I am on the T3 therapy and have been for almost a year .... I have more energy than I've ever had and I'm working a 40 hour work week.  

 
I'm happy to say, yes, I'm seeing improvements! What a blessing. Please know you will be in my prayers. I truly believe God is using you to heal me.

I'm 44 and suspect I've been experience bouts with WTS for at least three decades. My entire life has been fraught with severe fatigue, depression, anxiety, and many other of the symptoms you list on the website. Life has been very difficult. But I began ThyroCare two to three months ago. I had some results within a few weeks: higher temp, more energy, emotional balance, and mental clarity. But then I got my menses and had a pretty dramatic relapse. I added Adaptogen and quit eating grains that have not been soaked or fermented. My last menstrual cycle was so low in symptoms that if I hadn't been monitoring myself for symptoms, I wouldn't have noticed I had any. I had a minor drop in temp and energy, but in comparison to the last cycle, these are inconsequential.

Anyone who has suffered with symptoms of low body temp for any length of time knows all too well that life reeks of very serious consequences when you're living it from a base of continual health crises.

Thank you, your work is helping so many! I've passed the website on to as many people as I can and will continue to do so.

May God's best blessings find their way to your doors!++

Sincerely,
Anne K.  

 
I have been taking the T3 for Wilson's Syndrome for about 20 days. My body temperature was between 95.5 and 97 before treatment. Now it is 98.2 - 98.6. I feel 200% better. Fluid retention is almost gone. Before treatment I took 2 different blood pressure medications and a fluid pill and my blood pressure always ran 150/90 - 165/110. Now it runs between 114/76 - 135/89. I have also stopped taking one of the medications and cut the diuretic in half. I have doctored for my blood pressure for several years (10) with several doctors including a cardiologist. None of these "medical professionals" helped me. I was so glad when I found the Wilson's site on the Internet.

I would whole heartily encourage anyone who has been to several doctors and not had successful treatment to try Wilson's Temperature Syndrome. Also I drive 3 hours and 15 minutes one way for treatment and it is well worth it.

June B.  

 
Do you recommend reviewing T4 and T3 levels before determining if the WT3 protocol is an option?  

 
Is there a lab test that can distinguish between T3 and RT3? I am a lab tech. Or is the issue between what happens in the blood and what happens on the cellular level?

Gail in Washington  

 
I have yet to undertake the WT3 therapy but I am about to begin soon. I have heard many success stories and this gives me much hope. However, I was wondering about any unsuccessful stories. Does the treatment ever fail? If so, what circumstances or health conditions are indicative of a poor or failed treatment? Who is a poor candidate for WT3 therapy? I believe I will benefit greatly from the treatment. However, I do not want to get my hopes up too high. And I have only read success stories. I don't imagine the treatment is 100% successful, and I was curious about how and why the treatment might fail.  

 
I am on my first cycle of WT3 and developed tinnitus at 75 mcg, along with a persistent headache. Is this common? Will these symptoms go away after tapering off? (I have taken every dose exactly on time.)

Sue K.