
I’m Megan-Claire Chase, aka Warrior Megsie!
Breast Cancer Survivor, Advocate, Speaker, and Writer
Hi, I’m Megan-Claire, aka Warrior Megsie, a breast cancer survivor, patient advocate, writer, and speaker. Welcome to my blog, Life on the Cancer Train.
I didn’t set out to become an advocate. I became one because I had to.
This space is where I share the real story of survivorship, beyond diagnosis and treatment. I write about life after breast cancer, chronic illness, grief, mental health, and what it means to navigate the world as a Black woman, survivor, and professional.
My Breast Cancer Story – the cliff note version
On September 14, 2015, two months after my 39th birthday, I was diagnosed with Stage IIA invasive lobular breast cancer – something I never saw coming. I was introduced to another underrepresented category of Adolescent and Young Adult Cancer (AYA) because I was diagnosed just a hair under 40.
My treatment lasted 22 months, all while working full-time:
- 16 rounds of chemotherapy (4 AC, 12 Taxol)
- Blood transfusion
- 8 surgeries
- 33 radiation treatments
- Bilateral salpingo hysterectomy & oophorectomy (ovaries removed)
By the end, I was using a cane, unable to drive, and could barely walk, while also being beautifully bald and slowly developing my Warrior Megsie persona.
On October 25, 2016, I was declared NED (No Evidence of Disease). I don’t use “cancer-free” or “in remission” because those words don’t fully capture the reality of survivorship. So, NED is my boyfriend, and we’ve been together for 10 years this year!
Life After Breast Cancer: The Reality of Survivorship
I’m now in my 40s, still in a long-term relationship with NED, and yes, still chronically single.
I share my life with my cat-daughter, Phoebe Nell, and carry with me the love of my heart, my cat-son, Nathan Edgar (Baby Natey), who passed away at 20 in 2024.
Life after cancer comes with lasting effects, including:
- Chemo-induced peripheral neuropathy (CIPN)
- Fibromyalgia
- Surgically induced menopause
- Loss of fertility
- Chronic, often debilitating back pain
After five years of advocating to be taken seriously, I received a nerve ablation in 2022 that provided only four months of relief. I was getting injections every 4–6 months, but it was hard to manage, so I stopped for now. Now that I finally have professional help to lose weight (post-menopausal weight is awful), I can tolerate the pain better, but I continue to search for real, lasting solutions.
Some days, my body feels 900 years old. I’ve often wished I could get a refund for this body and get an upgraded, pain-free version.
Breast Cancer Advocacy, Race & Health Equity
My experience is not just about cancer—it’s about navigating systems that often fail patients like me.
As a Black woman, I’ve faced delayed diagnoses, dismissed symptoms, and systemic inequities in healthcare; that reality drives my advocacy. We all deserve quality care and quality of life.
I speak and write about:
- Health equity and racism in cancer care and this country
- The experiences of Black breast cancer patients
- Survivorship beyond treatment
- The need for better resources and representation
- Career transitions and microaggressions
My work has been featured on PBS (Stories from the Stage) and in The New York Times, People Magazine, Cancer Today, CURE, and Patient Power.
Why I Created Life on the Cancer Train
I created this blog to give you a raw, unfiltered, humorous, and authentic insight into what it was like to go through breast cancer as a single woman, as a Black woman, as a professional.
I bring the Breast Cancer REAL – the full, complicated, human experience of cancer and survivorship, sprinkled with stories from my youth.
Here, you’ll find honesty, advocacy, and community because I don’t sugarcoat the experiences. Whether it’s through writing or videos, I’m here to share my story in the hope that it will resonate with others.
If You’re Here
Whether you’re a patient, survivor, caregiver, or simply trying to understand…
You’re in the right place.
Welcome to Life on the Cancer Train with Warrior Megsie.
Photo credit: Patricia Alvarez, World Channel
