My gp is concerned and wants to refer me to an endo as I'm on t3 and t4 and my tsh is undetectable and I'm over 60. Does anyone know if this is a problem?
I'm an ex dr Skinner patient and although I feel a lot better she is not confident treating me. My t3 is at the top of the range but t4 not at the top. I wanted to increase t4 and decrease t3 but because of undetectable tsh she will not agree to any increase.
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jeans
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I have just had back very similar results and I am on NDT and over 60. I am also a former Dr Skinner patient and of course he taught us to listen to our bodies and take little notice of blood tests. My GP phoned me to say I was over replaced because TSH was 0.02 (0.27 - 2.2). She said we like it to be around 2. I replied not when taking a T3 product. I also pointed out that T4 is low in range and T3 is just in range, plus I told her I am feeling the best I have in years. She very quickly replied, "oh, we'll leave it then" I was amazed and very thankful. I am sure that as long as T4 and T3 are not over range, you are fine. In fact I think the book accepted as gospel by GPs by Dr Toft states this too. It is available in chemists but someone may see this and send you a copy of the relevant page. If you are feeling good, do not reduce your dose, unless you have known heart problems. Good luck.
Someone will correct me if I'm wrong, but I don't think raising T4 would help, given the active hormone T3 is already top of the range.
There's definitely no problem with your TSH being suppressed - that's normal when on T3.
Gp was concerned re undetectable tsh so I wanted to decrease t3 and increase t4 just because t3 suppresses tsh. I thought I had room to increase t4 and decreasing t3 may help tsh
Don't risk your health and wellbeing just because your ill informed GP wants one of the numbers on your blood test result to be a bit different. Having undetectable TSH would be risky (increased risk of heart problems and osteoporosis) if you were not being medicated for hypothyroidism, but because you are there is no associated risk. However lots of doctors don't know this.
A bit concerned about the article that states over replacement and osteoporosis.
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from the article : "Levothyroxine sodium monotherapy at an appropriate daily dose provides uniform levels of both thyroxine and triiodothyronine in the circulation" - does that mean that Levo contains T3 as well as T4? Or what is the triodo..... component?
All I can offer on this is that my wife has been post-Hashimoto's for 43 years, is on T4 (125-150) and has never had a detectable TSH in all that time. She's now 75, has perfectly good bones, occasional AF controlled by minimum dose beta blockers - but this may have nothing whatever to do with the T4 dose. Our doc leaves us to get on with it, which is all that can be done because our local hospital does TSH only and so no useful results can be obtained. Our response is if my wife feels well, then she is. She knows well enough if hypo symptoms occur - eg eyebrows going, skin roughening etc. A classic case of carrying on without routine testing - OK only if you are stable.
Taking T4 when your TSH is very low is actually blocking the T3 from working. I was like this for years, so much so that my brain has become damaged with Alzheimer like symptoms. The Endo was an absolute waste of space, but eventually I was recommended taking just T3 as I dont have a TSH at all. This has made a world of difference and I am so much better, being able to play tennis 3 times a week and do lots of exercise. As a result I have lost 3 and a half stone and its still slowly going down. More importantly my brain is now functioning much better, although the damage done will never improve and I still a diagnosis of Dementia. My T4 is absolutely zero, so I am dependant on taking T3 in small doses throughout the day.
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