Hello Lawman,
I was diagnosed with prostate cancer (Gleeson score 9 & Tumour T3B)
just a year ago and I am no in remission. Age 70.
There are two types of cancer patients; those who want to know everything about it and those who dont.
I belong to the former kind but some of my friends who have had prostate cancer for a few years just
dont want to know very much about it and simply leave it to their urologist and/or their radiation oncologist.
In my case I researched and studied the condition and sought second opinions.
My progress was as follows
-PSA test indicated 4 (doubled in 2 years)
-My GP referred me to a Urologist
-digital exam , could not feel anything
-he said that the usual proceedure was watchful waiting for 6 mos & then another blood test.
-he also offered an MRI scan which showed 35 shadow on the left hemisphere
-then had a biopsy which indicated 60% of prostate effected (Gleeson 9 & Tumour T3B)
-had bone & soft tissue body scans and all were clear.
-Then offered radiation (surgery had similar prognosis in my case but possible more side effects)
-Then given androgen injections for 6 months (reduced testosterone from 8 to virtually zero)
(testosterone feeds prostate cancer and androgen therapy reduces tumour)
-after 4 months had gold seeds implanted to guide radiation.
-then had 39 sessions of radiation (5 per week) @ 2 Grays per session.
-6 weeks after radiation I had blood test (PSA 0.5 & Testosterone 0.03)
-declared by Radiation Oncologist that I am in remission)
-put on a further 12 months androgen injections with review every 4 months.
Side effects:
-nil until the last week of radiation; more frequent peeing and loose bowel movements
-5 months later and these side effects still persist , albeit abit less"
Comment:
I have found that it of benefit to take ownership of one's own health; ask questions , read about
prostate cancer, talk to others who "have been there and done that". I'm keenly aware that
urologists who are the first specialist port of call tend towards radical surgery because that's their
specialty remedy. In my case I had team of 6 made up of my urologist, radiation-oncologist, the
lab specialist who did the biopsies, a radiation scientist & two others.
In surgery there is convertional surgery or the robotised Divinci machine proceedure, Both can be nerve saving.
In Radiation there is External Beam,(which I had) Bracky Seeds or Bracky Rods .
The best advice that I can offer 12 months after my diagnosis is:
(a) talk about it
(b) dont over-think it once you have done the research
(c) seek professional psychological advice if needed
(d) join a gym and keep fit and stay socially in touch with friends and family.
(e) Athough there is no emperical evidence to show that diet or vitamins are of any use; just eat
well and relish your food and dont consume alcohol. Green tea is great.
In my case I volunteered as a Volunteer Carer in the Cancer Ward of my local hospital and i find that
very rewarding.
Hope that helps.
Cheers
ZOL
... View more