Hi, i'm currently on 3 grains of NDT and 1 x 25mcg T3 daily. I would like to try T3 only. I was doing wonderfully on NDT for 4 long lovely months but sadly since the New Year my hypo symptoms have returned. Have tried increasing NDT/T3 in different ratios but it just doesn't seem to have any improvement but it does send my heart rate above 100bpm, so i drop back down.
Would like to switch to T3 but am unsure how to dose and my brain won't function despite reading several posts about it. Please help!
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Ticklek
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Your combined dose of NDT and T3 was quite high - equal to around 400mcg of levothyroxine.
Maybe that's the reason you weren't feeling so good.
The usual way to introduce NDT is to start off on 1/2 gr (Unless you were already on levo and then you just take the equivalent of NDT) you then increase by 1/4 to 1/2 gr every 2 weeks till you feel well.
When you said you were fine on NDT was that before you added T3?
Have you had a recent blood test as that would allow members to give their responses. If you've not had one for a while I would advise a new one so that you can start afresh with your hormones i.e. TSH, T4, T3 Free T4 and Free T3. Also vitamins/minerals if you've not had them for a while.
Are you aware of the best procedure to take in having blood tests?
To be completely frank i'm all over the place. I feel like I'm losing the plot. I had tried t3/t4 combo's for hashi's for the last 3 years since diagnosis (self medicating). Usually the case was i found a level i felt great on but a few months later the hypo symptoms were back, so I increased and the symptoms abated once again. Then i tried NDT for the first time last year and felt amazing. Hair and nails grew lovely. Could lose a lb or 2 a week with a healthy diet (a first!), felt well, looked well. Skin was great, body temps great. Etc etc. Really thought i'd found 'the one'.
But Straight after christmas last year everything went to pot. So i tried NDT and t3, a different type of NDT, i even went back to levo and t3 which I didn't think i'd ever do. But the symptoms (cold, tired, brain fog, weight gain, constipation, poor urine output, fluid retention) etc continues. Yet...my bpm is 80+ and i feel hyper sometimes. So thought perhaps i have high rt3?
Haven't had a blood test for about 6 months. To be honest I darent as my TSH i fear will be hyper.
TSH is likely to be suppressed on the doses you are taking. It's not important as long as FT3 remains within range. Ideally you'll have a blood test after every change of medication and dose adjustment to check FT3 remains within range and you are optimally medicated.
It may be a good idea to have ferritin, vitamin D, B12 and folate which are commonly low/deficient in hypothyroid patients tested too.
You can order private tests if you are reluctant to ask your GP to test. GP is unlikely to do FT3 anyway.
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