On October 8, 2024, I was diagnosed with acute lymphoblastic leukemia. It changed everything in an instant. Since then, my treatment has included multiple rounds of chemotherapy, blood and platelet transfusions, lumbar punctures, and bone marrow biopsies. The physical toll has been intense — I’ve experienced hair loss, memory issues, anxiety attacks, early menopause, and was newly diagnosed with diabetes. My immune system is fragile, so hospital visits are restricted. I often can’t walk or even get dressed without help. Eating is difficult, and I’ve missed out on countless family gatherings and holidays.
Right now, I’m starting my third cycle of immunotherapy. My doctors delayed this round because of concerns about memory changes — they’ve done a lumbar puncture and an MRI to check whether the treatment or the leukemia is affecting my brain. I still have another cycle ahead and two more bone marrow biopsies before we know what comes next.
Being a young adult with cancer means never having the time to fully process what’s happening. From the moment you’re diagnosed, you’re launched into treatment — flight mode kicks in and everything becomes a blur. But through all of it, I’ve tried to hold on to hope. I miss my family, especially my nephew, who was born just a month before I was diagnosed. I dream of doing something fun and meaningful with them again.
Mia’s LifeList:
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Meet the Broncos cheerleaders
- Tickets to take her family to a Broncos game