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Scott Colcord's avatar

What do you remember when the doc said you have prostate cancer?

I was told over the phone, which is all right, but not offered any other information than I could wait for treatment later, and probably years later.

What happened next …. ?

I said I was intrested in waiting for treatment. Then the urologist told me of the monitoring protocols. A PSA test every 6 months, and a follow up biopsy in one year. I agreed to both of those.

Did the urologist offer support? Did a nurse?

No. No support.

Were you pointed to a support group?

No.

Were you on your own?

Yes.

Can you comment below? Please. Need your help.

Looking back, upon diagnosis five years ago this January, I greatly increased my drinking and went into a slump, My girlfriend said to find a support group. After one year I looked for a support group, found two, tried both of them, and chose one of those two.

Because of advise in the support group, I cut way back on alcohol, changed my diet to mostly plant based, and exercise regularly. I have, for other reasons, engaged in much more social activities, and consider that an important part of my new lifestyle.

The support group has helped a lot. I am the only one on AS, and I think the leader resents my presence, but that is not my problem. The others in the group are great.

After one year in the support group, my anxiety lessened. I find a lot of education on the internet.

Gleason 3+3, January 2017, one core, I can't find what percentage, PSA 8+, up from 4. 12 core transrectal ultrasound

Follow up biopsy february 2018, ASAP Atypical Asinar , 12 core transrectal ultrasound

Prostate size 35 grams, so above 4 needs to be monitored. Last PSA Feb 2022, still 4.4.

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Scott Colcord's avatar

I was told of the diagnosis, and told I could wait, probably wait for years, until treatment. No explaination of why I could wait. No information to help me decide.

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