Resources & Relief for Caregivers of Rare Blood Cancer Patients

Supporting Waldenström’s

Caregivers, One Day at a Time

Practical tools, printable planners, and real-world guidance—created by a WM caregiver, for caregivers.

Welcome to Waldenström Strong from one WM caregiver to another...

This site is here to help you stay organized, supported, and steady—even on the hardest days.

New here?

Let’s get you started.

“Feeling overwhelmed? You’re not alone. Your caregiver journey has already begun—whether you were ready for it or not. Let’s take the next step together by helping you find the tools, clarity, and encouragement you need to face each day with more confidence.

What Is

Waldenström’s Macroglobulinemia?

“Feeling overwhelmed? You’re not alone. Your caregiver journey has already begun—whether you were ready for it or not. Let’s take the next step together by helping you find the tools, clarity, and encouragement you need to face each day with more confidence.

Just How Rare Is

(WM)

Waldenström’s macroglobulinemia is very rare, with fewer than 1,500 U.S. cases each year. If you feel alone, you’re not imagining it—support is limited, but you’re not alone anymore.

Fewer Than 1,500 Cases Per Year

WM affects a very small number of people annually in the U.S.

Under 3 Million Living with WM

Even across decades, the total number remains extremely low.

Support Can Be Hard to Find

Especially in rural areas, resources for WM caregivers are nearly nonexistent.

Less Than 1 in 200,000

That’s how rare this disease is—making it hard to find others who understand.

Free Download

Caregiver Survival Starter Kit

You’re Not Alone

Let’s Navigate This Together

Waldenström’s may be rare, but your need for support is real. Start your journey with tools and encouragement designed by someone who understands.