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Dr.Mani

Susan, having enjoyed the power of social networks in spreading word about something I care about passionately - helping children born with congenital heart defects - http://www.chdinfo.com/mission/ - I have a fair idea about how this works... and also that it goes far, far beyond the individual.

It's the MESSAGE.

That's what gets 'buy in'. Not the peas. Not your story. At least, not primarily. It's the thought that by sharing in the awareness effort, people are indirectly helping save millions of lives touched by cancer, probably generating awareness and funding for cancer cure research, and making the world a better place.

Sure, everyone feels a certain empathy and bond with you - but the viral nature of the spread of such a message across networks is rarely linked to one person or one story... more the thought that flits subliminally through every mind - It might have been me!

It is fascinating and heartening to hear just how far and wide your awareness building effort has spread, and it will certainly have a long lasting and meaningful impact. I wish you strength and health to not only fight the menace of breast cancer, but to also capitalize on the momentum you have built with the 'Peas Movement' and create a lasting, definitive and sustainable effort to fight cancer and help other sufferers.

You continue to be in my prayers.

All success
Dr.Mani

Beth (AKA Splashgirl)

I don’t talk about ‘it’ and glare at anyone who brings it up. I went in for 2nd surgery on Friday and broke down crying. Not for the reason you’d think. Every woman in the women’s center was in their 60’s/70’s. Why was I here? I didn’t fit in and I was angry/sad I was there.
I applaud you w/ your Twitter and your blog for getting it out there that we have to do more for Cancer/Research. Neither you nor I want to be a member of this club but you are making a difference. Until I can deal, I’ll hide behind that big rock in the corner, and follow your writings.

ChazFrench

Susan you are an inspiration to so many people (and PEAple). You are giving hope to others who are battling breast cancer, and inspiring many of us to raise money for research.

Charles

B.L Ochman

Susan - your writing is so clear and you are helping so many pea-ple by sharing your experience.

Now we need you to get better and kick cancer's nasty ass.

Peas on earth
xo
BL

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About My Cancer

  • Invasive Lobular Carcinoma
    My form of breast cancer is less common than others. In fact only about 6 to 8% of cases of breast cancer are the invasive form that is based in the lobules, not in the milk ducts.

    Invasive, sometimes called Infiltrating, is a scary word. In most cases this form of breast cancer has been present for 8–10 years when detected by a mammogram or physical exam.

    In my case there was clearly an area that felt thickened or dense on December 6, 2007. A mammogram the next afternoon was not able to detect it but it clearly appeared on ultrasound and was confirmed by multiple biopsies the same day.

    During those 8 to 10 years the cancer took to become apparent to me, there has been plenty of opportunity for those invasive cells to get out of the breast and spread to the rest of the body.

    It is after all, by definition, an invasive form of cancer.

    Each year about 190 thousand women are diagnosed with invasive breast cancer in the US and about 40 thousand women will die of the disease. The larger the mass is when discovered the more risk. Mine had tentacled almost 5cm into the surrounding tissue and two other areas in the breast were discovered as well.

    My chances of living another 10 years without cancer in another area are about 40%. The likelihood of one of my other underlying health conditions doing the job before that is 20%. it took a few months to get used to that idea.

    Now though my attitude is that at least I know what I'm facing. It's just not what I expected. Life changes in an instant.

Funding Cancer Research


  • We Will Not Apeas Cancer

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