I expect some of you have been discouraged from taking T3 by doctors telling you that it can thin your bones (and increase the risk of a heart attack).
Four years ago, my (NHS) endo wrote to my GP and suggested that because I was taking NDT, that I should have a DEXA scan in a two years time. (I had been taking T3/NDT for around 13 years already!)
Early this year, I had an appointment wi h a GP about another matter, but while I was there, I asked him when I could expect a DEXA scan. He asked me why, and I told him about the letter from the endo. He told me that he didn't have time to look up the letter, and if I had a copy, could I email it to him. I did that as soon as I got got home, but heard nothing at all from the practice.
Last month I made a written complaint to the practice. Not only were they ignoring a letter from a specialist, but they were also not testing me for B12 levels (also requested by a specialist, they had also ignored a request to test my PSA as the prostate cancer specialist had asked them to do.
I was asked to book an appointment for blood to be drawn for the B12 and PSA, but after a couple of weeks they wrote to me saying that my GP had checked the 'test' for patients needing a DEXA scan, and I didn't qualify. I looked at the test on-line, and there was no mention of hypothyroidism, or taking T3, so no wonder I didn't qualify for a scan.
I will discuss this matter with my endo in a couple of weeks, but it has got me wondering if the bit about T3 thinning the bones is valid or not. We all know that 'they' want us all on thyroxine, and will tell us what they like to put us off T3. What do you think?