Where on Earth can you get 15mg pills. Largest I've seen were in Costa Rica where they are still "controlled" except outside the metro area and those are 6 mg
My prostate cancer was diagnosed in 2017. After much google scholar, other internet searches, and 2nd doctor opinions I came to the conclusion that surgeons cut. Not surprised. My urologist suggested a shot of Lupron and after 5 months Brachytherapy using Polladium 103. I went with this treatment. Prior to this I had PSA tests every year for 10 years. My PSA went from 2.5 to just over 4 then tested every 6 mo o 6.5 then over 11. My urologist then said you just earned yourself a biopsy. Biopsy showed both lobes had cancer cells. Additional tests including MRI did not reveal cancer outside of the prostate capsule.
Lupron does reduce the size of the prostate but I had more and higher severity "hot flashes" than my wife ever had while going through menopause. The bottom line is that one year after treatment, my PSA went to non-detect and currently still non-detect. The treatment made if difficult to have full erection so Tadalafil (Cialis) is taken several time a week to make it easier to pee.
Just wanted all to know that PSA screening is still important as well as a digital rectal exam. But only by a urologist. Most GPs do not have a "magic finger."
Where on Earth can you get 15mg pills. Largest I've seen were in Costa Rica where they are still "controlled" except outside the metro area and those are 6 mg
hi there. are u still doing the trial. has
ivermectin been successful for BPH thank you
Got the Viber app on my phone but could not access the group "A Prostate Community Trial" I would very much like to get in on this trial.
Also here is a new "invite link" from DoorlessCarp. https://invite.viber.com/?g2=AQAFgUnAnHbxg0%2BclrQDsqjsOsdzJHLCRt1ts8Yv96WUZnbPDYCpD5b5tQoQ0EHy
And this is a VIBER download link for those who don't have it yet. https://www.viber.com/en/download/
I'm new to the Viber app. I believe I had to scan a code to get into the group. I'm not sure if this link will work for you. Let me know if it doesn't. https://invite.viber.com/?g2=AQAFgUnAnHbxg0%2BclrQDsqjsOsdzJHLCRt1ts8Yv96WUZnbPDYCpD5b5tQoQ0EHy&lang=en
My prostate cancer was diagnosed in 2017. After much google scholar, other internet searches, and 2nd doctor opinions I came to the conclusion that surgeons cut. Not surprised. My urologist suggested a shot of Lupron and after 5 months Brachytherapy using Polladium 103. I went with this treatment. Prior to this I had PSA tests every year for 10 years. My PSA went from 2.5 to just over 4 then tested every 6 mo o 6.5 then over 11. My urologist then said you just earned yourself a biopsy. Biopsy showed both lobes had cancer cells. Additional tests including MRI did not reveal cancer outside of the prostate capsule.
Lupron does reduce the size of the prostate but I had more and higher severity "hot flashes" than my wife ever had while going through menopause. The bottom line is that one year after treatment, my PSA went to non-detect and currently still non-detect. The treatment made if difficult to have full erection so Tadalafil (Cialis) is taken several time a week to make it easier to pee.
Just wanted all to know that PSA screening is still important as well as a digital rectal exam. But only by a urologist. Most GPs do not have a "magic finger."
I like your trial on using IVM. Good luck.
I would be curious to know if those who rushed to volunteer for the jabs would volunteer for something that actually is safe and might help them!