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In Conversation With Community: Boobs in the Washington Post

Today the Washington Post ran an article - How Frozen Peas Started a Movement - about my experience with cancer and how the virtual world of people on the other end of computers all over the world have felt somehow moved to reach out to me. 

What does this mean to me, to someone with cancer, to have others walk towards me instead of away? Approach me with interviews, blog posts, interaction on twitter and more?

PhotowarticleIt's not a cure. But can it help ease the pain, the worry, the doubt?

In some ways of course not, but in other ways I'm reassured, and most of all I feel a supportive wall of people at my back - and distraction from the pain when it's not relieved by traditional medications.

It also means a lot to me just to have people talking. I only found that out after the fact - when people started interacting with me and with other people not just about their support but also about their experiences.

One of the most surprising facets of this for me is that men are talking to me about cancer more than women.

Maybe women already have people to talk with about boobs - or other delicate topics. But it's most often men who tell me about their mothers, sisters, grandmothers, aunts, daughters, wives struggles with breast cancer or other less well known cancer.

For the most part it sounds like they haven't really communicated this information to anyone before. And most of the stories are things that have really impacted them on a personal level.

I guess its true - it's hard to go to work and chat up your coworker on the topic of your aunt's wasting away with breast cancer - but that is something I hadn't thought of before.

What have I concluded from these conversations?

Rather than suggesting we need to have special programs to get a man - or anyone - to join a group or move too far outside their comfort zone, I  would like to just start the conversation with anyone who will listen and maybe talk back or talk to someone else about the issues surrounding prevention, diagnosis, treatment and finding a cure.

I hope that I can simply let these all people young and old, of whatever sex, know that we do appreciate them mentioning that they had an experience with cancer. I hope to remind them that just speaking about it a little - one sentence even - has potential to do good. To encourage a new patient to discuss more, to ask questions. It reassures that someone understands at least part of our story.

Their words might get someone else talking, and thinking, and remembering that they wanted to keep up to date with cancer signs or symptoms like this excellent article from the American Cancer Society, or to do a self-exam.

But how do we use this information and the ability to draw people out and encourage them to communicate?

I don't know - this is all really sudden for me so master-plans or long term strategies are hard to come by.

For now I'm thinking it needs to be part of my mission statement down the road when I get that far. For now it's good to file away and remind ourselves in the future that we want to make sure to keep the issue of encouraging communication on the table, however that happens.

I hope you will help.

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What a great article and photo of you today in the Post. I can just imagine people sitting around the breakfast table reading their morning paper and trying to figure out what the heck is this Twitter thing?

I have a feeling their curiosity is going to get the better of them and they will be clicking on the Frozen Pea Fund and showing a little love this week.

Hugs to you..terrific job!

Just did a blog piece on the pea brigade. Thanks for sharing your story.

Hello! A friend of mine found this blog through the Washington Post article online... I had elective breast surgery about 7 years ago and was inspired at that time to develop a product to fully encompass the entire breast area for cold therapy with ONE application. I found relief from frozen peas, but because of the nature of my surgery, I needed relief for my ENTIRE breast. I also felt this would be good during breast engorgement (experienced twice with two children) or for breast cancer patients. I've patented a gel pack design for this purpose and manufacturing will be complete soon. I am told that they should be ready for sale by March or April. I've already had an opportunity to provide these to a number of women for use after surgery with great results. I would love to find out ways to promote my product for breast cancer surgery and donate percentages of sales to a reputable organization. I think I may find some good information on this blog and I will check in from time to time... Please keep in mind when you view my website, that it is a test site and is not operational yet. I will need to make a number of small changes to the site, including text changes. Let me know your opinion on whether or not you feel my product is appropriate for women undergoing radiation treatment or mastectomy. I know reconstruction patients would benefit, but I would like recieve education on other breast cancer procedures and surgeries...

www.breastcomfort.com/index_2.php

Great article, I never really thought of it that way. carpenterz@tamu.edu

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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.

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