My urologist told me I was beyond surgery and into CRPC .. A year later he told me I may have to remove my testicles .
The problem is I wanted to trust my life to my doctor. Turns out I was able to lower my PSA from 31 to 4.5 now for 2 years using PCSPES and POMI10x. I take everything my doc tells me as an opinion and will always have second or even third opinions from now on.
Prostate Surgery May 2021,(PSA was 18.5) - last PSA – 0.48 (03/21) - PSADT 4.6 months•Time to recurrence – 1.10 @ 9 mths; 2.2 @14 mths•Pathological Gleason score – 4+3 (7)+T5 •Stage: p2Tc – PNI - (clear margins, SV, lymph nodes) After 6 months 8 pills of PCSPES per day and 4 pills of POMI10X , PSA is holding at .81 for 5 months now. No Lupron. Truly amazing results.
After being diagnosed with metastatic PC about 4 years ago, my 70 year old brother passed away in a hospice house on Labor Day. He tried everything, but nothing seemed to stop his prostate cancer! While he didn’t follow this website, I would often tell him of my protocol of 8 PCSPES and 4 POMI10x per day or procedures I had read about on this site, trying to offer him hope amidst a dire prognosis. Fortunately, he never suffered from the side effects of his Docetaxel chemo, but he never really got any substantial improvement from any of his treatments either. After stopping his last infusions, he deteriorated rapidly, suffering from extreme pain, confusion, incontinence, weakness and falls. His quality of life was what impacted me. But my brother was the eternal optimist and comic but a cynic of natural therapies like PCSPES. I believe his stage 4 diagnosis could have been avoided and prolonged as it has done for me. My PSA went from 16.9 and is holding at 3.2.
I stopped Lupron January 2021 after the terrible side effects. I April 2021 my PSA was 0.19 and T < 20. On November 2021 my PSA has increased to 6.9 and T is 170. Bone scan is clear, CT shows all pelvic and abdominal lymph nodes avid in PET/CT scan are normal size. I started with 9 pills of PCSPES 3 times per day and for about 6 months PSA is holding steady at .97
I did Xtandi and Lupron and was hoping for the cure. I had some durable remission maybe 5 months and plan to rechallenge after chemo or immunotherapy. I tried three months of 8 pills per day and my PSA dropped 50%. Docs say to just keep doing what i'm doing and that sometimes natural supplements interact in a positive way.
My urologist told me I was beyond surgery and into CRPC .. A year later he told me I may have to remove my testicles .
The problem is I wanted to trust my life to my doctor. Turns out I was able to lower my PSA from 31 to 4.5 now for 2 years using PCSPES and POMI10x. I take everything my doc tells me as an opinion and will always have second or even third opinions from now on.
Prostate Surgery May 2021,(PSA was 18.5) - last PSA – 0.48 (03/21) - PSADT 4.6 months•Time to recurrence – 1.10 @ 9 mths; 2.2 @14 mths•Pathological Gleason score – 4+3 (7)+T5 •Stage: p2Tc – PNI - (clear margins, SV, lymph nodes) After 6 months 8 pills of PCSPES per day and 4 pills of POMI10X , PSA is holding at .81 for 5 months now. No Lupron. Truly amazing results.
After being diagnosed with metastatic PC about 4 years ago, my 70 year old brother passed away in a hospice house on Labor Day. He tried everything, but nothing seemed to stop his prostate cancer! While he didn’t follow this website, I would often tell him of my protocol of 8 PCSPES and 4 POMI10x per day or procedures I had read about on this site, trying to offer him hope amidst a dire prognosis. Fortunately, he never suffered from the side effects of his Docetaxel chemo, but he never really got any substantial improvement from any of his treatments either. After stopping his last infusions, he deteriorated rapidly, suffering from extreme pain, confusion, incontinence, weakness and falls. His quality of life was what impacted me. But my brother was the eternal optimist and comic but a cynic of natural therapies like PCSPES. I believe his stage 4 diagnosis could have been avoided and prolonged as it has done for me. My PSA went from 16.9 and is holding at 3.2.
I stopped Lupron January 2021 after the terrible side effects. I April 2021 my PSA was 0.19 and T < 20. On November 2021 my PSA has increased to 6.9 and T is 170. Bone scan is clear, CT shows all pelvic and abdominal lymph nodes avid in PET/CT scan are normal size. I started with 9 pills of PCSPES 3 times per day and for about 6 months PSA is holding steady at .97
I did Xtandi and Lupron and was hoping for the cure. I had some durable remission maybe 5 months and plan to rechallenge after chemo or immunotherapy. I tried three months of 8 pills per day and my PSA dropped 50%. Docs say to just keep doing what i'm doing and that sometimes natural supplements interact in a positive way.
My urologist told me I was beyond surgery and into CRPC .. A year later he told me I may have to remove my testicles .
The problem is I wanted to trust my life to my doctor. Turns out I was able to lower my PSA from 31 to 4.5 now for 2 years using PCSPES and POMI10x. I take everything my doc tells me as an opinion and will always have second or even third opinions from now on.
Prostate Surgery May 2021,(PSA was 18.5) - last PSA – 0.48 (03/21) - PSADT 4.6 months•Time to recurrence – 1.10 @ 9 mths; 2.2 @14 mths•Pathological Gleason score – 4+3 (7)+T5 •Stage: p2Tc – PNI - (clear margins, SV, lymph nodes) After 6 months 8 pills of PCSPES per day and 4 pills of POMI10X , PSA is holding at .81 for 5 months now. No Lupron. Truly amazing results.
After being diagnosed with metastatic PC about 4 years ago, my 70 year old brother passed away in a hospice house on Labor Day. He tried everything, but nothing seemed to stop his prostate cancer! While he didn’t follow this website, I would often tell him of my protocol of 8 PCSPES and 4 POMI10x per day or procedures I had read about on this site, trying to offer him hope amidst a dire prognosis. Fortunately, he never suffered from the side effects of his Docetaxel chemo, but he never really got any substantial improvement from any of his treatments either. After stopping his last infusions, he deteriorated rapidly, suffering from extreme pain, confusion, incontinence, weakness and falls. His quality of life was what impacted me. But my brother was the eternal optimist and comic but a cynic of natural therapies like PCSPES. I believe his stage 4 diagnosis could have been avoided and prolonged as it has done for me. My PSA went from 16.9 and is holding at 3.2.
I stopped Lupron January 2021 after the terrible side effects. I April 2021 my PSA was 0.19 and T < 20. On November 2021 my PSA has increased to 6.9 and T is 170. Bone scan is clear, CT shows all pelvic and abdominal lymph nodes avid in PET/CT scan are normal size. I started with 9 pills of PCSPES 3 times per day and for about 6 months PSA is holding steady at .97
I did Xtandi and Lupron and was hoping for the cure. I had some durable remission maybe 5 months and plan to rechallenge after chemo or immunotherapy. I tried three months of 8 pills per day and my PSA dropped 50%. Docs say to just keep doing what i'm doing and that sometimes natural supplements interact in a positive way.