In January I was taking 150 T4 daily and 2x5mg T3, my bloods were T4=18.1 (9-19) T3 4.98 (2.6-5.7) TSH <0.03(0.35-4.94). I have been taking T3 since Oct 2019 because I felt so ill, tired, hair loss, dry skin, muscle and joint problems. With the help of much advice on here I started taking supplements and regularly get my vit &min checked. I then discovered that T3 helped me enormously (initially paid for by me, then prescribed on NHS via endo). My TSH has been suppressed since 2014 when I had my thyroid removed (cancer) and RAI treatment. I have been discharged by my oncologist and referred to an endocrinologist with instruction to reduce my dose to stop my TSH being suppressed. In September my dose was reduced to T4 150, 3 days and 125 4 days, plus T3 2x5mg daily. I have recently started developing some of the symptoms I had before I started T3 so asked for a blood test, my results are currently T4=14.5(9-19) T3=4.46 (2.6-5.7) TSH ,0.03 (0.35-4.94).
I have been told I will get osteoporosis and atrial fibrillation if my TSH doesn't go up , is this true ?
I am starting to get muscle/joint problems, which led to me needing trigger finger surgery before, the GP doesn't seem to get the connection, but I'm sure there is one as my fingers wont bend in the mornings, this happened before when my dose was too low, has anyone else experienced this ?
I will be speaking to my GP again shortly, and may speak to the endocrinologist if I can, as I was feeling great before my dose was reduced. Any advice anyone can offer would be very welcome.
Thank you for your opinions and advice.