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| Links to WTS Website |
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Compounds T3 Therapy Accepts over 200 insurance plans |
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| Low Temp Symptoms |
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Fatigue |
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Headaches & Migraines |
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PMS |
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Easy Weight Gain |
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Depression |
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Irritability |
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Fluid Retention |
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Anxiety & Panic Attacks |
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Hair Loss |
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Poor Memory |
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Poor Concentration |
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Low Sex Drive |
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Unhealthy Nails |
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Dry Skin & Hair |
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Cold Intolerance / |
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Heat Intolerance |
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Low Motivation |
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Low Ambition |
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Insomnia |
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Allergies |
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Acne |
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Carpal Tunnel Syndrome |
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Asthma |
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Hives |
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and many others... |
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| ++ Disclaimer |
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These statements have not been evaluated by the Food and Drug Administration. These products are not intended to diagnose, treat, cure or prevent any disease.
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# 1003287 |
WTS Newsletter: ''I am unspeakably grateful'' |
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WTS Newsletter: "I am unspeakably grateful"
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| Upcoming Conference: |
October 17-21st, 2010 |
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| Moab, Utah (offers WTS Certification) |
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| Success Stories |
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I'm having great results with ThyroCare, Healthy Foundation, and Adaptogen (less constipation, more energy, a great sense of well-being, much calmer, have stopped menstruating every two weeks!), and thank you so much for putting the manuals on-line. I have begun eating five or six small meals spaced throughout the day and doing short work-outs three to five times daily as discussed in the book. This morning my temp was 98.3! That's a first! For as long as I can remember when I'd have a checkup and ask the doc about my temp, it would always be around 97. I am unspeakably grateful and thank God for your commitment to free people from this stifling condition. Thank you so much, Anne K. Hermon, Maine
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I've been checking my temps for 4 weeks now. Just started on the WT3 protocol this past Friday and am feeling better already! I have ordered the Doctor's Manual - I sure wish it would come in so I can learn more about this! Thanks, Jacki
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That's great Jacki. For now, you can read the Doctor's Manual online for free.
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I must say I wasn't for sure, if and how much, ThyroCare and Adaptogen were helping me until about a month ago. I had a thyroidectomy in 1988 and was put on Synthroid. It worked a few years, I thought, until I broke out on the entire body (including head) with severe itching hives, along with hair loss, weight gain, constipation, low energy, low temperature (94.5), and other symptoms which lasted for 9+ years. All the doctors I went to (including about a year of treatment in a glandular research center) just took tests (which showed normal) and left me on some form of Synthroid. Finally last year I found a medical doctor who also uses alternative medicines, and though she hesitated, I insisted that I be put on Armour or some natural hormone. At that time I also started taking ThyroCare and Adaptogen on my own, since she wouldn't prescribe them for me. I began to improve immediately and within ten days my itching had stopped and the hives disappeared. It was like a miracle. In time my temperature went up to normal and stayed there. Feet and hands no longer cold; other symptoms disappeared also. So I continued the Armour hormone and the ThyroCare and Adaptogen until about a month ago when I ran out of the ThyroCare and Adaptogen products. I thought maybe it was the change to Armour that gave me the relief and probably not the herbs at all. So, I decided just not to re-order them. Well, to my surprise, about 7 days later, two areas on my body began to itch constantly and break out in a rash as before. I checked my temperature and it had dropped to an average of 95.5. I immediately re-ordered the products (which you delivered promptly) and within four days the itching and rash started clearing, and is now clear. My temperature is slowly going back up too. Sorry this is so long but just wanted to explain how ThyroCare and Adaptogen have made a believer out of me. By the way, I'm a retired research scientist and clinical laboratory manager. Thus, I test things for myself and am now convinced that I'm on the right path to better health through these products. Sincerely, Cleste H.
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| Question & Answers |
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I am being treated for Hypothyroidism but had not heard about Wilson's Temperature Syndrome until now. I thought I heard something about a reverse T3 test to determine if you have WTS or not. Is that correct? I have been on a couple of different medications through the years but I feel like my symptoms get worse every year even though my Dr says my levels are fine and tells me I am depressed. I feel that I am depressed from the total exhaustion I experience a good 95% of the time. It would be an answer to prayer if I could finally be treated correctly! Thank you, Kathy
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Hi Kathy, You can click here to read why WTS is undiagnosable with thyroid blood tests. I hope you get well soon! Denis Wilson, MD
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I have had many hypothyroid symptoms for several years, but never had the blood results to warrant medication according to the 30+doctors I have seen. I found a doctor who gave me medication to improve my symptoms anyway, and the medication was quite helpful. I have been taking Westhroid for about 20 months now and it's positive effects seem to be diminishing. I asked my doctor about trying the T3 and he was supportive of me trying it. When I implemented the protocol, I had side effects even at 7.5 mg and did not receive the guidance I needed from my doctor to successfully follow through. I know you offer him help, but he requested I go back on the Westhroid. There are no doctors listed on your website within a reasonable driving distance. So my plan at this point is to slightly increase my Westhroid dosage (30mg. to 45 mg.) and try it on any empty stomach. I was also thinking about trying Thyrocare in addition. Do you have any advice as far as which of your products would best suit my needs, dosage, timing of the dosages,etc.? The most troublesome symptoms right now are the fatigue, increased cholesterol, hair thinning,and increased prolactin. I seem to experience side effects from a lot of treatments, so I would need to start with one product and proceed cautiously at first. Thank you for your informative newsletters and all of the help you offer. Brenda
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ThyroCare supports normal functioning of the thyroid gland and is very well tolerated and is available directly to the public on our website. Thyroid Px is available only through qualified health care practitioners. It is a stronger formula than ThyroCare and is generally well tolerated. However, more care is needed with Thyroid Px because it contains a lot of Iodine (which is often very helpful). Some people can notice an increased awareness of their heartbeat with Thyroid Px.++ Hope that helps, Denis Wilson, MD
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Does WTS cause low blood pressure, or does it impact blood pressure? Thank you, Rita R.
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Some people with low temperatures have tended to have low blood pressure that normalized when their temperatures were normalized. On the other hand, some people with low temperatures have tended to have high blood pressure that normalized when their temperatures were normalized. So it can go either way. Warmly, Denis Wilson, MD
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Is it true that a person that has Wilson's Temperature Syndrome shouldn't take copper, like for instance in a multivitamin supplement? I was diagnosed with WTS but never heard anything about not taking copper. Claudia M.
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Dear Claudia, I believe that someone may have confused Wilson's Temperature Syndrome with Wilson's Disease. Wilson's Disease is an inherited disease of copper storage metabolism wherein people are unable to excrete copper normally. Consequently, the copper can accumulate in their bodies often causing liver damage. These patients often collect copper in their corneas (eye) as well, causing a greenish or golden brown ring discoloration of the cornea (known as Kayser-Fleischer rings). You may have Wilson's disease if you have Kayser-Fleisher rings, low serum ceruloplasmin (a few WD patients have normal ceruloplasmin levels), and increased amounts of liver and urinary copper. You may have Wilson's Temperature Syndrome if you have a low body temperature. If you don't have WD and you do have WTS then I see no particular reason you would have much more trouble with copper than anyone else. WD is very rare. WTS is very common. Hope that helps, Denis Wilson, MD
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