Went to my GP today and he has put my dose up from 150mg to 175mg. So not my old dose of 200mg but he wants to do it incrementally, and re-do bloods in 8 weeks time. Didn't want to look at T3 dose, wants to see how I go. He did say he had read the latest reaseach before I went in 😳 Which I was pleasantly surprised to hear. He has suggested that if symptoms do not improve will yes look at dose, but may also refer me to a neurologist as he would not want to put all of symptoms down to hypothyroid just in case something else is going on. Seems fair to me. I plan to see how I am in 8 weeks and than maybe seek a referral ( possibly private) to an endocrinologist.
I am angry though, as with any practice there are lots of GP's and I generally just see whoever is available. I decided whilst I was there to get my previous blood results taken in April as ordered by his colleague, to try and see why he came back and said all was normal with my thyroid function. I had reported to him the same symptoms (which are now far worse six months on) and as far as I can see from what I have gleaned so far from this forum he missed some red flags for a patient with no thyroid gland and a 'recently' reduced dose:
April 2016 October 2016
TSH 4.5 mu/L (0.4-5.5) 4.7 same range
T4 16.7 pmol/L (11.5-22.7) 18.1 same range
No T3 done 2.9 (3.5-6.5)
Ferritin 56ug/L (10.0-307.0) 76 same range
Calcium concentration 2.19 mmol/L (2.25-2.65) 2.36 same range
Vit D 37.0 nmol/L 30-50 = vit D insufficiency 105.8 (supplements taken)
Mean cell haemoglobin 33.0 pg (27.0-32.0). 32 same range
Hopefully now on the right path though to getting sorted 😀