Ed’s 2021 Walk for WM

After dealing with the symtoms of Waldenstrom’s for years, undetected, I was diagnosed by a perceptive emergency room doctor in June, 2019, most likely saving my life. Now, after more than two years of treatment, I’m ‘on the mend.’

Since WM is so rare, there is still so little known about it, explaining why it was never caught from the dozens of bloodtests I received during my knee replacement surgeries. Please consider joining me in supporting the research, and maybe even doing the walk on 10/29!

The IWMF is dedicated to supporting and educating everyone affected by Waldenstrom's macroglobulinemia (WM) while advancing the search for a cure. Help us raise awareness and support for Waldenstrom’s macroglobulinemia by donating to the Walk for Waldenstrom’s. All donations will support WM patients and caregivers and bring us closer to a World without WM.

Funds raised during the Walk for Waldenstrom's will directly support the mission of the IWMF.

Join us and help raise awareness and support that will be used by the IWMF for patients, caregivers, and families affected by WM and to find a cure.