I had a test a week ago that was TSH 2.2 (range 0.27-4.2) FT4: 14.5(11-24.0) FT3: 3.4 (3.6-6.7)REVERSE T3:26.8(9-35.0) FT3/RT3 INDEX: 8.2(<15.0) this was also taken in the evening(my mistake)
I'm confused because I'm experiencing night sweats which i read is a sign of hyper - despite this I am freezing all day and constipated, the usual hypo symptoms basically. I have hashimotos and was diagnosed with hypothyroidism I had a T3 of MINUS 2.8 and even then the doctors and endo sent me home as it being something else due to my tsh being normal..
they said that my t3 was likely due to me being sick from something else, as I had extremely high inflammation at the time(despite having been diagnosed hashimotos by a functional doctor and antibody test???)
I have had to resort to taking a natural glandular (supplement) while I'm waiting to see an endo who will listen to me. I was having great improvements on this supplement for a month or so, then it started to plateau and decline again, so the FT3:3.4 is my most recent test only two weeks ago.
I'm trying to figure out if this has caused me to have hyper like symptoms (the night sweats)or is it more likely the night sweats are due to low cortisol thanks to being hypo?
I am freezing all day, tired but wired can't stay asleep longer than a few hours, its typically at 1-3 am I wake up very hot with what feels like adrenaline and sometimes sleep apnea like symptoms. It's worth mentioning I was keto during this period due to SIBO. I've stopped it temporarily as I think it's stressing my body even more.
I am seeing a functional endocrinologist in a few weeks as I'm sick of this! It's leading me down some dark places. It's been going on for 2 months now but in the mean time I have school and I'm trying to discern if I need to lower or increase, or come off all together until I see this endo, thank you . Please any advice is appreciated
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ratqueenxo
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I was taking erfa for a few weeks, before that it was T3 only. Both I was having side effects when trying to increase (he told me i'd need a higher dose) which is why I transitioned into a glandular "supplement" which I had no side effects with and was improving. Anytime I had side effects my functional doctor was quite dismissive. I could not see someone consistently to treat my levels unfortunately. I am waiting now to see an offical endo who specialises in hashimotos. I've never taken just levothyroxine it's never been offered to me. I'm not sure what my B12 is right now and it's been a while since my ferritin was tested. Does it sound likely I am still hypo? I will raise this when I see her.
OK thank you. It's so frustrating because I have no doctor I can requests these tests for at the moment. My gp is very combative but I will ask my endocrinologist when I see her in a few weeks. Again thank you for clarifying that
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