Monday, April 1, 2013


The banner of this blog has been changed, yet again.  April Blog Follies on April Fool's Day.  I decided it was time to do some sort of an "About Me" page that reflects ME.  It's up in the banner.  Since I don't expect anyone to realize there has been an update, I'm adding as a blog post.  Expect it will be changed, rearranged and who knows what else in the days and weeks to come.

It's up there for the clicking but it's here today, too......


This blog was launched in July of 2011.  It's barely two years old.  I would love to attempt to update a narrative bio, but I think bullet points may be easier.


  • I was diagnosed with invasive lobular breast cancer in July of 2006 after four months of imaging, in office biopsies and ultimately, the surgical biopsy that found what is known as the *sneaky* cancer.  I thank the tenacity of the initial radiologist, the radiologist at MSK for her persistence in finding that *density* when doing the core biopsy.  "If he saw it, it was there, I'll find it."  The surgeon who skillfully removed the area and the pathologist, THE PATHOLOGIST, who read those slides.
  • It was two months of running around and researching options before I ultimately had a bilateral mastectomy with tissue expanders that were exchanged for cohesive gel implants (gummi bears) which were still in clinical study at the time and approved (quietly) by the FDA in late 2012.
  • Yes, I have a family history of breast cancer.  There are, for all intents and purposes, five diagnoses of breast cancer among my mom, my sisters and me.  Four of those were pre-menopausal.  
  • Our family genetics is a mess.  I have mutations of unknown significance on both BRCA1 and 2 which as I understand, is sort of unusual to return that kind of result on both genes.  Oh well.  I also understand one or both of these genes may have been declassified but I have little faith in that information since only one lab using one methodology is, at the present time, able to verify any of this.  Also, I've not received any official notification which makes me even less confident in the integrity of The Lab. (The Supreme Court case will be heard within weeks so this may or may not be relevant if I fail to update)
  • I did eight rounds of chemotherapy (CMF) which was believed to be a gentler treatment protocol.  I never lost my hair.  I feel like a chemo fraud.  It's all about the hair.  However, I have ongoing cognitive issues that seem to have worsened and some seem to have jumped on the scene later.  My chemo was complete in March of 2007.
  • I am presently NED
  • My mom had primary breast cancer in 1987 and a second primary in August of 2007.  She had aggressive treatment in 1987 as there was nodal involvement.  In 2007, she had early stage disease.
  • My mom is now a metastatic patient.  Somehow, despite hitting the 5 year *celebratory* date, her cancer progressed to a rib.  There is no way of knowing if this was a dormant cell from 1987 or from 2007.  Each scenario is equally horrifying: A stage IIB cancer resurfacing after 25 YEARS or a stage 1 cancer of an area that was being watched closely because of her history (and then more closely after my diagnosis) spawning a rogue cell that took over five years to activate. 


  • I have two grown kids.
  • I was working in a high level accounting, managerial position (NYC commercial construction, unions, etc.. it doesn't really get much crazier than that) and had to step away because of chemobrain.
  • I spent at least two years beating myself up over my inability to perform at my job.  I blamed a changing work load, constant interruptions and a host of other things before I realized "There may be a problem."
  • I had a neuropsychological evaluation, was deemed to have issues "primarily around numbers," entered a clinical study (results not yet published) and realized I had to switch directions in life.
  • I began this blog with the help of the Visible Ink writing program offered at no charge to all patients at Memorial Sloan Kettering Cancer Center.
  • I embarked on a journey of volunteerism and I am well aware how fortunate I am to have the means to have done this for these past two years.
  • It may be time to start thinking about ways to earn a living.


  • The blog, which began as a means of me unclogging my brain became a vessel to the outside world.  This is the 415th post on this blog.
  • People began reading and commenting and I became very active in Social Media.  So-Me which was just reframed to me as "So-WE" is the essence of So-Me: Community and collaboration.
  • I'm getting tired of being the spam police but I suppose that means the blog has legs.  And fingers.
  • My preferred platform is twitter and the blogs, recently added Linked In, have had a G+ account dating back to the days of "you need an invitation" but I haven't embraced that platform fully. Facebook WAS a means of stalking my kids, then became a means of keeping up with peripheral family things but now, worlds have officially collided.  There are no lines.  They are blurry enough to have moved seamlessly and now they are blended together.  "What I do" and "Who I am" are one and the same and that's just fine by me.
  • I stepped into the world of advocacy.  I began as a patient volunteer at MSKCC, a role I love.  Shortly after that, I sought active volunteer roles within the Love/Avon Army of Women.
  • I am now actively involved with METAvivor and Breast Cancer Action, too.
  • I support the #BCSM community on twitter in every way possible.  People helping people.  Doctors helping patients.  
  • Those volunteer roles opened many doors.  I found my voice.  I became the cliche.  I changed my entire life, completely switched paths at a point in one's life when you simply don't do that.  Except, if you do.  And I did.
  • There is a page with my "guest appearances" where you can see some of the places I've been, 2D and 3D.  And some writing.
  • I am passionate about research.  All research.  Across all diseases.  Once I discovered that passion, I found my true voice and I won't be silenced until I see REAL and MEANINGFUL change.

  • I live in NY where I have lived my entire life.
  • I prefer beaches to mountains, although a five day stay at Miraval in Tucson, AZ, the mountains are pretty damn awesome, too.  Proper attire is key.  I'd love to zipline but I wonder, "Will it dislodge my implants?"
  • I support the research of Dr. Susan Love and her quest to understand the reason why some of us develop breast cancer.
  • I KNOW the metastatic community at large deserves far better than we have given them.  We should be funneling more of the research dollars into determining how to stop a metastasis from progressing.  Prevent death is not a priority and that upsets me.  Stopping mets in the first place is important but staking claims that this is going to help those whose disease has already metastasized is speculative at best and it troubles me.
  • I ONLY support organizations whose missions and beliefs align with mine.
  • I don't disparage against organizations with whom I don't agree.  This doesn't mean I won't say something.  It just means I will be respectful.  Always agree to disagree and ALWAYS with respect that we are all different and each of us has a right to our own beliefs.
  • That entire statement does NOT apply to snake oil.  Those people/organizations are committing murder.  Doctor Oz is coming very close.
  • I tend to take things to an extreme when I know I'm right.  When it comes to evidence based medicine and good science, I know I'm right.
  • I abhor headlines and sound bites.  If it sounds too good to be true, it's definitely NOT true.  So far, I've found no exceptions so I live by that rule.  Call me jaded.  It's the New Yorker in me.
  • Nothing on this blog has been put here because I've been paid or enticed in any way.  If I believe something is worthy of sharing, I will share.  Just because I like something, doesn't mean it works for anyone else.  The opinions are my own.  Respectful comments, regardless of oppositional viewpoints are always welcome.  It's how I learn.
  • I believe I am empathetic.
  • I live with passion.
  • I do have chemobrain, I defy anyone to challenge that statement.
  • I AM a breast cancer patient and I will be for the rest of my life.  Ditto above on the defy thing.
  • I love shoes.  The more impractical they are, the more I like them.  I may snap an ankle one day.
  • Yoga DOES count as exercise.  And meditation.  Effective use of time and multi-tasking, too.
  • I can no longer multi-task thanks to chemobrain.
  • I was the person with an alphabetized spice cabinet.  Today, I may not bring my mail in for three days.  Might not open it for another three.... 
  • Rhett Butler on all of that: Frankly, I don't give a damn.
  • Everything on this earth can be fixed if we try hard and work together.  Except death.  
  • Death is part of life but I can still be pissed off about what should be preventable or untimely deaths.
  • I love deeply.
  • I have nothing against the color pink aside from the fact that it's really not a flattering shade for me.
  • The pervasive pink culture?  Not for me.
  • I'm probably not militant enough for many but I've found that militant stances are most effective when tempered with a calmer approach.  In other words, some of my beliefs may be militant but if I don't speak in ways others may hear, being militant serves absolutely zero purpose.  Ditto judgmental.
  • I am judgmental.  Not in a bad way, at least I hope note, but as a means to change things I think can be made or done better.
  • I don't judge.
  • Each day, every day, I try to make a small difference in any way I can.
  • The only way to see the change is to BE the change.
  • I love those in my "virtual world" as deeply as I would if they were in my every day 3D world.
  • YES, that is possible.
  • I spend lots of time shaking my head in disbelief at where I am today and where I was in May of 2011 before I was evaluated for cognitive issues.
  • Collaboration is not a topic or a buzzword.  It's a call to action.
  • Patient engagement is an idea whose time should have been here a long time ago.  We still have far to go.  I'm all in.
  • Somehow, I already see how this "Just Stuff" list is going to continue to grow and evolve.
  • Stagnant stinks in every form. 
  • I'm REALLY pissed off about my mom's metastasis. Lots.  And then some.
  • I miss my dad.  Lots.  And then some.  And some more......


  1. dear annemarie,

    this is fabulous, such a great idea for all about you to be in the form of a blog post. i loved reading it and am asking myself what i would write all about ME! i think that would be a very interesting exercise.

    i particularly like what is so you - that you try to make a small difference every day in any way you can. boy - do you ever! and i got a funny picture of you worrying about if ziplining might dislodge your implants!

    i can only imagine how pissed off you are about your sweet mom's mets - nothing but a big bullshit. and i know missing you dear dad must just ache so bad. i continue to send you my most powerful vibes, dear friend, to comfort you, to inspire you, and to give you fulfillment and feelings of accomplishment - with all of who you are and all that you do.

    i love you, XOXOXOXOXOXO


  2. AnneMarie:
    Didn't get a chance to read this until today. I'm so glad I did. No wonder I felt like I found a kindred spirit when I first discovered your blog. We have a LOT in common. I'm originally from NY (State), I have two grown kids (one a jr. in college), love the beach, live with passion, love shoes, am a breast cancer patient and will be one for the rest of my life, did the CMF regimen - twice, lost my dad (esophageal cancer) who I miss terribly (we were both big Giants fans), work with numbers (I'm an engineer), and have mush for brains. Scared every day that someone at the office is going to realize how incompetent I've become and let me go. I HAVE to work - I'm the sole provider for our family and have a kid in college. I'm also starting to wonder about Dr. Oz - he seems to have sold his soul. There is one difference - pink (especially HOT pink) is my favorite color and I can wear it. But I'm sick of companies coloring their products pink and pretending to support BC research.

    Anyway, I love the blog, I love how you are so open and honest with us, and how you've connected with those of us out here whom you've never met. I hope you continue with it. You will make advocates out of many of before long. Hope I get to meet you in person one day. Think it would be fun. Meanwhile, I will continue to be connected to you through the blog and twitter.

    Love you!!! xoxox

  3. Anne Marie,
    You a really an inspiration. I have absolutely nothing in common with you beside being Italian & having breast cancer. I do love she's but the higher the heel the worse my back hurts. I think of your mom & will keep her in my prayers. I agree with Ellen. I have never met you in 3D but feel your care & love through whatever waves link us. Keep on keeping' on. I admire your courage.

    With love,


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