HeidiBR
May 16th, 2010, 06:53 PM
I wonder what you all think?
I received the Hashimoto’s diagnosis in March 2010 based on symptoms, minimally positive Thyroid Peroxidase antibodies, and positive family history. No other major health issues.
Labs
March 2010 compared to May 2010 after 6 weeks on Synthroid .25 & .50
TSH was 3.42 in March – decreased to 1.7 [range = 0.4 – 4.5] in May
FT3 was 2.9 in March – decreased to 2.61 [range = .2.0-4.4]* in May
FT4 was 1.21 in March – stayed the same at 1.2 [range = .82-1.77]* in May
*I'm not 100% sure of the ranges for FT3 and FT4.
Vitamin D increased from 30.5 to 77 with prescription supplementation.
After 6 weeks on Synthroid .50, most of my symptoms have abated, except for the hair loss/thinning which has gotten worse. Which makes this interesting: why have my symptoms mostly abated, if the FT3 actually decreased and my FT4 stayed the same? Yes, the TSH was cut in half, but my endo is not concerned with the TSH – he is looking at the FT3 and FT4 levels.
Since it is not clear why the FT3 decreased and FT4 stayed the same, my Synthroid dosage was increased from .50 to .75 in an attempt to increase to FT3 and FT4 to upper third of the range. It is not clear whether or not my body is not 1) converting the T4 properly to T3, or; 2) not able to use the T3, or; 3) I have not yet been prescribed enough T4 replacement hormone. My endo said we’ll consider adding synthetic T3 if needed.
Any thoughts on all of this? I am pleased with my endo’s handling of this so far. It is reasoned, prudent, and rationale.
I hope I am able to just stick with one pill and not add another!
I received the Hashimoto’s diagnosis in March 2010 based on symptoms, minimally positive Thyroid Peroxidase antibodies, and positive family history. No other major health issues.
Labs
March 2010 compared to May 2010 after 6 weeks on Synthroid .25 & .50
TSH was 3.42 in March – decreased to 1.7 [range = 0.4 – 4.5] in May
FT3 was 2.9 in March – decreased to 2.61 [range = .2.0-4.4]* in May
FT4 was 1.21 in March – stayed the same at 1.2 [range = .82-1.77]* in May
*I'm not 100% sure of the ranges for FT3 and FT4.
Vitamin D increased from 30.5 to 77 with prescription supplementation.
After 6 weeks on Synthroid .50, most of my symptoms have abated, except for the hair loss/thinning which has gotten worse. Which makes this interesting: why have my symptoms mostly abated, if the FT3 actually decreased and my FT4 stayed the same? Yes, the TSH was cut in half, but my endo is not concerned with the TSH – he is looking at the FT3 and FT4 levels.
Since it is not clear why the FT3 decreased and FT4 stayed the same, my Synthroid dosage was increased from .50 to .75 in an attempt to increase to FT3 and FT4 to upper third of the range. It is not clear whether or not my body is not 1) converting the T4 properly to T3, or; 2) not able to use the T3, or; 3) I have not yet been prescribed enough T4 replacement hormone. My endo said we’ll consider adding synthetic T3 if needed.
Any thoughts on all of this? I am pleased with my endo’s handling of this so far. It is reasoned, prudent, and rationale.
I hope I am able to just stick with one pill and not add another!