Shauna’s Story

Site created on January 9, 2022

Welcome to our CaringBridge website.  We are using it to keep family and friends updated in one place. 
We appreciate your support and words of hope and encouragement. Thank you for visiting.

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Shauna was diagnosed with early-stage breast cancer in November 2021, received a single left-sided mastectomy with immediate reconstruction January 2022.
Following surgery, they can learn a lot more about the type of cancer I had, etc. and we also discovered I had another cancer called "Paget's Disease of the Nipple" and I'm grateful we had not kept it (as we were planning to in surgery but then right before surgery I said only if it was a very viable vein).
Had multiple infections & skin necrosis which resulted in implant loss and irrigation surgery March 2022.
Due to the type of breast cancer, ER+/PR-/HER2-, Invasive Ductal Carcinoma, no lymph node involvement & "clear margins" after the single tumor was removed, they ran a test called "Oncotype Score" which indicated the benefit for chemotherapy would outweigh the costs of chemo treatment to reduce my likelihood of cancer recurrence.
I had a high score. so I underwent chemotherapy from late April 2022 to July 1, 2022. 


I completed a gradual return to work in January 2023 where I was back on full-time hours as of March 2023, with incredible support from my entire company, family, & friends, with some modified duties and accommodations in place. 


I did a mammogram in February 2023 that showed no signs of cancer in my right (remaining) breast, and read my results through the new AHS Connect platform in Alberta, Canada.
I get emails for all my test results as soon as they are published, which can be a mixed blessing for sure. Thankfully, all looked good, except I was given a NEW classification of "C" heterogeneously dense breasts and with a new protocol/recommendation in Canada/Alberta - women should now receive an Ultrasound if they have dense breast tissue C or D, as small tumors would appear the same as dense breast tissue in a mammogram. So I received a breast exam & ultrasound in March 2023, indicating no sign of cancer. 


I knew I was experiencing pain, fatigue, but a lot of these things all could be explained by somewhat recent cancer treatment during the prior year, as well as transitioning back to full time hours, adjusting to my new normal while still grieving so much loss.


Alas, in May 2023 - a few weeks before my 2nd attempt at reconstruction surgery - I had a follow up Bone Scan (from cracked ribs in Oct 2022) where they ran additional testing. 
From there, my life would change forever as I was diagnosed with Metastatic Breast Cancer - Stage 4 - innumerable lesions (tumors) in BOTH my lungs. 
For 5 or so weeks I underwent a series of CT's, MRI's, New Biopsy, etc. - where I learned my type of cancer had changed to  "Triple Negative" 


AKA = mTNBC = metastatic Triple Negative Breast Cancer
This has the worst prognosis, and even worsened by the fact I'm under 40 and we know TNBC is VERY aggressive in younger people, and I know my original cancer was very aggressive, especially since my naturopath (who specialized in oncology) advised me I had the highest Oncotype Score she had ever seen. 


It's been a whirlwind, I am completely exhausted and overwhelmed - so much uncertainty ahead of me, but what we know for sure if I don't have that much time left - years, if we are lucky.


I start treatment for mTNBC tomorrow, Tues June 20th, 2023 and I'm terrified but holding onto hope and faith for as much time and pain-free days as possible. 


Hoping this will be a space where my loved ones can come and stay up-to-date on how I'm doing, and share information with one another, support one another.
As an empath and Highly Sensitive Person, sharing these updates is not only devastating for myself, having to hear it aloud and relive it, but then also manage the emotional impact and response from those who care about me, my husband, and one another. 


I am hopeful this median will ensure people feel looped in when they have capacity and can read as much or as little as they like.


DISCLAIMER: This may be a bit of a therapeutic journal if that's what I end up needing as well, so please just know I am well supported and just in complete survival mode and wanting to navigate this as authentically and real as possible for me, but I do seem to embellish/dramatize a little by nature. Your prayers & loving wishes are welcome always. 


Thanks for reading

Newest Update

Journal entry by Shauna Henson

TW: Cancer - Health Update
In May 2023, I had posted about a bone scan, which was to follow up on the status of my cracked ribs following chemotherapy last summer.
It was a huge relief that there was no sign of cancer in the bones (healing observed was consistent with a rib fracture).
However, they did notice, "multiple lung nodules, highly suspicious for lung metastases. Additionally, soft tissue lesion left anterior third intercostal space, also worrisome."
Holy. Shit.
In the month that followed, I underwent rigorous testing where my medical team determined I have Stage 4 Triple-Negative Breast Cancer that has metastasized into both of my lungs ("innumerable lesions").
Prognosis is not great, particularly for "young adults" (under 40) as the cancer tends to be more aggressive. Moreover, my hormone status changing to "triple-negative" also means that there are less treatment options available to me (my cancer won't respond to hormone related treatment options).
However, I am determined to fight - in mind and body - and am leaning into "hope" over fear, as much as possible. With my oncologists support, it is our sincerest hope that I'll have "years" ahead of me.
In early June, with the incredible & overwhelming support from my manager Holly Milena, people & culture team, and all of my amazing colleagues at LivingWorks, I made the difficult decision to return to Long-Term Disability status while I restart treatment and navigate what's ahead of me.
So far, I've received 2 rounds of systemic treatment (immunotherapy & chemotherapy) which have not gone smoothly with various complications (all manageable thus far).
Today, I'm starting my 3rd cycle - with chemo meds only... and at a lower intensity than first round.
We currently believe my immunotherapy drug (pembro) made it so that my immune system attacked my liver (making it very, very unhappy), one of my chemo drugs made my platelets crash, and the other chemo drug greatly exacerbated carpal tunnel issues making daily life painful and sleep difficult. Thus, continued adjustments have been made to balance quality of life with effective treatment for as much time as possible.
Over the last few months I've learned that adaptability, flexibility, and patience are critically important elements which I will continue to work on... Planning is extremely difficult as things can quickly change on a dime, or so it feels some days.
And TIME is invaluable.
Right now I feel fairly good - I have an amazing support system and am focused on my health, my family, making the most of today (esp the "good days") and trying to sort through the complexities that come with such a devastating diagnosis.
As an empath and highly sensitive person (HSP), I have an exceptionally difficult time navigating others' emotional responses to this news as I struggle to come to terms with it myself. It's partly why I think it's taken me so long to share this information publicly. It's also very overwhelming, exhausting, and constantly evolving, so keeping people updated has been more challenging than I had personally anticipated. Not to mention - denial, anyone?
It is my hope to share high level updates on facebook periodically with my network. After 4 cycles, for example, I'll have another CT of my lungs to see how the treatment is going (aka are we kicking some butt or do we need to change things up).
Thank you for any prayers, best wishes, gifts, cards, and loving vibrations you have sent to me over the last couple years since my initial diagnosis in Oct/Nov 2021 & ongoing.
I truly thought I'd be "getting back to normal" (or a "post-cancer new normal") & would eventually have the energy to reconnect with my network more after transitioning back to work, but alas! My body had another plan in mind and I continue to focus on one day at a time, sometimes one hour at a time.
I'm transitioning to a place of acceptance that I won't ever be going back to the life I knew before cancer, or the brief version of me that existed in between remission and metastatic diagnosis. The future plans me and my husband made together now must be adjusted (hello grief), and the rediscovering of who I am & what I'll do now - will be an ongoing learning process.
It's been a hell of a ride! I look forward to making the most of what time lies ahead.
Remember to take care of your health, y'all! Much Love Always! &
-Shauna
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