Henry's Story
If you lose your libido, make sure your partner knows that it seems to be a side effect of the treatment.
Do whatever resistance exercise you can, to combat the loss of muscle and increase in fat. This will also work against the effects of androgen deprivation (ADT) therapy on cholesterol, risk of diabetes, and can give you some small sense of agency with regard controlling the side effects. Ask for liver function tests when on ADT.
ADT really removes my "umph" - not only my libido (sexual "umph" - but my motivation to do much at all. This was particularly irritating when it came to exercise - I had intended to be consistent with thrice-weekly weights, but couldn't get around to it. I got runners knee, which I put down to loss of muscle, and I really missed running. I felt very bad about the cancer and its treatment causing a decline. This decline has gradually reversed since coming off the ADT (which was temporary, for some radiotherapy) but when you are experiencing it, you can't be sure it's going to be temporary.
Not sure
I could deal with a specified brief time on ADT. I'd check for other options than Zoladex.
Radiotherapy to lymph node close to my oesophagus (20 treatments over 4 weeks) inflamed my oesophagus, causing swallowing difficulty and pain. Treated with peptobysmol and a mouthwash containing local anaesthetic and effervescent paracetamol. Started 2 weeks into RT and resolved 2 weeks after it finished. It was uncomfortable, and a reminder of my PC having spread, making it hard to minimise the seriousness of my condition.
Not sure
Soon after the treatment to this lymph node, my PSA is going up again so I am due more scans. The chasing of each metastasis involves a lot of investigations and treatment. I would want to know of other options for the treatment of future metastases, in order to try and choose the least harmful, yet effective, option.
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