I’ve been on T3 only for about 6 months now, started off on 5mcg/day, then 10mcg/day, went onto 15mcg/day about 6-8 weeks ago. At my last appt the ending said he wasn’t keen on going to a higher dose but I feel like I need it and my bloods from last week seem to indicate I do too - here are my bloods from Dec 17 to last week:
15/12/17
TSH 1.23 (0.35 - 4.5)
Free T3 3.4 (3.9 - 6.8)
Free T4 15.2 (11 - 26)
24/2/18
TSH 1.65 (0.35 - 4.5)
Free T3 3.1 (3.9 - 6.8)
Free T4 15 (11 - 26)
8/5/18 (10mcg T3 only/day)
TSH 2.33 (0.35 - 4.5)
Free T3 4.3 (3.9 - 6.8)
Free T4 12.4 (11 - 26)
2/8/18 (15mcg T3 only/day)
TSH 1.55 (0.35 - 4.5)
Free T3 3.7 (3.9 - 6.8)
Free T4 8.2 (11 - 26)
So my TSH, FT3 and FT4 have all dropped since my last increase, even though I feel a little bit better??
Should my TSH not be higher as my body should be trying to increase my below range FT3 and FT4? Does this mean there’s an issue with my feedback loop/pituitary?
Any advice very gratefully received! I should be seeing the endo again shortly and want to be well informed about what these results mean and to have an argument to back up my request to increase the T3!
Many thanks!
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cazzaleo
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Thanks SlowDragon. Endo said there wasn’t a problem with my FT4 or TSH when I first saw him and that I wasn’t strictly hypothyroid but he was prepared to give me a trial of T3 to see if it helped anyway. Do you think I should’ve been on Levo as well from the start then?
I agree with SlowDragon that your T3 dose is too low. I suppose Endo is fixated with the TSH which will be low on T3 only. 25mcg of T3 is equal approx - in its effect to 100mcg of levo so your dose isn't sufficient. The action of T3 is to saturate all of our T3 receptor cells - we have millions - and it is the only Active thyroid hormone needed in our millions of T3 receptor cells. This enables our metabolism to work normally when we are on a dose which permits this.
Also the blood tests were introduced along with levothyroxine, so if we add in T3 or take T3 alone then the blood tests cannot correlate and it should all be about 'how the person feels on their dose of hormones'. One of our advisers increased by patient's dose by 1/4 tablet every two weeks until the patient was symptom-free. The patient also took their temp/pulse several times a day when introducing increases and if either went high they reduced to previous dose and that seemed to be their optimum.
Thanks shaws. The endo told me I was on quite a high dose already! I knew that wasn’t the case from what I’ve seen on here, but maybe he was talking specifically about dosing in what he considers to be an unconventional case I.e. because he says I’m not really hypo?
Either way, it seems to me from the results (and what you guys in the know are telling me!) and how I feel that I need a higher dose. Fingers crossed I can convince him!
Otherwise I suppose I can buy some without prescription to top up!
Tell him also that some people have Thyroid Hormone Resistance in that they need larger doses than 'ordinary' people and greygoose knows more than most doctors/endos. This is some info:-
I would suggest that you suggest to your endo that the reason your TSH was never 'a problem' was that you have a pituitary problem - Central Hypo, when the Frees are low, but so is the TSH because the pituitary can't produce enough - for one reason or another. I doubt he knows enough about thyroid to have thought of it for himself, but he could go away and google it. And, your FT4 was low enough to warrant a little levo.
He tested those to see if he could blame your problems on menopause. Your prolactin is near top of range and high prolactin is often indicative of a pituitary problem.
Thanks. I had a short synacthen test back around Feb/March too, apparently didn’t show anything out of the ordinary. I’ll look into those other ones. Thanks for your help.
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