Morning thyroid friends
I am taking Levothyroxine, (T3) 125 MLS daily. I have been on this dose for around 6 months.
My symptoms are several PEM, dry skin and hair loss.
A year ago before the current regime I was taking T4 -75 mls and T3 -10 ml. My blood tests showed up fine.
However this time last year. , because I have debilitating chronic fatigue, (5 years) I thought I would ask my Endo to change my script.
He wouldn't allow more of T3 and T4 as a daily dose so I thought I would try, (with his permission) an increase in T4 to 125 with no T3.
6 months or so later there was no noticable difference. So I went back to Endo in October to request a return to the 75 ml daily of T4 and an increased 20 ml of T3.
Endo refused because my TSH is 0.01. he said if anything I should reduce my 125 of Levo to 100.
So. I am wondering what to do next.
Do I look for a new endo? Accept that 0.01 is too low?
Maybe my PEM and chronic fatigue is nothing to do with my thyroid meds.
I also take a therapeutical, (tiny) dose of Buprenorphine for Restless Legs and am aware that may affect my HPA Axis and the effectiveness of my thyroid meds absorption.
The reality is though that I just don't know.
I haven't put my blood results down because I haven't the energy at the moment to sort them out.
The T4 and T3 however are in sinc' and around three quarters of the way along the range.
I am wondering whether to source my own T3 and 'go it alone'
I am aware of Tom Robinson's books and thought of trying T3 only however it looks too complicated for me to use his system.
So I thought if I could buy some T3 online I could try the T4 and T3 combo myself.
Unless anyone out there knows of a private endocrinologist that is prescribing T3.
Apologies for the long post.
Ps. I take high dose Vit D. Thorne B, B12, vits. SI B12 and Selenium. Along with Ubiquinone. Lions Mane and Ashwsanger. My Folate and iron levels are fine.
Jane 😊