That’s from Cornell, of course we want the PSA to drop to .01 but unfortunately as stated it went up from .20 to .26 not happy, we are both concerned of the rise as insignificant as it appears, he has ductal with cribform features and it’s alarming to us, any rise in psa
This is cut/copy from the portal as Cornell reports the psa
Your ValueStandard RangeFlagProstate Specific Antigen
0.26 ng/mL<=3.99 ng/mL
As of February 2017, this test is performed on the Siemens Centaur using Chemiluminescent Immunoassay. Values obtained with different assay methods or kits cannot be used interchangeably. The results cannot be interpreted as absolute evidence of the presence or absence of malignant disease.
Totally agree. The more sensitive tests can cause emotional trauma without adding information. My brother (we both have PCA) is on abiraterone and Lupron. His MO uses a very sensitive assay and his PSA came back as 0.02. This caused a lot of pain as he assumed resistance to abiraterone. So far it is just bouncing around below 0.07. Maybe it will go up soon but it is not helpful to know early.
I am very happy that nobody from my family is following closely my prostate cancer journey.
They just ask how are you if even that. They may thought 4 years ago that I will die sooner but now after 4.5 years after my diagnosis they may say, oh well you live long.
I believe that your husband is doing well and that he is getting the best treatments and scans.
I didn't have any scan for almost 4 years and I am only on ADT Degarelix injections only. I had an early docytaxel chemotherapy 6 cycles and I had 15 plus bone mets in my spine.
Now I don't have any visible mets on my PSMA PET/CT.
My biggest concern now is that I am osteoporotic. I have to go to the endocrinologist for that.
I just finished radiation of my prostate and mu PSA dropped from 1.4 to 1.2.
I don't want that they are preoccupied with my cancer. I am more than capable making decisions and happier if they don't interfere with my desissions.
I believe it would be unproductive and just unnecessary burden on them. I am so happy that I am not under guardianship and that I can make my own decisions without pressure from outside.
I see that I am probably the only one who is going to the doctor alone and I couldn't be happier.
Ok, my son is pushing me to exercise and that is ok. Otherwise even that is not necessary. I know what I can and can't.
yes I agree it is hard or impossible to talk to someone not going through the same thing. My younger brother just happens to be going through the exact same illness only he is a couple of years ahead. I would not wish it on him but it has been great to have him by my side on the walk.
Hi, Do you have Advanced Metastatic Prostate Cancer? We are trying to find a medication for sever plague psoriasis, my husband was on Stelera and then Tremfya for years, his MO took him off because he didn’t want my husband on any suppressants….I found a study possibly going to trial that IL-23 inhibitors which Skyrizi is may be used for prostate cancer as an aide…see thisicr.ac.uk/news-archive/immu...
I have stage 4 prostate cancer, diagnosed in March 2020. Psoriasis started when I was a teenager. Currently I take Skyrizi for psoriasis; if it has an effect on the cancer, so much the better.
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