intolerance” the list is longer and included beef and pork (thus the bovine gelatin was out and so was my idea of returning to natural dessicated thyroid medication as it is porcine). Just to bore you with more detail than you want I will list all the items in the this category: apple (even apple cider vinegar included), asparagus, bay leaf, beef, brazil nut, canola oil, cayenne pepper, celery, cherry, chicken liver, cumin, fava bean, guava, mung bean, nutmeg, paprika, pork, red/green lettuce, sesame and turmeric. Those items can be consumed once a week but if I consume them I should note how they make me feel.

There are three blue boxes included in the test results. These list your blood’s reaction to candida, gluten/gliadin and casein/whey. Of those three I had a mild reaction to candida albicans, so no honey, cane sugar, fructose or maple sugar for three months. I had no response to casein or whey. I had no response to gluten/gliadin and I really don’t know what to make of that but I am going to assume that is because I haven’t had it in any quantity in a long time. I admit to being perplexed regarding my non-reacton to gluten/gliadin, so stay tuned for more information after I talk to the nutritionist.

That is the last, but not least, recommended thing I will do, talk to their nutritionist. Included in the price of the test is that 30 minutes with Dr. Lane and 30 minutes with one of their nutritionists. I am hopeful that the nutritionist can fill in some of the blanks especially why I had no adverse reaction to gluten/gliadin.


I am still digesting all of the information I now have in my hands. I look over my results every day and learn something new (for instance just now I learned what trichoderma was). I was relieved that tea and coffee were not to be eliminated but still their nutritional recommendation is no food or herb or drink is ever repeated more than once every fourth day. I have tea every day, more than once, and coffee is one of those social things that I am not very willing to give up even though I do not drink it every day (normally). I can give up the offending items for the required amount of time and I can even rotate them back in to my diet but a rotation diet of all the other foods may be really painful, too painful. Time will tell and so will my gut.



Discovering Your Genetic Code

???????????????????????????????My last post was at the end April and here we are nearing the middle of June. I will not repeat the same old tired phrase regarding the passing of time but I will say it has been a busy and kind period of my life.

After my Sidney died I started investigating adoption options as my heart and home felt empty and in need of a poodle. I contacted Sidney’s breeder in Oregon and I had friends investigating options for breeders in Minnesota. One fateful inquiry led to adopting our new furkid, Vienna, a miniature poodle.Vienna

Vienna, age 4 almost 5, belonged to the family who run the kennel where my boys have boarded for almost 10 years. Mark, one of the owners, grew up with miniature poodles and wanted to raise them and sell them responsibly. Vienna was going to have a litter or two of puppies but when the first litter turned out a bit wild and incorrigible they felt it was best not to have any more puppies and they considered finding a good home for Vienna. As Mark was to say later, “We have had our eye on you for awhile” and when I contacted him about responsible breeders of miniature poodles in our area he had a gift for me.

Vienna is a sweet little girl and while I still get misty over Sidney she has become part of the family. My heart and my home feel whole again and I like to think that Sidney would approve of her wholeheartedly.


On the topic of health, I may or may not have mentioned that a few months ago I bought a kit from 23andMe. I did it with some hesitation because the company often comes under criticism for invasion of privacy, collecting data to sell, etc. Also, the SU was not wholly behind me doing it but I really wanted to know more about me. A friend of mine was going to place an order for two kits and was willing to order one for me (they are slightly cheaper that way), so I asked her to order one for me. When I got my kit I deposited my saliva in the tube supplied, closed the kit up as instructed and sent the kit in to be analyzed.

The results were confusing and absolutely mind boggling at first as the government has essentially hogtied 23andMe making it impossible for them to tell you anything important about your results. They do compare your results to a person named Lilly Mendel, part of the Mendel family, and from that you can deduce some details about your health.

On the other hand, your ancestry is more clear cut and not illegal for them to tell you. I am 100% European. 34.7% Scandinavian (no surprise there, my mother’s mom immigrated from Sweden and her father was born to Swedish parents here in America) 16.1% Irish and British (Dad always told us he was a mutt, meaning he had a little of everything and he may have been right, at least as far as Europe was concerned), 4.5% French and German, 3.7% Finnish. Oh, and 2.7% Neanderthal. I might have hoped for something more amazing but this was confirmation that I already knew where I came from (although the Neanderthal was a bit of a surprise).

But what of the rest of the test?

Ugh, the rest of the test. The first thing you need to do is contact other sites to analyze your genetic results. I bought the Sterling App and eventually I purchased results from I got free results from, and Overall, I use Livewello more than any other because it is more complete. Geneticgenie, Nutrahacker and Sterling are more about MTHFR issues and while I wanted to know the totality of my MTHFR issue I already intuitively knew I had a methylation issue, so I was curious about the rest of the data. I feel Livewello shows me more information not just methylation issues.

Fascinating or depressing?

When Nutrahacker summed up my results they reported that they found a total of 17 mutations out of the 58 polymorphisms assessed. These were in the Detox and methylation mutation report only. I don’t know about you but that seems like a lot of mutations. Some might find this disturbing but I like having the knowledge at my fingertips and I feel empowered.

Anyone who knows genetics knows we are not prisoners of our genes. Epigenetics teaches us that the way the mutations are expressed or not expressed can depend on a host of things. Knowing what mutations exist I can do all I am physically and mentally able to do to keep them from being expressed. Energy medicine also would say that positive thinking can change the expression. In other words, if you think sick you will be sick. Think healthy and your chances of being healthy are greatly increased.

Is 23andMe for every body?

Simply put, no, 23andMe is not for everybody. My daughter does not find my results comforting and she has no interest in knowing her genetic make-up. I think most young people would find the results more disturbing than someone who is already considered a senior by many. At 61 I feel like I have beat the odds already and if I can continue to stave off one thing or another I have won the lottery of life.

Most of my immediate relatives found my results interesting but had no interest in doing their own genetic testing. My SU is not at all interested in testing. His old but frequent statement is “What will be, will be.” He has little interest in his genes nor in preventing any disease or premature death.

One friend told me she would be concerned about the results and it might negatively affect her outlook on life. Obviously, it is not for that person.

Here is the type of person who I think might benefit from doing a 23andMe test:

  • You genuinely feel you have some control over your fate.
  • You have a keen interest in health and the human body.
  • You have no fear of your future and live life as if each day is your last
  • You or a loved one has a dis-ease of the body and you want to know if it is an inherited tendency

Maybe someday I will share more of my results. I find myself very inhibited when it comes to revealing anything on the internet that you might not want an insurance company or the government to get ahold of. My blog is open to the public and they, the people who are interested in such things, already know I have thyroid issues. I may or may not want them to know anymore.

What do you think of genetic testing? Have you done a genetic test? I would love to know how many people with thyroid issues in particular have tested their genetic code and want their family to be tested.



A Departure

IMG_1448Happy May to my readers. With the passing of a full moon, and its resultant power, our nights will get darker and our souls will once again relax and calm before the power of the next full moon is upon us.

Life and death are closely knitted together in our world, much like the full moon and new moon. I accept these relationships and honor the need for both but this woman has never accepted death quite as easily as I accept life, so last Thursday was a harrowing day for me. I was, as I have been recently, home with my standard poodle, Sidney.

For almost a year, Sidney had suffered from a nerve demylenization somewhat akin to Multiple Sclerosis in humans but called Degenerative Myelopathy. He had lost the feeling in his hind quarters and one side effect was his tail didn’t wag, nor stand erect anymore. When you can’t really feel your hind legs, stairs and uneven surfaces become a challenge. His vocal cords had been somewhat paralyzed as well making his bark a mere shadow of its former self and his breathing loud.

Probably, as a result of his hindquarter lameness he now had a very sore front right leg, so was really relying on one strong leg to maintain his mobility. Despite these maladies, he always had a sparkle in his eyes and a willingness of spirit. I depended on that sparkle in his eyes to help guide me and hopefully to show me when he had had enough. I knew his days were numbered but I was determined to make them joyful.

Thursday in the dark of early morning hours I made my way to the bathroom. Right behind me Sidney hobbled in, unsure of the tile floor beneath his paws, clearly favoring his right leg again but still moving forward not to be deprived of his third eye kiss and his ear rub. We then headed outside for his morning wee and then inside for his food and medicine (he who never needed any medicine had spent the last two weeks on one med or another). Then back to bed, me to read, Sidney to rest and let his food digest.

That fateful morning, after I had read and Sidney had rested he followed me to the kitchen, but limping badly and clearly in pain. He did make it down the two stairs he needed to navigate to go outside but he hesitated to even wee, much less other more difficult movements, and soon headed back inside, done with being outside on his feet that didn’t work very well.

He headed for his spot by my computer because even having to lift his legs to his cushiony bed seemed too much effort. I think he looked to me for safety in the storm, so wherever I went he wanted to be there glued to my hip. I always have things to do but that morning I eventually gave up and just sat by my computer reading, investigating, thinking, all the while letting Sid rest his weary legs.

That morning, unlike most normal mornings, he was restless but listless, moving from place to place trying to find comfort but always within eyesight of me. I became concerned because this was not my Sidney. Eventually I called Dr. Winter his veterinarian for advice on our next step. We had been visiting his office almost weekly in the last month because there was always something changing.

Dr. Winter was in surgery that morning, so I was told he would call me back around noon. While we waited for the call I had Sidney go to his crate where he could rest and stay off his feet as I moved around a bit to get some things done. I even went out for a couple of hours to clear my head and talk to a friend of mine knowing that the longer he was safely ensconced in his crate the better his hurt paw would feel.

While my friend and I walked and talked Dr. Winter called but I didn’t hear his call and, in the end, this was a good thing. Had he answered Sidney would have had a painful trip to the office for an equally unwelcome x-ray of his right front leg that was causing him to limp so badly. It would all have been for naught, it wasn’t his leg that was plaguing him.

Dr. Winter left his cell phone number and when I got home I called him. He was unavailable, so I left a message to please call me back. Then I took my boy outside because I knew he must be desperate for a nature call, which he was, but on the way back to the house he suddenly stopped as if he couldn’t walk another step.

I looked at him and clapped my hands, trying to make a game of walking inside but he wasn’t having anything to do with my games. I detected a certain sadness in his look and he looked at me as if to say “Have a heart Mom, help me here, I am miserable.” A little later in the afternoon, Dr. Winter called. I told him his limp was really bad, we decided on an x-ray in the morning, 8 a.m. sharp.

The rest of the afternoon is a blur but I remember that Sidney would not quit fidgeting and I knew all his movement was irritating that right front leg that either had a ligament pull or a bone tumor, the x-ray would decide which it was but not until morning. I set his crate up next to my computer, so he could keep his eye on me but stay still and keep weight off his bad leg. He tossed and turned even in his confined space and I finally gave him another Tramadol for pain but the restlessness continued until I suddenly sensed something had changed.

He was trying to stand up but his hind quarters were slack. I looked at his sparkling eyes and they were dull and listless. My first thought, silly mom, was get him a treat and he will get up and be okay. I got a treat and while he took it he couldn’t even eat it and it crumbled down his chest onto the floor where he valiantly attempted to pick up the crumbs.

Those eyes were the worst part for me and they haunt me today as I grieve his loss. When Sidney’s eyes had no sparkle left and the lids hung limply I madly called family looking for a second opinion but got no response from anyone. With a sense of finality and a very heavy heart I called Dr. Winter and asked him if he would come and bring some peace to my beloved furkid. While we waited I did some Reiki for Sidney just for his peace of mind and reduction of any pain he might be in but also hoping if he was ready to go Reiki would help him make that final journey.

I will not gnaw at this moment much longer but please bear with me, I have an inner need to tell his story. Dr. Winter arrived almost at the same time a friend arrived to hold my hand and lend support. We brought Sidney outside to the soft green grass and placed him on his beloved blankie. As I held his head, and kissed his face, telling him over and over that I loved him he crossed the Rainbow Bridge to a place where he can run again.

I like to believe that across the Rainbow Bridge he will forever eat all the food he wants. There will be mountains of meaty beef bones to clean his teeth. He will once again be able to dive in to the snow and come up frosted with its rime. He will stot through the sage covered mountainsides of Idaho just like the deer he used to chase (yes, its true but they were always faster).

He will have joy and his spirit will be renewed across that bridge. Farewell my big guy. You had a mighty fine life for 13 1/2 years. When Dad and I are at the cabin I will cast your ashes in the same spot with Stanley (July 2001) and Fitzy (December 2013). The mountainside on Elk Ridge will be alive with poodles as the three of you run free, stotting across the sage, your adorable faces wind blown and happy.

God bless the poodles of my life.



The Itch of Eczema

???????????????????????????????Spring has sprung across the United States but on the very first full day of spring in Minnesota winter reared its icy cold soul and surprised us with snow the next day. This reversal of the seasons is expected here in the tundra, so if spring gives you snow I guess you might as well make a snowman (or so my grandson thought).

As the earth yawned and lifted its winter weary head earlier in March I optimistically started thinking that this spring might bring something new and different in to my life. You know what I mean, something with flair and perhaps exciting? Well something new happened and it was a flare but somehow the exciting part got lost in translation.

Eczema Goes Walk About

That’s right it was a flare, an all out attack on my epidermal layer, eczema on crack or some such thing. My eczema that previously had partied only on my legs decided to ask all its friends to come and visit, so they could itch together and cause crimson exudate. Ugh.

Anyone with eczema knows the pleasure of the initial itch, it must be akin to the way addicts feel the first time they take an illicit drug. It is intensely pleasurable but there is a fine line that can and will be crossed and pretty soon you regret your weakness. Once you start itching your eczema you cannot stop and very soon you regret that initial itch much like a junkie must regret they ever took that first hit.

Stop the Itch

What does one do when a problem arises? Honestly? I turn to the internet and others who have suffered a similar fate. I also did consult with my homeopath, Dr. Kim Lane. She suggested Rhux Tox and/or Urtica Urens and I started one and then the other but while I waited for the remedies to kick in I needed something for the itch. I really wanted instant relief and I didn’t want to apply steroid creams having read too many horror stories of steroid withdrawal.

After reading all the information I could get my hands on I came upon a solution that made perfect sense to me, apple cider vinegar and coconut oil.

One more use for apple cider vinegar and coconut oil

Yes, yet another use for household ingredients like apple cider vinegar and coconut oil. Apparently apple cider vinegar sprayed on the itchies takes the itch away and coconut oil serves as a protective layer and moisturizer. Not just any ACV will do but the kind that has a mother and is alive with probiotics, so off I went to my cupboard and pulled out the Bragg’s ACV and poured it in to a spray bottle I had on hand.

I sprayed it on every itchy spot I could see and while the sting was intense the itching immediately subsided. The sting was so much better than the itch I cannot tell you and for about 24 hours every time the itch threatened to be scratched I sprayed more ACV. Each time, after the ACV was dry I applied liberal coats of coconut oil.

The next day the positive results were noticeable. The patches that were really bad had scabbed over, the itch had greatly diminished. The best news was the partying stopped, no new attendees showed up or if they did they got sprayed and chased off.

I am sure the homeopathic remedies were doing most of the work but the ACV and coconut oil were a God send. This past weekend I could even shave my legs, something I haven’t been able to do without intense itching for months.


I know there are many facets to eczema and other skin conditions that plague millions of people worldwide. I do not think for one minute that all you need do is spray some apple cider vinegar on your skin and eczema and all its causes will go away. What I did want to share is that apple cider vinegar and coconut oil took away the itch of eczema and hastened the healing for me. If you have no known allergies to either ingredient, they will do no harm and they might just help.

Until next time, take care of yourself and I hope spring brings you something exciting with a flair and not a flare.




T3 Update

???????????????????????????????Just a quick update on my order of T3. It arrived today. It took about a month and a half but it is here and I was one jubilant woman when the postman brought it to the door.
If you haven’t received your email from the pharmacy, know that they are very embarrassed by this debacle and are offering 17% your pharmaceutical orders according to an email I received last week.
I hope you all are well.


Winter Blues

???????????????????????????????Last night, I sat outside with my SU while soft, white flakes of frozen precipitation gently fell on my shoulders. The water in our spa was warm. The air was quiet. It was that kind of hush that only comes with freshly fallen snow. It was sublime.

Suddenly the quiet of the evening was interrupted by a very distinctive and recognized sound, a certain woosh of feathers and a coo. I identify birds by their calls, so I looked around for the source because I knew it sounded like mourning doves but this it too early.

If this were the halcyon days of spring instead of the dead of winter “my” doves, letting their presence be known, would not be unusual but doing so on February 3 is most uncommon. I finally spotted four of them, one lone scout and three fluffy companions resting comfortably in a decorative crab tree not far from where we lounged.

This morning, I was somewhat relieved to read that while they prefer to spend all year in the Greater Antilles and most of Mexico  (and who doesn’t?) they will also stay as far north as central Minnesota even through our nasty winters. I like to think they know they will be safe at my house where the feeder is always full and the bird bath is warm but still winter is winter and we have months of it left to endure.

In the middle of our winter blues spring tries to sneak in with the coo of one of the loveliest birds I know. Winter is here to stay for a while but seeing my doves has given me a certain confidence that spring will arrive sooner or later.


I was spurred to action on my blog by the recent conversations on Facebook. If any of my readers are not on Facebook and are not participating in the conversations on the thyroid groups you should know that our supply of T3 from south of the border has dried up.

I do not know all the details but here is what I do know. I placed an order the first of January 2015. Payment was accepted and I received a note that it had been shipped. I paid no more attention until this discussion came up on Facebook.

After I read several comments it seemed clear that yes, payments are being accepted but it doesn’t mean they have T3 on their shelves. One person who has been in touch with the pharmacy said they told her their credit card system is antiquated and doesn’t know how NOT to accept payment.

That comment prompted me to check the email that had been sent right after my order was placed in January. I clicked on the “track your package” link provided and much to my surprise it took me to my last order that had indeed been delivered. In November. It was not, as I thought, an email regarding my January order it was an automatically generated email from months ago.


There I said it, I think those of us who order from this pharmacy are screwed. I don’t think they are being intentionally dishonest but their supplies ran out and they don’t know how to handle the situation. There aren’t just one or two people not getting their T3, their lifeline, there are many of us who placed orders as far back as November who are not going to be getting our T3.

Many folks are now reporting that they have been sent an email saying that the transaction “failed”. Those folks feel that this means the problem is not temporary it is permanent. Why the manufacturer would suddenly stop making Cynomel, I do not know but it is starting to point in that direction. Fingers crossed that this an erroneous conclusion and they will fill their shelves again and we will receive our T3.


Okay, so now that those of you who get your T3 from Mexico know your T3 supply is in danger it is time to pursue another source. I have resorted to begging my doctor to provide a prescription for an American made T3 from Perrigo (formerly Paddock). It is gluten-free unlike the American Cytomel which, by the say, is not guaranteed to be gluten-free. She will not be willing to prescribe the dose I need but anything is better than nothing until I figure this out. At the moment I have three months of Cynomel left and I can supplement what she is willing to prescribe to get my normal dose.

I suppose another choice is to try a natural desiccated thyroid med again. The most popular one right now is Westhroid. It is gluten-free and most people are feeling really good taking it.

Armour is another choice but most people feel it doesn’t  work as well as it used to. Armour has never recovered their reputation after they apparently made a formula change several years ago that they would not acknowledge but the humans taking it noticed a decline in their health.

ERFA (Canadian NDT) has reportedly been causing a return of hypo symptoms, just like Armour. Seriously, if a pharmaceutical company makes a formulation change why not tell the consumer that they have made a change no matter how slight or inconsequential. Patients need to be told before they start feeling a return of hypo symptoms, or worse, are sick on the couch again.

Thyrogold is an over-the-counter natural thyroid med that Dr. Lowe (who died three years ago after a bad fall and trauma to his head) developed and it is now being sold by his widow, Tammy. It sounds great but the cost might make it prohibitive. The general starting point is 2-3 capsules a day and 90 capsules are $54.95 plus shipping. That is approximately $60 a month if taking 3 capsules a day.

If you know of other possibilities please let me know. I will share the ideas on the Facebook groups but it will also help those who read Krisinsight and are not on Facebook.


This blog entry has been almost entirely my viewpoint but let me share one more thought with you. Allopathic medicine is seriously damaged. Our system is so dysfunctional that it is harming the patients who have to use it. Doctors simply do not understand the thyroid and how it affects our bodies when it doesn’t work properly. They go by the book and the book is old and out of touch with reality.

We are forced to treat ourselves because our doctors look at low FT3 numbers and say all is well. They do not understand RT3 ratios and as long as you don’t have Wilson’s syndrome they tell you all is well when your ratio is revealing a thyroid resistance issue. When you take NDT or T3 your TSH will most likely be suppressed when you finally feel good. However, when your doctor sees a suppressed TSH they assume you are over medicated even when your body temperature is low, your pulse is low and your blood pressure is low. Come on, doc, you should know better.

Sadly, too many doctors tell patients who say they just don’t feel good on their current dose of T4 thyroid meds that they may need psychiatric help. Or worse than that, if a patient asks too many questions they are rudely informed that they are Google experts and will be dismissed as patients if they continue with this nonsense.

Ugh. This is our reality. I faced it five years ago and solved my heart problems (inappropriate release of adrenaline) by treating myself with T3-only. It wasn’t easy and I don’t recommend it to anyone but I did solve my problem so effectively that the SU has completely forgotten how ill I was 5 years ago today.

My wish for all of us. That some day this will change. I pray that “some day” is just around corner.



The Dark Days and Your Thyroid

???????????????????????????????Yesterday, winter officially arrived here in central Minnesota. I care not what the calendar says the season is, it is winter. My deck is covered in an icy mix. That is winter. My driveway is horrific. That is winter. It is bloody cold and windy. That is winter, so we might as well move from Halloween to Christmas as far as I am concerned and, in fact, I did yesterday.

Other than our premature introduction to Old Man Winter everything is pretty normal and chugging along. In the last few weeks I would not have been so bold as to report anything like “normal” but finally things seem a wee bit better and the short, cold days have a lot to do with the changes I experienced.

Old Man Winter and your thyroid

You see a couple of months ago my hands and feet started feeling cold again. My sleep was poor and I was feeling sluggish. After a night’s sleep I would get up and feel like a nap within an hour. One could put this all down to getting older but as you may know I don’t accept that excuse.

So I started taking my temperatures again and was horrified to see my daily high was under 98F degrees (one day it was 97.6) and my low or basal temperature was good if it hit 97F. What???? Needless to say, I increased my T3 by 6.25 mcg.

I stayed at that dose (56.25 mcg) for a week or more and kept checking my temperatures, erratically, but at least once a day. They were still really low, so after a number of weeks I increased again and was now taking 62.5 mcg of T3. I let that dose stabilize for a few weeks and then checked my temperatures again. Ridiculously low. Crikey!

At this point, I opened a new bottle of T3 thinking that perhaps my old bottle had sat unsupervised at customs too long and was rendered ineffective or less effective (probably neither were true). With the new bottle in hand I increased my dose by 6.25 mcg (6.25 mcg being 1/4 of a tablet). That was just a week ago and I recently checked my temperatures at 3:49 in the afternoon, it was 98.6 F. Yea! The next day I checked it in the morning and it was 98.4 F, double hooray. My current dose is 68.75 mcg per day and my temperature at 9:00 this morning was 98.

Why the need to increase thyroid meds and the big fluctuation? Most likely nothing to do with ineffective bottles of your meds nor anything else your mind can conjure up. It is primarily down to the shorter, colder days of autumn and winter. Perhaps because in order to stay warm your body is working harder and that increases the need for T3 or NDT.

Just remember, not only do you need to support your thyroid (meds, exercise, diet, sleep, etc.) through the dark days your adrenals need added support. One way to do this is to add the adrenal cocktail. After all if you increase thyroid meds you put a strain on the adrenals and they,too, will need extra support.


So the other thing my mind conjured up as a culprit for my sudden need for more T3 is the iodine I started taking about a month ago. I started at a really low dose of 225 mcg which according to Iodine experts is way too low. I justify my low dose because I had a very real concern about taking Iodine after taking large doses several years ago and having my TSH rise to 13, something it has never done before or since.

Little by little I have increased my dose of potassium iodide and am now up to 1000 mcg or 1 mg of Iodine and other than the lowering of my temperatures there are no apparent side effects. It is possible that by detoxing bromide (something that Iodine does) I cleared the receptors in my thyroid and my thyroid suddenly could accept and needed more T3 to run my body efficiently.

This is all pure conjecture as I did not do an Iodine Loading test before I started the Iodine supplementation. If it weren’t for the acknowledged need to increase thyroid meds during autumn and winter and the fact that I started needing more T3 in September (the 17th to be exact and well before I started the Iodine) I might question Iodine’s role in my recent increased need for T3. What is more likely is that Iodine supplementation has contributed to my thyroid needing more T3 but is not the sole reason for my increased needs.

Before I go I must tell you that I have now been attuned to Reiki Master. “Master” to me means I can now teach others how to do Reiki on themselves, their loved ones or their beloved pets in addition to using Reiki’s healing energy when the need arises. I am most grateful to my Reiki Master, Donna Murray and our healing circle which includes Lynette VerBout, Jane Russo and myself. Namaste.

Stay warm and be sure to feed your body what it needs to get you through the dark days of the year.