Experiences with

Antagon

Hi, I'm contemplating going for Bepiroversin jabs, to reduce my HbsAg levels, which currently stands at 1012 iu/mL, with treatment (from a starting level of 3k+ 12 years ago). I understand Bepiroversin treatment especially works on people with a low HbsAg level. What number/s is considered a low?

I received a text from the WIFE of a buddy. She said he has been diagnosed with advanced PC. She had no real particulars other than it was in his spine, pelvic area and lymph nodes, bladder, etc. The really scary part of the text was she sounded upbeat because the doctor was very optimistic- just

abiraterone+predni failed after 2 yrs 10 months. Had SBRT and VMAT 33 sessions one year ago to swat L1 lesion .. pSA gradually rising ,now at 6.7. what can I do as a next step to fight the beast. Any recoms? Anyone have the same situation?

Just the things are messy rn. And if i get accepted, i try and get overwhelmed and sick. For everyone telling me to get a work as if it's the magical cure for everything

After PCa reoccurence, after Proton therapy in 2009, started Doublet therapy.. Firmagon & Nubeqa in August 2024 and PSA just tested January 16th, is .75. Wondering when I should have 2nd PSMA-Pet scan to check on bone & lymph node mets which lit up scan in August 2024?Thanks for any input.

I had RP nine years ago, salvage radiation 4 years ago, my psa test results have been less than .02 after treatment with radiation. Current side effects minor incontinence, maybe one leak per day, and one small passing blood in urine event during the past year due to radiation damage to the bladder

My dad (72) was diagnosed in 02/24 with multiple bone mets, Gleason 9 an initial PSA of around 4000. He had triplet therapy with Docetaxel, Lupron and Nubeqa. His nadir was 26.1 in September 2024. His PSMA in November 2024 showed moderate to high activity in his prostate and in one area on his spine.

Got a battery of tests going on to understand why my immune system is not as good as our blog’s humor guy (starts with a J) In reviewing some of the ancient history I found that my PSA was 1.14 in January, 22. In late July, 22 I had a brain MRI but my legs blew up a week later to twice their size

First off, a status of my situation: I am hormone sensitive and have been doing BAT myself using different testosterones at times. Been doing BAT for 16 months. Recently had a one month PSA spike ( 1.4 to 6.3) along with uric acid/ kidney stone/gout. I attribute the PSA and uric acid spike to one

Hi Everyone, Firstly want to say thanks for all the responses to my last post regarding my husbands dreadful side effects of Doxcetaxel. Each reply was encouraging and informative. After 3 infusions with Doxcetaxel and horrendous side effects, my husbands psa has climbed to 900 which is alarming. The

Been a while since I posted, Long story short. Radiation 2019/2020. Psa was lower than a snakes guts. then it started to rise and was advised by urologist to have salvage surgery. Our friend TA advised against this. Sorry TA but to keep my Sheriff happy went through with it on 15 february 2023. I ended

I have an aggressive and somewhat rare form of metastatic prostate (super low PSA, high CEA). Being treated at Duke. I went off Pluvicto after two doses. Duke is putting me into their CHAMP trial. https://clinicaltrials.gov/study/NCT04709276 Has anyone out there participated in this trial? Thanks

My husband has been on Nubeqa for 3 1/2 years now. His PSA is rising again, so MO has ordered another PSMA scan and also did a Guardant 360 liquid biopsy blood test, to hopefully find out what's going on. MO said if something shows up on his scan, he will probably start him on Olaparib (Lynparza) and

How long does it take abi to start reducing PSA? I started 4 weeks ago and PSA is still rising.

I was on TRT prior to my diagnosis. When my PSA was over 4, my doctor took me off of TRT. That was in March 2023. I experienced and continue to experience the typical side effects of low T. My Gleason Score was 4+3 and the cancer was localized and confirmed by a PSA- PET scan. My PSA never exceeded 5.7

74 yrs old, initial PSA 16. Biopsy Gleason 4+3 with mets to presacral lymph nodes as per PSMA scan. 45 radiation treatments ended Dec. 2 started Eligard Oct 8. December 23rd PSA 0.16, T <10. Urologist wants to add abi+ prednisone to Eligard for total of 24 months. Currently only minor SE with Eligard

For many of us learning about the various initial and recurring cancer options etc can be very confusing. In my journey I am at the point where I am past all the work up data and have already had my initial treatment and am now looking into potential identification of recurrence. Just some things that

As you know from my recent BAT posts I had to stop due to Kidney Stones, gout and high uric acid at 5.6 along with a big spike in PSA from 1.4 to 6.36 in 30 day period while on High T. I contribute it to not drinking enough water and a PSA spike causing high uric acid. In any event this was fortuitous

Hi ! I thought that I could share some good news. I’ve had my PSA result; 9 month PSA measurement after radiation (with ongoing Orgovyx and Abi) and it was < 0.1 again (in Sweden and Finland they don’t do ultrasensitive PSA). Well, anyway I wanted to share good news with all fantastic members

Hi-I apologize if I am taking up your time to simply satisfy my curiousity. My post is not seeking advice or suggestions just thoughts on what think is a bit strange. I am curious about my most recent PSA test after being treated on Lupron and Abirarterone for more than 12 years. My PSA started rising