Last winter I spent 24/7 on a sofa almost unable to walk with a diagnosis of fibromyalgia, which I put down to 12 years of poorly treated hypothyroidism. My Gp had tested my TSH only yearly. Research brought me to Dr. Lowe's treatment.... I upped my levothyroxin to 133 mcg to take FT4 over range (12-22) at 22.60, and still my FT3 was 4.72. I was not converting T4 to T3 adequately ( in 2006 my conversion ratio, which was ignored by doctors, was 5.39:1, now it was 4.79:1). I had also checked my VitD, B12, folate and ferritin, and started supplementing to get them to optimum.
I reduced my levothyroxin to 125mcg, started to keep records of basal body temperature ( with glass thermometer by mouth), and Bp and heart rate. I noted that members suggested decreasing T4 by 25 mcg for every 10 mcg of T3 added. I was hoping to add, gradually, a whole 25 mcg T3, Tiromel pill, so knew that this might mean an 'exchange' of 62.5 mcg levothyroxin, but realised as a bad converter this might not hold true. Anyway I introduced T3 initially at 1/8 th of a pill in May increasing the dose slowly...I got some high Bp and pulse results, no temperature differences...and reduced my levothyroxin down to 100 then 75 mcg, and kept on this dose for 6 weeks. About a month on this dose the Bp went down nearly overnight from as high as 169/90 to 117/56, and stayed as this 'normal' level. I feel much better- I can walk 10,000 steps daily, but a still get very tired, have aches, hair falling out, still no weight loss, and despite the hot weather can feel the cold.
My recent blood tests from Medichecks showed:
TSH 0.015 ( 0.27-4.2). From 0. 175 on 133 T4
FT4 12.70 (12-22). from 22.6 on 133 T4
FT3 4.57 ( 3.10-6.8) From 4.72 on 133 T4
Antibodies, though Hashi, been normal both May and July tests.
So what happened to my FT3, going down though adding 25 mcg of T3? I have read that suppressed TSH can lead to poorer conversion of T4 to T3, the more you reduce the TSH the less you are able to convert. So I presume I am no longer converting any , or next to nothing, of the levothyroxin to T3, and the 4.57 is largely the T3. I still need to raise my FT3 so presumably I cannot do this by tinkering with an increase of levothyroxin but will have to add more T3. Any suggestions re levothyroxin dose etc. Any comments in general about what has happened to my FT3?
Many thanks