Hi Everyone,
I've recently been prescribed T3 by an endocrinologist for the first time having been on T4 only for 20 years or so. I've been stable on a dose of 175 micro grams for a couple of years now (having had it reduced from 200), but haven't been feeling great - mental slowness / brain fog, extreme tiredness, and more recently very dry eyes and poor vision.
I recently paid for DNA testing (via ancestry) and found out that I have two faulty copies of the DIO1 gene, and one faulty copy of the DIO2 gene which would perhaps suggest a predisposition to conversion challenges?
I've noticed looking back over my historic blood tests over the last 20 years, where FT4 has been tested it is consistently above 20 and has been as high as 30. Where T3 has been tested (infrequently!) its typically in the range of 3.5-4.0
Could anyone give an opinion on whether or not my recent results (plus DNA results) suggest a conversion problem, and whether it is worth trying the combination therapy? Also it would be good to get some advice on the dose - the Endocrinologist has suggested reducing the T4 down to 125 mcg and adding 10 mcg of T3 (split into two does of 5 mcg). Does this sound sensible, I don't want to get even worse on this treatment, 125 mcg of levothyroxine seems very low!
I've attached my recent blood test results - its probably worth ignoring the most recent ferritin as I had just recovered from an e-coli water infection, so my inflammation markers were off the scale (CRP 55.1).
Another piece if information that came up in the DNA result, which I wonder if it could be relevant relates to how my body could have impaired ability to convert phenylalanine to tyrosine. Given tyrosines role as a building block of thyroid hormone, I wonder if this could be linked? Also it would perhaps seem relevant in terms of another common symptom of hypothyroidism that I have suffered from almost continually - depression. I appreciate that things that come up in DNA results do not mean that you'll 100% have or develop an issue, but as again I have two defective copies of this gene my chances of having an issue would be elevated. Not sure if this one has come up before?
Any advice much appreciated