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Photography by Patient Voice.
March 14, 2023
14.3.2023
Photography by Patient Voice.
Photography by Patient Voice.
14.3.2023
March 14, 2023
Photography by Patient Voice.
14.3.2023
March 14, 2023
Photography by Patient Voice.
Photography by Patient Voice.
Photography by Patient Voice.

Alyssa’s story

Multiple myeloma

Toronto, ON

I’m a stay-at-home mom to my seven-year-old, Elliot. He’s an outgoing, high-energy kid. He loves playing soccer with his friends at recess. He’s also very sensitive and caring. Kids pick up vibes – they can sense what’s happening around them.

I’m trying to spend as much time with Elliot as I can. And to be there for him. It’s so important to me that we bond and create memories – whether it’s playing, practising his reading, or doing activities he enjoys. With my diagnosis, I’m always worried that there will be a day I won’t be there and I want him to remember me.

I was diagnosed with multiple myeloma, a rare bone marrow cancer, in 2010. It’s not considered curable. There’s treatment, but you’re told to expect periods of relapse and remission for the rest of your life. I was 32 when I was diagnosed and I’d been having unexplained symptoms for years. Doctors attributed my frequent infections, fatigue, anemia, and pain to IBS, migraines, low iron, or stress. I was brushed off by specialist after specialist. Multiple myeloma isn’t difficult to diagnose, but it’s a rare disease and I didn’t fit the typical patient profile, being so young.

“With my diagnosis, I’m always worried that there will be a day I won’t be there and I want him to remember me.”

A few years into my search for answers, after my third ER visit in one month, the doctors looked a little deeper. They finally connected the dots. I was admitted as an inpatient, had an emergency bone marrow biopsy, and started treatment that day. After my first stem cell transplant, it took over a year before I regained the energy to restart my life as a 32-year-old. I discovered yoga and strength training, which have helped me not only physically but also mentally, and they’ve been a key part of my recovery.

I’ve only relapsed once in the past 13 years, and I was luckily able to have my son via IVF before my relapse. My husband and I are so grateful for Elliot. He completes our family. And I’m so grateful my oncologist recommended I preserve my fertility up front. But my cancer could be back any month. It’s always in the back of my mind. I’m in remission, but I’m not cured. And so I can never just ‘be.’ Creating legacy and memories will always be something I’m working at.”