Patient experience, advocacy and communityPersonal experience — not medical or legal advice
A patient’s voice since 2016

Multiple myeloma changed my life. It did not end it.

Real experience, honest conversation and hard-earned perspective for people living with MGUS, smoldering myeloma and multiple myeloma — and for the families who walk beside us.

More than laboratory numbers and treatment plans

Medical websites explain the disease. MMWarrior focuses on what the medical handouts often cannot: fear, fatigue, family, identity, purpose, treatment decisions and building a meaningful life while living with uncertainty.

For patients

First-person experience from diagnosis through treatment, transplant and long-term survivorship.

For families

Recognition that cancer reaches spouses, children, grandchildren and caregivers too.

For veterans

A Marine’s perspective on service, resilience, Camp Lejeune and navigating illness after the uniform.

The journey

Smoldering multiple myeloma

A routine physical began a chain of appointments, conflicting opinions and a diagnosis that changed everything.

Progression to active disease

Worsening symptoms and further evaluation led to treatment and a new phase of the fight.

Autologous stem-cell transplant

A day-by-day journal documented preparation, melphalan, engraftment, fear, humor, setbacks and recovery.

Advocacy and long-term survivorship

Patient representation at Mayo Clinic’s Myeloma and You Day, active participation in online myeloma communities, and continuing to share the realities of living with MM.

The archive is part of the story

Original MMWarrior posts can be restored as WordPress posts with their original publication dates and historical context.

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