Prostate Cancer- getting help-questions answered

Posted by cony2 @cony2, Aug 16, 2022

Approximately 20 years ago a Urologist after listening to my symptoms and without doing procto or anything said I had prostate cancer and would schedule me for surgery next week-- my response was lets talk and chose to go on the blue pill and wait.
Since then after biannual tests and blood count going from 4 to 7 now 14, suggests getting a bone marrow test to see if any cancer cells show up.
My question is: should I consult a cancer specialist now???

Interested in more discussions like this? Go to the Prostate Cancer Support Group.

Profile picture for dirtdancer @dirtdancer

I was on abirateron for two years. Now on apaulutimein (?) (Ebearlea) for no apparent reason. I could not take the recommended dose as it made. Me very nauseous and so I split the medication two pills in the morning and two pills at night
I have become convinced that my doctors are treating me, and not trying to cure me . So I have started my own research into cancer cures and have added more vitamins, even more stringent, diet changes, prayer, etc. My numbers have been on a downward trend since I started my cancer cure. Thanking I’m not putting this out there to criticize, but to bring awareness. I do think these huge cancer center buildings have to pay for themselves and the way they do it is treating you not curing you.

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Please share more

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Profile picture for dirtdancer @dirtdancer

Honestly your dr or drs need to be more aggressive in their treatment! I sought multiple opinions at 11 PSA
I first cut out sugar including very little fruit ( so I could eliminate natural sugars as well)
I restricted carbs a lot, but I did not eliminate them. I increased salads with olive oil, vinaigrette, type dressings. No sodas, no, french fries, almost no beef, or processed red meat of any kind, increased consumption of fish. Then I saw a naturopathic person and added magnesium glycinate (specifically) a super B complex, double the daily dose of vitamin C, with rose hips. Multiple vitamins, saw palmetto, iron, D3, melatonin, and two I don’t remember how to spell. I take the majority in the morning with a small breakfast. The chemo pills I take have the side effects of increasing belly fat in men or women, it’s just a side effect and so you have to eat less and exercise more. Walking is good dumbbells are good. I am still researching minerals to take and I am going to add a broccoli pill or a plankton pill I am going to continue this research on cures. No sugar seems to be the most beneficial first step

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If diagnosed as stage 4 castrate sensitive metastatic cancer in spine, how can it be cured, but only controlled.

I am on Zolodex again after L2 lumbar nuked taking out 1 inch PC 5 years ago had 40 sets of radiation and WAS FINE psa <.02 Now 1.2 RISING TO 5.23

concerned GETTING CT SCAN AND BONE SCAN AGAIN DEC 5TH

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Profile picture for Ski Rossi @ford1929

Would you mind sharing what vitamins you are taking?
I was on Bilutamide for 2 months, PSA 72 down to 28 then switched to Zytiga
and my blood pressure increased and PSA up to 37

Jump to this post

Honestly your dr or drs need to be more aggressive in their treatment! I sought multiple opinions at 11 PSA
I first cut out sugar including very little fruit ( so I could eliminate natural sugars as well)
I restricted carbs a lot, but I did not eliminate them. I increased salads with olive oil, vinaigrette, type dressings. No sodas, no, french fries, almost no beef, or processed red meat of any kind, increased consumption of fish. Then I saw a naturopathic person and added magnesium glycinate (specifically) a super B complex, double the daily dose of vitamin C, with rose hips. Multiple vitamins, saw palmetto, iron, D3, melatonin, and two I don’t remember how to spell. I take the majority in the morning with a small breakfast. The chemo pills I take have the side effects of increasing belly fat in men or women, it’s just a side effect and so you have to eat less and exercise more. Walking is good dumbbells are good. I am still researching minerals to take and I am going to add a broccoli pill or a plankton pill I am going to continue this research on cures. No sugar seems to be the most beneficial first step

REPLY
Profile picture for dirtdancer @dirtdancer

I was on abirateron for two years. Now on apaulutimein (?) (Ebearlea) for no apparent reason. I could not take the recommended dose as it made. Me very nauseous and so I split the medication two pills in the morning and two pills at night
I have become convinced that my doctors are treating me, and not trying to cure me . So I have started my own research into cancer cures and have added more vitamins, even more stringent, diet changes, prayer, etc. My numbers have been on a downward trend since I started my cancer cure. Thanking I’m not putting this out there to criticize, but to bring awareness. I do think these huge cancer center buildings have to pay for themselves and the way they do it is treating you not curing you.

Jump to this post

Would you mind sharing what vitamins you are taking?
I was on Bilutamide for 2 months, PSA 72 down to 28 then switched to Zytiga
and my blood pressure increased and PSA up to 37

REPLY
Profile picture for philnob @philnob

Hello,
I was on Zytiga, and noticed a slight breathing problem which over a short period of time became more serious. When I couldn’t walk one block without feeling a heaviness in my chest I called my nurse and told her I would no longer be taking Zytiga. My Doctor told me that when her patients complain about this problem she recommends another medication. I don’t understand why we all can’t get out in front of the wrecking ball, but that seems to be the way it is. I have been using Relugolix for 11 months with no breathing issues.

Jump to this post

I was on abirateron for two years. Now on apaulutimein (?) (Ebearlea) for no apparent reason. I could not take the recommended dose as it made. Me very nauseous and so I split the medication two pills in the morning and two pills at night
I have become convinced that my doctors are treating me, and not trying to cure me . So I have started my own research into cancer cures and have added more vitamins, even more stringent, diet changes, prayer, etc. My numbers have been on a downward trend since I started my cancer cure. Thanking I’m not putting this out there to criticize, but to bring awareness. I do think these huge cancer center buildings have to pay for themselves and the way they do it is treating you not curing you.

REPLY
Profile picture for dd2312 @dd2312

Colleen, it says there is a prostate cancer support group meeting right now but there is no Zoom link posted.

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Hi @dd2312, I'm sorry that I'm only seeing this now. I will ensure that the future meeting have the link included.

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Profile picture for Colleen Young, Connect Director @colleenyoung

DD, I don't see a Zoom support group specifically for prostate cancer listed in the Events. Many inperson support groups at Mayo moved to Zoom over the past couple of years. @muradangie might know more.

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Colleen, it says there is a prostate cancer support group meeting right now but there is no Zoom link posted.

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Profile picture for dd2312 @dd2312

Colleen, I was fortunate enough to be at Mayo Rochester for radiation therapy last week when the prostate cancer support group met in person for the first time since COVID. Interesting, they also did it on Zoom but the Zoom didn't work. IT (information technology) was not involved but I think they could have easily fixed it.

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Dang. Thanks for letting me know. We'll work to get that fixed.

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Profile picture for Colleen Young, Connect Director @colleenyoung

DD, I don't see a Zoom support group specifically for prostate cancer listed in the Events. Many inperson support groups at Mayo moved to Zoom over the past couple of years. @muradangie might know more.

Jump to this post

Colleen, I was fortunate enough to be at Mayo Rochester for radiation therapy last week when the prostate cancer support group met in person for the first time since COVID. Interesting, they also did it on Zoom but the Zoom didn't work. IT (information technology) was not involved but I think they could have easily fixed it.

REPLY
Profile picture for cilong @cilong

My husband’s oncologist prescribed Abirateron (Zytiga) treatment assuring us there was no risk of seizure side effects. Three to four weeks into treatment, husband had a gran mail seizure and was transported to ER. Thankful he was home and not driving, etc. Three of his doctors (oncologist, pcp, and now neurologist) still say this is not a side effect. They don’t like it when we do our own research, My husband has been seizure free for over forty years. He will be having an MRI and EEG just to be sure something else isn’t going on, but it seems the Abiraterone was the culprit. Any thoughts? Thank you.

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I’ve been taking low-dose (250mg/day with a light breakfast )abiraterone for over two years and never experienced any seizure side effects. However, I did experience a moderately increased blood pressure and an increase in blood lipids due to the abiraterone.

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