Hi everyone
I had my 2nd Surgery on September 17th, which went very well, at first I lost all function of my pituitary and was on full replacements. I also had DI for a while but luckily that was transient.
Since surgery I have had bloods done and am now just on Levothyroxine and Testosterone replacement. There’s a good chance I will be able to drop those also, but for how long remains to be seen. I yesterday started Radiotherapy treatment. 25 doses over a 5 week period to cover the entire pituitary fossa. So inevitably I will probably lose some if not all pituitary function through Radiotherapy damage. I’m ok with that and accept if that’s what it takes to stop another regrowth then so be it. I’m just hoping and praying that DI doesn’t result as it’s not a pleasant experience at all as I’m sure some of you are all to aware.
Anyway I just thought I’d share my 2nd experience with you and if anyone has any questions they want to ask then please feel free, I consider myself fairly seasoned now with regard to surgery, hormone replacement and soon Radiotherapy experiences, so would be more than happy to talk if anyone has any anxieties.
On both occasions mine has been a non-functioning Macroadenoma
All the best
Karl