I have an Endo appointment coming up this week, I just wanted to share my latest results and see if anyone wanted to comment on them, I feel better than I have done for years.
I take 75/87.5 mcg on alternate days of Levothyroxine and I take 12.5mcg of T3 ( tiromel) split into two doses , one at night with my levo and the other first thing in the morning.
These are my results:
TSH 0.005 ( 0.27-4.2 ) this have been suppressed since I started T3, endo doesn't seem to mind !
T4 total 107 (66-181)
Free T4 20.6 ( 12-22)
Free T3 6.57 (3.1-6.8)
TPO <9 (<34)
Tg A 11 (<115) used to be around 450 prior to going GF
Vitamin D 123 (50-175 ) I take 3000iu daily all year round to maintain this.
Vitamin B12 510 ( consider reducing dose if above 569 ) I take a bit B complex
Folate 30.2 ( 8.83-60.8 )
Ferritin117 ( 13-150)
Magnesium 1. 0 (0.7-1.0)
Hs CRP 3.6 (<5) This was 7.something a few months back so I'm guessing that any inflammation is reducing.
Is there anything I need to be aware of that might be flagged up at my appointment so I can be ready, the endo has commented before that TSH will be suppressed if taking T3.
Many thanks in advance.
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knitwitty
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Was test done as early as possible in morning before eating or drinking anything other than water and last dose levothyroxine 24 hours before test and last 6.25mcg of T3 8-12 hours before test
Did you stop vitamin B complex a week before blood test
Yes I stopped B12 10 days before, and I did the test first thing before eating or drinking , last dose of levo 24 hours before and last dose of T3 10 hours before.
I feel great , better than I have in years.
I haven't used BH so I was unsure what the total T4 refers to and my magnesium is on 1.0 ( 0.7-1.0) so I wasn't sure if I should reduce the amount I take.
I only take a B Complex and I stopped that 10 days before the test.
The Endo seems to be more knowledgeable than most and was on the list from Dionne but he is still refusing to prescribe the T3 on the NHS ( despite me having the DIO2 gene mutation and despite me feeling so much better on the T3) and even though he has written to my GP 3x to ask them to prescribe it, they are refusing on the grounds that they don't feel "comfortable" prescribing a medication they have not prescribed before, ridiculous I know.
I'm guessing the magnesium is fine and I don't need to reduce my current dose.
Agree completely, but I'm glad he at least acknowledges that TSH is suppressed on T3.
I'm still badgering him on the NHS prescription, have also been in touch with my MP about the problem of being unable to access T3 on the NHS, but have not followed that up in recent months due to covid.
I just wanted to thank yourself, Greygoose , Hellvella, Shaws and SeasideSuzie for all your help in the last couple of years I wouldn't have made any progress without you all.
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