On Tues June 11, I was diagnosed with advanced metastatic prostate cancer (lymph nodes from pelvis to aorta).
A few days later I got a Firmagon injection (now Zoladex 10.6 every 12 wks) and on June 23rd received my first Docetaxel drip. I take 10mg of Prednisone in the morning.
June 12, PSA - 450
Aug. 2, PSA - 3.0
My Oncologist is happy, I'm happy.
Cheers
Written by
kcamH
To view profiles and participate in discussions please or .
I was diagnosed a year ago. I did the same drugs and treatment as you with a similar response. After my sharp PSA drop to 2.0, I have continued to have a slow and steady decline on Zoladex. I'm now at 0.17. Best of luck to you through the rest of your chemo.
Sleeping much better, turned my bedroom into a dark freezer and got the brain working on stuff again. Like driving in traffic, does wonders to the emotional despair of high anxiety and fear by redirecting to road warrior.
Although, based on my recent bone scans, may go back to the NYMets handle.
Bueno Cumpa! I’d never forget you . What did your bone scans say? I just had a dexa and got a shot of prolia because I’m in osteopenia ..who hoo. No signs of pc just my hips are degrading rapidly . Se la ve ....it’s good that you’re sleeping .. I’m a road rage animal 1/2 the time .. the other half is when I’m a passenger ..Take care
No bone mats showed up in my MRI, just lymph nodes. Side effects from Docetaxel are: Tongue feels swollen and interfered with speech.
Mouth lining seems thick.
Finger tips numb but painfully sensitive to pressure. Makes buttoning a shirt difficult.
Same but to a lesser degree for toes.
Bright pink across knuckles. Sensitive to temperature and pressure.
Light red areas on temple and cheeks.
Skin peeling on fingers.
Occasional wheezing, cough and throat clearing
Stuffy nose. Fewer nasal hairs mean more dust hits my sensitive nasal membranes causing sneezing and runny nose with interestingly shaped clotted blood sculptures.
Fewer eyelashes mean more dust gets into my eyes so eyes water a lot.
Sleep disruption, waking up often usually because of a blocked nose.
These symptoms come and go with no rhyme or reason and I consider them trivial
compared to fatigue and nausea of which I've had none.
After the second Docetaxel I started loosing hair so shaved my head. I shave my head everyday but don't need to shave my face.
I have learned the value of hair in the groin region. Have to use baby power now that mine is gone.
Could not sleep a week before first infusion because of the chemo stigma.
My cheeks felt like having a sore and taste buds left the house for awhile.
My scalp looked like I had mange, so told the hair cutter it's chemo OK, so no need to quarantine the shop and electric shaver. She laughed and told me about some of the breast cancer customers, had to quickly change the subject, as her compassionate concern for cancer patients was evident.
Anyway, my scalp feels sore, can't sleep, as the pillow irritates, weird, perhaps nothing.
Still have eyebrows and eyelashes, hope will last.
The groin hair is holding out, maybe the chemo got sympathetic because of the ADT outcome with the raisins.
"These symptoms come and go with no rhyme or reason and I consider them trivial"
Yes, same here, I choose life, had a fun run, the brain does gets amazing orgasims!
My second Docetaxel is in a few days, as you say Onwards!
Well no, it's not fun, but it's a small price to pay for a few more years. And it could be much worse. My side effects are trivial discomforts. I could be in bed with a bucket.
My dx was Friday the 13th 3-15 ..... how that sticks with us . You are on the right pathway to healing it seems to me . Time to celebrate any good news .. Keep up the resistance and faith in your beliefs .. 🥳
Congrats! Got my psa today. Still 0.1. But it's in the bones. Chemo knocked lymph nodes out. Hit it hard now. Don't let it get the chance of getting in your bones. Consider Tall_Allen's advice. Enjoy.
Alas there are so many different outcomes from a few rounds of Doxetaxel because everyone is different. For some, they will come out of Chemo with a low PSA, and it will stay low. For others, the low PSA merely reflected a low kill rate of the cancer because the immune system had been shut down, and a couple of weeks later the true situation re-appears with the PSA doubling every few days as the immune system recovers. Remember the PSA is not a direct measure of how much cancer is there, but a measure if how many are being killed - which in turn gives an indication of how well your immune system is working. I do hope you are one of the lucky ones where it works like a charm!
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.