Two days after second BCG treatment and not feeling too bad. I did notice this AM some debris in my urine and I am going to assume that this is normal for this stage of the BCG treatment. This is based on the posts that I have read at this site and again I can't stress how grateful I am for the input I have received thus far.
I do feel a little guilty about feeling uncomfortable with not allowing an unsupervised trainee to administer my second treatment. She did not even display competence in telling me she was going to perform the treatment. Well Que Cera it's my junk she was going to deal with.
Thanks to all of you for sharing your experiences.
One of the main reasons I have for taking the aggressive route with cancer is my family history. I have had a
brother who died from throat cancer and another brother who is a survivor of various forms of cancer. I believe if one is not aggressive then the cancer will be aggressive. Just my thoughts anyway.
An off the wall question that has come to my head is that my sleep pattern is way off kilter. Does that ever go back to normal? Please share your thoughts.
Just received a reminder call for treatment number two (who's counting?) on Friday.
Really, I am not an expert on this....sort of been there, done that, and, like all of you, read everything I could get my hands on.
I believe that the deal with BCG is that it is more effective against high grade, or CIS, than against low grade bladder cancer. The problem with all of these is that THEY COME BACK. Many patients with low grade, where BCG was not recommended at the beginning, end up trying it when they tumors return for the third or fourth time.
In my case, I had CIS to start, so there was no question.
Ray, you sound like the right kind of patient. One who finds out everything he can and then makes joint decisions with his doctor. IMHO, that is the only way to go.
Diagnosis 2-08 Small papillary TCC; CIS
BCG; BCG maintenance
Vice-President, American Bladder Cancer Society
Making the decision to go for the BCG treatments was a joint decision between my urologist and myself after a discussion on the odds of re-ocurrence. Not sorry that I'm taking the treatments but just wanted to know what to expect. This forum is already providing me with an enormous amount of information. Information that is real time with live experiences is a whole lot better than a lot of the historical data that is out there. I am grateful for that. Be interesting to hear Sara Anne's comments.