Archive for the ‘Heartbeat irregularity’ Category

Wind in My Sails

IMG_1917 (2)I have just arrived home after a whirlwind trip to northern Minnesota. It was one of those last-minute decisions that worked out perfectly, something that often doesn’t happen with those bees up-the-rear-end- type of events.

It was not a happy occasion but a necessary one. Our aunt died in October and left no children just nephews and nieces (by marriage) who loved her and cared what happened to her. My SU was ultimately responsible for her estate, so he and I spent all day Saturday emptying a house of Janet. We had moments when we laughed and moments when we cried. We had some difficult moments when something precious just had to go in the dumpster but others when we could think of a place for something else that will always remind us of her life.

In the end, I have to question the acquisition of things.  I keep thinking if someone came to my house today to empty it of “me” where would all of “me” go? Unfortunately, I know all too well after this weekend. I am trying to find solace in knowing that our life’s accumulation might help someone, somewhere, furnish a home. I know Janet would, but still, I think I will be more careful about adding things to my life in the future.

Updates galore

Or perhaps just, updates, would be more accurate. I have had a rough month now. It started as a rough week when Janet died, and then other things fell apart but it just keeps coming at me, so now I will call it a rough month. This on top of a trip abroad in September, which I love, but it always takes its toll. Have you noticed that you don’t recover as well from time change holidays? I sure do. First it takes me a week to get back on my time. Secondly, my adrenals get shaky and that’s not a good thing for someone whose endocrine system is already challenged.

By the end of October, I was feeling pretty good but there were blips. One blip was my irregular heartbeat. Everything was pretty stable in the morning but by afternoon and my second dose of T3 at noon my heart races at the slightest provocation and then it blips every so often. I hate that, I really do and it was happening frequently by the third week of October. My sleep was pretty good but the daylight hours from 1-3 p.m. were often marred by an occasional bur-blip, bur-blip and a cough. It varies by the day and by the stress in my day.

Here is what I noticed, warm hands and feet, something that is abnormal for me, so I randomly checked my temperatures. They were running really normal and slightly above. Hurrah! Perhaps I was slightly hyper but in any case things were better than average. My sleep was fair to good, also a good measure of thyroid output. My aches and pains were lessening.

What to do when it seems your world is falling apart

In general, I think things were/are pretty good despite the heart blips (sometimes called arrhythmia). Then just when you think things are going right with your world again something comes along to shake your foundation. Within the last week a family member informed me that I was difficult to be around and we needed a “break”. This is beyond upsetting to me and I wouldn’t normally share such goings on with the world but I think it is important for thyroid folks to know that family arguments, like deaths of loved ones, are very destructive and you need time to recover. The recovery will not happen overnight.

For two days my limbs visibly shook if I faced any tense moments (getting behind schedule at work for instance). I heard from this person via email and just reading the email caused me to shake and feel weak all over. As I read through the email I found that some of what was said was very true (I do comment on thyroid health a lot. I do try to be sympathetic to this person’s family situation.) Some statements were patently untrue and the untruths undid me even more. By the time the day ended I had that “wired but tired” feeling that I had when I had taken myself off all my thyroid medication (By the way, not something I ever recommend. I have been recovering for about 8 years now).

My nights were and are restless. I am waking early in the morning (around 3:30). As soon as my brain is awake it is recalling all the things I might have said and/or done and I get up and start my day. There is always a positive side to our ups and downs and my early morning schedule worked really well this weekend as we started both Saturday and Sunday around 4 a.m. We accomplished in one and a half days what would have taken much longer had things been normal.

What the……..?

So I would say my world kind of went topsy-turvy, wouldn’t you? You want to know something interesting? My heart has quit acting up, The breathless feeling I was getting walking upstairs or chasing dogs has gone. The heartbeat that wanted to race at the least amount of exertion has all but gone.

Krisinsight

In summary, it is obvious my adrenal health is not perfect. I think my adrenals are still a problem and that causes this roller coaster when presented with day-to-day stresses or worse, family issues. I know I need a cortisol test so that I can adjust my CT3M dose of T3 and heal them completely but I am still trying to catch up from my September holiday and subsequent unexpected days off due to the death in our family. In other words, it will be awhile.

I have not scheduled any other blood tests but I did schedule an appointment with my Homeopath/MD. My energy feels more positive after a few days of mulling over my course of action and getting back in charge of my emotions but I feel Dr. Lane will help me right now more than a blood test. She can help me work through my emotions and connect with the deeply buried hurt that now exists and is draining my endocrine system.

I also have not been taking my slow release potassium regularly. I forgot to take it at all last week. I was feeling an acute need this weekend, so I did eat bananas (something I normally don’t do) because I had forgotten to bring my potassium tabs along for the trip. In addition to my adrenal short comings I am sure my electrolytes are off and that always affects my heartbeat

Over the course of the past month my aches and pains have decreased.  I rode all morning today in a Ford F-250 and when I got out of the vehicle for a rest stop I could walk without stalling while my joints got in gear. Up until now I have had to stand for a few minutes to get my body to work properly and propel myself forward. This would also point to a more optimally treated thyroid. If you are hypothyroid everything gets stiff with inflammation and aches. That is one reason there is a general feeling that many fibromyalgia cases have their roots in under-treated thyroid disease.

The facts stated, now comes my latest experiment and my insight. The decrease in pain and the feeling of being optimal started when I started taking two capsules of Vital Choice Curcumin every day approximately two weeks ago. It is known that curcumin reduces inflammation but finding the right formula to optimize the effects of the turmeric is difficult. I looked at various formulas and decided this one was right for me as it’s base is Alaskan salmon oil. In subsequent blog entries I will try to update you on how the old aches and pains are doing.

The current turbulence in my life continues.  Just when I think I am in calm winds a gust of wind speeds me along my way and then the wind changes  and knocks the wind out of my sails. Believe me the wind will fill my sails again and things will be on an even keel again very soon but this only happens when you take charge of your life.  One thing this disease has proven to me is I am the captain of my ship and what happens is ultimately up to me.

See you the first Monday of December.

Santé,

Kris

P.S. I have edited this because I felt it was necessary. This gives me the opportunity to tell my readers that I had a really good night’s sleep last night. I went to bed at 8:30 and basically slept until 5:30, my normal time to get up. My mind did not race nor did it seem troubled BUT I did have an Epsom salts (3 pounds because we have a big Jacuzzi style tub) soak last night with 2 cups of baking soda and I wore some detox foot pads to bed. Did that make the difference? I don’t know but it sure felt great.

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Food Sensitivities

IMG_1917 (2)This has been a week dominated by fire watching from afar. We have watched fire consume acres of land around our private bit of Idaho ravishing livestock and wildlife as it raged through. For the last few days we have watched as hungry flames quite literally eat the landscape around Hailey, Ketchum, and Sun Valley but for now our cabin and land remain untouched.

We, my SU and I, watch our computer monitors with mouths agape as fire fighting helicopters wrestle with what they are calling “Fire-nadoes”. These are virtual whirlwinds made entirely of fire fueled by summer dried trees and sagebrush. Fire fighters on the ground are filthy with soot but keep doing their job of saving lives and structures.

They have done their job very well indeed, as few structures have been lost and no humans have perished thus far. Even the animal shelter near Hailey, Idaho was protected so well you can see the burn came right down to the structures but nothing was touched, it wasn’t even licked by flame and that, my friends, is fire fighting at its best. Just so you know, all the animals (including some bomb sniffing dogs) were safely removed and re-housed in other locations until the fire danger passed.

Meanwhile, here in Minnesota it is dry and warm. It is mostly stereotypically August although we often are much warmer than we have been. I don’t hear anyone complaining (with possible exception of those who own boats who shall remain nameless). Today, smoke from the western fires will waft over us but mostly it will be a Sunday like many others, me writing my blog for publication tomorrow morning bright and early and John catching up with unfinished business from Friday.

Food sensitivities

MSG

I have talked about food sensitivities on this site many times and it is still a subject of some curiosity for me. You all know about my burning mouth syndrome and irregular heartbeat issues. I explored numerous food issues from MSG (excitotoxins) to gluten in the past. Through very unscientific research I concluded that MSG wasn’t causing my irregular heartbeat but excitotoxins (as described by Dr. Russ Blaylock) are not good for us whether or not we have obvious reactions and I avoid them if at all possible.

Bioactive Amines, Salicylates,Nightshades and others

I found this great article titled “Natural Food Toxins” in my research this week. Chloe, research assistant and friend, and I were talking this week about aches and pains and causes of said A&Ps. She brought up nightshade vegetables and the fact that eating potatoes makes her feel quite upset. Nightshades are notorious for reacting this way on people and sure enough they are included in the article “Natural Food Toxins”.

You all know about my Burning Mouth Syndrome and I remain perplexed by the causes but I am starting to narrow down some of the culprits. I am not sure of their connection, if any to each other, but coffee is a definite culprit. Ground peppercorns on my eggs this morning caught my mouth on fire. I believe that supplements with rosemary extract ignite the issue as well. Any kind of mint be it peppermint, spearmint or wintergreen will make my mouth burn for days. What do all of these things have in common? Yup, you guessed it, they are all natural food toxins.

This is a broad category of foods including some dairy, meats, fruits, vegetables, nuts and herbs. The article at Healthknot.com is well worth reading and the link is there if you click on the first mention of “Natural Food Toxins”.

Gluten

Gluten free has become the new buzzword for food sensitivities and allergies. For some, the mere hint of gluten in their food can cause their throats to tighten and swallowing impossible.  Others are more intolerant than allergic. For me it is a culprit behind many negative health issues including ensuing malaise and seemingly irregular heartbeat. I cannot tell you, the reader, how or why gluten affects my heart but I think and have had it confirmed by others in the thyroid groups that being “glutened” can and does cause autoimmune attacks and since my heart is prone to irregularity an autoimmune attack seems to be a trigger.

Lactose

Lactose intolerance is the number one food people have trouble with. Whether it is a true allergy or an intolerance doesn’t really matter to the person who is having issues with a food. My friend Chloe totally eliminated dairy from her diet to see if it was a culprit in her fibromyalgia and found, perhaps to her delight, it really didn’t seem to make any difference. Nothing changed and she was true to no dairy for months. I can’t see that dairy affects me negatively. I never ache after consuming dairy products. My heart never bothers me (no change in pulse even). I cannot see that dairy is a negative for me in any way other than calorie content. That is not true for others and for them lactose causes too much distress to make consuming it worthwhile.

Krisinsight

Consuming gluten causes me to ache all over, have autoimmune issues within weeks of consumption and my heart reacts negatively within hours of consumption. The odd thing (at least it seems odd to me) is for most Celiac patients coffee has a similarly negative effect. They cannot tolerate coffee and this week after two episodes of achy joints I connected the dots.  I don’t have coffee very often but I do have it as a treat once in a while particularly on weekends and at my daughter’s house.

Last Saturday, we had coffee and that night I had a ruined night’s sleep as I tossed and turned with aches and pains in my knees like you wouldn’t believe. Sunday night was okay and I slept well but then I didn’t have coffee on Sunday. Monday I had coffee at my daughters and unbelievably I hurt all night long again. My knees ached and my hip ached. I got up during the night and I could barely walk my ankles were so stiff (I thought this was from running barefoot on my driveway at the time). I was starting to feel very old for 59. Then Tuesday, Wednesday and the rest of the nights this week were full of good sleep with no achiness. Of course, I have avoided coffee ever since Monday.

I mentioned that my ankles were stiff and they were and I did blame the running but it suddenly went away with no residual soreness or stiffness once I had the coffee at least 48 hours out of my system. I have since run barefoot all over my driveway and yard with no issues. Yesterday, I even did lunges across our backyard in addition to jogging. This did affect my left hip-joint last night but nothing else ached, so I conclude coffee is as bad for me as gluten.

I don’t know about you but I keep wondering what will be next and why. Do people with autoimmune issues just have more aches and pains? Or, as I tend to think, do we know that this is not normal? Do we just not accept? I know that aches and pains are not a normal part of aging, that they represent a problem. The problem is inflammation. That inflammation is a result of some thing that your body is missing, is reacting to and/or to which your body just wants you to pay attention.

I think it is important to pay attention to these aches and pains before you need a hip replacement, before your fingers are crooked with arthritis. Pay attention before your cells go crazy and multiply and some doctor tells you that in order to live you need chemotherapy and radiation. Hello Kristin!!!! Are you paying attention now? I sure hope I am. I am going to try really hard to do as I say and stop doing as I have been doing and get rid of these aches and pains.

Santé,

Kris

 

 

Heat, Rapid Heartbeats and Me

IMG_1917 (2)I wasn’t going to post anything this week because I am at my mountain retreat, or as one of my dentists called it, my compound. It’s no compound but it is a retreat, a small dollhouse cabin with a blue tin roof  in the middle of the National Forest in Fairfield, Idaho. When we hike around our land and look back at our tiny footprint of a house in the middle of this gigantic  mountain it always leaves me in wonder.

That said, this time it is hotter than I remember it ever being. It is a scorcher everywhere in the west, southwest. I read today that planes aren’t taking off from LAX because of the extreme heat. It seems planes can’t get aloft as easily when it is hot and must either take a much smaller load or not fly at all. I think I must be related to airplanes because this heat is grounding me.

The thyroid person and debauchery

Ever since I started the CT3M my oral temperatures have been coming up nicely but I am now always warm. I really don’t know if this means I am slightly hyper or if this is just the way people feel when their body temperature at the end of the day is 99. What I do know is even though I am better medicated I am still not as “normal” as I want to be nor able to handle what seems like normal activity to everyone else.

The past day we were really warm for a mountain location and by bedtime last night I was just miserable. During the day we went to an altitude of 9100 feet which may have had some effect. We took a two-hour hike early in the day and that left me feeling slightly drained. While we were at 9100 feet I had two drinks containing alcohol (gin and tonic to be exact) because they just seemed refreshing at the time but they may have had an effect.

When we got home (back to 6000 feet) from our day of play at a slightly higher altitude in Ketchum, Idaho we had another icy drink and that may have had some effect. Whatever the cause I think the effect is a bit of a storm for my body and it isn’t up to the upset. I knew it when I went to bed and  I know it now at midnight as I write this blog entry heat, debauchery, high altitude and thyroid disease do not make for a happy body.

What I do when I wake up with a rapid heartbeat

My main issue as I write is that I am up at midnight with an elevated heart beat. When I was eating gluten and not being particularly careful I would wake up with this horrible rapid heartbeat, a pounding head and the overwhelming feeling of sweatiness. In the past few months, after swearing off gluten entirely (not even in lotions or potions) I have managed to avoid these episodes.

What I have now is not that miserable. When I awoke I was sweaty and my heart beat was elevated but the pounding head wasn’t an issue and the rapid beat was only mildly elevated; perhaps as in a hot flash. I was having rather vivid dreams but nothing disturbing and when I finally got up I realized I had been dreaming the book I had read until I turned off the light, as in I was dreaming every word and every action of the pages I had been reading. I also needed to go to the bathroom and I won’t bore you with details but this type of evacuation is not abnormal when my heart is beating fast.

Anyway the only thing I can do when this happens is get up, drink 1 teaspoon of Celtic Sea Salt in water and wait to get tired again. Now, as I always do when I am awake and it seems the rest of the world is sleeping,  I wonder if anyone else has experienced this reaction and what they do when it happens.

Krisinsight

There isn’t much insight from me at midnight on a too warm, too still night. I am guessing this bit of a storm my body is experiencing is a combination of factors, no one of which would be a problem but combined they add up to a sleepless night. Everyone has a sleepless night now and then and as my mother-in-law told my SU when he was a sleepless little boy, no one ever died of not sleeping one night.

Before I close (and hopefully go back to bed) I did want to share a snack idea with you that I think is really tasty and good for your thyroid.

Toasted Chips of Coconut

Heat your oven to 350°. Once the oven is hot place the coconut oil in a 9×13 pan and melt it in the oven. Add the coconut chips and toss well to coat the chips with coconut oil. If you are a thyroid person, salt liberally and toss again. If your adrenals don’t need salt, salt less liberally. Place the pan in the oven and bake for 10 minutes. Watch carefully as the chips will brown very quickly. As soon as they are lightly golden remove from the oven and toss again, adding more salt if you want. Let cool in the pan and then store in an airtight container.

The taste is salty/sweet and satisfies that need for a snack such as chips or popcorn in a slightly more healthful way.

On that note, she says with a yawn, I think I will leave my garage (where we cook and have our computers) and head back to the dollhouse. Night, night.

Santé,

Kris

 

How Do You Know When to Increase?

I am writing this post on the day before Mother’s Day because I get the honor of having my daughter, her husband and my grandson with me tomorrow, Mother’s Day. What a great gift she is giving me as I know my daughter hates getting in the car and traveling across town but she is doing it to honor me and that makes me feel very humbled and grateful.

On bold moves

This week I made the bold move of increasing my T3 dosage. To many that may seem like no news. For someone like me who went through an entire year of incremental increases of T3 gradually exceeding the dose my body could tolerate it is a bold move indeed.

I will try to provide a short timeline for those who are interested otherwise skip down to “Along came T3”. I started my T3 only in April 2010. I decided to try T3 only because nothing was helping an irregular heartbeat I had suffered with for about a year prior to starting T3-only.

When I was first diagnosed with hypothyroidism about 15 years ago I was prescribed what I now call Syncrap, T4-only. Then around 2005 I got tired of always needing to increase my thyroid meds and stopped taking them. Just for the record, that was not a good idea. This in turn eventually caused my adrenals to burn out, a.k.a. adrenal fatigue. Finally in about 2007 I started seeing Dr. Robert Bruley in Linden Hills, MN. He put me on compounded T3 and T4 adjusting the T4 according to my symptoms but keeping the T3 very low.

I stayed on T3/T4 for a year or two but my heart continued to give me troubles. I knew from my symptoms that this was not a weak heart or blocked arteries. It would come on at certain times of day and certain times of day it would be non-existent. Exercise didn’t bring it on, stress didn’t bring it on but when it came on it was so severe it would make me cough as if I had asthma.

Finally in late 2009, I convinced Dr. Bruley to let me try Armour. I felt a drug that supplied me with T1, T2, T3 and T4 was superior to one that was mostly T4 with a tiny bit of T3. I was probably correct but it still didn’t solve the problem. My palps were disturbing but thankfully not life threatening.

Along came T3

Then in April of 2010 I took a really bold step and started T3-only. I did so without Dr. Bruley but with the wonderfully helpful people on a thyroid forum who looked at my RT3 blood test and told me I had thyroid resistance and needed T3-only to clear the T4 that was blocking the all important T3 from entering my cells. These folks had all been under treated by allopathic doctors and some had come very close to dying as a result of T4-only thyroid drugs. They had found help in taking T3-only but first they had to clear the T4 out of the thyroid cell receptors and that my friends is the bit of Hell I mentioned earlier.

It took me 9 months to finally feel normal again after starting T3. That was about 4 months of checking my temperature three times a day. 5 months of hand tremors. 6 months of horrible sleepless nights. All that but my heart was beating quite regularly at this point, not all the time but more and more it was not beating irregularly and no more coughing, none. Finally at 9 months came a realization that I had to dramatically decrease my T3 dosage. I couldn’t take the sleepless nights nor shaking hands. I gradually dropped my dose to 37.50 mcg at dose where I felt comfortable and my heart still beat normally.

At that point I felt good and decided I just couldn’t keep concentrating on the negative. I needed to be well. I quit taking my temperature three times a day and got on with my life. I knew 37.5 mcg wasn’t enough but it was okay for a while. About 7 months ago I increased gradually to 50 mcg and have been at that dose ever since.

At 50 mcg I had almost normal energy, my hair loss decreased, my sleep was reasonably good. I even slept on my left side at night (on your left side you can hear your heartbeat and when it is irregular that is disturbing). However, I knew I should wake up feeling more aware and sharp than I was. Even when I started my B12 shots, instead of feeling much better I felt only marginally better and, as time passed I felt even more lethargic than I had been feeling.

The good news

I think this makes a short blog a long one and I am sorry for the verbosity but we now move onward. This week I finally took a basal temperature and when it read 97.3 I knew it was time to increase my T3 and I felt certain my body could handle an increase. On Tuesday I added 6.25 mcg to my 11 a.m. dose. The first day I felt no change whatsoever. The second day I could tell my pulse was slightly higher and my sleep was better.

So far things are working rather well. My temperatures were up on the second day but now four days later they are down again.  My blood pressure is closer to normal (109/70). My pulse is normal (70). I don’t feel so muzzy headed when I get up in the morning. With my temperatures hovering around 98 during the day I know I am not done. I need more T3 and will aim for 75 mcg as that is the level that most people need to feel really good but if at anytime the tremors return or I feel hyper the dose will change. That is the beauty of T3-only, you can lower it and see quick improvement.

Kris Insight

Here is why I think it is working this time. It is only a theory mind you but I think taking the B12 shots and increasing my cellular levels of B12 has contributed to allowing what T3 I take to actually get in to the cells. When the T3 is finally allowed in to the cells you go quite hypo (slight weight gain, sluggishness) because you are using it all and need more.

I also think my inadequate levels of selenium, zinc, CoQ10 and Inositol were possibly keeping my cells from clearing all the T4 out and/or allowing all the T3 in to the receptors. I am now taking therapeutic doses of all those nutrients to get my cellular levels up where they belong.

I could be wrong so don’t take me to task about my insight. I am not a doctor, I am a dental hygienist who has successfully treated her thyroid resistance with the help of the “village”. With that said, if you are still having troubles with getting your T3-only treatment to work for you (or any thyroid treatment for that matter) may I make a suggestion? Get a Spectracell Nutrient test. It is clear to me that we really must test everything we can at the cellular level not just a normal blood test.

If you want more information on the trials and tribulations of going it alone just go here. I have pages and pages of experience you can read through. Obviously I am still learning and I need to keep an open mind and an informed one but for today increasing a minute amount has made a difference and I feel good.

Santé,

Kris

Got Greens?

It has been a dark and gloomy week in Minnesota with intermittent spring-like thunderstorms and warmer temperatures. If barometric pressure bothers you this has been a bad week and many are complaining of renewed pain and restless nights.

Personally I have an ache in my head that is constantly there above my eyes and in the occipital portion of my skull, aka sinus/allergy headache, and I wish it would abate. I take comfort in knowing, this too shall pass like the waxing and waning cloud cover and the budding and blooming trees and shrubs.

Speaking of budding and blooming trees, allergies and headaches, reminds me of the color green. The color green reminds me that I wanted to tell you that I may have finally found a green powder that doesn’t turn my world inside out. A green food that doesn’t wreak havoc but has all the benefits of a super green powder.

Why think green?

My interest in greens started a few years ago when Mercola extolled their virtues and recommended juicing lots of green vegetables as a breast cancer preventive measure (of particular interest having lost a sister-in-law to breast cancer and another sister-in-law having had a double mastectomy). Most of dis-ease is a result of uncontrolled inflammation and greens reduce inflammation.

They have visibly reduced inflammatory responses in my body. What do I mean by visible change in my body? When I started with Boku Superfood years ago there was a large cyst on my right ring finger that was impinging on the growth of my fingernail and causing a deformed nail. One doctor suggested a trip to a surgeon to have it removed but I resisted.

I tried numerous experiments to get rid of the cyst (thinking it might be a ganglion cyst I hit it hard several times to no avail) and then I started on Boku Superfood, a nutrient dense powder with lots of greens, and over time the cyst disappeared along with one that was on a toe and a small one on my left hand. In my opinion, these cysts were inflammatory in nature and as inflammation decreased they were resorbed.

The only trouble was Boku Superfood caused some major tummy upsets. I just didn’t know it was Boku at the time, I thought it was something else. I also ignored the heavy reliance on brassicas in Boku but eventually I had to admit to myself and now to you my reader that the powder was messing with my delicate innards. I just hadn’t quite figured out what ingredient was responsible.

So when do you admit defeat?

Actually I admitted defeat for reasons other than my upset tummy. My endocrine system got really messed up about 7 years ago when I took myself off my thyroid meds and unbeknownst to me this eventually caused adrenal fatigue and an irregular heartbeat that was, let’s just say, bothersome.

I looked for every reason under the sun for that erratic, unpredictable and  irritating heartbeat as many of you may know. Thanks to all my research I am more knowledgeable than I was but in the process I did come to some erroneous (but potentially correct) conclusions. One was that the brassica vegetables were causing my thyroid to be under productive (check out this blog post) and that Boku Superfood was ultimately responsible because it was largely composed of the dreaded brassica veggies. Don’t get me wrong, brassica vegetables are a problem for those with hypothyroidism but I now know green powder was not the culprit responsible for my irregular heartbeat.

Long story, short, for various and sundry reasons I quit drinking Boku Superfood and my tummy aches got better. I hated to give up my anti-inflammatory drink but I had  to admit defeat and move on.

On refusing to take chemicals

If you think green drinks are bad for your digestion and your thyroid what can you do for inflammation? Take ibuprofen? Acetaminophen? Aspirin? Ah, no. Not me anyway. I was determined to find a green powder that I could use, so my quest began. I would carefully scrutinize the ingredients and choose powders low in brassicas but the upset tummy persisted and the rumbling gas and loss of nutrients to diarrhea seemed to plague me.

I was and have been suspicious of flax-seed, particularly flax-seed meal, for some time. Flax and flax meal are both supposedly “so good for you” that I just couldn’t accept that flax was the offending ingredient. As time passed the light slowly dawned, if I took just Chlorella or Spirulina I didn’t have an upset tummy. I even tried E3Live and never had a moment of discord in the nether regions. As soon as I tried Garden of Life’s Perfect Food Super Greens I was running to the bathroom with that all too familiar discomfort again.

That did it, I ran in to the kitchen and tore the container out of the pantry, put on my reading glasses (yes, you read that right, reading glasses) and scrutinized the list of ingredients. There it was. I had failed to see it in the online list of ingredients: flax-seed. Another green powder bites the dust.

Kris Insight

At last I know I need a green powder that has no flax and is filled with greens from every green source and not a preponderance of brassica veggies. I don’t like fillers nor sweeteners in my green powder. I would prefer it blended easily in to water with a spoon but if it will blend with a whisk I am fine with that. Taste and texture are unimportant when compared with diarrhea and gaseous bloating.

Midori Greens seems to be the best answer for me. Midori Greens are sold at http://www.iHerb.com (WordPress won’t even allow a simple link to iHerb, urgh!). Admittedly, it seems expensive for the size of the container but one small scoop seems adequate, so the cost comes down. If you want more and don’t mind the cost, have several scoops a day.

The powder will whisk in to water easily and the taste, while not fabulous, is not bad. It tastes green and unadulterated and could easily be added to apple juice or juiced vegetables. There is a little residue at the bottom of the glass if I mix it with filtered water but if you add it to a smoothie it disappears and is undetectable.

For me the best part is I am getting my greens, my inflammation has not returned and wait for it……I’m not flatulent. Hurrah! Every day without bloating and gas is a great day. By the way, I thought you should know the sinus headache  that I spoke of in the beginning is a distant memory. I wonder if the barometer is finally rising?

Santé,

Kris

On Being Hypothyroid and Other Minutaie

Spring has sprung in Minnesota and as always I am reminded that with spring there is renewal and with that rebirth comes a certain amount of joy. Perhaps Anne Bradstreet said it best in Meditations Divine and Moral (1655)-“If we had no winter, the spring would not be so pleasant: if we did not sometimes taste of adversity, prosperity would not be so welcome”.

I thought as this week brings with it the first official day of spring it might be timely to update my thyroid buddies on my current state of health. I will preempt everything by asking you to understand if I seem a bit sardonic. I admit to still being very superstitious about what I say and I know many hypothyroid people, and other “spoonies” will relate.

That said, here we go……..

T3 only and what works for me

I am still taking 50 mcg of T3. This dose seems to work pretty well for me even though by the dictates of the RT3 thyroid group it is not enough. My pulse is pretty normal and I am happy with my blood pressure. I generally have a pulse around 75-78 bpm and my blood pressure is pretty consistently at 116/69. After being outside and pulling weeds it is 122/74 with a heart rate of 81 bpm.

How I feed my adrenals

I still take 1/2 teaspoon of Celtic Sea Salt every morning and every afternoon. I salt my food heavily and often take extra salt if I feel my pulse is too high or if I have reason to perspire more than normal. A hot bath, a FIR sauna or this warm summer-like winter weather increases my perspiration and thus my need for sea salt.

I can tell by how I feel if I suddenly stand up whether or not my adrenals need more support. If I get light-headed I know I need to increase my sodium intake. It seems my adrenals, while healthier than they used to be, still require plenty of salt to feed their “condition” . Reminds me of the old adage “feed a cold, starve a fever” I feed them salt but hopefully starve them of nothing.

How to increase cellular deficiencies

Overall I think I am doing quite well but as you know my Spectracell test showed some deficiencies. I increased my Ubiquinol to 100 mg twice a day. I am taking 200 mcg of Selenium twice per day and  close to 64 mg of chelated Zinc per day. I was taking about 750 mg of Inositol per day but for some reason I didn’t feel any particular improvement and maybe felt worse.

Here is my new dog and pony trick. I finally got things straightened out between my doctor and a very helpful pharmacist at The Prescription Center in LaCrosse Wisconsin and my injectable B12 arrived post-haste. I will tell you more about injecting B12 next week after I have finally perfected the technique with Chloe’s assistance. I expect great things from an increased level of B12 and I hope not to be disappointed.

Exercise and FIR sauna resumed

I took several months off my normal frenetic exercise regimen around this time last year and I am finally getting back in to the swing of things. I am very careful not to overdo. In fact, I do something totally foreign to the before-adrenal-meltdown-me. I actually ask the SU if he will slow down when we walk together just to avoid taxing my system. I strongly believe that my heart palps were stimulated by an unnatural release of adrenalin and if just cooling it a bit avoids a reenactment I am content to be a wimp (yes, I have a problem with not pushing to the max).

Along with mild exercise (T-Tapp Basic, PACE walking, rebounder, Schwinn Airedyne) I have resumed some brief FIR sauna sessions. My basic routine is to exercise enough to sweat. While I am working out my sauna is warming up and as soon as I finish I hop in there for 15-20 minutes, salt water in hand. I have missed my sauna sessions but when you have adrenal stress the FIR sauna pushes you over the limits of what you can stand.

Kris Insight

Does all this mean I am as good as I can be? In one simple word, no. My heart still thumps occasionally, especially if I have too much caffeine or external stimulation. I have restless nights when I get up and sleep elsewhere so I don’t wake up the SU. I can only handle a tiny glass of wine unless I don’t mind being awakened by a pounding heartbeat that is in excess of 100 bpm. My mouth burns or tastes metallic most days and I occasionally have a hot flash that causes my face to flush (sex hormones are still not perfect).

Overall though, I feel fine. Not fine as in I don’t want to say anymore but the kind of fine that has a bit of cockiness and swagger. I saw this great quote on Facebook today that I strongly identify with,  “Life is not about waiting for the storm to pass…..it is about learning to dance in the rain”. I have learned to dance in the rain and I feel fine.

Santé,

Kris

December Thyroid News:The Hypothyroid Heartbeat

It is trite I know but I will say it anyway, I simply cannot believe how time passes us by. One day you are 10 without a care in the world and the next you are 57 with all the cares of the world on your shoulders. Being  a person with autoimmune dis-ease does not make it simpler but there are few if any dull moments and you constantly learn something new and unusual. With that in mind I thought an update on my thyroid health would be timely.

On Sleeping on Your Left Side

Many of my readers and fellow hypo’s will know that my hallmark of thyroid health is being able to lie on my left side and without further ado let me say, I am sleeping on my left side. Not all the time but when my right side is sore from use I can turn to my left side and even if I hear my heart beat it is not irregular and it is not pounding. Just for the sake of feeding my thyroid health superstitions I will add that it is not consistent, there are times when my heartbeat blips or pounds (read below for other reasons) but for the most part I can turn to my left side and fall back in to a relaxing, rejuvenating sleep without any particular upset.

A Brief on the Hypo’s Heartbeat

The above statement may be hard to comprehend if you have never experienced the hypothyroid heartbeat, so let me briefly tell you. When your thyroid is not producing enough thyroid hormone to adequately feed the needs of your body your body produces unnatural amounts of adrenaline to compensate. This over compensation by your adrenal glands, in my opinion, not only causes adrenal fatigue it affects your heartbeat causing palpitations. This often ends with  you sitting in a cardiologist’s office, then being put through a myriad of tests only to be prescribed this and that medication and still suffering the palpitations.

Bear in mind, we “hypos” aren’t used to a normal heartbeat because our hearts often beat too slowly and too softly to be heard, so as we start medicating our thyroids adequately, either with a doctor’s assistance or on our own,  we suddenly hear a pounding heartbeat if we lay on our left side in particular. Add to this “pounding” (but probably normal) heartbeat any kind of irregularity and you have a person who never sleeps on their left side. Never, that is, when they are under-treated or incorrectly treated for thyroid resistance.

Life Changes

I hate to go so far as to say I live in fear of the irregular heartbeat but I have blogged on this subject ad nauseum, so I must dread it. A few weeks ago I found myself at my computer at midnight with a heartbeat in excess of 100 bpm. This always leads to researching online, first to my groups and then to other online comments or studies. This particular knowledge gleaning moment led me to a conclusion that was the end of my world as I knew it, after reading  a hundred entries or so on many different forums I realized what the problem was. I needed to cease my evening tipple.

Yes, you read that right and it pains me to say because I love my traditions (not addictions because I can give them up without bad side effects) many of which I learned while living in Europe, a time that is full of pleasant memories and custom. I love my English “tea ceremony” every morning and I thoroughly enjoyed two glasses of wine in the evening. What I didn’t realize is that my adrenal fatigue had reared its ugly head and adrenal fatigue and alcohol do not mix.

If you have adrenal fatigue alcohol acts as a stimulant akin to having caffeinated coffee or perhaps even Ephedra or other like stimulants (I have never taken Ephedra but I have read about its effects). I knew those were stimulants to avoid just like the nerve racking television which I avoid after 8 p.m. because the lights and noise stimulate me like a cup of coffee or worse.

What I didn’t seem to associate with my sleeplessness and racing heartbeat was the wine before supper that “relaxed” me. Seriously, how could it be a stimulant? It is specifically supposed to help me relax. I felt betrayed (not really) but clearly I needed to stop that long standing custom, so I did. If someone would have told me that putting that particularly bad nightmare scenario to bed was this simple I would have been all over it ages ago.

I know, I know, I can hear all the health conscious folks reading my soliloquy asking with wonder “Doesn’t she know alcohol is bad for her?” Mercola and many others preach and preach on the evils of alcohol but honestly I still don’t think a glass of wine is going to kill you but there is a time and place and I am not in either at the moment.

In Conclusion

With that admission behind me I feel like my shoulders are less rounded as if a weight has been lifted from them. I have to say that other than a few niggling issues I have been exceptionally well. I am still taking 50 mcg of T3 which results in normal energy and slightly below normal basal temperatures. I have recently started taking Ashwaghanda again and I added 5-HTP to my repertoire of supplements to elevate my moods slightly and help me sleep even better.

There are things that still need attention and the one that plagues me at the moment is my dry eyes and mouth. It could be Sjogren’s as that often accompanies Hashimoto’s Disease but I have never had that diagnosis, so my quest for an answer to that problem continues. If you have successfully treated this issue please share your experience by leaving a comment.

I conclude that with almost everything in my life I have come to expect the unexpected and I glean from all I experience what I can. I am fascinated by the stories of the world and the challenges we all face. If you come across this blog while on your own midnight quest for knowledge I hope you find it comforting that you are not alone. We are truly in this together and we share the weight of the world’s health issues on collective shoulders.

To your good health,

Kris