hi all. Back again 😬 my endo tells me this is really common and she sees it a lot with the surgeon I’m scheduled to see but that he’s a very good surgeon.
Do I need to look into seeing someone else?
My endo told me it happens in between 5 and 10 per cent of TTs. She never mentioned the possibility of having the parathyroid glands transplanted somewhere else.
She said if it happens it’s just a case of taking otc calcium supplements and there will be no adverse effect for me as long as my calcium is controlled.
I’ve been trying to trust her and take her word for it but I’m getting more and more worried after reading posts on here
thank you all