Absolutely, I fought the fight this morning with nhs endo and got nowhere. So def try it as directed. Before I knew what was what, I was on 80 t3 before I had rai. I’d have stocked up if I knew then what I know now. 😭
Hubby thinks it’s in my head and t3 won’t make diff but would love to see.
Try starting 'low and slow', by taking say, 5 mcg of T3 daily for a couple of weeks i.e. one table divided into four. You can get tablet cutters from Boots. Then increase by 5mcg every couple of weeks until your symptoms go. Synthetic hormones didn't work for me and I am now doing well on NDT. You won't find out if it works unless you try it.
Yes, that's the usual way Endocrinologists usually advise but remember your stomach has to be empty when you take tablets and wait about an hour before eating.
Personally, and I'm not medically qualified I would add one 5mcg to 75mcg levo and after a week or two would add the other 5mcg.
With T3 I have a pain-free symptom-free life. After all it is the only Active Thyroid Hormone, levo being inactive and has to convert to T3.
If you don't have an improvement and obviously give it a good trial at least you have tried. It cannot make you feel worse but sometimes the fillers/binders in the product (of any thyroid hormone replacement) may affect us. If it doesn't work, again you have tried.
My friend recently started t3 she is amazingly better than before. Now endo has increased her dose, I can't keep up with her! Lol
Her brain health has improved too. No longer stopping and starting trying to remember words during conversation.
Honestly? It seems as though she has woken up! I'm well jealous!, ha ha... she wasn't improving with old endo treatment.
She changed to my endo as I said mine was really caring (I waited 25 years to see one, and had one appointment so far). She has seen him twice! And, definitely fairing better than me!
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