Carol, the good news is that this "discomfort" tells you that the BCG is doing something!!! However, it is hard to take sometimes. If the side effects get to be too much, the dose of BCG can be lowered; even 1/10th the original strength has been shown to be effective. I was down to 1/3 by the time I was through the maintenance series.
My urologist told me something interesting. He said that the dose of BCG has no scientific basis (ie, clinical trials) behind it. That just happened to be the commercially available preparation at the time it was beginning to be used and shown to be effective in treating bladder cancer. So there is no "MAGIC" rule that says that you have to stay with the initial dose.
Diagnosis 2-08 Small papillary TCC; CIS
BCG; BCG maintenance
Vice-President, American Bladder Cancer Society
Thank you for sharing your most valuable information. I finally started the bcg on July 31st. The first one was a walk in the park compared to the 2nd one. This is not very pleasant to say the least! Once it came time to hit the bathroom it was on!! The razor blade/burning/urgency feeling was back!! I had to take a pain pill!! Today I feel whooped! My nurse said on Thursday that the 4th treatment gets pretty tough. I know I have to get through it but holy cow!
I will definitely ask my doctor about flexarill. I am starting to feel somewhat better after the addition of the myrbetrig. It has finally kicked in somewhat. Now just Anxiously waiting to start the bcg.
Carol, my hubby is a bladder cancer patient....but i have interstital cystitis which ia another painful bladder condition. I take flexeril a muscle relaxant when it flares. I am wondering if something like that might calm your bladder down...it could be spasming causing your frequent urge to urinate. The flexeril helps me with that, but i take it only at night as it makes me sleepy. Just a thought .
As I posted previously I was scheduled for a Doctor's visit on 6/24 to discuss my BCG treatments. Well it is not going to start until July 24th as I am having too much pain and the urge is aweful. My Dr said I have a very "Unhappy Bladder."it could be from the mytomyicin and then going back in to biopsy in June. He stated that the BCG would make it worse. This is extremely uncomfortable and I am tired all of the time. Maybe chalk some of the tiredness to getting up every night and going every hour. He did double the enablex and add myrbetrig. I don't feel that they are helping. It has been 2 months since the initial TURBT and 1 month since the biopsies and now I'm worried that something could be brewing while I wait.
Stage 1 grade 3 bc
TURBT with Mytomyicin
I had same diagnosis as you in 2006, and am still here and life is good. I had a series if mytomycin treatments, and have to say the side effects, whilst definitely not unbearable lasted for about 12 months( a day or two not good , but mild cistitis like effects for much longer).The most time I had to take off work was the afternoons of the treatment. Don·t worry about the " catheter part" of bcg treatment- the amount of the liquid they put in your bladder is very small, and a tiny,tiny tube is used to put it in. Side effects vary from person to person, but for me, so far have not been too bad.Good luck on the 24th, with the start of your treatment, and feel free to bend our ears whenever you fel like it!