As this is my first post I'm repeating my bio.
In 2013 I had RT & chemo for head & neck cancer (Nasopharyngeal Carcinoma which had spread to lymph nodes in neck). Lost 5 stone but survived and fought my way back.
Around 2018 was diagnosed with prostate cancer (PSA 70+). I was initially on Lupron for 4 months but had to quit because of panic attacks, anxiety and depression (suicidal) and was put on bicalutamide. I was on that for 2 years (with very few mental health problems) which along with RT brought the PSA down to < 0.1.
In 2023 my PSA started to climb again but because of my reaction to injections they told me they wouldn't start hormone treatment until they were sure the cancer had returned.
After numerous CT & bone scans which found nothing in Jan 2025 (by which time my PSA was 74) a CT scan showed swelling in 2 lymph nodes outside the prostate.
In Feb 2025 I was put on enzalutamide but gradually I got the exact same sides as I did on Lupron (anxiety, panic attacks, suicidal) and stopped after 2 months. This was devastating as the enzalutamide had taken my PSA from 74 to 2 in a short space of time. It was also puzzling because of its similarity to bicalutamide which I tolerated for 2 years.
The last 7 months I've been on the PATCHES trial. Treatment consists of 4 x 100 mcg Estraderm patches twice per week. Initially my quality of life was much better and it did keep my PSA low (currently 1.2). I was depressed but was free of the worst of the aforementioned affects. However, 3 or 4 months ago, my concentration went to hell and anxiety and panic attacks gradually increased in frequency. In the 2 weeks leading up to Xmas 2025 they've become a permanent fixture to the extent that today (24th Dec) I've ripped them off because I've had enough.
I'm autistic and my mind never rests. I have some terrifying thoughts.
So here I am in the early hours of Xmas 2025 with prostate cancer that's left the prostate, is in 2 lymph nodes and I've jacked in the treatment. Why did this all have to peak so close to Xmas? I can't contact oncology until after new year. As oestradiol only has a half life of 1 hour I already feel a bit better but I'm unsure if that's the placebo affect or maybe even just the distraction of typing all this out.
Anyway, the only way I could go back on HT is if they were able to give me some kind of anti-anxiety/depression tablet. Hence the question in the title. Anyone doing the same? Are they working? How are the sides? Also has anyone suffered effects as bad as this on HT?
Edited by member 25 Dec 2025 at 19:22
| Reason: Not specified