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To read the most complete version of my story, please read Part 1 as well as this part, Part II.

Here, I am writing a continuation after CT scan has shown more lesions, growth in
at least one liver lesion, and a possible lesion in a new location (with follow-up
testing recommended.) This while receiving Genzar and Taxol. Also, yesterday I
had a turbt (and am at home, with a catheter.) I don't know the exact dimensions of the calsified tumor removed, but it was a lot smaller than the "softball" sized one removed last year.)

I write with a subjective description of my almost-a-year since diagnosis.

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In 2006 and 2007, my wife and I took a road trip (motorcycles) for my birthday (around Memorial Day Weekend).  She rides my Suzuki Volusia VL800, and I ride my friends Honda Shadow 750cc.  During the trip last year (2007), I developed a bad migraine.  My wife offered a niproxin, and after verifying with my RN mother that this would be fine, I took the medication.  Within a few hours, I felt fine.  We rode for several hours during the next couple days, but over paved rode.  I ride my motorcycle to work each day (one hour each direction), so my body is very used to the ride.

The day after

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01-29-08  Results of recent CT Scans

I talked to my nurse on the phone, not so good a way to get results. I think I'll call back and ask to pick up a copy of the report today. I did hear that my largest liver lesion had grown from 4.0 to 4.9 CM since November. And it sounds as if I have more lung nodules than before. I am confused about what to do now. My urologist wants to do cystoscopy on TH and I am also scheduled to see my medical oncologist that day. One thing has to be deferred -- but which I don't know. I do want to know what impact the CT scan results will have on my treatment

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Going in for the Four monther tomorrow 1/29/2008.  Will update

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after 3 times with bladder cancer I have been cancer free for over 2 years. but I will never forget my friends here that have helped me thru the ruff times-* thank you so very much my prayers are with you

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In January 2007, the bleeding became continuous. I went to my present primary care doctor and was told that I should take antibiotics and see if it improved. I called back when the big clots started coming but was told (by a nurse) to just keep my regular appointment. I didn't get to that appointment because I had to go to the hospital with "frank bleeding."  I got a referral to a urologist while hospitalized and had a tur after being transferred to a hospital repaired enough to do it. Pathology: Stage 3 high grade tcc with sarcomatoid features. Some tumor remained after tur. The tumor has

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Susan - delayed diagnosis
A volunteer at my church helped me find WebCafe and its forum. My bladder cancer has spread to my liver and lungs, maybe a bone. i was supposed to have a radical cystectomy this month (Dec. '07), but we cancelled it after the MRIi report. Now, I'm getting chemotherapy (taxol and genzar). MVAC didn't work for me. Radiation did shrink my primary tumor.

I am told my case is "difficult" because of the late stage of discovery/tur/diagnosis (Stage 3, fat invasive) the sarcomatoid variant, and now the spreading. I know it is difficult -- I just want to be seen as important

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Hi everyone , in Jan 2006 we got a break in our weather,(I live in the  mountains) so I was doing an early spring cleaning in my horse barn. I had been moving alot of heavy junk out all day when I had to stop and pee.Surprise! alot of blood came out, so being me I went back to cleaning figuring I probly wasn,t going to drop over dead yet. That night I was still peeing blood so I went to the er. They did a cat scan and said I had a kidney stone, the Dr. ask me if my back was hurting ,and it was but I deal with back pain all the time so it wasn,t any big deal. Went home to strain my pee for a

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Home alone:

Now that the operation is all over I have no regrets for choosing to have the neo bladder. I would be lying if I said it was easy it certainly was not.

At times during my first few days I did have lots of regrets and thought I had made a big mistake for choosing the neo bladder. The other operation for the stoma bag would have been easier on my body and the recovery time much quicker. However I came through it all and I am alive and I am so very thankful and appreciative. I take my hat off to all of the people involved in helping and supporting me for getting through the last 6

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Home:

I spent 10 days at home with my two catheters and it was a very slow process building up my strength day by day. Walking around the living room or visiting the toilet was enough to feel exhausted.

During these 10 days at home I had a great support network to help me which is so important. Rest and relaxation was the order from the doctor and eating as much as possible to get my strength back. During my 22 day hospital stay I lost 14 kilo’s in weight and it took a good week before I noticed that I was filling out again and not so gaunt.

I truly believe that getting to your home environment

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