I’ve now got my blood results back so have now have a good baseline I think - all on NHS! 🙏
On the advice of a private consultant, my Levothyroxene has been reduced to 75mcg (from 100mcg), and T3 added - 2x5mcg - daily. I’m now on day 4. I feel ‘stronger’ but that may just be psychological as I feel more in control and slightly more knowledgeable about this disease- I will be forever in the debt of such kind, knowledgeable people on HealthUnlocked. Thank you. 😊
These results were on 100mcg of Levothyroxene before I dropped to the new regime. I will request thyroid tests in 6- 8 weeks with the new dose/Liothyronine. Fingers crossed the NHS consultant will support.
TSH 0.04. (range 0.27-4.20)
T4 23 (range 11-22)
T3 5 (range 3.1-6.8)
TPO negative <15
Cortisol 325 (133 - 537)
250H vit D 78 (range 51-)
B12 561 (range 197 771)
Serum Folate 5.7 (range 3.9 - )
Ferritin 94 (range 30 -150)
HA1c 38 ( range 20-41)
Blood test was done 8.20am, no Levothyroxene for 24 hours, no food/drink since 8pm the night before.
Other than Vit D being out-with the Vitamin D council recommendations of 125, could any one please comment if anything stands out.
There was also a comment on the pathology report list that said: clinical details illegible, PV (referred). Sample referred to ...(hospital name). Anybody know what that means?
Many thanks. Wishing everyone well.