Comprehensive information about DCIS (also known as ductal carcinoma in situ or intraductal carcinoma), the most common type of noninvasive breast cancer. This site is presented by the Northern California Cancer Center (NCCC).
Click here to skip to my latest posts. My heart sank, my head spun and my gut knew... The "standard of care" treatment options offered to me following a diagnosis of DCIS didn't feel right. My intuition led me on a highly motivated journey
I was diagnosed with DCIS in the summer of 2007. After having a lumpectomy in December of that same year, I decided to forgo radiation and tamoxifen after consulting with Dr. Michael Lagios, a world renowned DCIS expert and pathologist.Using the Van Nuys
Welcome to the DCIS My Story website. My name is Britta Wilk McKenna and I was diagnosed with DCIS (Ductal Carcinoma in Situ) on December 30, 2010. Since then I've undergone four surgeries, with Stage 2 reconstruction completed on November 18, 2011,
With 60,000+ women a year being diagnosed with DCIS (Ductal Carcinoma In Situ), it is estimated that by 2020 there will be 1 million women living with a DCIS diagnosis. The purpose of this site is to help alleviate the misconceptions, fear and confusion
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