Fiery Poops and Brain Fuzz

It still almost doesn’t feel real. Here I am, a week and a half after my first chemo treatment and it’s still hard to believe that I have to deal with this shit again. 

Last week was probably a lot harder than it needed to be, given that it was Christmas. I really wanted to have a normal Christmas, especially as it was Miles’s first Christmas, but also because I love this holiday and it brings me so much joy. It was still a lovely few days, but extra tiring from all the hubbub. Still got to spend it with family and friends, so it was worth it, but we’ll wait to see if round 2 brings the same about the same level of tiredness. 

Because oh man I was definitely tired. And had a lot of brain fuzz those first few days. There was even an instance where the brain fuzz was so bad that I was trying to change a diaper and it was all I could do to focus on how to do it. I got through it, but I ended up breaking down crying because it was so tough for me to concentrate on what the next steps were. 

My mouth has been on fire too. It lasted about a week, but now it’s broken out into mouth sores. My stomach felt like acid (though while taking the dexamethasone it was like my body could feel it and yet it was numbed?) and I had acidic/spicy pee and poops. I had a fair bit of back pain, too, to the point that I couldn’t lift the baby which made me extra sad. 

Yesterday was the first day that I actually felt mostly human, apart from the mouth sores. Though I’ve had diarrhea yesterday and today. And today I have a headache (though I might not have had enough fluids yesterday). 

My heart is still trying to wrap itself around the fact that my time on this planet is now short. I know in my heart that I’m going to fight this the best I can, and that I have accepted that this is what it is, but it’s hard to not sit in those moments. We spent the weekend with our best friends, and the kiddos had kiddo moments. I kept joking that “this is what we have to look forward to” in regards to Miles, but then my brain would add “if I live that long”. I know that as soon as we’re born everybody has a timer–nobody escapes death–but to have it so evident and obvious is so difficult to process. To know that yours is significantly shorter than the average person’s, that you might not get to experience those milestones with your kid weighs heavy. Then I have the added guilt that I want to be present and enjoy each day, but it’s exceptionally hard when you’re feeling like garbage. 

Deep breaths. One day at a time.

This is my “This is Bullshit” face

This is my “this is bullshit” face.

I never thought I’d be here the first time. I hoped I wouldn’t be here a second time. But here I am.

Last week we learned that my breast cancer has returned and has metastasized into my lung, liver, and bones. In March I had reached my 5 year survivorship milestone, so to have this news hit so soon after has been a big shock. Blair and I are pretty devastated, after everything we’ve been through these past 6 years since I was initially diagnosed. We’ve been taking the last week to digest and connect with family and close friends.

Today I start back on treatments. I told the oncologist I wanted to get on this right away to give me the best possible chance, so she was ON IT. I’ll be on chemo for the next six months, and then regular preventative treatments for the rest of my life or until it stops being effective (and then they’ll change up the treatments).

This is NOT a death sentence. It sucks bad and is really sad. But Blair and I are trying to treat this more like a chronic condition that I now have to live with. I may live 2 years, 5 years, 10+ years… who knows, but I am NOT dying tomorrow. I am choosing to live everyday to the best I can and I have so much to live for. So I am picking up that battle sword and I will just.. keep… going.

We are going to need all your love, support, and hugs, especially these first six months while the chemo takes it out of me. We have to keep working because Adventure Dice is our only source of income, and I’m not going to be at my best. We will likely be reaching out for childcare, home cooked meals, and Adventure Dice help. Blair needs lots of hugs.

Together, we’ve got this. There is nothing else to it.

Thank you all for your love and support. 💜 -Andrea, Blair, and Miles

Participant of Hope

This past weekend, I was honoured to be the Participant of Hope at the Fraser Valley Relay for Life for the Canadian Cancer Society. I got to share my story, so here it is!

This is a story about Dungeons & Dragons. And about Fundraising. Little of both.

The first time I fundraised for the Canadian Cancer Society, I was 12. My Pathfinder group sold daffodils outside the local IGA as our service project. At the time, I didn’t directly know anyone who had cancer. Cancer was just the Big Bad Evil Guy in the books I’d read growing up. It was something that other people, old people, got but nobody really talked about. I remember thinking how these pretty yellow flowers looked sitting in their water buckets just waiting to be chosen. I couldn’t figure out how something so cheerful and delicate could fight this Big Bad.

My senior year of highschool, I joined our school’s Mission: Possible crew, a group that was dedicated to raising funds and awareness at the school level. We sold yellow ribbons and pins in the foyer at lunch time and after school. Thanks to the club I learned more about what cancer was, that it wasn’t just old people who got it, but I definitely still felt like it happened to people I didn’t know. It was still just a storytale.

And then cancer came home. As I was studying for provincial exams and worrying about post-secondary, my dad was diagnosed with prostate cancer. My parents said it was Serious and yet Not Serious in the way that parents do, that he’d only need surgery and recovery. Surgery happened in June, so you can be sure that I studied for my exams under his watchful and very bored eye as he recovered at home. 

The next time I fundraised, I did it for my Dad. 

I was in university and my Dad’s work was sponsoring the Father’s Day Prostate Cancer walk. Team For Pete’s Sake came together and every step of that charity 5k walk had meaning because now I was fundraising for someone I loved. Cancer seemed like it could still be the Big and Scary Monster, but a little less so. My Dad was doing well, we were fundraising to ensure other Dads didn’t have to walk that path too. It was all going to be okay.

Big Bad laughed. 

My senior year in university, Big Bad came home again. This time it was my mom, diagnosed with breast cancer. Her lumpectomy, the chemo, the radiation, her bravery, her pain, her courage, her will to fight back: now the Big Bad felt real.  It was there everyday, showing me what real big and scary looked like. But my mom showed me what bravery looks like, where the adventurer picks up their sword every day and just. Keeps. Going. 

The next time Team for Pete’s Sake did the Father’s Day walk, every step meant that much more. I was doing it for both my parents.

And then 2017 happened. My husband Blair and I not-so-lovingly refer to it as “The Year From Hell”. It was a year that started with my husband being in two serious car accidents and ended with me being diagnosed with stage three breast cancer. At 31 and a newlywed, cancer was not on my character sheet. I can still remember that moment when I heard those words, “You have cancer.” I was at the Breast Health Clinic in Abbotsford and the nurse had lovely black hair with bright blue streaks. I went numb. I could hardly breathe. All I could do was stare across the room at my mom as my brain processed the fact that Big Bad had now come for me. 

All those years, all those kilometers walked, all those ribbons and flowers sold… was I doing it for me all along?


But also no. 

If you’ve never played Dungeons & Dragons, or D&D as it’s often called, it’s a tabletop game where the players work together to tell a story. The Game Moderator acts as the story narrator, setting the scene for the other players and giving them opportunities for adventure. The other players take on the role of the heroes of the story, needing to interact and work together in order to succeed and ultimately tell an awesome tale. While I was undergoing cancer treatments, the game allowed Me and Blair to connect with our friends on a regular basis, we were able to play online over Zoom when I was immunocompromised, and it allowed us to step away from “real life” for a bit as we wove tales of what our characters would do.

One of the big elements of D&D is that when the Big Bad Evil Guy arrives, the adventurer’s rise up to fight back. The Big Bad had come for me, and like the characters we get to play in our favourite game, it was our turn to roll. 

Across that room in the Breast Health Clinic my mom looked at me and nodded. That one look told me I could do this. That I wouldn’t be alone. That it didn’t matter how small and fragile and scared I was feeling. Because I had my Mom and Dad, warriors who had tread this path before me. I had my husband, who has the biggest shoulders to carry me–emotionally, and yes there were times he had to literally carry me. I had my friends, who donned their armor and brought their swords to fight next to me. I had the Canadian Cancer Society and the connections I made with others who were on this journey, too. 

In 2018, Team Andrea’s Adventurers participated in our first Relay for Life. We fundraised for me, yes, but also for every person who has been in our shoes. Because in Dungeon and Dragons when one party member is attacked, we all roll for initiative. 

For a while, COVID-19 tried to be the scariest monster on the table. But just like the Big Bad Evil Guy in stories, cancer doesn’t stop just because there’s another monster around. Over the pandemic, Andrea’s Adventurers Charity RPG Weekend launched online. Nine Game Moderators and 30+ players played nine games of Dungeons and Dragons over 40 hours and three days. We raised $10,000 by telling stories together. When such a kind, caring community teams up with you for this common goal—people who are willing to do shots of Hot Sauce…numerous shots of hot sauce on what is essentially live television–I truly feel like one of the brave adventurers in the stories we tell.

In 2021, my mom was diagnosed with cancer again. My mom continues to fight with a fierness found in most prairie folk and wise warriors. She is the bravest, kindest, strongest, most loving person I know. Even in her most pain-filled days, she always has joy and love to share. Those are the weapons she wields to tell Big Bad that it hasn’t won yet.  

This past weekend was our third year running our online D&D event. On Sunday as I thanked all my volunteers, I cried happysad tears. I was reminded of those cheerful daffodils from my very first fundraiser. I finally understood why something so delicate could fight a Big Bad like cancer. Because it’s a reminder that no matter how fragile I feel, I can be brave, too. That with every flower, ribbon, and step, my adventuring party is with me. And that together, we will win this fight against cancer. 

Today is for you Mom.


cw: body image, cancer, infertility

“I didn’t know you were expecting!”

Well-meaning words, the speaker wanting to share in your happiness. They come from a place of joy, not malicious intent.

And yet, they cut deep.

Five years ago, I was diagnosed with stage 3 breast cancer. I had a single mastectomy then to remove the cancer from my body. I made the decision then to not get reconstructive surgery. It would have meant two to three more surgeries, plus no guarantee of a successful reconstruction.

Last year, I had a prophylactic (preventative) mastectomy to reduce the risk of cancer returning. I still decided to forgo plastic surgery. I’d always felt a little uncomfortable with my breasts. They drew attention I didn’t always want. Men would talk only to my chest and not to me. Bras were annoying and never fit quite right, sometimes they chafed. They got in the way a lot. Not having breasts felt freeing.

I have prosthetics that I can wear, but most of the time I don’t bother. I was mostly content in my new flatness. This is my body now, literal scars and all.

Then the pandemic restrictions started to lift. I had to go back to the office. I had to go out more and more. I saw more people. The well-meaning comments about my possible pregnancy began.

My weight tends to go to my belly. Not having breasts makes my belly really obvious.

The last five year have been exceptionally difficult for me and my husband. One difficult circumstance after another has landed in our laps, in addition to a global pandemic. Trauma does things to bodies, and I’ve put on more weight.

I’ve always been self-conscious about my belly. I look at photos of myself from ten and twenty years ago and feel sad for the person I was who thought she was fat. I hate that feeling fat made me feel bad about myself then, that I felt ugly and unworthy. I hate that it still makes me feel bad about myself. I’ve been working hard to untangle these feelings about my weight and my looks, to repair some of my learned beliefs. To feel like my body is worthy.

And while the pregnancy comments do trigger my self-esteem regarding my weight, they cut even deeper than that. They’re a reminder of a dream that is just out of my grasp right now.

Blair and I have been trying to expand our family with a kiddo for six years. A year of trying ourselves before the cancer bomb went off. Then having my eggs harvested in between having a traumatic surgery and starting chemotherapy. Then learning that the hormones a body needs to make a baby are exactly what my cancer likes to eat. Years of processing this grief that my body won’t do what it should do, working through the guilt and the loss. Making the big (and expensive) decision to pursue surrogacy. Putting our hearts on our sleeves to find a surrogate. Trying once, twice, three times with no success. Still putting our hopes out into the universe and putting our hearts into someone else’s hands.

My belly is a reminder of grief and loss, of pain and struggle and sacrifice. It’s a reminder of a story not yet finished; a reminder of dreams not yet reached.

No, I’m not expecting. I’m hoping and hanging on.

The healing power of games

Hey interwebs! It’s been awhile!

The healing power of gaming
My last chemo treatment!

Life threw me a major curveball in 2017. I’ve shared bits of it over on twitter, but if you don’t follow me there: I was diagnosed with stage 3 breast cancer, and spent the last year and a half going through treatment. I’m officially considered a cancer survivor, but as any survivor will tell you, it’s something that will echo through the rest of my life.

And thus for my first post back I’m going to talk about… the healing power of gaming!

There are a lot of benefits to tabletop gaming, even if you aren’t suffering a major illness. But reflecting back, gaming really was a positive factor that got me through the bad times. My husband and I wouldn’t have made it through this past couple of years if it hadn’t been for our family, and for our awesome friends who kept our spirits up through gaming.

TCTC 2018 with my hair just barely starting to grow back.

Since I’m a big fan of lists these days, here are my ways that gaming helped me heal:

  • Distraction. Gaming gave me the chance to think about something else. Whether it was an immersive RPG or just a quick five minute party game, it gave me something totally different to focus on than my medical issues.
  • Escape. With Dungeons & Dragons and role-playing games, I was able to become someone else for a while. For a few hours I wasn’t “Andrea the cancer patient”, I was Ocoria the Goliath Monk, Ellie the vampire, or Wren the Starfleet Security Officer. It also gave me the chance to feel their strength even when I wasn’t feeling strong in my own life.
  • Connection. My friends wanted to be supportive and present in my life, but sometimes it was difficult for them to know what to do or say. Gaming gave our friends a way to bring some extra positivity into our lives when we desperately needed it. I think this really solidified our friendships in many ways.
  • Accessibility. New technology in the gaming sphere allowed me to continue playing, even when some of the side effects of my treatment would have otherwise prevented me. I could still participate in our regularly scheduled D&D games on roll20 without having to leave our house.
  • Mental focus. Chemo brain is this fuzz that rolls into your mind and memory. Some days it feels like you’re in a heavy fog. Some days it’s like your short term memory has taken a vacation. But gaming gave me something specific to focus and concentrate on, to help me keep my mental acuity as sharp as I could.
  • Laughter. It really is the best medicine. Even on the worst days, laughter was possible. (And laughter releases endorphins, which makes you feel happier.)