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I agree with Anettemartinrn, whether the original story of Kathy West is true or not is trivial. Ovarian cancer is true and the fact that it is almost a totally silent cancer is just as true. How do I know? I have it. And I had no signs in the beginning. Most of you will not recognize my name - I used to post here years ago and only recently began lurking again. Last fall, I started to have serious pain when having a bowel movement. Thinking I had Irritable bowel syndrome, I let it go for a few weeks before finally making an appt. with a gastroenterologist. It was only then discovered after a series of tests that I have advanced cancer. By the time I found out I had it, it had already spread throughout my peritoneal cavity. I immediately went to Memorial Sloan Kettering Cancer. The doctor told me most women 'present' as Stage 3 or even 4 because it's very hard to detect in the early stages. I had an extremely painful operation on January 2. They literally opened me from my groin to my rib cage, took every single organ out, and removed all the visible tumors. They were everywhere, my abdominal lining, my bladder, my colon (they had to resection a part of it), my diaghragm, and a tissue inside my abdomen called the 'omentum' which was also removed. I'm still not recovered from the operation, yet had to start my first round of chemo on February 5. I will have to go through 6 rounds of chemo. The first round has sucked; I cannot imagine what it's going to be like to go through the next 5. Once this cancer is in Stage 3, the return rate is really high and the 5-year survival statistics are not good. I can't even begin to express how depressed and angry I've become, how in fear for my life I am every single day, not knowing what's going to happen with me. I've never been sick in my life, always healthy. I ate right and exercised. I'm only 43 years old. I too was discouraged by my gynocologist from taking the CA125, because of the false positives. If I had the chance do it again, I'd take that CA125 anyway, false positive or not, even if I had to pay for it out of my own pocket. I would have insisted. I wish it would become a mandatory test.

That was me Kathleen. I am an 8 year Inflammatory Breast Cancer Survivor. It is a very aggressive cancer. I'm not out of the woods yet, still being treated but so far it is very well controlled. I show no evidence of disease. I was never promised a cure but they said they hoped to control it. Control is good! Cherryfizz has a sister who has survived it about twice as long as I have. Anne gave me so much hope when she told me about her sister, it meant the world to me. I thank you everyday Anne for giving me the hope I needed. Fortunately I knew about IBC before I was diagnosed. My doctor was very surprised that I diagnosed it and he was sure it was mastitis. Knowing helped saved my life. If you haven't watched the video, I urge you to see it. It is a rare cancer, but it happens. The youngest gal I know to get it was 13 years old. BTW Men get it too.

Well, the main word in all of this "what to eat" information...is "healthy"...I'm trying my best to stay away from junk food and it's paid off in the weight department. Staying as healthy as possible through diet is very important. I "couldn't" have my entire kidney removed so they had to go in and remove the tumor and leave as much kidney as possible...it is functioning. I think maybe I would have felt a little better if they could have removed the whole kidney and been done with it. But...I had had to have the adrenal gland removed on my other kidney and there wouldn't have been any place for the remaining adrenal gland to rest had they removed the kidney. They told me that..if the cancer comes back, it will most likely be in my lungs or bones...it is still called kidney cancer even if it comes back in those places. After this length of time, the doctors feel that I don't need routine CAT scans. They consider me cured...I don't know if "I" consider me cured, but I try every day to be positive.....and now...I'm too old to die young :o)