My breast cancer story starts like so many others, with a short trip, this one to get a routine mammogram.
Breast Cancer Biopsy
Over the years, many of my mammograms have come back with issues that necessitated follow up, and so did this one –it revealed a spot.
I didn’t give much thought to it, even when I was told I’d need a biopsy. I’d already had a number of biopsies and they hadn’t turned up cancer.
Lumpectomy Surgery
I was lulled into further quietude when the surgeon reassured me there was only a 10% chance this tiny spot in my breast was cancerous. I knew I would ace this test like I aced everything else. Or so I thought.
Discovering Cancer
Little did I realize I had already begun my safari into the Breast Cancer Jungle. We’d left “civilization” and I was now a passenger in the process of discovering a strange exotic thing growing in my body.
The first leg of this expedition took a couple of months. From the time of that mammogram to the day my surgeon left me marooned in a lagoon of words I did not ever want to hear –invasive lobular carcinoma, which was just a clunky way of saying it was CANCER.
Cancer Family History
Other family members preceded me as passengers on this unwanted journey.
My family history of cancer includes my father, a survivor of stage 3d colon cancer, and his mother, my grandmother, who had breast cancer at a youngish age, and a single mastectomy to go along with it.
Hereditary Cancer
This unfortunate right of passage had reached down into the third generation, and now I too was included.
What decisions would I make? How would I withstand the pressure of this disease and the grind of the Cancer Industrial Complex?
I’m still figuring it out. The most challenging part has been going through the mental and emotional parts of this journey.
Breast Cancer Genetics
It all began when I was diagnosed with the BRCA genetic mutation in 2008. Ever since I’ve been under high surveillance for breast cancer.
Breast Cancer BRCA Gene
Still, when I was diagnosed with breast cancer, late in the summer of 2021, like many patients, I went into physical and emotional shock. First came the overwhelm, then meltdown.
I lost myself as the Cancer Industrial Complex swung into high gear.
The Cancer Industrial Complex
Waves of treatment options flooded my world.
I received calls from the radiation center and was scheduled for radiation before I had the cancer staged. It was as if I vanished when the cancer crystallized.
They were looking out for me, taking care of me, but still, I was “disappeared.” In addition to taking a pause to find myself, I needed time to gather more information.
Multiple Sclerosis and Cancer
When I came up for air, a couple of weeks later, I put on my medical detective hat and began researching the safest cancer treatments.
This was critical for me since I suffer from several autoimmune conditions including MS.
How Many Breast Cancer Stages Are There?
Meanwhile, during my search for the best treatment for me, I was making plans to get the cancer staged. There are four stages of cancer.
Staging would require surgery for the second time in less than two months.
In late September, my phenomenal breast surgeon, Dr. Stephen Johs dissected my lymph node, after a radioactive dye was injected into my nipple. I awoke to learn the cancer had not spread. It was stage 1 cancer –considering things could be so much worse, I felt great relief.
That lasted for two weeks. Then the treatment options came home to roost, and I was faced with a series of tough choices and insomnia inducing dread along with them.
Disease of Decisions
Cancer is a disease of what can seem like never ending stress and a long string of difficult decisions. Chemo or radiation? Lumpectomy or mastectomy? Single mastectomy or double mastectomy? Implants or flat closure?
Cancer Treatment Options
I was swimming in confusion and at times, buried in denial.
Ultimately, when it came to treating the cancer, I decided not to do radiation.
The MTHFR genetic mutation combined with a heaping dose of electromagnetic sensitivity and certain studies I had read made me realize this was not the right choice for me.
Mastectomy vs Lumpectomy
Rather than lumpectomy with radiation, I chose amputation –to have my breasts taken off.
This decision further made sense because the BRCA mutation gave me a high likelihood of recurring breast cancers.
Breast Implants or Flat Closure?
Now that I had resolved to remove my breasts to save my life, I faced a new set of unyielding decisions.
The impending double mastectomy meant I had to figure out whether to do reconstruction with implant surgery or have my breasts removed without replacement, referred to as flat closure.
How to Make the Right Decision?
As my research continued, I found myself vacillating between flat closure and breast implants, swinging back and forth repeatedly, and somewhat neurotically, for a couple of months.
The decision kept me up many sleepless nights.
Yes, I knew I would have my breasts amputated, but I could not decide whether to leave them with a flat amputated look or undergo reconstruction after they were taken off.
Oddly, I felt like whichever choice I made was the wrong one.
Perky New Breast Implants?
Truly, the idea of having perky “new” breasts to replace the old ones I would lose was tantalizing and I spent a couple of months researching it.
Along with this research came a stream of endless assurances from every single doctor I spoke to about silicone or saline breast implants. They’re totally safe. I was told over and over again, without fail.
Yet I never believed this would be true for me.
General Anesthesia and MTHFR Mutation
Still, if I could put aside my own fears about the risk of breast implant illness that had gained a strong toehold in both my mind and gut, I remained concerned due to the fact that reconstruction surgery would mean more procedures and as a consequence, more general anesthesia.
Given that I have the MTHFR genetic mutation, clearing toxins out of my body is far more difficult than for the average person, so this was of grave concern.
Furthermore, I worried that placing a foreign object in my body would pose a potential risk to me, given MS and a multitude of environmental allergies.
Breast Implant Illness
Along those lines, the last thing I wanted was the risk of breast implant illness (BII), a condition regarded with a fair amount of skepticism and disbelief by the medical establishment, but not at all uncommon on an anecdotal level.
Breast Implant Cancer
Another concern? Breast implant cancer, known as anaplastic large cell lymphoma (ALCL).
Breast Implant Recall
This cancer of the immune system is caused by an Allergan implant1 recalled in 2019.2
Allergan Implants and Explants
As an aside, I am absolutely horrified thinking of the women who struggled to overcome breast cancer, undergoing mastectomy surgery and opting for implants.
Can you imagine going through all that and then discovering that a cancer-causing substance was placed inside your body? I can’t!
The idea terrified me, along with the thought of facing another surgery to explant a cancer causing implant.
Going Flat
Ultimately I chose flat closure, not to have my breasts reconstructed in any way.
Note to readers: If you are considering flat closure, Kim Bowles’ website, Not Putting on A Shirt is a must visit; you can also read more about her mastectomy and flat denial in Cosmopolitan magazine.
How Breast Cancer Feels
In the end, offering your breasts in any form to the Gods of Cancer is a terribly personal decision.
I did so for my own physical health and peace of mind, and I understand that this is only my decision in a very bad situation, one that worked for me.
There are many paths and forks in the road on the voyage into the Breast Cancer Jungle. If you are hanging from its branches, only you will know what’s right for you.

Double Mastectomy Surgery
In early February I underwent a double mastectomy, my third surgery in six months. At that point, I was physically spent, emotionally exhausted, and full of hope.
Post Mastectomy Life
Thrilled to put the surgical component of the double mastectomy behind me, my relief was short lived.
Unfortunately, the surgery on the non-cancerous side of my chest was aggressive, I was hollowed out to the point of concavity. The surgical result was asymmetrical, unexpected, and painful.
Although I inquired a couple of times, I was given no explanation.
Both the physical pain and aesthetic result do not make sense to me at this point and are a bit of an additional trauma on top of cancer and losing my breasts.
The confusion and misunderstanding around this situation makes the healing process and emotional resolution around this surgery a bit more challenging.
Putting the cancer experience behind me when I live with pain as a near constant reminder is not an easy process.
Post Mastectomy Pain Syndrome (PMPS)
Today, at more than six months out, the right side of my chest and armpit are filled with a burning neuropathic pain, referred to as post mastectomy pain syndrome (PMPS).
In the world of breast cancer, it’s easy to convince yourself that after your breasts come off, you will simply move on. I myself was under this illusion.
Breast Cancer PT and Axillary Webbing Syndrome (AWS)
I’m now heading to my fourth physical therapist for treatment of the burning neuropathic pain, along with an armpit and portion of my back that are numb, and axillary webbing syndrome (AWS), a condition also referred to as cording.
In my quest for sensation, pain relief, and healing, the helpful and caring physical therapists tell me to speak with my surgeon since there is not much more they can do for me. We will see where this leads.
On that note, I’ve found solace in Meghan O’Rourke’s book, The Invisible Kingdom, a fantastic primer on the revolving door that is women’s health care today in the US, and which I once again find myself in.
Ovary Removal
Thankfully, life goes on as I swing from branch to branch in the Cancer Jungle, wondering what will become of me since this trying year is not over.
In the fall I will have my fourth surgery in just over a year, this one a hysterectomy to remove my ovaries, tubes, and more, while hoping for a negative biopsy.
A Collection of Symptoms
And so, to the diagnoses of multiple sclerosis, celiac disease, and autoimmune thyroiditis, I now add breast cancer.

My One Year Cancerversary
July 2022 was the month of my one year cancerversary, and I’ve spent almost every day of the last year dealing with the medical system.
Some days I’m reduced to feeling like a collection of symptoms.
On the worst days, I feel like I’m breaking apart. Other days, I go on a hike and feel like I look in the photo above –happy to get outside and drink in nature.
Cancer and Toxic Positivity
As one of the survivors in a Facebook group for flat folks like myself said:
I’m not brave, thriving, happy. I’m scared, scarred, and numb.
She goes on to say that being shown only smiling women, all those brave warriors and happy survivors, burdened her with a toxic positivity that added to her anguish.
I understand this –being told you’re strong and brave when you’re falling apart can cause a bit of cognitive dissonance.
The Dark Side of Breast Cancer
Yes, I know this is an incredibly dark piece of writing for me to share with you.
I’m generally optimistic. But for me, everything about breast cancer is dark. As they say, “cancer sucks” and this writing is about that experience, that part of my life.
Life and Death in the Cancer Jungle
That wraps up this summary of my trip into the Breast Cancer Jungle.
Many with a cancer diagnosis wrestle with imminent annihilation, grasping for life itself. Even for those not at death’s door, the struggle is exhausting, stressful, and burdensome.
Once you’ve entered, the Cancer Jungle will chew you up and spit you out. There are no silver linings here.
I am one of the absolutely incredibly lucky ones, and still, this is very, very hard.
I first published this post on August 8, 2022.






Erin says
Elana,
Blessings to you and your family as you walk through this journey together. Thank you for always sharing about your health challenges openly and honestly.
Elana says
Erin, thanks so much for your support.
Lisa says
My heart and prayers reach out to you! I admire you so much.
Elana says
Lisa, thank you for your sweet comment.
Lorain says
Oh dear, I was shocked to read your story. I am so terribly sorry that you are suffering some side effects from the surgery and hope they resolve themselves. I too was diagnosed with breast cancer last year and luckily it was DCIS with a small micro invasion. I opted for lumpectomy and partial breast radiation (just a five day course so totally doable)…I just finished the rads on Friday.
My thoughts are with you as you continue your fight. Thanks for your thoughtful post,I hope it encourages other women to get checked! Catching it early is the best.
Hugs
Elana says
Lorain, thanks for your comment and sorry to hear about your diagnosis. Yes, catching it early is key.
Diane J Corbman says
Oh Elana, did I miss something you wrote during this past year regarding this new situation for you? I am so grateful to you as a human being, someone who is real and who really speaks to me as though I was (am) a human being. Do I tell you that my heart is with you and that all my thoughts of you, always, are filled with love and gratitute. How do I tell you how much you mean to me and how much loving energy I send to you every time I think of you.
You are the most “woke” person I know, with a spirit and truly good nature, so intelligent, so generous in sharing your experiences — good and bad — with us all. I cannot express the loving hug with which I embrace you. You are important, a voice for us all — of reason, of explanation, on good health habits and food intake –there isn’t anything that could make you more critical to all of us, to ME, as you are the only “real” person in my life. How do I tell you how much I value and love you? Your strength puts me to shame — you are the example of what a good, intelligent, informed, honest human being should be. You give so much. I wish only the good you give to us all is returned to you manyfold. And yet, how does this happen to someone like you? We share a common heritage, so HOW can I, or anyone ask this question. But I do. And I love you. Everything — you are so adept and patient to be able to express your experiences to us. How can we, I, do anything, something, to help you?
Elana says
Diane, what an unbelievably, incredibly supportive comment. I am overwhelmed in such a good way in reading it and receiving your love. Wow, to be seen is a beautiful gift (for anyone) and I thank you for seeing me and reflecting your thoughts back to me. As for how could this happen to me, I spent so much time thinking about that and will be writing about it in the future. We do our best as we live in a world that is becoming more toxic every day. Add some genetic mutations, genealogical trauma, and abuse to that and, well, the body can only take so much. Still, I work every day to become stronger and more resilient whether that means hiking a mountain or taking a nap. Finally, you did not miss anything! It took me a while to digest this new diagnosis and compose my thoughts so that I could write about it. Sending you big hugs and much gratitude!
Pamela says
Love and Blessings to you, Elana.
Elana says
Pamela, right back to you.
Jane says
Elana, I too am a BRCA 1 previvor- 8 years out. Your piece resonated deeply with me. The hysterectomy and the hormonal aftermath is it’s own unique challenge too. All I can say is that all this does get easier with time and recovery. When I look at my kids, I know I made painful choices but the right choices for me and for them. My grandmother did not have the option available to her and she died in her 50s, missing so much. Sending you strength and love on your journey.
Elana says
Jane, not the club we wanted to be in but knowing we are BRCA+ might have saved our lives –you are a previvor and I was lucky enough to catch my cancer at stage 1.
Sheryl says
I’m sending you love and prayers. Your inner spirit will carry you through this journey.
Elana says
Thank you Sheryl.
Julie Ann Westwater says
Wellness Warrior, you continue to be an inspiration. Thank you for using the words, so eloquently, that only you can do, to share your story. I am one grateful soul to have gained so much wisdom, so many delicious recipes, and what I can only call “virtual love” from you, Elana. Many blessings as you continue on in this journey of life.
Elana says
Julie, sending virtual love right back to you. Thanks for your sweet support.
Barb says
Elana
My first thought when I saw the title was “Oh no, not something else”. You don’t deserve another challenge in your life. I’m sure all your readers appreciate your posting about your experience especially those who are going through the jungle as well. I am sending you love and healing vibrations for your mental and physical pain. I feel your pain and pray that you can overcome this as well as you did your other life challenges. Please know that your willingness to share has impacted thousands of people. Praying for your quick return to good health.
Elana says
Barb, thanks so much for your support.
Miriam Kearney says
I have always been grateful that “it seems” my family doesn’t get cancer; we get heart disease and diabetes! I married a man who had 3 bouts of cancers before he died. It was a very difficult time in our lives and pain was a big part of it, along with the fear.
What I really related to in your story was the pain you are going through. 30 years ago I had an accident which result in spinal fusion in the middle of my back. And 4 years ago I became aware that for the first time in my life I was having low back pain. I didn’t realize for a while what the cause was but it was finally diagnosed as a low lumber stenosis. Stenosis grows slowly and encompasses the nerves that in the area. The pain in my legs was intolerable and I was completely bedridden while I waited for surgery (which, because of Covid was delayed several months). Now a year post surgery I am still in pain every day (although not as much as pre surgery). But enough to make walking and moving around very painful which is quite debilitating. I’m sure you have days when that is true as well. I told me kids to make sure they keep a strong back and legs because mobility is everything! I have been trying to manage the pain with OTC dugs but have finally succumbed to Lyrica which is actually helping, thank the Lord. I wish you well and I know that you will look after yourself. Having read your posts in the past I know you to be a very sensible and aware person.
Elana says
Miriam, I’m so sorry to hear about the back pain, so frustrating. I’ve heard great things about Lyrica for chronic pain and I hope it gives you some relief. Keep me posted :-)