Forum Replies Created

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  • mike

    Member
    April 18, 2008 at 3:34 pm in reply to: Newly Diagnosed at 27!

    I too had a 6 month cystoscopy this morning and it was clear. I have much more discomfort than with the other ones though. But I am off to a ladies retreat on Lake Huron so I’ll deal with it! The sun is out and I’m ready for a couple of days away from it all. We had a devastating senior apartment fire recently in the community in which I work (made national news) and though the trauma didn’t happen to me, being there in the midst of it helping the 200 evacuated seniors has had an emotional affect on me and I am a little weary. I know I seldom post but I am always here listening and learning. There is so much knowledge here and not just about cancer, perhaps just as important, about living. Here’s to rest, relaxation and renewal.

  • mike

    Member
    April 5, 2008 at 1:04 am in reply to: Many times lurking first post

    I know this is about BC but I’m concerned about the statement “I don’t feel safe in my own home”. Are you OK? I’ll choose to not over react and assume you are venting as we all need to do, but really if you are not safe please know there are always options in our lives. It is just so hard to see them sometimes.

    Anyway, we care about you here and as it was said, someone is almost always on site to listen.

  • mike

    Member
    March 14, 2008 at 9:00 pm in reply to: Hollys father passed

    Though I do not know you or your father the tears started when I read of his passing. It has been 6 years since both my Mom and Dad died. I remember feeling like I had joined a club I didn’t want to belong to. (Perhaps the parentless child club…I don’t really know) I asked some older, wiser women than myself when I would stop missing them and they told me never. It is ix years later and I believe them to be right. But life is good (even with BC) and there are many, many years of memories and lessons learned and love to pass on to the next generation.

    I really didn’t mean for this to be about me. I really just want to offer my condolences to you and your family during this sad time.

  • mike

    Member
    March 7, 2008 at 9:59 pm in reply to: Finally, GOOD NEWS

    My urologist also recommends the Theralogix. I haven’t seen it mentioned on this forum before until you brought it up. (I’ve only been here a few months though). I was interested in ordering it but haven’t due to the cost. So I guess it’s extra carrots and sweet potatoes for me!

  • mike

    Member
    February 21, 2008 at 9:08 pm in reply to: Mitomycin-C Revisited

    Everyone responds different and my uro also did not make a big deal out of it. I was still a little concerned. However, I had 6 weeks of mitomycin, finishing in Dec 07 and didn’t have a moment of discomfort or any side effects. I was grateful as I know that is not everyone’s experience. Good luck to you. Hope you have an easy time of it.

  • mike

    Member
    February 5, 2008 at 3:00 pm in reply to: My Doctor gave us good news after a second Tur

    Hi Rosemary, the second one says it was high grade invasive cancer, present in the muscle bundles but not the muscle wall,they just told us that yesterday. I have a call in to my oncologist to see if he has any answers for us.

  • mike

    Member
    February 2, 2008 at 1:29 am in reply to: My Doctor gave us good news after a second Tur

    Rosemary,we have not seen the conflicting report, although we have requested it today probably get it next week when the offices are open. we were told by the second surgen that he saw no cancer in the muscle wall. so thats where we stand on one hand I would like to go with good report and just be happy, but Id like to be more sure. thanks

  • mike

    Member
    February 1, 2008 at 11:54 pm in reply to: My Doctor gave us good news after a second Tur

    Rosemary, no the second turb found no cancer in the muscle. The first lab that saw muscle invasive tumor was done with the specimen from the tumor of,my first turb. the conflicting report was done from a slide, could this fact effect the pathologists findings slide versis specimen? thank you sodacat

  • mike

    Member
    February 1, 2008 at 8:05 pm in reply to: My Doctor gave us good news after a second Tur

    thank you all for sharing I had my latest path report e mailed to me today. it says the tumor is mainly low grade with a focus of high grade carcinoma5% and there is no muscle or lamina invasion.what do you think? thanks sodacat this is nothing like the first report in dec.

  • mike

    Member
    January 31, 2008 at 9:27 pm in reply to: My Doctor gave us good news after a second Tur

    My first Doctor sent me to the second doctor who saw the pathology report and disagreed with the results and went in to remove the remainder of the tumors left by the first surgen, the first surgen said there was too much blood and was unable to see well enough to remove all the tumors that were present, I had two transfusions while in the hospital, so that part seems reasonable.

  • mike

    Member
    January 31, 2008 at 8:19 pm in reply to: My Doctor gave us good news after a second Tur

    Hi Pat, two different doctors and two hospitals.

  • mike

    Member
    January 31, 2008 at 6:08 pm in reply to: My Doctor gave us good news after a second Tur

    I want to be happy with the last pathology report but can they be so compleatly conflicting should I have a third

  • mike

    Member
    January 29, 2008 at 8:30 pm in reply to: Glad to know I’m not alone

    That’s what I had. Mitomycin immediately after my TURB and after I healed, 6 weekly treatments of it. I also had no side effects and my first 3 month check-up done this month was clear. I now graduate to monthly maintenance treatments. Best wishes to you for the procedure and treatments!

  • :Dhey Karen, Thank you .very helpful reading,have a great day :-*sodacat

  • mike

    Member
    January 22, 2008 at 12:16 pm in reply to: 34 year old newby in Seattle

    Pat, Im not Seattle,Im from Florida,but thanks for the info.sodacat :)I guess I got off tract in Lynns post, sorry,my friend

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