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BCG shortage again and lack of surveys?
Greetings. I had bladder cancer diagnosis March 2014 and apologize for not giving correct details – i will do that for next post. Generally it sounded scary – invasive but nothing in the muscle layer. Two types of cells, and nothing past stage 1 which was surprise. In July had good biopsy result. In September was supposed to have 3 BCG treatments but because of shortage only had 1 with 2 mitocyicin (sp?) treatments instead. I have continued to have minor discomfort when urinating (4 months later) but no complaints. Today was scheduled for second of 3 BCG treatments and cancelled again because of shortage. I read online last month that some places were rationing the BCG (not giving as much to some people as they would before). I asked my urologist about the shortage last month and he didn’t seem to be aware that it was much of a problem.
I see you have a thread about BCG but nothing since 2006 or did I miss it? The other thread I would be interested in is a national (international even better) survey of bladder cancer patients. I am a woman who never smoked so I would love to know whether I did something that could be avoided. It would not be that hard for the medical professionals to distribute such a survey as people get diagnosed so I don’t understand why that is not happening.
In my community there is a cancer center with all kinds of resources and support groups. I have never seen an oncologist and feel like I am outside of any loop that might get me answers to the above questions.
Thanks to everyone who started this site and continues to spend hours maintaining it.