Morning guys. I have my latest blood tests.
FT4 14.3 (10-20) 43% through range
FT4 6.0 (3.5 -6.5) 83.3% through range
TSH 0.03 (0.55-4.78)
So I’m seeing my GP later today to discuss the hand over of prescribing and also the fact that I need an increase in Levo. I have been super well since starting T3 in April, no sensitivity to adding Liothyronine to my Levo. I did not start it slowly, I just received my package and took 15mcg in 3 split doses from day 1. I then added another 5mcg after my first blood test because of a couple of remaining symptoms.
Now after nearly 4mths on combo treatment I have a couple of issues again. Constipation, lethargy in afternoon, numbness in left leg and left side of face and body odour. These are all very mild but they are my very specific symptoms that there is an imbalance.
I want to ask my GP to increase my Levo but I dont think she will because of this statement she wrote to my private endo in response to taking over the prescribing of T3
‘I would need reassurance that she would still be under your care for ongoing management and advice regarding changes. This is not something we are experienced in prescribing in general practise’
If she says no then I want to use this to ask her to do a vitamin and mineral check as my requests for these have been turned down.
I also want to ask her what happens if I can no longer afford to pay for private blood tests or Endo visits. And also more importantly what happens if my private endo retires or pops his clogs 😬
It’s all very well her saying that she isn’t experienced enough to deal with my condition but I think it still leaves me in a precarious position going forward.
What are your thoughts?