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Adrenal Px DHEA
Adrenal Px DHEA
Medaus
Compounds T3 Therapy Accepts
over 200 insurance plans
Adrenal Px LoBP
Adrenal Px LoBP
Low Temp Symptoms
Fatigue
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Cold Intolerance /
Heat Intolerance
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and many others...
 
ThyroCare
ThyroCare
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++ Disclaimer
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.
# 0908255 WTS Newsletter: ''WTS Newsletter: ''Unsolvable health issues solved''
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WTS Newsletter: "WTS Newsletter: "Unsolvable health issues solved"
Success Stories  
     
 
I finally have the energy to write and thank you for giving me a life. My Wilson's syndrome began c ...
I am on Doctor Wilson's treatment through my naturopath and am doing so great!! I am so thankful for ...
 
     
Question & Answers  
     
 
thyroid supplement
How do doctors get on the list of WTS Physicians?
Low cortisol and T3 therapy
 
     
Upcoming Conference: October 21-24th, 2009
Restorative Medicine Conference
Sedona, Arizona (offers WTS Certification)
Success Stories    
 
 
 
I finally have the energy to write and thank you for giving me a life. My Wilson's syndrome began classically...trauma, trauma, trauma. My best friend, sister, twin, killed herself when we were twenty four. I barely survived, spending months in bed, screaming and crying and withering away. Ten months later, I landed in a hospital for major surgery for 10 tumors, all bigger than tennis balls, which they excised and then burned away all the scar tissue my body had formed in an effort to contain the tumors. I never recovered. The pain was excruciating and unmanageable, even with maximum doses of morphine, for months and months. I then began to develop a whole plethora of horrible symptoms that I never had before:
-horrible periods....I bled for two weeks every month, going through ultra-plus tampons every hour to two hours, tons of unbearable pain, painful diarrhea, clots, fainting
-body odor that did not wash away...I could shower, bathe, shower and come out still stinking to high heaven.
-painfully cold hands and feet
-after never having had a cavity in my life, my next dental check up revealed eight
-night sweats....even though I never felt hot (or even warm) I would soak through four or fiver changes of pajamas every night
-never could I get enough sleep....I could easily sleep 12-14 hours every night and wake up exhausted, needed to nap during the day
-debilitating fear/anxiety/nightmares
-before the suicide and surgery, I was an avid and strong hiker, runner, biker, taught 11 hard core fitness classes every week. Now, I had to sit down to rest after half a flight of stairs, and my muscles would shake and give out when simply brushing my teeth or my hair
-developed asthma, hacking up phlegm almost continually, post nasal drip
-poor immunity...when I got colds, they developed into pnuemonia, lasting months at a time
-"hay fever" that lasted 9 months out of the year, so severe, I could not even drive because I could not see through the tears and sneezing...debilitating
-CRUSHING chest pains and heart palpitations...it felt like my heart beat would stop for 2 or 3 counts, ( I would sometimes collapse), then race wildly to 'catch up'
-painful digestion, embarrassing gas and belching
-arthritis, osteopenia........

Then, after 13 years of suffering , I developed excruciating pelvic pain. Went to emergency and was sent home, because there 'was no fever, therefore no infection'. My temp was 98 degrees. Two days of horrible agony later, I was rushed to the e.r. by ambulance. My fever was 104. I had Toxic Shock , which is often fatal, and spent three weeks in intensive care. My attending physician told me if I had waited even one hour longer before calling the ambulance, I would have died.

So after all this, I find your web site, and start taking my temp. I did have a fever at 98 degrees.....for me.....a big fever. My daily temps ranged as low as 94 (with a mercury thermometer) and averaged around 95. So, I began the T3 in earnest, and after only one pill, my heart palpitations were out of control. My physician would not prescribe the 'antidote' you recommend, so I fought for a few months, cycling up and down, feeling worse then ever, with a resting heart beat of 113!, but wanting so badly for this to work. Then I found one doctor's suggestion on your site for 'mini cycle up , mini cycle down' of taking only one pill each morning, that it would take longer, but was gentler for those not coping well with the standard protocol. It worked. My temp is holding steady after about a year of trying, and all of my symptoms have resolved.
Albert Einstein said there were only two ways of viewing life....either everything is a miracle, or nothing is. You have given me my miracle.
May you be given back threefold all the good you have granted so many others.

Bless you, Gina  
 
     
 
 
I am on Doctor Wilson's treatment through my naturopath and am doing so great!! I am so thankful for doctors like Dr. Wilson that went the extra mile to see why people were suffering who had no one to listen. It just takes a little "tweeking" and we can feel so well. Thank you for taking the time,

Sincerely,
Eunice  
 


Question & Answers    
 
 
 
I was diagnosed with Graves' disease at 13 and had a thyroidectomy, I have been on synthroid since and I am now 49 and currently take .212 mcg qd--- I have no sex drive, can't remember anything, dry rough skin and now am constantly gaining weight while dieting and exercising, I have chronic insomnia and when I do sleep and wake up I hurt all over with muscle aches. I have to take a very long hot shower before I can function. I know my body temp is typically low but I have not taken it through the day to trend it. Is there any correlation between Wilson's Syndrome and Graves' Disease? I am miserable with the symptoms I have described above and no one seems to take me seriously.

Tammy  
 
     
 

For sure Tammy,

Patients who have been treated for Graves' disease and who are taking thyroid replacement medication can be suffering from Wilson's Syndrome. People can be given plenty of T4 containing medication and still be suffering the effects of low body temperatures.

Thyroidectomies render people hypothyroid. If a person's body is not utilizing well the T4-containing medicine they are taking, they might benefit from T3 therapy instead.

Best regards,
Denis Wilson, MD  
 
     
 
 
I want to know how doctors get on the website list. I have an appointment with one in December and cannot wait. I wish it was sooner, but I am afraid it will be another disappointing appointment. I have recently ordered the book and think that I am one of those people that have had WTS my whole life. I am 39 years old and hope this will be my turning point. I am just glad I have a supportive family. They know I am not nuts. I have been to a lot of doctors and keep getting treated for my symptoms and talked to about diet and exercise. It is very frustrating. I had seen this on the internet, but decided to really pursue it when my Chiropractor brought it up to me. By the way, I have fair skin, freckles, light eyes and red hair. Yes I am very Irish.

Thanks,
Rosie (very hopeful in Illinois)  
 
     
 

Dear Rosie,

In order to be added to the WTS Physician List, physicians must:
-attend an Annual International Restorative Medicine Conference (covering the WT3 protocol and WTSmed Supplements).
- pass a certification exam.
-and agree with the WT3 Tenet.
(For those of you that don't yet know it, Rosie is referring to being Irish since WTS appears to be more common in patients whose ancestors survived famine...especially Irish and American Indian people).

Wishing you all the best,
Denis Wilson, MD  
 
     
 
 
DR Wilson

Here is my question. I have suffered from anxiety and shortness of breath along with low temp's (around 96.8 ~ 97.8) for most of my life. Recently , after many unexplained infections respiratory and urinary and elevated cholesterol, high CRP, Positive RA and high CCP, I was found to have Hashimoto's and a high level of RT3. I have been on Armour( 1~ 2 grains) for almost 3 years with almost no improvement and have actually gotten worse because my immune system is getting weak. I had a salivary cortisol test done and the results were stage 7 adrenal fatigue. This may explain why I was not making progress with the Armour. I was placed on T3 along with 15 mg of Cortef in divided doses throughout the day. Now , if feel more anxiety than ever , to the point of not wanting to try to treat this condition anymore. Other practitioners have conflicting opinions , but my question to you is this. Do you feel that the adrenals MUST be attended to first so that thyroid (T3) can actually work for me? I have begun to support my thyroid and adrenals with Thyrocare and Adaptogen as I go off T3 to see if I can "bank some cortisol" . Then I may be able to begin a cycle of T3 without feeling like I am jumping out of my skin. Your thoughts on this would be most helpful. I have read all of your patient and physician manuals and I noticed that you have very little on adrenals while attempting T3 therapy. My current doc feels that I need T3 and adrenal support at the same time, but I feel that I am speeding up cortisol clearance by taking T3 without adequate adrenal cortisol levels. My symptoms have gotten much worse while on both.

Thank you

Dr. Janet  
 
     
 

Dear Dr. Janet,

Very strong adrenal support (such as Adrenal Px Balance, Adrenal Px DHEA, and Adrenal Px LoBP) can be very helpful for many patients considering WT3 protocol.

Some physicians will not treat with T3 until patients' adrenal fatigue is addressed first with adrenal support. I feel that some patients will definitely need adrenal support in order to adequately tolerate the T3 treatment. On the other hand, the normalization of body temperature can sometimes improve adrenal function as well. Therefore, thyroid support will sometimes help patients with adrenal fatigue.

Hope that helps,
Denis Wilson, MD  
 


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